US20100022542A1 - Compounds exhibiting thrombopoietin receptor agonism - Google Patents
Compounds exhibiting thrombopoietin receptor agonism Download PDFInfo
- Publication number
- US20100022542A1 US20100022542A1 US12/504,604 US50460409A US2010022542A1 US 20100022542 A1 US20100022542 A1 US 20100022542A1 US 50460409 A US50460409 A US 50460409A US 2010022542 A1 US2010022542 A1 US 2010022542A1
- Authority
- US
- United States
- Prior art keywords
- optionally substituted
- hydrogen atom
- compound
- substituent
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 193
- 108010070774 Thrombopoietin Receptors Proteins 0.000 title claims abstract description 37
- 230000008484 agonism Effects 0.000 title claims abstract description 33
- 230000001747 exhibiting effect Effects 0.000 title claims abstract description 30
- 102000005763 Thrombopoietin Receptors Human genes 0.000 title claims abstract 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 170
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 97
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 93
- 125000003107 substituted aryl group Chemical group 0.000 claims abstract description 50
- 229940002612 prodrug Drugs 0.000 claims abstract description 47
- 239000000651 prodrug Substances 0.000 claims abstract description 47
- 150000003839 salts Chemical class 0.000 claims abstract description 41
- 239000012453 solvate Substances 0.000 claims abstract description 40
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 36
- 239000004480 active ingredient Substances 0.000 claims abstract description 12
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims abstract description 12
- 229910052801 chlorine Chemical group 0.000 claims description 389
- -1 amino, carboxy Chemical group 0.000 claims description 262
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 204
- 125000001424 substituent group Chemical group 0.000 claims description 191
- 125000005843 halogen group Chemical group 0.000 claims description 143
- 125000003545 alkoxy group Chemical group 0.000 claims description 95
- 125000004414 alkyl thio group Chemical group 0.000 claims description 62
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 61
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 48
- 125000003342 alkenyl group Chemical group 0.000 claims description 40
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 40
- 238000000034 method Methods 0.000 claims description 37
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 36
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 36
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- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
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- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 52
- 238000005160 1H NMR spectroscopy Methods 0.000 description 47
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- 239000000243 solution Substances 0.000 description 33
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 25
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- 238000006243 chemical reaction Methods 0.000 description 19
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 19
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- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 18
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 18
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- 229910052794 bromium Inorganic materials 0.000 description 17
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- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 9
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- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 125000006203 morpholinoethyl group Chemical group [H]C([H])(*)C([H])([H])N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- JUOLDYWXWRDNTB-UHFFFAOYSA-N n-[4-(3,4-dichlorophenyl)-1,3-thiazol-2-yl]-4-formylbenzamide Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CSC(NC(=O)C=2C=CC(C=O)=CC=2)=N1 JUOLDYWXWRDNTB-UHFFFAOYSA-N 0.000 description 1
- 125000006257 n-butyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])OC(*)=O 0.000 description 1
- 125000004888 n-propyl amino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006256 n-propyloxycarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])OC(*)=O 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 description 1
- 125000006327 phenyl hydrazinyl group Chemical group [H]N(*)N([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000012746 preparative thin layer chromatography Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- 125000001422 pyrrolinyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 238000003797 solvolysis reaction Methods 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 125000005302 thiazolylmethyl group Chemical group [H]C1=C([H])N=C(S1)C([H])([H])* 0.000 description 1
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Images
Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/433—Thidiazoles
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A—HUMAN NECESSITIES
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61P7/06—Antianaemics
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
- C07D231/40—Acylated on said nitrogen atom
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/82—Nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
- C07D285/18—1,2,4-Thiadiazines; Hydrogenated 1,2,4-thiadiazines
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- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Definitions
- the present invention relates to compounds exhibiting thrombopoietin receptor agonism.
- Thrombopoietin polypeptide cytokine composed of 332 amino acids, activates the production of platelets by stimulating the differentiation and proliferation of megakaryocytes through the receptor and is expected as a medicine for hemopathy accompanied with the unusual number of platelets, for example, thrombocytopenia and the like.
- DNA sequences encoding the thrombopoietin receptor have been described in Proc. Natl. Acad. Sci., 89, 5640-5644 (1992).
- Low molecular peptides having an affinity for the thrombopoietin receptor is also known (JP98/72492A and WO96/40750), but these peptide derivatives are not generally practical for oral administration.
- 1,4-Benzodiazepine derivatives as a low molecule compound having an affinity to the thrombopoietin receptor is described in JP99/1477A and JP99/152276A.
- the object of the present invention is to prepare pharmaceutical compositions exhibiting thrombopoietin receptor agonism and provide orally administrate platelet production modifiers.
- the present invention relates to:
- a pharmaceutical composition exhibiting thrombopoietin receptor agonism which contains as an active ingredient a compound of the general formula (I):
- X 1 is optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl;
- Y 1 is —NR A CO—(CR C R D ) 0-2 —, —NR A CO—(CH 2 ) 0-2 —V—, —NR A CR C ⁇ CR D —, —V—(CH 2 ) 1-5 —NR A CO—(CH 2 ) 0-3 —, —V—(CH 2 ) 1-5 CONR A —(CH 2 ) 0-2 —, —CONR A —(CH 2 ) 0-2 —, —(CH 2 ) 0-2 —NR A —SO 2 —(CH 2 ) 0-2 —, —(CH 2 ) 0-2 —, SO 2 —NR A —(CH 2 ) 0-2 —, —NR A —(CH 2 ) 0-2 —,
- Z 1 is optionally substituted phenylene, optionally substituted monocyclic heteroarylene, optionally substituted monocyclic non-aromatic heterocycle-diyl, or optionally substituted monocyclic cycloalkane-diyl;
- W 1 is a group represented by the formula:
- R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino;
- R 5 , R 6 , and R 9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
- a 1 is a optionally substituted aryl or optionally substituted heteroaryl; a broken line (---) represents the presence or absence of a bond, its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- the invention relates to the following II) to XXIX).
- R 10 and R 11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl;
- R 12 is a hydrogen atom or lower alkyl.
- W 1 is a group represented by the formula:
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 14 and R 15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A; a broken line (---) is as defined in I);
- substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy.
- XI A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IX), wherein W 1 is a group represented by the formula
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen a torn;
- R 26 is a hydrogen atom or lower alkyl; a broken line (---) is as defined in I);
- XII A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to XI), which is a platelet production modifier.
- XIII) Use of a compound of any one of I) to XI), for preparation of a medicine for modifying a platelet production.
- XIV) A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of I) to XI) in a pharmaceutically effective amount.
- XV) A compound represented by the general formula (II):
- X 2 is optionally substituted 5-member heteroaryl or optionally substituted pyridyl: Y 2 is —NR A CO—(CR C R D ) 0-2 —, —NR A CO—(CH 2 ) 0-2 —V—, —NR A CO—CR C ⁇ CR D —, —V—(CH 2 ) 1-5 —NR A CO—(CH 2 ) 0-2 , —V—(CH 2 ) 1-5 —CONR A —(CH 2 ) 0-2 —, —CONR A CH 2 ) 0-2 , —(CH 2 ) 0-2 —NR A SO 2 —(CH 2 ) 0-2 —, —(CH 2 ) 0-2- SO 2 —NR A —(CH 2 ) 0-2 —, —NR A —(CH 2 ) 0-2 —, —NR A —CO—NR A —, —NR A —CS—NR A —,
- R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino;
- R 5 , R 6 , and R 9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroaryl
- R 10 and R 11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl, its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XVII A compound described in XV) or XVI), wherein X 2 is a group represented by the formula:
- R 16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted aminocarbonyl
- R 17 , R 18 , R 19 , R 20 , R 21 , R 22 , and R 23 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
- substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alky
- XVIII A compound of any one of XV) to XVII), wherein Y 2 is —NHCO—; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XIX A compound of any one of XV) to XVIII), wherein Z 2 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XX) A compound of any one of XV) to XIX), wherein R 1 is a hydrogen atom or lower alkyl; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XXI A compound of any one of XV) to XX), wherein R 2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XXII A compound of any one of XV) to XXI), wherein W 2 is a group represented by the formula:
- R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and A 2 are as defined in claim XV); provided that R 2 is not imidazolyl, triazolyl, or tetrazolyl; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XXIII) A compound of any one of XV) to XXII), wherein W 2 is a group represented by the formula:
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 14 and R 15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
- substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- XXIV A compound of any one of XV) to XXII), wherein W 2 is a group represented by the formula:
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 36 is a hydrogen atom or lower alkyl
- a broken line (---) as defined in XV) as defined in XV
- XXV A compound represented by the general formula (III):
- R 16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted aminocarbonyl
- R 17 , R 18 , R 19 , R 20 , and R 21 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
- substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, ary
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 14 and R 15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic, heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
- substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
- R 24 is a hydrogen atom or lower alkyl;
- R 25 is lower alkyl, optionally substituted ary
- R 27 is a hydrogen atom, C1-C3 alkyl, trifluoromethyl, or halogen atom
- R 28 , R 29 , and R 30 are independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
- substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 14 and R 15 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
- substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
- R 24 is a hydrogen atom or lower alkyl; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
- R 28 , R 29 , and R 30 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
- substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl;
- R 13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom
- R 14 and R 15 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
- substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
- R 24 is a hydrogen atom or lower alkyl;
- T is —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —OCH 2 —, or —SCH 2 —;
- XXVIII A pharmaceutical composition containing as the active ingredient a compound of any one of XV) to XXVII).
- XXIX A pharmaceutical composition containing as the active ingredient a compound of any one of XV) to XXVII), which is exhibiting thrombopoietin receptor agonism.
- XXX A platelet production modifier which contains as the active ingredient a compound of any one of XV) to XXVII).
- XXXI Use of a compound of any one of XV) to XXVII) for preparation of a pharmaceutical composition for modifying a platelet production.
- XXXII A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of XV) to XXVII) in a pharmaceutically effective amount.
- halogen means fluoro, chloro, bromo, and iodo.
- alkyl employed alone or in combination with other terms means a straight- or branched chain monovalent hydrocarbon group having 1 to 15 carbon atom(s).
- alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, n-nonanyl, n-decanyl, n-undecanyl, n-dodecanyl, n-tridecanyl, n-tetradecanyl, n-pentadecanyl, and the like.
- C1 to C10 alkyl is preferred.
- C1 to C6 alkyl is more preferred.
- lower alkyl employed alone or in combination with other terms means a straight- or branched chain monovalent hydrocarbon group having 1 to 8 carbon atom(s).
- alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, and the like.
- C1 to C6 alkyl is preferred.
- C1 to C3 alkyl is more preferred.
- C1 to C3 alkylene include methylene, ethylene, propylene, and the like.
- cycloalkane employed alone or in combination with other terms means a mono cycloalkane having 3 to 8 carbon atom.
- examples of cycloalkane include cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, and the like.
- C3 to C6 cycloalkane is preferred.
- cycloalkyl employed alone or in combination with other terms means a mono cycloalkane having 3 to 8 carbon atom.
- examples of cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and the like.
- C3 to C6 cycloalkyl is preferred.
- lower alkenyl in the present specification means a straight- or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more double bond.
- alkenyl examples include vinyl, allyl, 1-propenyl, 2-propenyl, a variety of butenyl isomers and the like.
- C2 to C6 alkenyl is preferred.
- C2 to C4 alkenyl is more preferred.
- lower alkynyl used in the present specification means a straight or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more than two triple bond.
- alkynyl examples include ethynyl, 1-propynyl, 2-propynyl, 1-propenyl, 2-propenyl, crotonyl, isopentenyl, a variety of butenyl isomers and the like.
- C2 to C6 alkynyl is preferred.
- C2 to C4 alkynyl is more preferred.
- aryl employed alone or in combination with other terms means monocyclic or condensed ring aromatic hydrocarbons.
- aryl include phenyl, 1-naphtyl, 2-naphtyl, anthryl, and the like.
- aralkyl herein used means the above mentioned “lower alkyl” substituted with the above mentioned “aryl” at any possible position.
- examples of the aralkyl are benzyl, phenethyl (e.g., 2-phenethyl), phenylpropyl (e.g., 3-phenylpropyl), naphthylmethyl (e.g., 1-naphthylmethyl and 2-naphthylmethyl), anthrylmethyl (e.g., 9-anthrylmethyl), and the like.
- Benzyl and phenylethy are preferred.
- non-aromatic heterocyclic group employed alone or in combination with other terms means a 5 to 7 membered non-aromatic ring which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and the 5 to 7 membered non-aromatic ring may be condensed with two or more rings.
- non-aromatic heterocyclic group examples include pyrrolidinyl (e.g., 1-pyrrolidinyl, 2-pyrrolidinyl), pyrrolinyl (e.g., 3-pyrrolinyl), imidazolidinyl (e.g., 2-imidazolidinyl), imidazolinyl (e.g., imidazolinyl), pyrazolidinyl (e.g., 1-pyrazolidinyl, 2-pyrazolidinyl), pyrazolinyl (e.g., pyrazolinyl), piperidinyl (e.g., piperidino, 2-piperidinyl), piperazinyl (e.g., 1-piperazinyl), indolynyl (e.g., 1-indolynyl), isoindoinyl (e.g., isoindolinyl), morpholinyl (e.g., morpholino, 3-pyr
- morpholino morpholino, piperazino, pyrrolidino, teterahydrofuranyl, tetrahydropyranyl, and the like as “non-aromatic heterocyclic group” of R 17 , R 18 , R 19 , R 20 , R 21 , R 22 , R 23 , R 28 , R 29 , and R 30 .
- Non-aromatic heterocyclic group of substituent group B.
- Non-aromatic heterocyclic group of substituent group C.
- heteroaryl employed alone or in combination with other terms means a 5 to 6 membered aromatic heterocyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and may be fused with above mentioned cycloalkyl, above mentioned aryl, above mentioned non-aromatic heterocyclic group, and other heteroaryl at any possible position.
- heteroaryl examples include pyrrolyl (e.g., 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl), furyl (e.g., 2-furyl, 3-furyl), thienyl (e.g., 2-thienyl 3-thienyl), imidazolyl (e.g., 2-imidazolyl, 4-imidazolyl), pyrazolyl (e.g., 1-pyrazolyl, 3-pyrazolyl), isothiazolyl (e.g., 3-isothiazolyl), isoxazolyl (e.g., 3-isoxazolyl), oxazolyl (e.g., 2-oxazolyl), thiazolyl (e.g., 2-thiazolyl), pyridyl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl), pyrazinyl (e.g., 2-pyrazinyl), pyrimid
- thiazolyl Preferable are thiazolyl, isoxazolyl, thienyl, carbazolyl, benzothiazolyl, pyridyl, pyrazolyl, and the like as “heteroaryl” for X 1 . More preferable are thiazolyl, pyridyl, and the like.
- pyridyl thiazolyl
- benzothiazolyl and the like as “heteroaryl” for R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 .
- pyridyl pyridyl, thienyl, furyl, pyrimidinyl, imidazolyl, thiazolyl, oxazolyl, triazolyl, and the like as “heteroaryl” for R 10 and R 11 .
- imidazolyl Preferable are imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidinyl, and the like as “heteroaryl” for A 1 , A 2 , and A 3 .
- pyridyl pyrazolyl
- pyrimidinyl imidazolyl
- oxazolyl triazolyl
- furyl thienyl and the like as “heteroaryl” for substituent group B.
- pyridyl pyrazolyl, imidazolyl, and the like as “heteroaryl” for substituent group C.
- the term “5-membered heteroaryl” means a 5 membered aromatic heterocyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms.
- Examples of the 5-membered heteroaryl are thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolyl, thiazolyl, oxazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, and the like.
- Preferable is thiazolyl.
- heteroarylalkyl herein used means the above-mentioned “lower alkyl” substituted with the above-mentioned “heteroaryl” at any possible position.
- heteroarylalkyl examples include thienylmethyl (e.g., 2-thienylmethyl), thienylethyl (e.g., 2-(thiophen-2-yl)ethyl), furylmethyl (e.g., 2-furylmethyl), furylethyl (e.g., 2-(furan-2-yl)ethyl), pyrrolylmethyl (e.g., 2-pyrrolylmethyl), pyrrolylethyl (e.g., 2-(pyrrol-2-yl)ethyl), imidazolylmethyl (e.g., 2-imidazolylmethyl, 4-imidazolylmethyl), imidazolylethyl (e.g., 2-(imidazol-2-yl)ethyl
- heteroarylalkyl Preferable are 2-thienylmethyl, 2-furylmethyl, and the like as “heteroarylalkyl” for R 1 , R 2 , R 3 , R 4 , R 7 , and R 8 .
- phenylene herein used means a divalent group of the above-mentioned “phenyl”.
- examples of the phenylene are 1,2-phenylene, 1,3-phenylene, 1,4-phenylene, and the like. Preferable is 1,4-phenylene.
- heteroarylene herein used means a monocyclic heteroaryl divalent group of the above-mentioned “heteroaryl”.
- heteroarylene examples include thiophene-diyl, furan-diyl, pyridine-diyl, and the like.
- non-aromatic heterocycle-diyl herein used means a divalent group of an above-mentioned “monocyclic non-aromatic heterocyclic group”.
- non-aromatic heterocycle-diyl examples include pyrrolidine-diyl, piperidine-diyl, pyrazine-diyl and the like.
- cycloalkane-diyl herein used means a divalent group of the above-mentioned “monocyclic cycloalkyl”.
- examples of the cycloalkyl-diyl are 1,4-cyclopentane-diyl, 1,4-cyclohexane-diyl and the like.
- alkyloxy herein used are methyloxy, ethyloxy, n-propyloxy, 1-propyloxy, n-butyloxy, i-butyloxy, sec-butyloxy, tert-butyloxy, n-pentyloxy, n-hexyloxy, n-heptyloxy, n-octyloxy, n-nonanyloxy, n-decanyloxy, and the like. Methyloxy, ethyloxy, n-propyloxy, i-propyloxy and n-butyloxy are preferred.
- lower alkyloxy herein used are methyloxy, ethyloxy, n-propyloxy, i-propyloxy, n-butyloxy, i-butyloxy, sec-butyloxy, tert-butyloxy, and the like. Methyloxy, ethyloxy, n-propyloxy, i-propyloxy and n-butyloxy are preferred.
- lower alkylthio herein used are methylthio, ethylthio, and 1 the like.
- lower alkyloxycarbonyl herein used are methyloxycarbonyl, ethyloxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, t-butyloxycarbonyl, n-pentyloxycarbonyl and the like.
- aryloxycarbonyl herein used are phenyloxycarbonyl, 1-naphthyloxycarbonyl, 2-naphthyloxycarbonyl, and the like.
- acyl employed alone or in combination with other terms means alkylcarbonyl in which alkyl group is the above-mentioned “lower alkyl” and arylcarbonyl in which aryl group is the above-mentioned “aryl”.
- examples of the acyl are acetyl, propyonyl, benzoyl, and the like.
- “Lower alkyl” and “aryl” may be substituted respectively with substituents mentioned below.
- halo(lower)alkyl employed alone or in combination with other terms means the above-mentioned “lower alkyl” which is substituted with the above mentioned “halogen” at 1 to 8 positions, preferably, at 1 to 5.
- halo(lower)alkyl are trifluoromethyl, trichloromethyl, difluoroethyl, trifluoroethyl, dichloroethyl, trichloroethyl, and the like. Preferable is trifluoromethyl.
- halo(lower)alkyl herein used are trifluoromethyl, trichloromethyl, difluoroethyl, trifluoroethyl, dichloroethyl, trichloroethyl, and the like. Preferable is trifluoromethyl.
- acyloxy herein used are acetyloxy, propionyloxy, benzoyloxy and the like.
- lower alkylsilyl examples are triethylsilyl, t-butyldimethylsilyl, and the like.
- optionally substituted amino employed alone or in combination with other terms includes amino substituted with one or two of the above mentioned “lower alkyl”, “aralkyl”, “heteroarylalkyl” or “acyl”.
- the optionally substituted amino are amino, methylamino, dimethylamino, ethylmethylamino, diethylamino, benzylamino, acetylamino, benzoylamino and the like.
- Preferable are amino, methylamino, dimethylamino, ethylmethylamino, diethylamino and acetylamino.
- aminocarbonyl examples include aminocarbonyl, methylaminocarbonyl, dimethylaminocarbonyl, ethylmethylaminocarbonyl, diethylaminocarbonyl and the like. Preferable are aminocarbonyl, methylaminocarbonyl, and dimethylaminocarbonyl.
- the term “optionally substituted ureide” includes ureide substituted with one or more than two of the above mentioned “lower alkyl”, “aryl”, “aralkyl”, “heteroaryl”, “heteroarylalkyl” or “acyl”.
- substituents of “optionally substituted lower alkyl” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g., phenyloxy), aralkyloxy (e.g., benzyloxy), lower alkylsulfonyl, guanidino, azo group, optionally substituted ureide, ⁇ N—O— (acyl) and the like. These substituents are able to locate at one or more of any possible positions.
- halogen atom or halo(lower)alkyl, as substituents of “optionally substituted lower alkyl” for R C and R D .
- cycloalkyl, lower alkenyl, lower alkylidene as substituents of “optionally substituted lower alkyl” for R 12 .
- substituents of “optionally substituted lower alkyloxy” and “optionally substituted lower alkylthio” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g.
- phenyloxy e.g., benzyloxy
- aralkyloxy e.g., benzyloxy
- lower alkylsulfonyl guanidino
- azo group optionally substituted ureide, ⁇ N—O— (acyl) and the like.
- substituents of “optionally substituted lower alkenyl” and “optionally substituted lower alknyl” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g., phenyloxy), aralkyloxy (e.g., benzyloxy), lower alkylsulfonyl, guanidino, azo group, optionally substituted ureide, and the like. These substituents are able to locate at one or more of any possible positions.
- halogen, nitro, cyano, lower alkyl, lower alkyloxy, and the like substituents of “optionally substituted phenylene”, “optionally substituted heteroarylene”, “optionally substituted 2,5-pyridine-diyl”, “optionally substituted 2,5-thiophehe-diyl”, “optionally substituted 2,5-furan-diyl”, “optionally substituted monocyclic non-aromatic heterocycle-diyl”, “optionally substituted monocyclic cycloalkyl-diyl”. Their unsubstituted one is preferred.
- substituents of “optionally substituted aryl” and “optionally substituted aralkyl” for X 1 are lower alkyl, hydroxy lower alkyl, hydroxy, lower alkyloxy, lower alkylthio, halogen, nitro, cyano, carboxy, lower halo(lower)alkyl, halo(lower)alkyloxy, aralkyloxy, unsubstituted or substituted amino, unsubstituted or substituted aminocarbonyl, aryl, heteroaryl, non-aromatic heterocyclic group, arylazo (e.g., phenylazo), and the like.
- arylazo e.g., phenylazo
- substituents are lower alkyl, hydroxy, lower alkyloxy, lower alkylthio, halogen, halo(lower)alkyl, halo(lower)alkyloxy, aralkyloxy, —N ⁇ N-(phenyl), alkylenedioxy, and the like.
- aryl for X 1 are phenyl, 3-methylphenyl, 4-methylphenyl, 3,4-dimethylphenyl, 4-ethylphenyl, 4-t-buylphenyl, 4-n-buylphenyl, 4-n-hexylphenyl, 4-n-octylphenyl, 3,5-di-t-butyl-4-hydroxyphenyl, 4-ethyloxyphenol, 4-fluorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl, 4-iodophenyl, 4-trifluoromethylphenyl, 4-methylthiophenyl, 4-phenylmethyloxyphenyl, 4-phenylazophenyl, 4-phenylphenyl, 2-naphtyl, benzodioxoyl (e.g., 1'-benzodioxolyl), and the like.
- substituents of “optionally substituted aryl” for R 10 and R 11 are halogen atom, optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted aminos optionally substituted aminocarbonyl, acyl, formyl, acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., pyridyl, imidazolyl), non-aromatic heterocyclic group (e.g., morpholino, piperazinyl), aralkyl, and the like.
- halogen atom optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl.
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, and heteroaryl.
- the aryl may be fused with C5-C7 cycloalkane (e.g., cyclopentane, cyclohexane) and non-aromatic heterocyclic group (e.g., tetrahydrofuranyl, 1,3-dioxolyl, 1,4-dioxynyl, pyrrolidinyl) to form indane, 1,2,3,4-tetrahydronaphthalene, 1,2,3,4-tetrahydroquinoline, 2,3-dihydrobenzo[1,4]dioxyline, benzo[1,3]dioxole, 2,3-dihydrobenzofuran, 2,3-dihydro-1H-indole.
- C5-C7 cycloalkane e.g., cyclopentane, cyclohexane
- non-aromatic heterocyclic group e.g., tetrahydrofuranyl, 1,3-dio
- substituents of “optionally substituted heteroaryl” and “optionally substituted heteroarylalkyl” for X 1 are optionally substituted alkyl, lower alkenyl (e.g., ⁇ CH—CH 3 , lower alknyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl (e.g., optionally substituted aryloxycarbonyl by halogen atom nitro, cyano, and the like) acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl, 3-thienyl, 5-methylpyridin-2-yl, 3-quinolyl, 5-ch
- heteroatom is nitrogen atom
- the nitrogen atom may be substituted by alkyl, oxo, and the like.
- substituents of “optionally substituted 5-membered heteroaryl” for X 3 are optionally substituted lower alkyl, lower alkenyl (e.g., ⁇ CH—CH 3 ), lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl (e.g., aryloxycarbonyl optionally substituted with halogen, nitro, cyano and the like), acyloxy, optionally substituted phenyl, aryl, optionally substituted heteroaryl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl, 3-thienyl, 5-methylpyridine-2-yl, 3-quinolyl, 5-chlorothiophene
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl,
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino non-aromatic heterocyclic group, and heteroaryl,
- substituents of “optionally substituted aryl” for R 10 and R 11 are halogen atom, optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, formyl, acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., pyridyl, imidazolyl), non-aromatic heterocyclic group (e.g., morpholino, piperazinyl), aralkyl, and the like.
- halogen atom optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl.
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, and heteroaryl.
- ( ⁇ ) ⁇ - ⁇ ” means that ⁇ is present of number of ⁇ to ⁇ .
- Examples of “( ⁇ ) ⁇ - ⁇ ” are (CR C R D ) 0-2 , (CH 2 ) 0-2 , (CH 2 ) 0-5 mean that CR C R D is present of number of 0 to 2, CH 2 is present of number of 0 to 2, CH 2 is present of number of 0 to 5, respectively.
- the term “hemopathy” means hemopathy accompanied with the unusual number of platelet,
- the hemopathy is thrombocytopenia (after bone marrow transplantation, after chemotherapy, anaplastic anemia, bone marrow dysplasia syndrome, acquired thrombopenia of intractable sudden thrombocy topenic purpura and the like, congenital thrombopenia of thrombopoietin deficiency and the like) and the like
- this medicine can be used as treating agent in the case of decreasing number of platelet by administrating antitumor agent, or as protecting agent in the case of expecting the decrease of number of platelet by administrating antitumor agent.
- modifying a platelet production means 1) increasing a number of platelet decreased by administrating antitumor agent and the like. 2) maintaining a number of platelet which may be decreased by administrating antitumor agent and the like. 3) reducing the ratio of the platelet number of decrease caused by administrating antitumor agent and the like.
- FIG. 1 The chart shows the stimulation activity of a present invention for the proliferation and differentiation of megakaryocyte precursor cells, by counting megakaryocyte colonies formed from human bone marrow cells.
- FIG. 2 The chart represents proliferation of the human TPO dependent cells bearing human TPO receptors by the present invention compound, wherein the x-axis is concentration of the present invention compound, and the y-axis is the absorbance as an indicator of cell proliferation. Open circles indicate a response of human TPO, and closed circles indicate a response of the compound (B-1).
- FIG. 3 The chart represents proliferation of the human TPO independent cells bearing no human TPO receptor by the present invention compound, wherein the x-axis is a concentration of the present invention compound, and the y-axis is absorbance as an indicator of cell proliferation. Open triangles indicate a response of human TPO, and closed circles indicate a response of the compound (B-1).
- Compounds (I) of the invention can be synthesized by the following methods A to B and the similar process.
- R 1 , R 2 , R 3 , and X are as defined above mentioned.
- This step is a process of protecting of carboxylic acid of 4-formyl-substituted or 4-acyl-substituted benzoic acid derivatives by R E .
- R E and R F are important in order to remove selectively protecting group of two carboxylic acid.
- RF is protecting group such as methyl and ethyl, which can be removed by basic condition, it is necessary that protecting group of R E can be removed by another condition except basic condition.
- R E examples include allyl (removed by palladium (0) complex), tert-butyl, p-methoxybenzyl, triphenylmethyl, diphenylmethyl (removed by acidic condition), trimethylsilylethyl, trimethylsilylethoxymethyl, tert-butyldimethylsilyl (removed by fluoride ion) and the like.
- Esterification condition can be used the method of reacting with considerable halo-compound in the presence of suitable base. And it can be synthesized by condensation reaction using a alcohol derivative as starting material.
- This step is a process of converting aldehyde or ketone to olefin
- the olefin can be syntesized by the reaction using phosphineylide such as Wittig reaction, Horner-Emmons reaction, or by dehydrated condensation reaction such as Knoevenagel reaction.
- This step is a process of removing the protecting group R E .
- the removal of protecting group R E is carried out under suitable reaction condition as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).
- This step is a process of preparing amide derivative (VIII) from carboxylic acid derivative (VII) and amine derivative (X 1 —NH 2 ) by the method such as active esterification, acid chloride, mixed acid anhydride. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, benzene.
- active esterification method it can be carried out by using 1-hydroxybenzotriazole, hydroxysuccinimide, dimethylaminopyridine, and the like and dicyclohexylcarbodiimide, 1-ethyl- 3- (3-dimethylaminopropyl)carbodiimide hydrochloride salt, and the like as condensation reagent.
- acid halide method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride.
- mixed acid anhydride method it can be carried out by converting carboxylic acid which is reacted with ethylchloroformate, isobutylchloroformate or the like to mixed acid anhydride.
- Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.
- This step is a process of removing protecting group R F .
- the protecting group R F is removed under suitable reaction condition by using the method as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).
- This step is a process of preparing amide derivative (I-A) from carboxylic acid derivative (IX) and amine derivative (R 3 —NH 2 ) by the method such as active esterification, acid chloride, mixed acid anhydride method. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, benzene.
- active esterification method it can be carried out by using 1-hydroxybenzotriazole, hydroxysuccinimide, dimethylaminopyridine, and the like and dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and the like as condensation reagent.
- acid halide method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride.
- mixed acid anhydride method it can be carried out by converting carboxylic acid which is reacted with ethylchloroformate, isobutylchloroformate or the like to mixed acid anhydride.
- Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.
- This method is another method for preparing compound (VIII) as described method A.
- R 1 , R 2 , and X 1 are as defined above mentioned.
- This step is a process of preparing carboamide derivative (X 1 ) in a manner similar to Step 4 of Method A.
- This step is a process of converting aldehyde derivative (X 1 ) to olefin derivative (XII) in a manner similar to Step 2 of Method A.
- Compound (XII) can be converted to compound (I-A) in a manner similar to Step 5 and 6 of Method A.
- a compound is represented by the formula wherein Y 1 is —N(-alkyl)-CO—; Z 1 is optionally substituted thiazole or the like:
- W 1 and Z 1 are as defined above mentioned; Alk is lower alkyl.
- R 1 , R 2 , R 3 , R 4 , X 1 , Y 1 , and Z 1 are as defined above mentioned.
- solvate includes, for example, solvates with organic solvents, hydrates, and the like.
- the term “compound of the present invention” herein used includes a pharmaceutically acceptable salt or solvate thereof.
- the salt is exemplified by a salt with alkali metals (e.g., lithium, sodium, potassium, and the like), alkaline earth metals (e.g., magnesium, calcium, and the like), ammonium, organic bases, amino acids, mineral acids (e.g., hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, and the like), or organic acids (e.g., acetic acid, citric acid, maleic acid, fumaric acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like).
- These salts can be formed by the usual method.
- These hydrates can coordinate with any water molecules when hydrates are formed.
- Prodrug is a derivative of the compound having a group which can be decomposed chemically or metabolically, and such prodrug is a compound according to the present invention which becomes pharmaceutically active by means of solvolysis or by placing the compound in vivo under a physiological condition.
- the method of both selection and manufacture of appropriate prodrug derivatives is described in, for example. Design of Prodrugs, Elsevier, Amsterdam, 1985), For instance, prodrugs such as an ester derivative which is prepared by reacting a basal acid compound with a suitable alcohol, or an amide derivative which is prepared by reacting a basal acid compound with a suitable amine are exemplified when the compounds according to present invention have a carboxylic group.
- esters as prodrugs are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, morpholinoethyl, and N,N-diethylglycolamido, and the like.
- prodrugs such as an acyloxy derivative which is prepared by reacting a basal hydroxy compound, with a suitable acyl halide or a suitable acid anhydride, or an amide derivative which is prepared by reacting a basal acid compound with a suitable amine are exemplified when the compounds according to present invention have a hydroxy group.
- acyloxy derivatives as prodrugs are —OCOC 2 H 5 , —OCO(t-Bu), —OCOC 15 H 31 , —OCO(m-COONa-Ph), —COCH 2 CH 2 COONa, —OCOCH(NH 2 )CH 3 , —OCOCH 2 N(CH 3 ) 2 , and the like.
- prodrugs such as an amide derivative which is prepared by reacting a basal amino compound with a suitable acid halide or a suitable acid anhydride are exemplified when the compounds according to present invention have an amino group.
- Particularly preferred amide as prodrugs are —NHCO(CH 2 ) 20 CH 3 , —NHCOCH(NH 2 )CH 3 , and the like.
- the compound of the present invention is not restricted to any particular isomers but includes all possible isomers and racemic modifications.
- the present invention compounds show excellent thrombopoietin receptor agonism as described in examples mentioned later, and may be used as a pharmaceutical composition (platelet production modifier) for hemopathy accompanied with the unusual number of platelet, for example thrombocytopenia and the like. And the present compound may be used as a peripheral blood stem cell releasing promoter, a differentiation-inducer of megakaryocytic leukemic cell, a platelet increasing agent of a platelet donor and the like.
- the compound of the present invention When the compound of the present invention is administered to a person for the treatment of the above diseases, it can be administered orally as powder, granules, tablets, capsules, pilulae, and liquid medicines, or parenterally as injections, suppositories, percutaneous formulations, insufflation, or the like.
- An effective dose of the compound is formulated by being mixed with appropriate medicinal admixtures such as excipient, binder, penetrant, disintegrators, lubricant, and the like if necessary.
- Parenteral injections are prepared by sterilizing the compound together with an appropriate carrier.
- the dosage varies with the conditions of the patients, administration route, their age, and body weight.
- the dosage can generally be between 0.1 to 100 mg/kg/day, and preferably 1 to 20 mg/kg/day for adult.
- THF tetrahydrofuran proppargyl, allyl, pyrazole, pyrimidine, piperidine, methyl, cyclohexylmethyl
- This ether solution was added to a THF solution of the acid chloride, and stirred at ice-cooling for 1 h.
- the reaction solution was partitioned between ethyl acetate and water.
- the organic layer was successively washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate.
- the solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane-10/1 to ethyl acetate) to obtain compound (B-1) (400 mg) as colorless crystals.
- TPO Thrombopoietin
- hTPO Human TPO
- murine TPO in TPO
- the TPO dependent BaF/hTPOR cell line which was established by introducing human TPO receptor (hTPOR) into BaF-B03 cells according to Collins et al (J. Cell. Physiol., 137:293-298 (1988)) was used to test the thrombopoietic activity of the present compound.
- the DNA sequences and encoded peptide sequences for human hTPOR have been described by Vigon et al (Proc. Natl. Acad. Sci. USA, 89:5640-5644 (1992)).
- TPO dose not have any ability to support proliferation of interleukin-3 dependent parental cell line BaF-B03.
- BAF/hTPOR cells were maintained in RPMI medium and WEHI-3B conditioned medium as a source of murine interleukin-3 (IL-3). These cells were washed and resuspended in RPMI medium without a source of murine IL-3 and seeded into each well of 96-well microtiter plates at a density of 5 ⁇ 10 4 cells per well in the absence or presence of various concentration of hTPO or the present compound. After incubation at 37° C. for 20 hours in the 5% CO 2 incubator, 10% WST-1 reagent (Takara Biomedicals, Japan) was added to each wells and the cells were further incubated for 4 hours. The absorbance at 450 nm was measured and the results are shown in FIG. 2 .
- FIG. 3 Effect of the present compound on the growth of BAF/mTPOR cell line which was established by introducing murine TPO receptor (mTPOR) into BAF-B03 cells is shown in FIG. 3 .
- Table 8 exemplifies the ED 50 for tested compounds of the present invention, wherein the ED 50 is the half concentration of the concentration showing the maximum thrombopoietic activity.
- addition of the compounds of the present invention induced forming megakaryocyte colonies and the number of colonies increased depending on the concentration of the compounds. This result revealed that the compounds of the present invention induced the differentiation of human bone marrow cells and produced megakaryocytes having ability of producing platelet.
- the compound supported the proliferation of TPO-dependent BaF/hTPOR in a dose-dependent manner as shown in FIG. 2 .
- BaF/mTPOR expressing murine TPOR was not induced the proliferation by compounds as shown in FIG. 3 .
- Granules are prepared using the following ingredients.
- the compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve.
- Corn starch is made pass through a 120 mesh sieve. They are mixed by a twin shell blender.
- An aqueous solution of HPC-L (low mucosity hydroxypropylcellulose) is added to the mixture and the resulting mixture is kneaded, granulated (by the extrusion with pore size 0.5 to 1 mm mesh), and dried.
- the dried granules thus obtained are sieved by a swing sieve (12/60 mesh) to yield the granules.
- Powders for filling capsules are prepared using the following ingredients.
- the compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve.
- Corn starch is made pass through a 120 mesh sieve.
- These ingredients and magnesium stearate are mixed by a twin shell blender. 100 mg of the 10-fold trituration is filled into a No. 5 hard gelatin capsule.
- Granules for filling capsules are prepared using the following ingredients
- the compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve.
- Corn starch is made pass through a 120 mesh sieve.
- an aqueous solution of HPC-L is added to the mixture and the resulting mixture is kneaded, granulated, and dried. After the dried granules are lubricated, 150 mg of that are filled into a No. 4 hard gelatin capsule.
- Tablets are prepared using the following ingredients.
- the compound represented by the formula (I), lactose, microcrystal cellulose, and CMC-Na (carboxymethylcellulose sodium salt) are made pass through a 60 mesh sieve and then mixed.
- the resulting mixture is mixed with magnesium stearate to obtain the mixed powder for the tablet formulation.
- the mixed powder is compressed to yield tablets of 150 mg.
- Intravenous formulations are prepared using the following ingredients.
- the compounds of the present invention have thrombopoietin receptor agonism and are useful as the treating or preventing agent for hemopathy accompanied with unusual count of platelet, for example, thrombocytopenia and the like
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Abstract
Pharmaceutical compositions containing as an active ingredient compounds of the general formula (I), prodrugs of the same, pharmaceutically acceptable salts of both, or solvates of them and exhibiting thrombopoietin receptor agonism:
X1—Y1-Z1-W1 (I)
wherein X1 is optionally substituted aryl, optionally substituted heteroaryl or the like; Y1 is —NRACO—(CH2)0-2— or the like (wherein RA is a hydrogen or the like); Z1 is optionally substituted phenylene or the like; and W1 is a group represented by the below formula:
wherein R1, R2, R3, and R4 are each independently a hydrogen atom, optionally substituted lower alkyl or the like, a broken line (---) represents the presence or absence of bond.
Description
- The present invention relates to compounds exhibiting thrombopoietin receptor agonism.
- Thrombopoietin, polypeptide cytokine composed of 332 amino acids, activates the production of platelets by stimulating the differentiation and proliferation of megakaryocytes through the receptor and is expected as a medicine for hemopathy accompanied with the unusual number of platelets, for example, thrombocytopenia and the like. DNA sequences encoding the thrombopoietin receptor have been described in Proc. Natl. Acad. Sci., 89, 5640-5644 (1992). Low molecular peptides having an affinity for the thrombopoietin receptor is also known (JP98/72492A and WO96/40750), but these peptide derivatives are not generally practical for oral administration.
- 1,4-Benzodiazepine derivatives as a low molecule compound having an affinity to the thrombopoietin receptor is described in JP99/1477A and JP99/152276A.
- The compounds having a similar structure of the present invention compound are described in JP98/287634A and the like, but the affinity for thrombopoietin receptor is not described therein.
- The object of the present invention is to prepare pharmaceutical compositions exhibiting thrombopoietin receptor agonism and provide orally administrate platelet production modifiers.
- In the above situation, the inventors of the present invention have found that the following compounds exhibit strong thrombopoietin receptor agonism.
- The present invention relates to:
- I) A pharmaceutical composition exhibiting thrombopoietin receptor agonism which contains as an active ingredient a compound of the general formula (I):
-
X1—Y1-Z1-W1 (I) - wherein X1 is optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl; Y1 is —NRACO—(CRCRD)0-2—, —NRACO—(CH2)0-2—V—, —NRACRC═CRD—, —V—(CH2)1-5—NRACO—(CH2)0-3—, —V—(CH2)1-5CONRA—(CH2)0-2—, —CONRA—(CH2)0-2—, —(CH2)0-2—NRA—SO2—(CH2)0-2—, —(CH2)0-2—, SO2—NRA—(CH2)0-2—, —NRA—(CH2)0-2, —NRA—CO—NRA—, —NRA—CS—NRA—, —N═C(—SRA)—NRA, —NRACSNRACO—, —N═C(—SRA)—NRACO—, —NRA—(CH2)1-2—NRA—CO—, —NRACONRANRBCO—, or —N═C(—NRARA)—NRA—CO—,
wherein RA is each independently a hydrogen atom or lower alkyl; RB is a hydrogen atom or phenyl; RC and RD are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino; V is an oxygen atom or a sulfur atom; - Z1 is optionally substituted phenylene, optionally substituted monocyclic heteroarylene, optionally substituted monocyclic non-aromatic heterocycle-diyl, or optionally substituted monocyclic cycloalkane-diyl;
- W1 is a group represented by the formula:
- wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino;
- R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
- A1 is a optionally substituted aryl or optionally substituted heteroaryl; a broken line (---) represents the presence or absence of a bond,
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof. - In more detail, the invention relates to the following II) to XXIX).
- II) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of I), wherein X1 is optionally substituted heteroaryl.
III) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of I), wherein X1 is a group represented by the formula: - wherein R10 and R11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl;
R12 is a hydrogen atom or lower alkyl.
IV) A pharmaceutical composition exhibiting thrombopoietin receptor agonism which contains a compound of I), wherein X1 is a group represented by the formula: - V) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IV), wherein Y1 is —NHCO—, —CONH—, —NHCH2—, —NHCO—CH═CH—, or —NHSO2—.
VI) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IV), wherein Y1 is —NHCO—.
VII) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to VI), wherein Z1 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl.
VIII) A pharmaceutical, composition exhibiting thrombopoietin receptor agonism of any one of I) to VII), wherein R1 is a hydrogen atom or lower alkyl.
IX) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IX), wherein R2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino.
X) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IX), wherein W1 is a group represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
a broken line (---) is as defined in I);
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy.
XI) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to IX), wherein W1 is a group represented by the formula: - R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen a torn;
R26 is a hydrogen atom or lower alkyl;
a broken line (---) is as defined in I); - XII) A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of I) to XI), which is a platelet production modifier.
- XIII) Use of a compound of any one of I) to XI), for preparation of a medicine for modifying a platelet production.
XIV) A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of I) to XI) in a pharmaceutically effective amount.
XV) A compound represented by the general formula (II): -
X2—Y2-Z2-W2 (II) - wherein X2 is optionally substituted 5-member heteroaryl or optionally substituted pyridyl:
Y2 is —NRACO—(CRCRD)0-2—, —NRACO—(CH2)0-2—V—, —NRACO—CRC═CRD—, —V—(CH2)1-5—NRACO—(CH2)0-2, —V—(CH2)1-5—CONRA—(CH2)0-2—, —CONRACH2)0-2, —(CH2)0-2—NRASO2—(CH2)0-2—, —(CH2)0-2-SO2—NRA—(CH2)0-2—, —NRA—(CH2)0-2—, —NRA—CO—NRA—, —NRA—CS—NRA—, —N═C(—SRA)—NRA—, —NRACSNRA—CO—, —N═C(—SRA)—NRACO—, —NRA—(CH2)1-2—NRA—CO—, —NRACONRANRB—CO—, or —N═C(—NRARA)—NRA—CO—,
wherein RA is each independently a hydrogen atom or lower alkyl; RB is a hydrogen atom or phenyl; RC and RD are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino; V is an oxygen atom or a sulfur atom;
Z2 is optionally substituted phenylene, optionally substituted 2,5-pyridino-diyl, optionally substituted 2,5-thiophene-diyl, or optionally substituted 2,5-furan-diyl;
W2 is a group represented by the formula: - wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino;
R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
A2 is a optionally substituted aryl or optionally substituted heteroaryl; a broken line (---) represents the presence or absence of a bond, its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XVI) A compound described in XV), wherein X2 is a group represented by the formula: - wherein R10 and R11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl,
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XVII) A compound described in XV) or XVI), wherein X2 is a group represented by the formula: - wherein R16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted aminocarbonyl;
R17, R18, R19, R20, R21, R22, and R23 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl;
substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, or heteroaryl; R16 and R17 taken together may form —CH2—, —CH2CH2—, —CH2CH2CH2—, —OCH2—, or —SCH2—;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XVIII) A compound of any one of XV) to XVII), wherein Y2 is —NHCO—;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XIX) A compound of any one of XV) to XVIII), wherein Z2 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XX) A compound of any one of XV) to XIX), wherein R1 is a hydrogen atom or lower alkyl;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXI) A compound of any one of XV) to XX), wherein R2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXII) A compound of any one of XV) to XXI), wherein W2 is a group represented by the formula: - wherein, R1, R2, R3, R4, R5, R6, R7, R8 and A2 are as defined in claim XV);
provided that R2 is not imidazolyl, triazolyl, or tetrazolyl; its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXIII) A compound of any one of XV) to XXII), wherein W2 is a group represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXIV) A compound of any one of XV) to XXII), wherein W2 is a group represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R36 is a hydrogen atom or lower alkyl;
a broken line (---) as defined in XV);
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXV) A compound represented by the general formula (III): - wherein R16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted aminocarbonyl;
R17, R18, R19, R20, and R21 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl; substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, or heteroaryl;
R16 and R17 taken together may form —CH2—, —CH2CH2—, —CH2CH2CH2—, —OCH2—, or —SCH2—;
R31 and R32 are each independently a hydrogen atom, lower alkyl, halogen atom, halo(lower)alkyl, lower alkyloxy, halo(lower)alkyloxy, or hydroxy;
W3 is represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic, heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
R24 is a hydrogen atom or lower alkyl;
R25 is lower alkyl, optionally substituted aryl, or optionally substituted non-aromatic heterocyclic group;
A3 is heteroaryl;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXVI) A compound represented by the general formula (IV-A): - wherein R27 is a hydrogen atom, C1-C3 alkyl, trifluoromethyl, or halogen atom;
R28, R29, and R30 are independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl; substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, or heteroaryl;
R31 and R32 are each independently a hydrogen atom, lower alkyl, halogen atom, haro(lower)alkyl, lower alkyloxy, halo(lower)alkyloxy, or hydroxy;
W4 is a group represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
R24 is a hydrogen atom or lower alkyl;
its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXVII) A compound represented by the general formula (IV-B): - wherein R28, R29, and R30 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl;
substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, or heteroaryl;
R31 and R32 are each independently a hydrogen atom, lower alkyl, halogen atom, haro(lower)alkyl, lower alkyloxy, halo(lower)alkyloxy, or hydroxy;
W4 is a group represented by the formula: - wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
R24 is a hydrogen atom or lower alkyl; - its prodrug, or their pharmaceutically acceptable salt, or solvate thereof.
XXVIII) A pharmaceutical composition containing as the active ingredient a compound of any one of XV) to XXVII).
XXIX) A pharmaceutical composition containing as the active ingredient a compound of any one of XV) to XXVII), which is exhibiting thrombopoietin receptor agonism.
XXX) A platelet production modifier which contains as the active ingredient a compound of any one of XV) to XXVII).
XXXI) Use of a compound of any one of XV) to XXVII) for preparation of a pharmaceutical composition for modifying a platelet production.
XXXII) A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of XV) to XXVII) in a pharmaceutically effective amount. - In the present specification, the term “halogen” means fluoro, chloro, bromo, and iodo.
- In the present specification, the term “alkyl” employed alone or in combination with other terms means a straight- or branched chain monovalent hydrocarbon group having 1 to 15 carbon atom(s). Examples of alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, n-nonanyl, n-decanyl, n-undecanyl, n-dodecanyl, n-tridecanyl, n-tetradecanyl, n-pentadecanyl, and the like. C1 to C10 alkyl is preferred. C1 to C6 alkyl is more preferred.
- In the present specification, the term “lower alkyl” employed alone or in combination with other terms means a straight- or branched chain monovalent hydrocarbon group having 1 to 8 carbon atom(s). Examples of alkyl include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, and the like. C1 to C6 alkyl is preferred. C1 to C3 alkyl is more preferred.
- In the present specification, the term “C1 to C3 alkylene” include methylene, ethylene, propylene, and the like.
- In the present specification, the term “cycloalkane” employed alone or in combination with other terms means a mono cycloalkane having 3 to 8 carbon atom. Examples of cycloalkane include cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, and the like. C3 to C6 cycloalkane is preferred.
- In the present specification, the term “cycloalkyl” employed alone or in combination with other terms means a mono cycloalkane having 3 to 8 carbon atom. Examples of cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and the like. C3 to C6 cycloalkyl is preferred.
- The term “lower alkenyl” in the present specification means a straight- or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more double bond. Examples of the alkenyl include vinyl, allyl, 1-propenyl, 2-propenyl, a variety of butenyl isomers and the like. C2 to C6 alkenyl is preferred. C2 to C4 alkenyl is more preferred.
- The term “lower alkynyl” used in the present specification means a straight or branched chain monovalent hydrocarbon group having 2 to 8 carbon atoms and one or more than two triple bond. Examples of the alkynyl include ethynyl, 1-propynyl, 2-propynyl, 1-propenyl, 2-propenyl, crotonyl, isopentenyl, a variety of butenyl isomers and the like. C2 to C6 alkynyl is preferred. C2 to C4 alkynyl is more preferred.
- In the present specification, the term “aryl” employed alone or in combination with other terms means monocyclic or condensed ring aromatic hydrocarbons. Examples of aryl include phenyl, 1-naphtyl, 2-naphtyl, anthryl, and the like.
- The term “aralkyl” herein used means the above mentioned “lower alkyl” substituted with the above mentioned “aryl” at any possible position. Examples of the aralkyl are benzyl, phenethyl (e.g., 2-phenethyl), phenylpropyl (e.g., 3-phenylpropyl), naphthylmethyl (e.g., 1-naphthylmethyl and 2-naphthylmethyl), anthrylmethyl (e.g., 9-anthrylmethyl), and the like. Benzyl and phenylethy are preferred.
- In the present specification, the term “non-aromatic heterocyclic group” employed alone or in combination with other terms means a 5 to 7 membered non-aromatic ring which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and the 5 to 7 membered non-aromatic ring may be condensed with two or more rings. Examples of the non-aromatic heterocyclic group are pyrrolidinyl (e.g., 1-pyrrolidinyl, 2-pyrrolidinyl), pyrrolinyl (e.g., 3-pyrrolinyl), imidazolidinyl (e.g., 2-imidazolidinyl), imidazolinyl (e.g., imidazolinyl), pyrazolidinyl (e.g., 1-pyrazolidinyl, 2-pyrazolidinyl), pyrazolinyl (e.g., pyrazolinyl), piperidinyl (e.g., piperidino, 2-piperidinyl), piperazinyl (e.g., 1-piperazinyl), indolynyl (e.g., 1-indolynyl), isoindoinyl (e.g., isoindolinyl), morpholinyl (e.g., morpholino, 3-morpholinyl), tetrahydrofuranyl, tetrahydropyranyl, and the like.
- Preferable are morpholino, piperazino, pyrrolidino, teterahydrofuranyl, tetrahydropyranyl, and the like as “non-aromatic heterocyclic group” of R17, R18, R19, R20, R21, R22, R23, R28, R29, and R30.
- Preferable are morpholino, piperazino, piperidino, tetrahydrofuranyl, tetrahydropyranyl, and the like as “non-aromatic heterocyclic group” of substituent group B.
- Preferable are morpholino, piperazino, piperidino, pyrrolidino, teterahydrofuranyl, tetrahydropyranyl, and the like as “non-aromatic heterocyclic group” of substituent group C.
- In the present specification, the term “heteroaryl” employed alone or in combination with other terms means a 5 to 6 membered aromatic heterocyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms in the ring and may be fused with above mentioned cycloalkyl, above mentioned aryl, above mentioned non-aromatic heterocyclic group, and other heteroaryl at any possible position. Examples of the heteroaryl are pyrrolyl (e.g., 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl), furyl (e.g., 2-furyl, 3-furyl), thienyl (e.g., 2-thienyl 3-thienyl), imidazolyl (e.g., 2-imidazolyl, 4-imidazolyl), pyrazolyl (e.g., 1-pyrazolyl, 3-pyrazolyl), isothiazolyl (e.g., 3-isothiazolyl), isoxazolyl (e.g., 3-isoxazolyl), oxazolyl (e.g., 2-oxazolyl), thiazolyl (e.g., 2-thiazolyl), pyridyl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl), pyrazinyl (e.g., 2-pyrazinyl), pyrimidinyl (e.g., 2-pyrimidinyl, 4-pyrimidinyl), pyridazinyl (e.g., 3-pyridazinyl), tetrazolyl(e.g., 1H-tetrazolyl), oxadiazolyl (e.g., 1,3,4-oxadiazolyl); thiadiazolyl (e.g., 1,3,4-thiadiazolyl), indolizinyl (e.g., 2-indolizinyl, 6-indolizinyl), isoindolyl (2-isoindolyl), indolyl (e.g., 1-indolyl, 2-indolyl, 3-indolyl), indazolyl (e.g., 3-indazolyl), puriyl (e.g., 8-puriyl), quinolizinyl (e.g., 2-quinolizinyl), isoquinolyl (e.g., 3-isoquinolyl), quinolyl (e.g., 3-quinolyl, 5-quinolyl), phthalazinyl (e.g., 1-phthalazinyl), naphthyridinyl (e.g., 2-naphthyridinyl), quinolanyl (2-quinolanyl), quinazolinyl (e.g., 2-quinazolinyl), cinnolinyl (e.g., 3-cinnolinyl), pteridinyl (e.g., 2-pteridinyl), carbazolyl (e.g., 2-carbazolyl, 4-carbazolyl), phenanthridinyl (e.g., 2-phenanthridinyl, 3-phenanthridinyl), acridinyl (e.g., 1-acridinyl, 2-acridinyl), dibenzofuranyl (e.g., 1-dibenzofuranyl, 2-dibenzofuranyl), benzimidazolyl (e.g., 2-benzimidazolyl), benzisoxazolyl (e.g., 3-benzisoxazolyl), benzoxazolyl (e.g., 2-benzoxazolyl), benzoxadiazolyl (e.g., 4-benzoxadiazolyl), benzisothiazolyl (e.g., 3-benzisothiazolyl), benzothiazolyl (e.g., 2-benzothiazolyl), benzofuryl (e.g., 3-benzofuryl), benzothienyl (e.g., 2-benzothienyl), 4,5-dihydronaphtho[1,2-d]thiazolyl, 4H-chromeno[4,3-d]thiazolyl, 4H-thiochromeno[4,3-d]thiazolyl, 4,5-dihydrothiazo[5,4-c]quinolyl, 8H-indeno[1,2-d]thiazolyl, 5,6-dihydro-4H-3-thia-1-aza-benzo[e]azurenyl and the like.
- Preferable are thiazolyl, isoxazolyl, thienyl, carbazolyl, benzothiazolyl, pyridyl, pyrazolyl, and the like as “heteroaryl” for X1. More preferable are thiazolyl, pyridyl, and the like.
- Preferable are pyridyl, thiazolyl, benzothiazolyl, and the like as “heteroaryl” for R1, R2, R3, R4, R7, and R8.
- Preferable are pyridyl, thienyl, furyl, pyrimidinyl, imidazolyl, thiazolyl, oxazolyl, triazolyl, and the like as “heteroaryl” for R10 and R11.
- Preferable are imidazolyl, triazolyl, tetrazolyl, pyridyl, pyrimidinyl, and the like as “heteroaryl” for A1, A2, and A3.
- Preferable are pyridyl, thienyl, furyl, pyrimidinyl, imidazolyl, thiazolyl, oxazolyl, triazolyl, and the like as “heteroaryl” for R17, R18, R19, R20, R21, R22, R23, R28, R19, and R30.
- Preferable are pyridyl, pyrazolyl, pyrimidinyl, imidazolyl, oxazolyl, triazolyl, furyl, thienyl and the like as “heteroaryl” for substituent group B.
- Preferable are pyridyl, pyrazolyl, imidazolyl, and the like as “heteroaryl” for substituent group C.
- In the present specification, the term “5-membered heteroaryl” means a 5 membered aromatic heterocyclic group which contains one or more hetero atoms selected from the group consisting of oxygen, sulfur, and nitrogen atoms. Examples of the 5-membered heteroaryl are thienyl, furyl, pyrrolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolyl, thiazolyl, oxazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, and the like. Preferable is thiazolyl.
- The term “heteroarylalkyl” herein used means the above-mentioned “lower alkyl” substituted with the above-mentioned “heteroaryl” at any possible position. Examples of the heteroarylalkyl are thienylmethyl (e.g., 2-thienylmethyl), thienylethyl (e.g., 2-(thiophen-2-yl)ethyl), furylmethyl (e.g., 2-furylmethyl), furylethyl (e.g., 2-(furan-2-yl)ethyl), pyrrolylmethyl (e.g., 2-pyrrolylmethyl), pyrrolylethyl (e.g., 2-(pyrrol-2-yl)ethyl), imidazolylmethyl (e.g., 2-imidazolylmethyl, 4-imidazolylmethyl), imidazolylethyl (e.g., 2-(imidazol-2-yl)ethyl), pyrazolylmethyl (e.g., 3-pyrazolylmethyl), pyrazolylmethyl (e.g., 2-(pyrazol-3-yl)ethyl), thiazolylmethyl (e.g., 2-thiazolylmethyl), thiazolylethyl (e.g., 2-(thiazol-2-yl)ethyl), isothiazolylmethyl (e.g., 3-thiazolylmethyl), isoxazolylmethyl (e.g., 3-isoxazolylmethyl), oxazolylmethyl (e.g., 2-oxazolylmethyl), oxazolylethyl (e.g., 2-(oxazol-2-yl)ethyl), pyridylmethyl (e.g., 2-pyridylmethyl, 3-pyridylmethyl, 4-pyridylmethyl), pyridylethyl (e.g., 2-pyridylethyl) and the like.
- Preferable are 2-thienylmethyl, 2-furylmethyl, and the like as “heteroarylalkyl” for R1, R2, R3, R4, R7, and R8.
- The term “phenylene” herein used means a divalent group of the above-mentioned “phenyl”. Examples of the phenylene are 1,2-phenylene, 1,3-phenylene, 1,4-phenylene, and the like. Preferable is 1,4-phenylene.
- The term “monocyclic heteroarylene” herein used means a monocyclic heteroaryl divalent group of the above-mentioned “heteroaryl”. Examples of the heteroarylene are thiophene-diyl, furan-diyl, pyridine-diyl, and the like. Mentioned in more detail, it is exemplified by 2,5-thiophene-diyl, 2,5-furan-diyl, 2,5-pyridine-diyl, 2,5-thiazole-diyl, 2,5-(1,3,4-thiadiazole)-diyl, 2,5-pyridine-diyl, 2,5-parazine-diyl, 3,6-pyridazine-diyl, 2,5-(4H-pyrane)-diyl, and the like. Preferable are 2,5-thiophene-diyl, 2,5-furan-diyl, 2,5-pyridine-diyl.
- The term “monocyclic non-aromatic heterocycle-diyl” herein used means a divalent group of an above-mentioned “monocyclic non-aromatic heterocyclic group”. Examples of the non-aromatic heterocycle-diyl are pyrrolidine-diyl, piperidine-diyl, pyrazine-diyl and the like.
- The term “monocyclic cycloalkane-diyl” herein used means a divalent group of the above-mentioned “monocyclic cycloalkyl”. Examples of the cycloalkyl-diyl are 1,4-cyclopentane-diyl, 1,4-cyclohexane-diyl and the like.
- The term “alkyloxy” herein used are methyloxy, ethyloxy, n-propyloxy, 1-propyloxy, n-butyloxy, i-butyloxy, sec-butyloxy, tert-butyloxy, n-pentyloxy, n-hexyloxy, n-heptyloxy, n-octyloxy, n-nonanyloxy, n-decanyloxy, and the like. Methyloxy, ethyloxy, n-propyloxy, i-propyloxy and n-butyloxy are preferred.
- The term “lower alkyloxy” herein used are methyloxy, ethyloxy, n-propyloxy, i-propyloxy, n-butyloxy, i-butyloxy, sec-butyloxy, tert-butyloxy, and the like. Methyloxy, ethyloxy, n-propyloxy, i-propyloxy and n-butyloxy are preferred.
- The term “lower alkylthio” herein used are methylthio, ethylthio, and 1 the like.
- The term “lower alkyloxycarbonyl” herein used are methyloxycarbonyl, ethyloxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, t-butyloxycarbonyl, n-pentyloxycarbonyl and the like.
- The term “aryloxycarbonyl” herein used are phenyloxycarbonyl, 1-naphthyloxycarbonyl, 2-naphthyloxycarbonyl, and the like.
- In the present specification, the term “acyl” employed alone or in combination with other terms means alkylcarbonyl in which alkyl group is the above-mentioned “lower alkyl” and arylcarbonyl in which aryl group is the above-mentioned “aryl”. Examples of the acyl are acetyl, propyonyl, benzoyl, and the like. “Lower alkyl” and “aryl” may be substituted respectively with substituents mentioned below.
- In the present specification, the term “halo(lower)alkyl” employed alone or in combination with other terms means the above-mentioned “lower alkyl” which is substituted with the above mentioned “halogen” at 1 to 8 positions, preferably, at 1 to 5. Examples of the halo(lower)alkyl are trifluoromethyl, trichloromethyl, difluoroethyl, trifluoroethyl, dichloroethyl, trichloroethyl, and the like. Preferable is trifluoromethyl.
- The term “halo(lower)alkyl” herein used are trifluoromethyl, trichloromethyl, difluoroethyl, trifluoroethyl, dichloroethyl, trichloroethyl, and the like. Preferable is trifluoromethyl.
- Examples of the term “acyloxy” herein used are acetyloxy, propionyloxy, benzoyloxy and the like.
- Examples of the term “lower alkylsilyl” herein used are triethylsilyl, t-butyldimethylsilyl, and the like.
- In the present specification, the term “optionally substituted amino” employed alone or in combination with other terms includes amino substituted with one or two of the above mentioned “lower alkyl”, “aralkyl”, “heteroarylalkyl” or “acyl”. Examples of the optionally substituted amino are amino, methylamino, dimethylamino, ethylmethylamino, diethylamino, benzylamino, acetylamino, benzoylamino and the like. Preferable are amino, methylamino, dimethylamino, ethylmethylamino, diethylamino and acetylamino.
- Examples of the term “optionally substituted aminocarbonyl” herein used are aminocarbonyl, methylaminocarbonyl, dimethylaminocarbonyl, ethylmethylaminocarbonyl, diethylaminocarbonyl and the like. Preferable are aminocarbonyl, methylaminocarbonyl, and dimethylaminocarbonyl.
- In the present specification, the term “optionally substituted ureide” includes ureide substituted with one or more than two of the above mentioned “lower alkyl”, “aryl”, “aralkyl”, “heteroaryl”, “heteroarylalkyl” or “acyl”.
- The substituents of “optionally substituted lower alkyl” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g., phenyloxy), aralkyloxy (e.g., benzyloxy), lower alkylsulfonyl, guanidino, azo group, optionally substituted ureide, ═N—O— (acyl) and the like. These substituents are able to locate at one or more of any possible positions.
- Preferable are halogen atom, or halo(lower)alkyl, as substituents of “optionally substituted lower alkyl” for RC and RD.
- Preferable are hydroxy, carboxy, halogen atom, alkyloxy, alkylthio, alkylsilyl, optionally substituted amino, cyano, acyl, and the like as substituents of “optionally substituted lower alkyl” for R1, R2, R3, R4, R5, R6, R7, R8, and R9.
- Preferable are lower alkyloxycarbonyl and halogen atom as substituents of “optionally substituted lower alkyl” for R10, R11, and R16.
- Preferable are cycloalkyl, lower alkenyl, lower alkylidene as substituents of “optionally substituted lower alkyl” for R12.
- The substituents of “optionally substituted lower alkyloxy” and “optionally substituted lower alkylthio” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g. phenyloxy), aralkyloxy (e.g., benzyloxy), lower alkylsulfonyl, guanidino, azo group, optionally substituted ureide, ═N—O— (acyl) and the like. These substituents are able to locate at one or more of any possible positions.
- The substituents of “optionally substituted lower alkenyl” and “optionally substituted lower alknyl” are cycloalkyl, lower alkenyl, lower alkyliden, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted non-aromatic heterocyclic group, aryloxy (e.g., phenyloxy), aralkyloxy (e.g., benzyloxy), lower alkylsulfonyl, guanidino, azo group, optionally substituted ureide, and the like. These substituents are able to locate at one or more of any possible positions.
- The substituents of “optionally substituted phenylene”, “optionally substituted heteroarylene”, “optionally substituted 2,5-pyridine-diyl”, “optionally substituted 2,5-thiophene-diyl”, “optionally substituted 2,5-furan-diyl”, “optionally substituted monocyclic non-aromatic heterocycle-diyl”, “optionally substituted monocyclic cycloalkane-diyl”, “optionally substituted aryl”, “optionally substituted phenyl”, “optionally substituted heteroaryl”, “optionally substituted 5-membered heteroaryl”, “optionally substituted pyridyl”, “optionally substituted non-aromatic heterocyclic group”, “optionally substituted cycloalkyl”, “optionally substituted aralkyl”, and “optionally substituted heteroarylalkyl” herein used are optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, alkyloxy, aralkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, acyloxy, optionally substituted aryl (which is substituted by halogen atom, carboxy, alkyl, or alkyloxy, and the like), optionally substituted heteroaryl (which is substituted by halogen atom, carboxy, alkyl, or alkyloxy, and the like), optionally substituted non-aromatic heterocyclic group, optionally substituted aralkyl, lower alkylsulfonyl, guanidino, azo group, —N═N-(optionally substituted phenyl) or optionally substituted ureide and the like. These substituents are able to locate at one or more of any possible positions.
- Preferable are halogen, nitro, cyano, lower alkyl, lower alkyloxy, and the like as substituents of “optionally substituted phenylene”, “optionally substituted heteroarylene”, “optionally substituted 2,5-pyridine-diyl”, “optionally substituted 2,5-thiophehe-diyl”, “optionally substituted 2,5-furan-diyl”, “optionally substituted monocyclic non-aromatic heterocycle-diyl”, “optionally substituted monocyclic cycloalkyl-diyl”. Their unsubstituted one is preferred.
- The examples of substituents of “optionally substituted aryl” and “optionally substituted aralkyl” for X1 are lower alkyl, hydroxy lower alkyl, hydroxy, lower alkyloxy, lower alkylthio, halogen, nitro, cyano, carboxy, lower halo(lower)alkyl, halo(lower)alkyloxy, aralkyloxy, unsubstituted or substituted amino, unsubstituted or substituted aminocarbonyl, aryl, heteroaryl, non-aromatic heterocyclic group, arylazo (e.g., phenylazo), and the like. Preferable substituents are lower alkyl, hydroxy, lower alkyloxy, lower alkylthio, halogen, halo(lower)alkyl, halo(lower)alkyloxy, aralkyloxy, —N═N-(phenyl), alkylenedioxy, and the like.
- The examples of “optionally substituted aryl” for X1 are phenyl, 3-methylphenyl, 4-methylphenyl, 3,4-dimethylphenyl, 4-ethylphenyl, 4-t-buylphenyl, 4-n-buylphenyl, 4-n-hexylphenyl, 4-n-octylphenyl, 3,5-di-t-butyl-4-hydroxyphenyl, 4-ethyloxyphenol, 4-fluorophenyl, 3,4-dichlorophenyl, 3,5-dichlorophenyl, 4-iodophenyl, 4-trifluoromethylphenyl, 4-methylthiophenyl, 4-phenylmethyloxyphenyl, 4-phenylazophenyl, 4-phenylphenyl, 2-naphtyl, benzodioxoyl (e.g., 1'-benzodioxolyl), and the like.
- The substituents of “optionally substituted aryl” for R10 and R11 are halogen atom, optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted aminos optionally substituted aminocarbonyl, acyl, formyl, acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., pyridyl, imidazolyl), non-aromatic heterocyclic group (e.g., morpholino, piperazinyl), aralkyl, and the like. Preferable are optionally substituted alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyloxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, optionally substituted non-aromatic heterocyclic group by one or more substituent(s) selected from substituent group C, and the like.
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl.
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, and heteroaryl.
- The aryl may be fused with C5-C7 cycloalkane (e.g., cyclopentane, cyclohexane) and non-aromatic heterocyclic group (e.g., tetrahydrofuranyl, 1,3-dioxolyl, 1,4-dioxynyl, pyrrolidinyl) to form indane, 1,2,3,4-tetrahydronaphthalene, 1,2,3,4-tetrahydroquinoline, 2,3-dihydrobenzo[1,4]dioxyline, benzo[1,3]dioxole, 2,3-dihydrobenzofuran, 2,3-dihydro-1H-indole.
- The substituents of “optionally substituted heteroaryl” and “optionally substituted heteroarylalkyl” for X1 are optionally substituted alkyl, lower alkenyl (e.g., ═CH—CH3, lower alknyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl (e.g., optionally substituted aryloxycarbonyl by halogen atom nitro, cyano, and the like) acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl, 3-thienyl, 5-methylpyridin-2-yl, 3-quinolyl, 5-chlorothiophen-2-yl, 5-bromothiophen-2-yl), non-aromatic heterocyclic group, aralkyl, ═N—O— (acyl) and the like. Preferable are optionally substituted lower alkyl, lower alkenyl, lower alkyloxycarbonyl, optionally substituted phenyl, heteroaryl, ═N—O— (acyl) and the like.
- In the case of heteroatom is nitrogen atom, the nitrogen atom may be substituted by alkyl, oxo, and the like.
- The substituents of “optionally substituted 5-membered heteroaryl” for X3 are optionally substituted lower alkyl, lower alkenyl (e.g., ═CH—CH3), lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, halogen, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl (e.g., aryloxycarbonyl optionally substituted with halogen, nitro, cyano and the like), acyloxy, optionally substituted phenyl, aryl, optionally substituted heteroaryl (e.g., 2-pyridyl, 3-pyridyl, 4-pyridyl, 3-thienyl, 5-methylpyridine-2-yl, 3-quinolyl, 5-chlorothiophene-2-yl, 5-bromothiophene-2-yl), non-aromatic heterocyclic group, aralkyl, ═N—O-(acyl), and the like. Preferable are optionally substituted alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyloxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted non-aromatic heterocyclic group by one or more substituent(s) selected from substituent group C, and the like.
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl,
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino non-aromatic heterocyclic group, and heteroaryl,
- The substituents of “optionally substituted aryl” for R10 and R11 are halogen atom, optionally substituted alkyl, cycloalkyl, lower alkenyl, lower alkynyl, hydroxy, lower alkyloxy, mercapto, lower alkylthio, nitro, cyano, carboxy, lower alkyloxycarbonyl, halo(lower)alkyl, halo(lower)alkyloxy, optionally substituted amino, optionally substituted aminocarbonyl, acyl, formyl, acyloxy, optionally substituted aryl, optionally substituted heteroaryl (e.g., pyridyl, imidazolyl), non-aromatic heterocyclic group (e.g., morpholino, piperazinyl), aralkyl, and the like. Preferable are optionally substituted alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyloxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, optionally substituted non-aromatic heterocyclic group by one or more substituent(s) selected from substituent group C, and the like,
- Substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl.
- Substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, and heteroaryl.
- In the present specification, the term “(α)β-γ” means that α is present of number of β to γ. Examples of “(α)β-γ” are (CRCRD)0-2, (CH2)0-2, (CH2)0-5 mean that CRCRD is present of number of 0 to 2, CH2 is present of number of 0 to 2, CH2 is present of number of 0 to 5, respectively.
- In the present specification, the term “hemopathy” means hemopathy accompanied with the unusual number of platelet, For example the hemopathy is thrombocytopenia (after bone marrow transplantation, after chemotherapy, anaplastic anemia, bone marrow dysplasia syndrome, acquired thrombopenia of intractable sudden thrombocy topenic purpura and the like, congenital thrombopenia of thrombopoietin deficiency and the like) and the like, For example this medicine can be used as treating agent in the case of decreasing number of platelet by administrating antitumor agent, or as protecting agent in the case of expecting the decrease of number of platelet by administrating antitumor agent.
- In the present specification, the term “modifying a platelet production” means 1) increasing a number of platelet decreased by administrating antitumor agent and the like. 2) maintaining a number of platelet which may be decreased by administrating antitumor agent and the like. 3) reducing the ratio of the platelet number of decrease caused by administrating antitumor agent and the like.
-
FIG. 1 : The chart shows the stimulation activity of a present invention for the proliferation and differentiation of megakaryocyte precursor cells, by counting megakaryocyte colonies formed from human bone marrow cells. -
FIG. 2 : The chart represents proliferation of the human TPO dependent cells bearing human TPO receptors by the present invention compound, wherein the x-axis is concentration of the present invention compound, and the y-axis is the absorbance as an indicator of cell proliferation. Open circles indicate a response of human TPO, and closed circles indicate a response of the compound (B-1). -
FIG. 3 : The chart represents proliferation of the human TPO independent cells bearing no human TPO receptor by the present invention compound, wherein the x-axis is a concentration of the present invention compound, and the y-axis is absorbance as an indicator of cell proliferation. Open triangles indicate a response of human TPO, and closed circles indicate a response of the compound (B-1). - Compounds (I) of the invention can be synthesized by the following methods A to B and the similar process.
-
- wherein R1, R2, R3, and X are as defined above mentioned.
- This step is a process of protecting of carboxylic acid of 4-formyl-substituted or 4-acyl-substituted benzoic acid derivatives by RE. In
step 3 combination of RE and RF is important in order to remove selectively protecting group of two carboxylic acid. In the case of RF is protecting group such as methyl and ethyl, which can be removed by basic condition, it is necessary that protecting group of RE can be removed by another condition except basic condition. Examples of RE are allyl (removed by palladium (0) complex), tert-butyl, p-methoxybenzyl, triphenylmethyl, diphenylmethyl (removed by acidic condition), trimethylsilylethyl, trimethylsilylethoxymethyl, tert-butyldimethylsilyl (removed by fluoride ion) and the like. - Esterification condition can be used the method of reacting with considerable halo-compound in the presence of suitable base. And it can be synthesized by condensation reaction using a alcohol derivative as starting material.
- This step is a process of converting aldehyde or ketone to olefin, For examples, the olefin can be syntesized by the reaction using phosphineylide such as Wittig reaction, Horner-Emmons reaction, or by dehydrated condensation reaction such as Knoevenagel reaction.
- This step is a process of removing the protecting group RE. The removal of protecting group RE is carried out under suitable reaction condition as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).
- This step is a process of preparing amide derivative (VIII) from carboxylic acid derivative (VII) and amine derivative (X1—NH2) by the method such as active esterification, acid chloride, mixed acid anhydride. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, benzene. At active esterification method it can be carried out by using 1-hydroxybenzotriazole, hydroxysuccinimide, dimethylaminopyridine, and the like and dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and the like as condensation reagent. At acid halide method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride. At mixed acid anhydride method it can be carried out by converting carboxylic acid which is reacted with ethylchloroformate, isobutylchloroformate or the like to mixed acid anhydride. Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.
- This step is a process of removing protecting group RF. The protecting group RF is removed under suitable reaction condition by using the method as described in Protective Groups in Organic Synthesis, Theodora W Green (John Wiley & Sons).
- This step is a process of preparing amide derivative (I-A) from carboxylic acid derivative (IX) and amine derivative (R3—NH2) by the method such as active esterification, acid chloride, mixed acid anhydride method. This step is reacted in the solvent such as tetrahydrofuran, dioxane, dichloromethane, toluene, benzene. At active esterification method it can be carried out by using 1-hydroxybenzotriazole, hydroxysuccinimide, dimethylaminopyridine, and the like and dicyclohexylcarbodiimide, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride salt, and the like as condensation reagent. At acid halide method it can be carried out by converting free carboxylic acid which is reacted with thionyl chloride or oxalyl chloride to acid chloride. At mixed acid anhydride method it can be carried out by converting carboxylic acid which is reacted with ethylchloroformate, isobutylchloroformate or the like to mixed acid anhydride. Triethylamine, pyridine or the like are used as base in these reaction according to be necessary.
- This method is another method for preparing compound (VIII) as described method A.
- wherein R1, R2, and X1 are as defined above mentioned.
- This step is a process of preparing carboamide derivative (X1) in a manner similar to Step 4 of Method A.
- This step is a process of converting aldehyde derivative (X1) to olefin derivative (XII) in a manner similar to
Step 2 of Method A. Compound (XII) can be converted to compound (I-A) in a manner similar to Step 5 and 6 of Method A. - A compound is represented by the formula wherein Y1 is —N(-alkyl)-CO—; Z1 is optionally substituted thiazole or the like:
- wherein W1 and Z1 are as defined above mentioned; Alk is lower alkyl.
- Under alkylation condition for preparing the above mentioned compound may be obtained below mentioned compound.
- wherein W1, Z1 and Alk are as defined above mentioned.
- Compound in formula (I), (II) and (III) wherein a broken line (---) represents the presence of a bond, contains cis-isomer, trans-isomer and their mixture, For example, compound wherein W1 is amide type possesses cis-isomer and trans-isomer blow mentioned.
- wherein R1, R2, R3, R4, X1, Y1, and Z1 are as defined above mentioned.
- The term “solvate” includes, for example, solvates with organic solvents, hydrates, and the like.
- The term “compound of the present invention” herein used includes a pharmaceutically acceptable salt or solvate thereof. The salt is exemplified by a salt with alkali metals (e.g., lithium, sodium, potassium, and the like), alkaline earth metals (e.g., magnesium, calcium, and the like), ammonium, organic bases, amino acids, mineral acids (e.g., hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, and the like), or organic acids (e.g., acetic acid, citric acid, maleic acid, fumaric acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like). These salts can be formed by the usual method. These hydrates can coordinate with any water molecules when hydrates are formed.
- Prodrug is a derivative of the compound having a group which can be decomposed chemically or metabolically, and such prodrug is a compound according to the present invention which becomes pharmaceutically active by means of solvolysis or by placing the compound in vivo under a physiological condition. The method of both selection and manufacture of appropriate prodrug derivatives is described in, for example. Design of Prodrugs, Elsevier, Amsterdam, 1985), For instance, prodrugs such as an ester derivative which is prepared by reacting a basal acid compound with a suitable alcohol, or an amide derivative which is prepared by reacting a basal acid compound with a suitable amine are exemplified when the compounds according to present invention have a carboxylic group. Particularly preferred esters as prodrugs are methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, morpholinoethyl, and N,N-diethylglycolamido, and the like, For instance, prodrugs such as an acyloxy derivative which is prepared by reacting a basal hydroxy compound, with a suitable acyl halide or a suitable acid anhydride, or an amide derivative which is prepared by reacting a basal acid compound with a suitable amine are exemplified when the compounds according to present invention have a hydroxy group. Particularly preferred acyloxy derivatives as prodrugs —OCOC2H5, —OCO(t-Bu), —OCOC15H31, —OCO(m-COONa-Ph), —COCH2CH2COONa, —OCOCH(NH2)CH3, —OCOCH2N(CH3)2, and the like, For instance, prodrugs such as an amide derivative which is prepared by reacting a basal amino compound with a suitable acid halide or a suitable acid anhydride are exemplified when the compounds according to present invention have an amino group. Particularly preferred amide as prodrugs are —NHCO(CH2)20CH3, —NHCOCH(NH2)CH3, and the like.
- The compound of the present invention is not restricted to any particular isomers but includes all possible isomers and racemic modifications.
- The present invention compounds show excellent thrombopoietin receptor agonism as described in examples mentioned later, and may be used as a pharmaceutical composition (platelet production modifier) for hemopathy accompanied with the unusual number of platelet, for example thrombocytopenia and the like. And the present compound may be used as a peripheral blood stem cell releasing promoter, a differentiation-inducer of megakaryocytic leukemic cell, a platelet increasing agent of a platelet donor and the like.
- When the compound of the present invention is administered to a person for the treatment of the above diseases, it can be administered orally as powder, granules, tablets, capsules, pilulae, and liquid medicines, or parenterally as injections, suppositories, percutaneous formulations, insufflation, or the like. An effective dose of the compound is formulated by being mixed with appropriate medicinal admixtures such as excipient, binder, penetrant, disintegrators, lubricant, and the like if necessary. Parenteral injections are prepared by sterilizing the compound together with an appropriate carrier.
- The dosage varies with the conditions of the patients, administration route, their age, and body weight. In the case of oral administration, the dosage can generally be between 0.1 to 100 mg/kg/day, and preferably 1 to 20 mg/kg/day for adult.
- The following examples are provided to further illustrate the present invention and are not to be constructed as limiting the scope thereof.
- Abbreviations described below are used in the following examples.
- Me: methyl
Et: ethyl
n-Pr: n-propyl
i-Pr: isopropyl
c-Pr: cyclopropyl
n-Bu: n-butyl
i-Bu: i-butyl
sec-Bu: sec-butyl
t-Bu: tert-butyl
i-Bu: i-butyl
n-Pen: n-pentyl
c-Pen: cyclopentyl
n-Hex: n-hexyl
c-Hex: cyclohexyl
i-Hex: i-hexyl
Ph: phenyl
Bn: benzyl
Bz: benzoyl
Py: pyridyl
Th: thienyl
Ac: acetyl
Z: benzyloxycarbonyl - THF: tetrahydrofuran
proppargyl, allyl, pyrazole, pyrimidine, piperidine, methyl, cyclohexylmethyl - The preparation of compound (A-1, A-2, and B-1)
- A solution of terephthaladehydic acid (7.5 g), allyl bromide (4.41 ml), and potassium carbonate (7.0 g) in DMF (100 ml) was stirred at 60° C. for 16 h. The reaction solvent was removed under reduced pressure, and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure to obtain compound (2) 9.2 g as colorless clear oil.
- 1H NMR (CDCl3, δ ppm): 4.87 (2H, dt, J= 1.2, 5.7 Hz), 5.30-5.47 (2H, m), 5.99-6.12 (1H, m), 7.94-7.98 (2H, m), 8.20-8.25 (2H, m), 10.11 (1H, s).
- A solution of compound (2) (4.37 g) and ethyl 2-(triphenylphosphoranilidene)propionate (10.63 g) in toluene (100 ml) was heated with stirring at 70° C. for 1 h. The reaction solvent was concentrated to ca. 30 to 40 ml, the precipitated triphenylphosphineoxide was filtered off. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane= 1/10) to obtain compound (3) 6.9 g as colorless clear oil.
- 1H NMR (CDCl3, δ ppm): 1.36 (3H, t, J= 7.2 Hz), 2.11 (3H, d, J= 1.5 Hz), 4.29 (2H, q, J= 7.2 Hz), 4.84 (2H, dt, J= 1.2, 5.7 Hz), 5.28-5.46 (2H, m), 5.98-6.11 (1H, m), 7.43-7.47 (2H, m), 7.69 (1H, d, J= 1.5 Hz), 8.06-8.10 (2H, m).
- A solution of compound (3) (6 g), tetrakistriphenylphosphinpalladium (1.27 g), and morpholine (2.68 g) in THF (100 ml) was stirred at 60° C. for 30 min. The reaction solvent was concentrated to ca. 30 to 40 ml, and ethyl acetate was added to the residue. The mixture was extracted with sodium bicarbonate aqueous solution three times. The combined sodium bicarbonate extract was acidified with 3M hydrochloric acid, and the precipitated crystals were extracted with ethyl acetate. The ethyl acetate layer was washed with brine, dried over magnesium sulfate. The solvent was removed under reduced pressure to obtain compound (4) 4.5 g as white crystals.
- 1H NMR (CDCl3, δ ppm): 1.37 (3H, t, J= 7.2 Hz), 2.13 (3H, d, J= 1.2 Hz), 4.30 (2H, q, J= 7.2 Hz), 7.49 (2H, d, J= 8.4 Hz), 7.71 (1H, s), 8.14 (2H, d, J= 8.4 Hz).
- To a solution of compound (4) (5.67 g), oxalyl chloride (1.3 ml) in THF (100 ml) was added catalytic amount of DMF, and then the reaction mixture was stirred at room temperature for 2 h. The reaction solution was removed under reduced pressure, toluene was added to the resulting residue, and toluene was removed under reduced pressure. The obtained carboxylic acid chloride was dissolved with dioxane (70 ml), was added 2-amino-4-(3,4-) dichlorophenylythiazole (1 g), and pyridine (970 μl) to the mixture. The reaction solution was heated with stirring at 100° C. for 16 h, and partitioned between ethyl acetate and water. The ethyl acetate layer was washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure to obtain compound (A-1) 1.5 g as white crystals.
- 1H NMR (DMSO-d6, δ ppm): 1.29 (3H, t, J= 7.2 Hz), 2.10 (3H, d, J= 1.2 Hz), 4.23 (2H, q, J= 7.2 Hz), 7.62 7.68 (3H, m), 7.72 (1H, d, J= 8.4 Hz), 7.91 (1H, s), 7.94 (1H, dd, J= 1.8, 8.4 Hz), 8.15-8.20 (2H, m), 8.21 (1H, d, J= 1.8 Hz), 12.84 (1H, br).
- A solution of compound (A-1) (1.7 g), 4M sodium hydroxide aqueous solution (5.5 ml) in THF (150 ml) was heated with stirring 85° C. for 18 h. The reaction solution was acidified with diluted hydrochloric acid, and the precipitated crystals were filtered. The obtained powder was washed methanol and ethyl acetate to obtain compound (A-2) (1.5 g) as white powder.
- 1H NMR (DMSO-de, δ ppm): 2.08 (3H, d, J= 0.9 Hz), 7.62-7.68 (3H, m), 7.72-(1H, cl, J= 8.7 Hz), 7.92 (1H, s), 7.95 (1H, dd, J= 2.1, 8.7 Hz), 8.16-8.20 (2H, m), 8.22 (1H, d, J= 1.8 Hz), 12.84 (1H, br).
- To a solution of compound (A-2) (690 mg), oxalyl chloride (420 μl) in THF (150 ml) was added catalytic amount of DMF, and then the reaction solution was stirred at 70° C. for 1 h. The reaction solution was removed under reduced pressure, toluene was added to the resulting residue, and toluene was removed under reduced pressure. To the obtained carboxylic acid chloride was added THF (100 ml), and cooled at ice-cooling. To a solution of 28% ammonia aqueous solution (20 ml) was added ether and sodium hydroxide (5 g) at ice-cooling, and stirred for 10 min, and stranded. This ether solution was added to a THF solution of the acid chloride, and stirred at ice-cooling for 1 h. The reaction solution was partitioned between ethyl acetate and water. The organic layer was successively washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane-10/1 to ethyl acetate) to obtain compound (B-1) (400 mg) as colorless crystals.
- 1H NMR (DMSO-d6, δ ppm): 2.04 (3H, d, J= 1.5 Hz), 7.18 (1H, br), 7.32 (1H, s), 7.52-7.58 (2H, m), 7.60 (1H, br), 7.72 (1H, d, J= 8.1 Hz), 7.91 (1H, s), 7.94 (1H, dd. J= 2.1, 8.4 Hz), 8.14-8.19 (2H, m), 8.22 (1H, d, J= 2.4 Hz), 12.81 (1H, br).
-
- To a solution of 4-acetylbenzoic acid (1.64 g), oxalyl chloride (1.31 ml) in THF (100 ml) was added catalytic amount of DMF, and then the reaction mixture was stirred at room temperature for 2 h. The reaction solution was removed under reduced pressure, toluene was added to the resulting residue, and toluene was removed under reduced pressure. To the obtained carboxylic acid chloride was added THF (50 ml), tert-butyl alcohol (1.15 ml), and pyridine (1.21 ml), and the reaction mixture was heated under reflux for 40 h, and partitioned between ice-water acidified with hydrochloric acid and ethyl acetate. The ethyl acetate layer was washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane-175) to obtain compound (7) (2.0 g) as white crystals.
- 1H NMR (CDCl3, δ ppm): 1.61 (9H, s), 2.64 (3H, s), 7.96-7.00 (2H, m), 8.04-8.09 (2H, m).
- To a suspension of 60% sodium hydride (360 mg) in THF (100 ml) was added 2-phosphonopropionic acid triethyl (2.14 g) at ice-cooling. After the reaction mixture was stirred for 30 rain, added dropwise a solution of compound (7) (1.9 g) in THF (15 ml) at ice-cooling. The reaction solution was stirred at 50° C. for 3 h, and partitioned between ice-water acidified with hydrochloric acid and ethyl acetate. The ethyl acetate layer was washed with sodium bicarbonate aqueous solution, water, and brine, and dried over magnesium sulfate. The solvent was removed under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/15) to obtain compound (8) (1.0 g) as a colorless oil.
- 1H NMR(CDCl3, δ ppm): 1.35 (3H, t, J=7.2 Hz), 1.60 (9H, s), 1.74 (3H, q, J=1.5 Hz), 2.24 (3H, q, J= 1.5 Hz), 4.27 (2H, q, J= 6.9 Hz), 7.18-7.22 (2H, m), 7.97-8.10 (2H, m).
- A solution of compound (8) (900 mg) in formic acid (98-100%, 10 ml) was stirred at room temperature for 3 h. The reaction solution was concentrated, toluene was added to the residue, and concentrated again. The obtained residue was washed with n-hexane to obtain compound (9) (680 mg) as white crystals.
- 1H NMR (CDCl3, δ ppm): 1.36 (3H, t, J= 7.2 Hz), 1.74 (3H, q, J= 1.5 Hz), 2.26 (3H, q, J= 1.5 Hz), 4.28 (2H, q, J= 7.2 Hz), 7.25-7.29 (2H, m), 8.10-8.14 (2H, m).
- Compound (A-7) was synthesized from compound (9) as starting material in a manner similar to Step 4 of Example 1.
- 1H NMR (CDCl3, δ ppm): 1.36 (3H, t, J= 7.2 Hz), 1.74 (3H, q, J= 1.5 Hz), 2.25 (3H, q, J= 1.5 Hz), 4.28 (2H, q, J= 7.2 Hz), 7.26-7.29 (2H, m), 7.44 (1H, d, J=8.4 Hz), 7.61 (1H, dd, J= 2.1, 8.4 Hz), 7.91 (1H, d, J= 2.1 Hz), 7.91-7.95 (2H, m), 10.09 (1H, br).
- Compound (A-3) to (A-6), (A-8) to (A-107), (B-2) to (B-46), (C-1) to (C-5), (D-1), (E-1) to (E-2), (F-1) to (F-3), (G-1) to (G-8), (H-1) to (H-8) and (I-1) to (I-6) were synthesized in a manner similar to Example 1 and 2.
- Their physical data of compound group A were shown in Tables 1 to 10, compound group B in Tables 11 to 17, compound group C in Tables 18, compound group D in Tables 19, compound group E in Tables 20, compound group F in Tables 21, compound group G in Tables 22 to 23, compound group H in Tables 24 to 25, and compound group I in Tables 26.
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TABLE I Com- pound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-3 H H Et 1.28 (3H, t. J = 7.2 Hz), 4.22 (2H, q, J = 7.2 Hz), 6.80 (1H, d, J = 16.5 Hz), 7.72 (1H, d, J = 8.4 Hz); 7.73 (1H, d, J = 15.9 Hz), 7.88-7.93 (3H, m), 7.94 (1H, dd, J = 2.1, 8.7 Hz), 8.12-8.18 (2H, m), 8.21 (1H, d, J = 1.8 Hz), 12.84 (1H, s). A-4 H H H 6.70 (1H, d, J = 15.9 Hz), 7.67 (1H, d, J = 15.9 Hz), 7.72 (1H, d, J = 8.7 Hz), 7.84 (2H, m), 7.92 (1H, s), 7.95 (1H, dd, J = 1.8, 8.1 Hz), 8.12-8.18 (2H, m), 8.21 (1H, d, J = 2.1 Hz). 12.57 (1H, br), 12.84 (1H, s). A-5 H Et Et 1.13 (3H, t, J = 7.2 Hz), 1.30 (3H, t, J = 7.2 Hz), 2.50 (2H, q, J = 7.2 Hz), 4.24 (2H, q, J = 7.2 Hz), 7.577 (1H, s), 7.60-7.63 (2H, m), 7.72 (1H, d, J = 8.7 Hz), 7.92 (1H, s), 7.95 (1H, dd, J = 1.8, 8.4 Hz), 8.16-8.20 (2H, m), 8.21 (1H, d, J = 1.8 Hz) 12.85 (1H, br). A-6 H Et H 1.13 (3H, t, J = 7.5 Hz), 2.47 (2H, q, J = 7.2 Hz), 7.55-7.60 (2H, m), 7.61 (1H, s), 7.72 (1H, d, J = 8.4 Hz), 7.91 (1H, s), 7.95 (1H, dd, J = 2.1, 8.4 Hz), 8.15-8.20 (2H, m), 8.21 (1H, d, J = 2.1 Hz), 12.76 (1H, br). A-8 Me Me H 1.71 (3H, d, J = 1.5 Hz), 2.22 (3H, d, J = 1.2 Hz), 7.37-7.42 (2H, m), 7.73 (1H, d, J = 8.4 Hz), 7.92 (1H, s), 7.95 (1H, dd, J = 2.1, 8.4 Hz), 8.13-8.18 (2H, m), 8.22 (1H, d, J = 2.1 Hz), 12.77 (1H, br). A-9 H Me Et 1.29 (3H, t, J = 6.9 Hz), 2.10 (3H, d, J = 1.8 Hz), 4.23 (2H, q, J = 6.9 Hz), 7.48-7.57 (1H, m), 7.62- 7.68 (3H, m), 7.78-7.85 (2H, m), 7.93-8.10 (1H, m), 8.15-8.20 (2H, m), 12.85 (1H, br). A-10 H Me H 2.07 (3H, d, J = 1.5 Hz), 7.47-7.57 (1H, m), 7.62- 7.67 (3H, m), 7.79-7.85 (2H, m), 7.93-8.01 (1H, m), 8.15-8.20 (2H, m), 12.81 (1H, br). A-11 H Cl Et 1.33 (3H, t, J = 7.2 Hz), 4.83 (2H, q, J = 7.2 Hz), 7.72 (1H, d, J = 8.1 Hz), 7.93 (3H, s), 7.94 (1H, dd, J = 2.1, 8.1 Hz), 8.04 (2H, d, J = 8.7 Hz), 8.08 (1H, s), 8.21 (1H, d, J = 2.4 Hz), 8.21 (2H, d, J = 8.7 Hz), 12.91 (1H, s). A-12 H F Et 1.26 (3H, t, J = 7.5 Hz), 4.27 (2H, q, J = 7.5 Hz), 6.91 (1H, d, J = 21 Hz), 7.22 (1H, s), 7.42 (1H, d, J = 8.1 Hz), 7.55 (2H, d, J = 8.1 Hz), 7.69 (1H, dd, J = 1.8 Hz, 8.1 Hz), 7.87 (1H, d, J = 2.1 Hz), 7.87 (2H, d, J = 8.1 Hz), 10.15 (1H, s) -
TABLE 2 Com- pound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-13 H NH Z Me 3.64 (1H, s), 5.12 (2H, s), 6.55 (1H, s), 7.32 (2H, d, J = 8.4 Hz), 7.35-7.42 (5H, m), 7.72 (1H, d, J = 8.7 Hz), 7.94 (1H, dd, J = 1.8 Hz, 8.7 Hz), 8.06 (2H, d, J = 8.4 Hz), 8.21 (1H, d, J = 1.8 Hz), 9.39 (1H, s), 9.39 (1H, s), 12.86 (1H, s) A-14 H Cl H 7.73 (1H, d, J = 8.4 Hz), 7.94 (1H, s), 7.95 (1H, dd, J = 2.1, 8.4 Hz), 8.04 (2H, d, J = 8.1. Hz), 8.05 (1H, s), 8.21 (2H, d, J = 8.1 Hz), 8.22 (1H, d, J = 2.1 Hz), 12.90 (1H, s), 13.84 (1H, bs) A-15 H Br Me 3.55 (3H, s), 6.84 (1H, s), 7.56 (2H, d, J = 8.4 Hz), 7.72 (1H, d, J = 8.1 Hz), 7.93 (1H, s), 7.95 (1H, dd, J = 8.4, 2.1 Hz), 8.15 (2H, d, J = 8.4 Hz), 8.22 (1H, d, J = 2.1 Hz), 12.90 (1H, s) A-16 H Br H 6.72 (1H, s), 7.58 (2H, d, J = 8.4 Hz), 7.72 (1H, d, J = 8.4 Hz), 7.93 (1H, s), 7.95 (1H, dd, J = 8.4 Hz, 1.8 Hz), 8.12 (2H, d, J = 8.4 Hz), 8.22 (1H, d, J = 2.4 Hz), 12.97 (1H, s), 13.97 (1H, bs) A-17 H Me Et 7.15-7.21 (1H, m), 7.26-7.84 (6H, m), 7.47- 7.54 (1H, m), 7.87 (1H, s), 8.24 (2H, d, J = 8.5 Hz), 12.97 (1H, s), 13.97 (1H, bs) A-18 H Me H 2.07 (3H, d, J = 1.4 Hz), 7.12-7.21 (1H, m), 7.47- 7.54 (1H, m), 7.64 (2H, d, J = 8.5 Hz), 7.66 (1H, s), 7.74-7.78 (1H, m), 7.80-7.84 (1H, m), 7.85 (1H, s), 8.18 (2H, d, J = 8.5 Hz), 12.63 (1H, bs), 12.85 (1H, s) A-19 H Me Et 1.30 (3H, t, J = 7.1 Hz), 2.10 (3H, d, J = 1.4 Hz), 4.23 (2H, q, J = 7.1 Hz), 7.33-7.36 (1H, m), 7.58 (1H, t, J = 8.0 Hz), 7.65 (2H, d, J = 8.5 Hz), 7.67 (1H, s), 7.91 (1H, s), 7.93 (1H, bs), 7.99-8.02 (1H, m), 8.19 (2H, d, J = 8.5 Hz), 12.85 (1H, s) A-20 H Me H 2.07 (3H, d, J = 1.4 Hz), 7.33-7.36 (1H, m), 7.57- 7.66 (4H, m), 7.91 (1H, s), 7.94 (1H, m), 7.99- 8.02 (1H, m), 8.18 (2H, d, J = 8.5 Hz), 12.68 (1H, bs), 12.85 (1H, s) A-21 H Me Et 1.29 (3H, t, J = 7.1 Hz), 2.10 (3H, d, J = 1.7 Hz), 3.89 (3H, s), 4.23 (2H, q, J = 7.1 Hz), 7.22-7.28 (1H, m), 7.63-7.66 (4H, m), 7.74-7.80 (2H, m), 8.18 (2H, d, J = 8.5 Hz), 12.80 (1H, bs) A-22 H Me H 2.07 (3H, d, J = 1.4 Hz), 3.89 (3H, s), 7.22-7.28 (1H, m), 7.63-7.67 (4H, m), 7.75-7.81 (2H, m), 8.18 (2H, d, J = 8.5 Hz), 12.80 (1H, bs) A-23 H Me Et 1.29 (3H, t, J = 7.1 Hz), 2.10 (3H, d, J = 1.7 Hz), 4.23 (2H, q, J = 7.1 Hz), 7.26-7.32 (4H, m), 7.63- 7.66 (3H, m), 7.69 (1H, s), 7.97-8.02 (2H, m), 8.18 (2H, d, J = 8.5 Hz), 12.83 (1H, bs) A-24 H Me H 2.08 (3H, d, J = 1.1 Hz), 7.26-7.32 (2H, m), 7.64 (2H, d, J = 8.5 Hz), 7.06 (1H, s), 7.704 (1H, s), 7.98-8.03 (2H, m), 8.18 (2H, d, J = 8.5 Hz), 12.85 (1H, bs) -
TABLE 3 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-25 H Me Et 1.29 (3 H, t, J = 7.1 Hz), 2.10 (3 H, d, J = 1.4 Hz), 4.23 (2 H, q, J = 7.1 Hz), 7.64-7.67 (3 H, m), 7.83 (2 H, d, J = 8.5 Hz), 7.95 (1 H, s), 8.17-8.20 (4 H, m), 12.93 (1 H, bs) A-26 H Me H 2.07 (3 H, d, J = 1.1 Hz), 7.65 (2 H, d, J = 8.2 Hz), 7.66 (1 H, s), 7.83 (2 H, d, J = 8.5 Hz), 7.96 (1 H, s), 8.17 (2 H, d, J = 8.2 Hz), 8.18 (2 H, d, J = 8.5 Hz), 12.93 (1 H, s) A-27 H Me Et 1.29 (3 H, t, J = 7.1 Hz), 2.10 (3 H, d, J = 1.4 Hz), 4.23 (2 H, q, J = 7.1 Hz), 7.64-7.72 (5 H, m), 7.97 (1 H, s), 8.19 (2 H, d, J = 8.5 Hz), 8.25-8.28 (1 H, m), 8.33 (1 H, s), 12.80 (1 H, bs) A-28 H Me H 2.08 (3 H, d, J = 1.1 Hz), 7.68 (2 H, d, J = 8.2 Hz), 7.66 (1 H, s), 7.71 (1 H, d, J = 5.2 Hz), 7.91 (1 H, s), 8.18 (2 H, d, J = 8.2 Hz), 8.26-8.28 (1 H, m), 8.33 (1 H, bs), 12.87 (1 H, s) A-29 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.32 (2 H, q, J = 7.1 Hz), 7.15-7.21 (1 H, m), 7.47-7.54 (1 H, m), 7.81- 7.83 (1 H, m), 7.86 (1 H, s), 8.05 (2 H, d, J = 8.5 Hz), 8.09 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.92 (1 H, bs) A-30 H Cl H 7.16-7.21 (1 H, m), 7.47-7.54 (1 H, m), 7.75- 7.78 (1 H, m), 7.81-7.84 (1 H, m), 7.86 (1 H, s), 8.04 (2 H, d, J = 8.2 Hz), 8.06 (1 H, s), 8.21 (2 H, d, J = 8.2 Hz), 12.91 (1 H, s) A-31 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.33 (2 H, q, J = 7.1 Hz), 7.34-7.36 (1 H, m), 7.57-7.63 (1 H, m), 7.92 (1 H, s), 7.94 (1 H, s), 7.99-8.02 (1 H, m), 8.05 (2 H, d, J = 8.5 Hz), 8.08 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.92 (1 H, bs) A-32 H Cl H 7.33-7.36 (1 H, m), 7.57-7.63 (1 H, m), 7.93 (1 H, s), 7.93 (1 H, m), 8.04-8.06 (4 H, m), 8.21 (2 H, d, J = 8.2 Hz), 12.92 (1 H, s) A-33 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 3.88 (3 H, s), 4.33 (2 H, q, J = 7.1 Hz), 7.22-7.28 (1 H, m), 7.67 (1 H, s), 7.74- 7.80 (2 H, m), 8.05 (2 H, d, J = 8.5 Hz), 8.09 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.88 (1 H, bs) A-34 H Cl H 3.89 (3 H, s), 7.22-7.28 (1 H, m), 7.67 (1 H, s), 7.76-7.81 (2 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.87 (1 H, bs) A-35 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.32 (2 H, q, J = 7.1 Hz), 7.48-7.57 (1 H, m), 7.80-7.85 (1 H, m), 7.83 (1 H, s), 7.94-8.01 (1 H, m), 8.05 (2 H, d, J = 8.5 Hz), 8.08 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.91 (1 H, bs) A-36 H Cl H 7.48-7.58 (1 H, m), 7.80-7.85 (1 H, m), 7.83 (1 H, s), 7.94-8.01 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.92 (1 H, bs) -
TABLE 4 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-37 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.32 (2 H, q, J = 7.1 Hz), 7.26-7.32 (2 H, m), 7.71 (1 H, s), 7.98-8.02 (2 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.09 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.91 (1 H, bs) A-38 H Cl H 7.26-7.33 (2 H, m), 7.72 (1 H, s), 7.98-8.03 (2 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.92 (1 H, bs) A-39 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.32 (2 H, q, J = 7.1 Hz), 7.83 (2 H, d, J = 8.4 Hz), 7.97 (1 H, s), 8.05 (2 H, d, J = 8.5 Hz), 8.09 (1 H, s), 8.18 (2 H, d, J = 8.4 Hz), 8.22 (2 H, d, J = 8.5 Hz), 13.00 (1 H, s) A-40 H Cl H 7.83 (2 H, d, J = 8.5 Hz), 7.96 (1 H, s), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.18 (2 H, d, J = 8.5 Hz), 8.22 (2 H, d, J = 8.5 Hz), 12.97 (1 H, bs) A-41 H Cl Et 1.33 (3 H, t, J = 7.1 Hz), 4.33 (2 H, q, J = 7.1 Hz), 7.70-7.72 (2 H, m), 7.98 (1 H, s), 8.05 (2 H, d, J = 8.5 Hz), 8.09 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 8.25-8.28 (1 H, m), 8.33 (1 H, bs), 12.92 (1 H, s) A-42 H Cl H 7.70-7.72 (2 H, m), 7.98 (1 H, s), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 8.24-8.28 (1 H, m), 8.33 (1 H, bs), 12.92 (1 H, bs) A-43 H F H 7.15 (1 H, d, J = 36.3 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.86 (2 H, d, J = 8.7 Hz), 7.97-7.94 (2 H, m), 8.18 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.89 (1 H, s) A-44 H F H 7.20 (1 H, d, J = 23.1 Hz), 7.68 (2 H, d, J = 8.5 Hz), 7.70 (1 H, s), 7.97 (1 H, s), 8.12 (2 H, d, J = 8.5 Hz), 8.25-8.28 (1 H, m), 8.33 (1 H, bs), 12.84 (1 H, bs) A-45 H F H 7.19 (1 H, d, J = 22.8 Hz), 7.33-7.56 (1 H, m), 7.57-7.63 (1 H, m), 7.68 (2 H, d, J = 8.5 Hz), 7.91 (1 H, s), 7.94 (1 H, bs), 7.99-8.02 (1 H, m), 8.11 (2 H, d, J = 8.5 Hz), 12.83 (1 H, bs) A-46 H F H 7.20 (1 H, d, J = 22.9 Hz), 7.68 (2 H, d, J = 8.5 Hz), 7.83 (2 H, d, J = 8.5 Hz), 7.96 (1 H, s), 8.12 (2 H, d, J = 8.5 Hz), 8.18 (2 H, d, J = 8.5 Hz), 12.91 (1 H, s), 13.87 (1 H, bs) A-47 H Cl H 7.39-7.45 (1 H, m), 7.48-7.54 (2 H, m), 7.67- 7.73 (3 H, m), 7.77-7.81 (2 H, m), 8.03-8.07 (3 H, m), 8.19-8.25 (3 H, m) A-48 H Cl H 1.32 (9 H, s), 7.47 (2 H, d, J = 9.0 Hz), 7.64 (1 H, s), 7.89 (2 H, d, J = 9.0 Hz), 8.01-8.06 (3 H, m), 8.22 (2 H, d, J = 8.1 Hz), 12.89 (1 H, s), 13.90 (1 H, bs) A-49 H Cl H 0.87 (3 H, t, J = 7.2 Hz), 1.26-1.36 (4 H, m), 1.60 (2 H, quint, J = 7.8 Hz), 2.60 (2 H, t, J = 7.5 Hz), 7.27 (2 H, d, J = 8.4 Hz), 7.64 (1 H, s), 7.87 (2 H, d, J = 8.1 Hz), 8.02-8.05 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.88 (1 H, s), 13.79 (1 H, bs) -
TABLE 5 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-50 H Cl H 7.30-7.46 (3 H, m), 7.63 (1 H, d, J = 2.4 Hz), 8.03- 8.07 (3 H, m), 8.12 (1 H, td, J = 1.8 Hz, 7.8 Hz), 8.22 (2 H, d, J = 8.7 Hz), 12.93 (1 H, s), 13.85 (1 H, bs) A-51 H Cl H 7.19-7.28 (2 H, m), 7.47-7.57 (2 H, m), 8.01- 8.05 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.97 (1 H, s), 13.80 (1 H, bs) A-52 H Cl H 3.82 (3 H, s), 6.89-6.94 (1 H, m), 7.36 (1 H, t, J = 8.1 Hz), 7.53-7.56 (2 H, m), 7.75 (1 H, s), 8.02- 8.06 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.88 (1 H, s), 13.82 (1 H, bs) A-53 H Cl H 6.60 (1 H, dd, J = 1.8 Hz, 3.3 Hz), 6.75 (1 H, d, J = 3.3 Hz), 7.44 (1 H, s), 7.75 (1 H, d, J = 1.8 Hz), 8.01-8.04 (3 H, m), 8.21 (2 H, d, J = 8.7 Hz) A-54 H Cl H 7.37 (1 H, m), 7.49-7.58 (3 H, m), 7.65 (1 H, dt, J = 1.8 Hz, 8.1 Hz), 7.71-7.76 (2 H, m), 7.88 (1 H, s), 7.97 (1 H, dt, J = 1.8 Hz, 7.5 Hz), 8.03-8.06 (3 H, m), 8.23 (2 H, d, J = 7.8 Hz), 8.28 (1 H, t, J = 1.8 Hz), 12.90 (1 H, s), 13.82 (1 H, bs) A-55 H Cl H 0.92 (3 H, t, J = 7.5 Hz), 1.34 (2 H, sext, J = 7.5 Hz), 1.60 (2 H, quint, J = 7.5 Hz), 2.64 (2 H, t, J = 7.5 Hz), 7.17 (1 H, d, J = 7.8 Hz), 7.35 (1 H, t, J = 7.5 Hz), 7.70 (1 H, s), 7.76 (1 H, d, J = 7.8 Hz), 7.81 (1 H, s), 8.02-8.05 (3 H, m), 8.22 (2 H, d, J = 8.4 Hz) 12.86 (1 H, s), 13.84 (1 H, bs) A-56 H Cl H 7.24 (1 H, dt, J = 5.8 Hz, 2.5 Hz), 7.40 (1 H, ddd, J = 11.9 Hz, 9.4 Hz, 2.5 Hz), 7.59 (1 H, d, J = 2.5 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.09-8.20 (1 H, m), 8.21 (2 H, d, J = 8.5 Hz), 12.93 (1 H, s), 13.82 (1 H, bs) A-57 H Cl H 7.55 (1 H, t, J = 8.0 Hz), 7.77-781 (2 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 8.37-8.42 (1 H, m), 12.99 (1 H, s), 13.85 (1 H, bs) A-58 H Cl H 7.22-7.30 (1 H, m), 7.37-7.46 (1 H, m), 7.72 (1 H, d, J = 2.5 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s), 13.82 (1 H, bs) A-59 H Cl H 0.92-0.97 (3 H, m), 1.41-1.49 (2 H, m), 1.67- 1.75 (2 H, m), 4.01 (2 H, t, J = 6.3 Hz), 7.00 (2 H, d, J = 8.5 Hz), 7.54 (1 H, s), 7.87 (2 H, d, J = 8.5 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.85 (1 H, s), 13.76 (1 H, bs) A-60 H Cl H 7.74-7.76 (1 H, m), 7.82 (1 H, d, J = 2.7 Hz), 7.80- 7.84 (1 H, m), 8.03-8.05 (3 H, m), 8.22 (2 H, d, J = 8.5 Hz), 8.31 (1 H, t, J = 7.6 Hz), 13.01 (1 H, s), 13.79 (1 H, bs) A-61 H Cl H 3.83 (3 H, s), 6.91-6.98 (2 H, m), 7.45 (1 H, d, J = 2.5 Hz), 8.00 (4 H, m), 8.21 (2 H, d, J = 8.5 Hz), 12.88 (1 H, s), 13.81 (1 H, bs) -
TABLE 6 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-62 H Cl H 7.68 (1 H, d, J = 2.5 Hz), 7.68-7.76 (1 H, m), 7.80- 8.07 (4 H, m), 8.20 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s) A-63 H Cl H 7.48 (1 H, t, J = 8.8 Hz), 7.85 (1 H, s), 7.98-8.03 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 8.30 (1 H, dd, J = 6.9 Hz, 2.2 Hz), 12.88 (1 H, s), 13.82 (1 H, bs) A-64 H Cl H 0.89 (6 H, d, J = 6.7 Hz), 1.87 (1 H, seven, J = 6.7 Hz), 2.48 (2 H, d, J = 7.3 Hz), 7.23 (2 H, d, J = 8.2 Hz), 7.64 (1 H, s), 7.87 (2 H, d, J = 8.2 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.88 (1 H, s), 13.79 (1 H, bs) A-65 H Cl H 8.02-8.05 (4 H, m), 8.05 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 8.27 (1 H, s), 8.64 (2 H, s), 12.94 (1 H, s), 13.84 (1 H, bs) A-66 H Cl H 3.86 (3 H, s), 7.17 (1 H, t, J = 7.5 Hz), 7.25 (1 H, t, J = 7.5 Hz), 7.38 (1 H, s), 7.50 (1 H, d, J = 8.4 Hz), 7.78 (1 H, s), 8.03-8.06 (3 H, m), 8.17 (1 H, d, J = 7.8 Hz), 8.22 (2 H, d, J = 8.4 Hz), 12.79 (1 H, bs) A-67 H Cl H 2.85 (6 H, s), 3.52 (2 H, t, J = 5.4 Hz), 4.41 (2 H, t, J = 5.4 Hz), 7.09 (2 H, d, J = 8.7 Hz), 7.60 (1 H, s), 7.93 (2 H, d, J = 8.7 Hz), 8.01-8.05 (3 H, m), 8.21 (2 H, d, J = 8.7 Hz), 12.84 (1 H, bs) A-68 H F H 7.15 (1 H, d, J = 36 Hz), 7.24-7.33 (2 H, m), 7.70 (1 H, s), 7.86 (2 H, d, J = 8.4 Hz), 7.96-8.03 (2 H, m), 8.18 (2 h, d, J = 8.7 Hz), 12.86 (1 H, s) A-69 H Cl H 7.57 (1 H, dd, J = 8.7 Hz, 1.8 Hz), 7.67 (1 H, d, J = 2.4 Hz), 7.70 (1 H, dd, J = 11.4 Hz, 2.1 Hz), 8.02- 8.09 (4 H, m), 8.21 (2 H, d, J = 8.7 Hz), 12.97 (1 H, s), 13.69 (1 H, bs) A-70 H Cl H 2.36 (3 H, s), 7.13-7.19 (2 H, m), 7.54-7.55 (1 H, m), 7.98-8.06 (4 H, m), 8.22 (2 H, d, J = 8.4 Hz), 12.89 (1 H, s), 13.80 (1 H, bs) A-71 H Cl H 7.39-7.45 (1 H, m), 7.51 (2 H, t, J = 7.8 Hz), 7.67- 7.72 (3 H, m), 7.79 (2 H, d, J = 8.4 Hz), 8.03-8.07 (3 H, m), 8.19-8.25 (3 H, m), 12.97 (1 H, s), 13.86 (1 H, bs) A-72 H Cl H 7.30-7.48 (2 H, m), 7.72 (1 H, d, J = 2.4 Hz), 7.88- 7.93 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.96 (1 H, s), 13.83 (1 H, bs) A-73 H Cl H 2.00-2.10 (2 H, m), 2.86-2.94 (4 H, m), 7.29 (1 H, d, J = 7.7 Hz), 7.61 (1 H, s), 7.72-7.75 (1 H, m), 7.82 (1 H, s), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.84 (1 H, s), 13.84 (1 H, bs) -
TABLE 7 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-74 H Cl H 3.24 (2 H, t, J = 8.5 Hz), 4.57 (2 H, t, J = 8.8 Hz), 6.83 (1 H, d, J = 8.2 Hz), 7.49 (1 H, s), 7.73 (1 H, dd, J = 8.2 Hz, 1.6 Hz), 7.82 (1 H, s), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.20 (2 H, d, J = 8.5 Hz), 12.83 (1 H, bs) A-75 H Cl H 7.51 (1 H, t, J = 9.1 Hz), 7.86 (1 H, s), 7.95-8.00 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.16 (1 H, dd, J = 7.4 Hz, 2.2 Hz), 8.22 (2 H, d, J = 8.5 Hz), 12.90 (1 H, bs) A-76 H Cl H 7.46 (2 H, d, J = 8.8 Hz), 7.72 (1 H, s), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.09 (2 H, d, J = 8.8 Hz), 8.22 (2 H, d, J = 8.5 Hz), 12.96 (1 H, s), 13.86 (1 H, bs) A-77 H Cl H 7.76 (1 H, d, J = 2.4 Hz), 7.81-7.91 (1 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.04 (1 H, s), 8.20 (2 H, d, J = 8.5 Hz), 12.95 (1 H, s), 13.81 (1 H, s) A-78 H Cl H 2.52 (3 H, s), 7.34 (2 H, d, J = 8.5 Hz), 7.69 (1 H, s), 7.91 (2 H, d, J = 8.5 Hz), 8.04 (2 H, d, J = 8.8 Hz), 8.06 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.91 (1 H, bs) A-79 H Cl H 7.58-7.64 (1 H, m), 7.79 (1 H, d, J = 2.5 Hz), 7.79- 7.83 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 8.52 (1 H, dd, J = 6.9 Hz, 2.2 Hz), 12.93 (1 H, s), 13.72 (1 H, bs) A-80 H Cl H 7.39-7.55 (5 H, m), 7.56-7.62 (2 H, m), 8.05 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.13 (1 H, td, J = 7.8 Hz, 1.8 Hz), 8.23 (2 H, d, J = 8.5 Hz), 12.96 (1 H, s), 13.82 (1 H, bs) A-81 H Cl H 7.30 (1 h, t, J = 8.1 Hz), 7.68-7.74 (2 H, m), 8.02- 8.05 (3 H, m), 8.10 (1 H, td, J = 7.8 Hz, 1.8 Hz), 8.21 (2 H, d, J = 8.7 Hz), 12.96 (1 H, s), 13.82 (1 h, bs) A-82 H Cl H 3.89 (2 H, s), 7.14-7.27 (2 H, m), 7.60-7.68 (2 H, m), 8.02-8.06 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.92 (1 H, s), 13.80 (1 H, bs) A-83 H Cl H 2.32 (3 H, d, J = 1.8 Hz), 7.21 (1 H, t, J = 7.5 Hz), 7.25-7.31 (1 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.94 (1 H, td, J = 7.5 Hz, 1.8 Hz), 8.02-8.06 (3 H, m), 8.21 (2 H, d), 12.91 (1 H, s), 13.80 (1 H, bs) A-84 H Cl H 0.84-0.90 (3 H, m), 1.30-1.37 (4 H, m), 1.56- 1.66 (2 H, m), 2.68 (2 H, t, J = 7.3 Hz), 7.20-7.30 (2 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.95 (1 H, td, J = 7.3 Hz, 2.1 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.88 (1 H, s), 13.89 (1 H, bs) -
TABLE 8 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A85 H Cl H 0.86-0.90 (3 H, m), 1.30-1.37 (4 H, m), 1.56- 1.66 (2 H, m), 2.65 (2 H, t, J = 7.6 Hz), 7.18-7.24 (1 H, m), 7.69 (1 H, s), 7.79-7.84 (1 H, m), 7.87- 7.91 (1 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s), 14.00 (1 H, bs) A-86 H Cl H 7.28 (1 H, td, J = 9.1 Hz, 1.8 Hz), 7.64 (1 H, s), 7.81-7.89 (1 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.20 (2 H, d, J = 8.5 Hz), 13.01 (1 H, s), 13.93 (1 H, bs) A-87 H Cl H 2.31 (3 H, s), 2.41 (3 H, s), 7.08 (1 H, dd, J = 7.7 Hz, 1.4 Hz), 7.18 (1 H, d, J = 7.7 Hz), 7.33 (1 H, s), 7.49 (1 H, d, J = 1.4 Hz), 8.05 (2 H, d, J = 8.5 Hz), 8.20 (2 H, d, J = 8.5 Hz), 12.85 (1 H, bs) A-88 H Cl H 7.31-7.44 (3 H, m), 7.49 (td, J = 7.5 Hz, 1.8 Hz), 7.62-7.68 (3 H, m), 8.03-8.06 (3 H, m), 8.12 (1 H, td, J = 7.5 Hz, 1.8 Hz), 8.22 (2 H, d, J = 8.4 Hz), 12.96 (1 H, s), 13.81 (1 H, bs) A-89 H Cl H 7.31-7.37 (1 H, m), 7.41-7.66 (7 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 13.00 (1 H, bs) A-90 H Cl H 7.49 (1 H, s), 7.70 (1 H, d, J = 8.5 Hz), 8.02-8.10 (4 H, m), 8.19 (2 H, d, J = 8.5 Hz), 12.97 (1 H, s), 13.82 (1 H, bs) A-91 H Cl H 7.48 (1 H, t, J = 7.9 Hz), 7.69 (1 H, dd, J = 7.9 Hz, 1.5 Hz), 7.74 (1 H, s), 7.81 (1 H, dd, J = 7.9 Hz, 1.8 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.21 2 H, d, J = 8.5 Hz), 12.99 (1 H, s), 13.87 (1 H, bs) A-92 H Cl H 7.47 (1 H, dd, J = 8.6 Hz, 2.7 Hz), 7.62 (1 H, d, J = 8.4 Hz), 7.88 (1 H, s), 8.02-8.05 (4 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.93 (1 H, s), 13.88 (1 H, bs) A-93 H Cl H 0.86 (3 H, t, J = 6.9 Hz), 1.27-1.30 (6 H, m), 1.55- 1.62 (2 H, m), 2.68 (2 H, t, J = 7.5 Hz), 7.19-7.30 (2 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.94 (1 H, dt, J = 7.0 Hz, 2.0 Hz), 8.03 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s), 13.86 (1 H, bs) A-94 H Cl H 13.70 (bs, 1 H), 12.93 (bs, 1 H), 8.21 (d, 2 H, J = 8.2 Hz), 8.06 (s, 1 H), 8.04 (d, 2 H, J = 8.2 Hz), 7.94 (dt, 1 H, J = 7.5, 2.0 Hz), 7.61 (d, 1 H, J = 2.7 Hz), 7.32 (m, 1 H), 7.25 (t, 1 H, J = 7.5 Hz), 2.90 (m, 1 H), 1.20-1.90 (m, 10 H) A-95 H Cl H 0.85-0.89 (3 H, m), 1.27-1.35 (4 H, m), 1.53- 1.60 (2 H, m), 2.63 (2 H, t, J = 7.7 Hz), 7.11-7.17 (1 H, m), 7.34-7.41 (1 H, m), 7.51 (1 H, s), 8.03 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.20 (2 H, d, J = 8.5 Hz), 12.96 (1 H, s), 13.78 (1 H, bs) -
TABLE 9 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-96 H Cl H 0.96 (3 H, t, J = 7.4 Hz), 1.41-1.54 (2 H, m), 1.70- 1.78 (2 H, m), 4.08 (2 H, t, J = 6.4 Hz), 7.13-7.24 (2 H, m), 7.61-7.66 (2 H, m), 8.03 (2 H, d, J = 8.6 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.6 Hz), 12.92 (1 H, s), 13.81 (1 H, bs) A-97 H Cl H 1.23 (3 H, t, J = 7.5 Hz), 2.72 (2 H, q, J = 7.5 Hz), 7.21-7.33 (2 H, m), 7.61 (1 H, d, J = 2.5 Hz), 7.95 (1 H, dd, J = 7.5 Hz, 2.0 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s), 13.85 (1 H, bs) A-98 H Cl H 0.88 (6 H, d, J = 6.6 Hz), 1.19-1.26 (2 H, m), 1.53- 1.66 (3 H, m), 2.66 (2 H, t, J = 7.7 Hz), 7.20- 7.30 (2 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.95 (1 H, dd, J = 7.5 Hz, 2.2 Hz), 8.04 (2 H, d, J = 8.4 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.4 Hz), 12.92 (1 H, s), 13.86 (1 H, bs) A-99 H Cl H 0.94 (3 H, t, J = 7.5 Hz), 1.63 (2 H, sext, J = 7.5 Hz), 2.67 (2 H, t, J = 2.67 Hz), 7.20-7.31 (2 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.95 (1 H, td, J = 7.5 Hz, 24 Hz), 8.02-8.06 (3 H, m), 8.22 (2 H, d, J = 8.4 Hz), 12.92 (1 H, s), 13.79 (1 H, bs) A-100 H Cl H 0.92 (3 H, t, J = 7.5 Hz), 1.35 (2 H, sext, J = 7.5 Hz), 1.59 (2 H, quint, J = 7.5 Hz), 2.69 (2 H, t, J = 7.5 Hz), 7.19-7.30 (2 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.94 (1 H, td, J = 8.2 Hz, 2.4 Hz), 7.99-8.06 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.92 (1 H, s), 13.80 (1 H, bs) A-101 H Cl H 0.98 (1 H, t, J = 7.5 Hz), 1.60 (2 H, sext, J = 7.5 Hz), 2.77-2.83 (2 H, m), 7.59 (1 H, d, J = 8.4 Hz), 7.66 (1 H, d, J = 3.0 Hz), 7.91 (1 H, t, J = 8.4 Hz), 8.01-8.07 (3 H, m), 8.21 (2 H, d, J = 8.7 Hz), 12.94 (1 H, s), 13.80 (1 H, bs) A-102 H Cl H 7.46 (1 H, t, J = 8.1 Hz), 7.54-7.60 (2 H, m), 7.70 (1 H, d, J = 2.7 Hz), 7.99-8.07 (4 H, m), 8.17 (1 H, dd, J = 8.2 Hz, 1.8 Hz), 8.21 (2 H, d, J = 8.4 Hz), 8.66 (1 H, bs), 8.83 (1 H, bs), 12.97 (1 H, s) A-103 H Cl H 1.39 (3 H, t, J = 7.0 Hz), 4.15 (2 H, q, J = 7.0 Hz), 7.13-7.25 (2 H, m), 7.62-7.67 (2 H, m), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.94 (1 H, s), 13.86 (1 H, bs) A-104 H Cl H 2.89-2.98 (4 H, m), 7.17-7.61 (7 H, m), 7.61 (1 H, d, J = 2.5 Hz), 7.95 (1 H, dt, J = 7.4 Hz, 2.2 Hz), 8.04 (2 H, d, J = 8.6 Hz), 8.05 (1 H, s), 8.21 (2 H, d, J = 8.6 Hz), 12.92 (1 H, s), 13.86 (1 H, bs) A-105 H Cl H 0.97 (9 H, s), 1.45-1.50 (2 H, m), 2.62-2.68 (2 H, m), 7.19-7.30 (2 H, m), 7.62 (1 H, d, J = 2.4 Hz), 7.94 (1 H, dt, J = 7.5 Hz, 2.1 Hz), 8.04 (2 H, d, J = 8.5 Hz), 8.06 (1 H, s), 8.22 (2 H, d, J = 8.5 Hz), 12.92 (1 H, s), 13.85 (1 H, bs) -
TABLE 10 Compound No. R6 R1 R2 R5 1H-NMR (DMSO d-6) A-106 H Cl H 1.10 (3 H, t, J = 6.9 Hz), 2.93 (2 H, t, J = 6.9 Hz), 3.46 (2 H, q, J = 6.9 Hz), 3.62 (2 H, t, J = 6.9 Hz), 7.24 (1 H, t, J = 7.5 Hz), 7.33 (1 H, td, J = 7.2 Hz, 1.8 Hz), 7.61 (1 H, d, J = 2.7 Hz), 7.97 (1 H, td, J = 7.2 Hz, 1.8 Hz), 8.02-8.06 (3 H, m), 8.21 (2 H, d, J = 8.4 Hz), 12.93 (1 H, s), 13.89 (1 H, bs) A-107 H Cl H 4.06 (2 H, s), 7.18-7.35 (7 H, m), 7.61 (1 H, d, J = 2.7 Hz), 7.98 (1 H, td, J = 7.5 Hz, 2.1 Hz), 8.02- 8.05 (3 H, m), 8.21 (2 H, d, J = 8.7 Hz), 12.92 (1 H, s), 13.86 (1 H, bs) -
TABLE 11 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-2 H H —NH2 6.77 (1 H, d, J = 15.9 Hz), 7.20 (1 H, br), 7.50 (1 H, d, J = 15.9 Hz), 7.60 (1 H, br), 7.72 (1 H, d, J = 8.7 Hz), 7.72-7.76 (2 H, m), 7.91 (1 H, s), 7.95 (1 H, dd, J = 1.8, 8.4 Hz), 8.14-8.18 (2 H, m), 8.22 (1 H, d, J = 1.8 Hz), 12.82 (1 H, br). B-3 H H —NHMe 2.73 (3 H, d, J = 4.8 Hz), 6.75 (1 H, d, J = 15.6 Hz), 7.50 (1 H, d, J = 15.6 Hz), 7.72 (1 H, d, J = 8.1 Hz), 7.72-7.75 (2 H, m), 7.91 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.09-8.18 (3 H, m), 8.21 (1 H, d, J = 2.1 Hz), 12.81 (1 H, br). B-4 H Me —NHMe 2.06 (3 H, d, J = 1.5 Hz), 2.72 (3 H, t, J = 4.5 Hz), 7.27 (1 H, s), 7.53-7.58 (2 H, m), 7.72 (1 H, d, J = 8.7 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 1.8, 8.1 Hz), 8.07 (1 H, q, J = 4.2 Hz), 8.13-8.18 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.81 (1 H, s). B-5 H Me —N(Me)2 2.05 (3 H, d, J = 1.5 Hz), 3.32 (6 H, s), 6.57 (1 H, s), 7.54-7.58 (2 H, m), 7.72 (1 H, d, J = 8.4 Hz), 7.91 (1 H, s), 7.95 (1 H, dd, J = 1.8, 8.4 Hz), 8.13-8.18 (2 H, m), 8.22 (1 H, d, J 1.8 Hz), 12.79 (1 H, br). B-6 H Me —NHEt 1.10 (3 H, t, J = 7.2 Hz), 2.05 (3 H, d, J = 1.2 Hz), 3.17-3.26 (1 H, m), 7.25 (1 H, s), 7.54-7.58 (2 H, m), 7.72 (1 H, d, J = 8.4 Hz), 7.91 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.1 Hz), 8.09 (1 H, t, J = 5.4 Hz), 8.13- 8.18 (2 H, m), 8.21 (1 H, d, J = 2.1 Hz), 12.80 (1 H, s). B-7 H Me —NH(n-Pr) 0.89 (3 H, t, J = 7.2 Hz), 1.51 (2 H, sextet, d = 7.2 Hz), 2.06 (3 H, d, J = 1.5 Hz), 3.11- 3.18 (2 H, m), 7.25 (1 H, s), 7.54-7.59 (2 H, m), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.10 (1 H, t, J = 5.4 Hz), 8.14-8.19 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.82 (1 H, s). B-8 H Me 2.06 (3 H, d, J = 1.2 Hz), 3.53-3.58 (4 H, m), 3.60-3.64 (4 H, m), 6.60 (1 H, s), 7.54- 7.61 (2 H, m), 7.72 (1 H, d, J = 8.7 Hz), 7.91 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.7 Hz), 8.13-8.19 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.80 (1 H, br). -
TABLE 12 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-9 H Me —NHBn 2.10 (3 H, d, J = 1.5 Hz), 4.41 (2 H, d, J = 6.0 Hz), 7.52-7.38 (6 H, m), 7.56-7.61 (2 H, m), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.14-8.20 (2 H, m), 8.22 (1 H, d, J = 2.4 Hz), 12.82 (1 H, br). B-10 H Me 2.22 (3 H, t, J = 1.2 Hz), 7.34 (1 H, dt, J = 1.2, 8.1 Hz), 7.47 (1 H, dt, J = 1.2, 8.4 Hz), 7.65-7.71 (3 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.78 (1 H, d, J = 7.8 Hz), 7.94 (1 H, s), 7.96 (1 H, dd, J = 2.1, 8.4 Hz), 8.02 (1 H, d, J = 8.2 Hz), 8.19-8.24 (3 H, m), 12.63 (1 H, br), 12.89 (1 H, br). B-11 H Me 2.18 (3 H, d, J = 1.5 Hz), 7.27 (1 H, d, J = 2.4 Hz), 7.56 (1 H, d, J = 3.3 Hz), 7.59 (1 H, br), 7.63-7.68 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.96 (1 H, dd, J = 2.1, 8.4 Hz), 8.17-8.22 (2 H, m), 8.23 (1 H, d, J = 2.1 Hz), 12.36 (1 H, br), 12.87 (1 H, br). B-12 H Me 2.18 (3 H, d, J = 1.2 Hz), 7.37-7.43 (2 H, m), 7.64-7.69 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.94 (1 H, s), 7.96 (1 H, dd, J = 1.8, 8.4 Hz), 8.15 (1 H, td, J = 1.5, 6.9 Hz), 8.18-8.24 (3 H, m), 8.31 (1 H, dd, J = 1.5, 4.5 Hz) 8.89 (1 H, d, J = 2.4 Hz), 12.87 (1 H, br). B-13 H Me 2.11 (3 H, d, J = 1.2 Hz), 4.49 (2 H, d, J = 6.0 Hz), 7.36 (1 H, br), 7.52-7.62 (4 H, m), 7.69-7.74 (3 H, m), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.1 Hz), 8.15-8.20 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 8.79 (1 H, t, J = 6.3 Hz), 12.83 (1 H, br). B-14 H Me 2.09 (3 H, d, J = 1.2 Hz), 4.38 (2 H, d, J = 5.7 Hz), 7.13-7.20 (2 H, m), 7.32-7.39 (3 H, m), 7.55-7.61 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.14-8.19 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 8.71 (1 H, t, J = 6.0 Hz), 12.84 (1 H, br). B-15 H Me 2.08 (3 H, d, J = 1.5 Hz), 4.55 (2 H, d, J = 5.7 Hz), 6.96-7.03 (2 H, m), 7.31 (1 H, br), 7.40 (1 H, dd, J = 1.5, 5.4 Hz), 7.55- 7.60 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.14-8.19 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 8.80 (1 H, t, J = 6.0 Hz), 12.84 (1 H, br). -
TABLE 13 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-16 H Me 2.07 (3 H, d, J = 1.2 Hz), 4.39 (2 H, d, J = 5.7 Hz), 6.28 (1 H, d, J = 3.6 Hz), 6.41 (1 H, dd, J = 1.8, 3.3 Hz), 7.30 (1 H, br), 7.55-7.61 (3 H, m), 7.73 (1 H, d, J = 8.1 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.14-8.18 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 8.63 (1 H, t, J = 6.0 Hz), 12.84 (1 H, br). B-17 H Et —NH2 1.07 (3 H, t, J = 7.2 Hz), 2.47 (2 H, q, J = 7.2 Hz), 7.20 (2 H, br), 7.48-7.53 (2 H, m), 7.65 (1 H, br), 7.73 (1 H, d, J = 8.1 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.13-8.18 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, br). B-18 H Et —NHMe 1.05 (3 H, t, J = 7.5 Hz), 2.48 (2 H, q, J = 7.5 Hz), 2.72 (2 H, d, J = 4.5 Hz), 7.11 (1 H, s), 7.48-7.53 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.4, 8.1 Hz), 8.08-8.18 (3 H, m), 8.22 (1 H, d, J = 2.4 Hz), 12.82 (1 H, br). B-19 H Et —NHEt 1.05 (3 H, t, J = 7.5 Hz), 1.10 (3 H, t, J = 7.2 Hz), 2.48 (2 H, q, J = 7.2 Hz), 3.16- 3.26 (2 H, m), 7.09 (1 H, s), 7.48-7.53 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.14-8.20 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.84 (1 H, br). B-20 H Et —NHBn 1.08 (3 H, t, J = 7.5 Hz), 2.52 (2 H, q, J = 7.8 Hz), 4.41 (2 H, d, J = 6.3 Hz), 7.18 (1 H, s), 7.22-7.40 (5 H, m), 7.50-7.54 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 1.8, 8.4 Hz), 8.14-8.18 (2 H, m), 8.22 (1 H, d, J = 1.8 Hz), 8.75 (1 H, t, J = 6.0 Hz), 12.84 (1 H, br). B-21 Me Me —NH2 1.70 (3 H, d, J = 1.2 Hz), 2.04 (3 H, d, J = 1.2 Hz), 7.21 (1 H, br), 7.35-7.41 (2 H, m), 7.52 (1 H, br), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.13-8.18 (2 H, m), 8.22 (1 H, d, J = 1.8 Hz), 12.80 (1 H, br). B-22 Me Me —NHMe 1.69 (3 H, d, J = 1.2 Hz), 1.99 (3 H, d, J = 1.5 Hz), 2.69 (3 H, d, J = 4.5 Hz), 7.36- 7.41 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 7.99 (1 H, q, J = 4.8 Hz), 8.13- 8.18 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.80 (1 H, br). -
TABLE 14 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-23 Me Me —NHEt 1.10 (3 H, t, J = 7.2 Hz), 1.69 (3 H, d, J = 1.2 Hz), 2.00 (3 H, d, J = 1.5 Hz), 3.14- 3.23 (2 H, m), 7.36-7.41 (2 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1, 8.4 Hz), 8.06 (1 H, t, J = 5.4 Hz), 8.13-8.17 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.80 (1 H, br). B-24 Me Me —NHBn 1.73 (3 H, d, J = 1.5 Hz), 2.00 (3 H, d, J = 1.5 Hz), 4.39 (2 H, d, J = 5.7 Hz), 7.22- 7.42 (7 H, m), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 1.8, 8.4 Hz), 8.12-8.18 (2 H, m), 8.22 (1 H, d, J = 1.8 Hz), 8.62 (1 H, t, J = 6.3 Hz), 12.80 (1 H, br). B-25 H Me —NH2 2.04 (3 H, d, J = 1.2 Hz), 7.20 (1 H, br), 7.32 (1 H, br), 7.48-7.64 (4 H, m), 7.79- 7.86 (2 H, m), 7.94-8.02 (1 H, m), 8.14- 8.18 (2 H, m), 12.83 (1 H, br). B-26 H Me —NHMe 2.06 (3 H, d, J = 1.2 Hz), 2.72 (3 H, d, J = 4.8 Hz), 7.26 (1 H, s), 7.47-7.58 (3 H, m), 7.78-7.87 (2 H, m), 7.94-8.02 (1 H, m), 8.08 (1 H, q, J = 4.5 Hz) 8.13-8.18 (2 H, m), 12.82 (1 H, br). B-27 H Me —NH(CH2)2—N(CH3)2 2.05 (3 H, d, J = 1.2 Hz), 2.19 (6 H, s), 2.39 (2 H, t, J = 6.9 Hz), 3.28 (2 H, q, J = 6.9 Hz), 7.26 (1 H, br), 7.55 (2 H, d, J = 8.7 Hz), 7.72 (1 H, d, J = 8.1 Hz), 7.91 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.1 Hz), 8.01 (1 H, t, J = 5.7 Hz), 8.16 (2 H, d, J = 8.7 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, br) B-28 H Me —NH(CH2)2—COOH 2.05 (3 H, d, J = 1.5 Hz), 2.49 (3 H, t, J = 7.5 Hz), 3.39 (2 H, q, J = 6.0 Hz), 7.26 (1 H, br), 7.56 (2 H, d, J = 8.7 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 1.8 Hz, 8.4 Hz), 8.16 (2 H, d, J = 8.7 Hz), 8.22 (1 H, d, J = 1.8 Hz), 12.90 (2 H, br) B-29 H Me —NHN(CH3)2 2.05 (3 H, s), 2.56 (6 H, s), 7.14 (1 H, s), 7.56 (2 H, d, J = 8.1 Hz), 7.73 (1 H, d, J = 8.1 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 1.8 Hz, 8.1 Hz), 8.16 (2 H, d, J = 8.1 Hz), 8.22 (1 H, d, J = 1.8 Hz), 9.08 (1 H, s), 12.83 (1 H, br) B-30 H Me —NHPh 2.17 (3 H, d, J = 1.1 Hz), 7.07-7.11 (1 H, m), 7.32-7.37 (3 H, m), 7.65 (2 H, d, J = 8.5 Hz), 7.73 (3 H, d, J = 8.5 Hz), 7.93 (1 H, s), 7.96 (1 H, dd, J = 2.2 Hz, 8.5 Hz), 8.20 (2 H, d, J = 8.5 Hz), 8.22 (1 H, d, J = 2.2 Hz), 10.01 (1 H, s), 12.85 (1 H, s) -
TABLE 15 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-31 H Me —NHCH2CF3 2.09 (3 H, d, J = 1.1 Hz), 4.02 (2 H, m), 7.34 (1 H, s), 7.60 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.5 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 2.2 Hz, 8.5 Hz), 8.18 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.2 Hz), 8.75 (1 H, t, J = 6.0 Hz), 12.85 (1 H, s) B-32 H Me —NH(CH2)3—SCH3 1.76 (2 H, qn, J = 6.9 Hz), 2.06 (6 H, s), 2.49-2.53 (2 H, m), 3.26 (2 H, q, J = 5.7 Hz), 7.26 (1 H, s), 7.57 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 8.15 (1 H, t, J = 4.8 Hz), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, br) B-33 H Me —NHCH(CH3)—Ph 1.46 (3 H, d, J = 7.2 Hz), 2.08 (2 H, d, J = 1.5 Hz), 5.08 (1 H, qn, J = 7.2 Hz), 7.21- 7.41 (6 H, m), 7.69 (2 H, d, J = 8.4 Hz), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 8.17 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 8.48 (1 H, d, J = 8.4 Hz), 12.83 (1 H, br) B-34 H Me —NHCH2Si—(CH3)3 0.06 (9 H, s), 2.06 (3 H, d, J = 1.2 Hz), 2.72 (2 H, d, J = 5.4 Hz), 7.18 (1 H, s), 7.57 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 7.99 (1 H, t, J = 5.4 Hz), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, s) B-35 H Me —NH(i-Bu) 0.87 (3 H, t, J = 7.1 Hz), 1.11 (3 H, d, J = 6.6 Hz), 1.41-1.57 (2 H, m), 2.06 (3 H, d, J = 1.4 Hz), 3.83 (1 H, sexth, J = 6.6 Hz), 7.21 (1 H, s), 7.57 (2 H, d, J = 8.4 Hz), 7.72 (1 H, d, J = 8.4 Hz), 7.80 (1 H, d, J = 8.1 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 8.17 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.82 (1 H, s) B-36 H Me —NH(c-Pr) 0.52-0.70 (4 H, m), 2.04 (3 H, d, J = 0.8 Hz), 2.74-2.80 (1 H, m), 7.56 (2 H, d, J = 8.1 Hz), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 8.11 (1 H, d, J = 4.2 Hz), 8.16 (2 H, d, J = 8.1 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.82 (1 H, s) -
TABLE 16 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-37 H Me —NH(CH2)3O—CH3 0.87 (3 H, t, J = 7.1 Hz), 1.11 (3 H, d, J = 6.6 Hz), 1.41-1.57 (2 H, m), 2.06 (3 H, d, J = 1.4 Hz), 3.83 (1 H, sexth, J = 6.6 Hz), 7.25 (1 H, s), 7.57 (2 H, d, J = 8.7 Hz), 7.73 (1 H, d, J = 8.1 Hz), 7.95 (1 H, dd, J = 2.1 Hz, 8.1 Hz), 8.11 (1 H, t, J = 6.0 Hz), 8.16 (2 H, d, J = 8.7 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, s) B-38 H Me —NH(c-Pen) 1.46-1.58 (4 H, m), 1.63-1.71 (2 H, m), 1.81-1.90 (2 H, m), 2.05 (3 H, s), 4.10- 4.15 (1 H, m), 7.20 (1 H, s), 7.57 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.1 Hz), 7.92- 7.96 (3 H, m), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 1.8 Hz), 12.82 (1 H, s) B-39 H Me —NH(t-Bu) 1.35 (9 H, s), 2.03 (3 H, d, J = 1.5 Hz), 7.13 (1 H, s), 7.56 (2 H, d, J = 8.4 Hz), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 2.1 Hz, 8.4 Hz), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.82 (1 H, s) B-40 H Me —NHpropargyl 2.06 (3 H, d, J = 1.2 Hz), 3.12 (1 H, t, J = 2.4 Hz), 3.98 (2 H, dd, J = 5.4 HZ, 2.4 Hz), 7.30 (1 H, s), 7.58 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.20 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 8.57 (1 H, t, J = 5.4 Hz), 12.83 (1 H, s) B-41 H Me —NHallyl 2.08 (3 H, d, J = 1.2 Hz), 3.83 (2 H, t, J = 5.7 Hz), 5.07-5.21 (2 H, m), 5.94-5.81 (1 H, m), 7.29 (1 H, s), 7.58 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.7 Hz), 7.92 (1 H, s), 7.94 (1 H, dd, J = 8.4 Hz, 1.8 Hz), 8.17 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 1.8 Hz), 8.31 (1 H, t, J = 5.7 Hz), 12.83 (1 H, s) B-42 H Me —NH(CH2)2O—CH3 2.06 (3 H, d, J = 1.2 Hz), 3.28 (3 H, s), 3.37-3.46 (4 H, m), 7.27 (1 H, s), 7.57 (2 H, d, J = 8.7 Hz), 7.72 (1 H, d, J = 8.4 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.15 (1 H, s), 8.17 (2 H, d, J = 8.7 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.83 (1 H, s) B-43 H Me —NHNHAc 1.91 (3 H, s), 2.08 (3 H, d, J = 1.5 Hz), 7.32 (1 H, s), 7.59 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.95 (1 H, dd, J = 8.4 Hz, 1.8 Hz), 8.18 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 1.8 Hz), 9.81 (1 H, s), 9.95 (1 H, s), 12.85 (1 H, s) -
TABLE 16 Compound No. R6 R1 R2 R 1H-NMR (DMSO d-6) B-44 H Me —NHNHPh 2.13 (3 H, d, J = 1.2 Hz), 6.73 (1 H, t, J = 7.5 Hz), 6.80 (2 H, d, J = 7.8 Hz), 7.17 (2 H, t, J = 8.1 Hz), 7.38 (1 H, s), 7.63 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.1 Hz), 7.82 (1 H, d, J = 2.7 Hz), 7.93 (1 H, s), 7.96 (1 H, dd, J = 8.1 Hz, 1.8 Hz), 8.19 (2 H, d, J = 8.4 Hz), 8.23 (1 H, d, J = 1.8 Hz), 10.04 (1 H, d, J = 2.7 Hz), 12.86 (1 H, s) B-45 H Me —N(CH3)NH2 2.10 (3 H, s), 3.11 (3 H, s), 4.84 (2 H, bs), 6.59 (1 H, s), 7.53 (2 H, d, J = 8.1 Hz), 7.71 (1 H, d, J = 8.1 Hz), 7.85 (1 H, s), 7.94 (1 H, dd, J = 8.1 Hz, 1.8 Hz), 8.15 (2 H, d, J = 8.1 Hz), 8.21 (1 H, d, J = 1.8 Hz), 12.63 (1 H, br) B-46 H Me —NHOCH3 2.03 (3 H, d, J = 1.5 Hz), 3.68 (3 H, s), 7.20 (1 H, s), 7.57 (2 H, d, J = 8.4 Hz), 7.72 (1 H, d, J = 8.1 Hz), 7.95 (1 H, dd, J = 8.1 Hz, 2.1 Hz), 8.16 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 2.1 Hz), 11.43 (1 H, s), 12.84 (1 H, s) -
TABLE 18 Com- pound No. R10 R1 R2 R5 1H-NMR (DMSO d-6) C-1 H Me Me 2.08 (3 h, d, J = 1.2 Hz), 3.64 (3 H, s), 6.87 (1 H, s), 7.38 (2 H, d, J = 8.7 Hz), 7.72 (1 H, d, J = 8.7 Hz), 7.91 (1 H, s), 7.95 (1 H, dd, J = 8.7 Hz, 2.1 Hz), 8.08 (2 H, d, J = 8.4 Hz), 8.21 (1 H, d, J = 2.1 Hz), 12.79 (1 H, s) C-2 H Me H 2.06 (3 H, d, J = 1.2 Hz), 6.69 (1 H, s), 7.46 (2 H, d, J = 9.0 Hz), 7.72 (1 H, d, J = 8.7 Hz), 7.92 (1 H, s), 7.94 (1 H, dd, J = 8.4 Hz, 1.8 Hz), 8.08 (2 H, d, J = 8.7 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.77 (1 H, s), 12.91 (1 H, s) C-3 H Br Me 3.76 (3 H, s), 7.48 (2 H, d, J = 8.7 Hz), 7.69 (1 H, s), 7.72 (1 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.11 (2 H, d, J = 8.4 Hz), 8.21 (1 H, d, J = 2.1 Hz), 12.86 (1 H, s) C-4 H Br H 7.47 (1 H, s), 7.54 (2 H, d, J = 8.7 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.11 (2 H, d, J = 8.4 Hz), 8.21 (1 H, d, J = 1.8 Hz), 12.83 (1 H, s) C-5 H F H 7.19 (1 H, d, J = 23.1 Hz), 7.68 (2 H, d, J = 8.4 Hz), 7.73 (1 H, d, J = 8.1 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 8.1 Hz, 2.1 Hz), 8.11 (2 H, d, J = 8.1 Hz), 8.22 (1 H, d, J = 1.8 Hz), 12.84 (1 H, s) -
TABLE 19 Com- pound No. R10 R1 R2 Het 1H-NMR (DMSO d-6) D-1 H Me 2.35 (3 H, d, J = 0.9 Hz), 7.12 (2 H, bs), 7.32 (1 H, s), 7.58 (2 H, d, J = 8.1 Hz), 7.72 (1 H, d, J = 7.8 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.17 (2 H, d, J = 8.4 Hz), 8.22 (1 H, d, J = 1.8 Hz), 12.31 (1 H, s), 12.79 (1 H, s) -
TABLE 20 Com- pound No. R10 R1 R2 R 1H-NMR (DMSO d-6) E-1 H Me anti OH 12.80 (bs, 1 H), 11.20 (s, 1 H), 8.21 (s, 1 H), 8.15 (d, 2 H, J = 8.3 Hz), 7.95 (m, 1 H), 7.93 (s, 1 H), 7.90 (s, 1 H), 7.72 (d, 1 H, J = 8.5 Hz), 7.57 (d, 2 H, J = 8.3 Hz), 6.83 (s, 1 H), 2.10 (s, 3 H) E-2 H Me syn OH 10.60 (bs, 1 H), 8.12 (d, 1 H, J = 1.9 Hz), 8.03 (d, 2 H, J = 8.5 Hz), 7.87 (dd, 1 H, J = 8.5, 1.9 Hz), 7.58 (d, 1 H, J = 8.5 Hz), 7.26 (s, 1 H), 7.16 (d, 2 H, J = 8.2 Hz), 6.56 (d, 1 H, J = 7.1 Hz), 3.20 (m, 1 H), 2.51-2.80 (m, 2 H), 0.98 (d, 3 H, J = 6.9 Hz) -
TABLE 21 Com- pound No. R10 R1 R2 R 1H-NMR (DMSO d-6) F-1 H Me —N(Me)2 (CDCl3) 2.24 (d, 3 H, J = 1.5 Hz), 2.92 (s, 6 H), 7.24 (s, 1 H), 7.47 (d, 1 H, J = 8.2 Hz), 7.52 (s, 1 H), 7.53 (d, 2 H, J = 8.5 Hz), 7.64 (dd, 1 H, J = 8.2, 1.8 Hz), 7.93 (d, 1 H, J = 1.8 Hz), 8.00 (d, 2 H, J = 8.5 Hz), 9.85 (brs, 1 H). F-2 H Me —NH(t-Bu) (CDCl3) 1.38 (s, 9 H), 2.28 (d, 3 H, J = 1.4 Hz), 4.19 (s, 1 H), 7.24 (s, 1 H), 7.49 (d, 1 H, J = 8.2 Hz), 7.53 (d, 2 H, J = 8.5 Hz), 7.62 (brs, 1 H), 7.66 (dd, 1 H, J = 8.2, 1.9 Hz), 7.96 (d, 1 H, J = 1.9 Hz), 8.03 (d, 2 H, J = 8.5 Hz), 9.80 (brs, 1 H). F-3 H Me —NH2 2.25 (d, 3 H, J = 1.2 Hz), 7.17 (s, 2 H), 7.42 (brs, 1 H), 7.64 (d, 2 H, J = 8.2 Hz), 7.73 (d, 2 H, J = 8.2 Hz), 7.92 (s, 1 H), 7.95 (dd, 1 H, J = 8.2, 2.1 Hz), 8.18 (d, 2 H, J = 8.2 Hz), 8.22 (d, 1 H, J = 2.1 Hz), 12.90 (brs, 1 H). -
TABLE 22 Com- pound No. R10 R1 R2 R5 1H-NMR (DMSO d-6) G-1 H H Me 2.67 (2 H, t, J = 7.7 Hz), 3.02 (2 H, t, J = 7.7 Hz), 3.69 (3 H, s), 7.20 (1 H, s), 7.26 (1 H, s), 7.29 (2 H, d, J = 8.2 Hz), 7.41 (1 H, d, J = 8.5 Hz), 7.58 (1 H, dd, J = 8.5 Hz, 2.2 Hz), 7.82 (2 H, d, J = 8.2 Hz), 7.86 (1 H, d, J = 2.2 Hz), 10.15 (1 H, bs) (CDCl3) G-2 H H H 2.61 (2 H, t, J = 7.3 Hz), 2.92 (2 H, t, J = 7.3 Hz), 7.42 (2 H, d, J = 8.5 Hz), 7.41 (1 H, d, J = 8.5 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.5 Hz, 2.1 Hz), 8.05 (2 H, d, J = 8.5 Hz), 8.22 (1 H, d, J = 2.1 Hz), 12.27 (1 H, bs), 14.73 (1 H, bs) G-3 H Me H 1.07 (3 H, d, J = 6.6 Hz), 2.68-2.77 (2 H, m), 2.94-3.03 (1 H, m), 7.39 (2 H, d, J = 8.5 Hz), 7.72 (1 H, d, J = 8.5 Hz), 7.95 (1 H, dd, J = 8.5 Hz, 2.2 Hz), 8.06 (2 H, d, J = 8.5 Hz), 8.21 (1 H, d, J = 2.2 Hz), 12.19 (1 H, bs), 12.69 (1 H, bs) G-4 H Cl H 3.19 (1 H, dd, J = 14.3 Hz, 8.2 Hz), 3.42 (1 H, dd, J = 14.3 Hz, 6.3 Hz), 4.83 (1 H, dd, J = 8.2 Hz, 6.3 Hz), 7.48 (2 H, d, J = 8.2 Hz), 7.72 (1 H, d, J = 8.5 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.5 Hz, 1.9 Hz), 8.08 (2 H, d, J = 8.2 Hz), 8.22 (1 H, d, J = 1.9 Hz), 12.77 (1 H, bs), 13.46 (1 H, bs) G-5 H Cl Me 3.21 (1 H, dd, J = 14.3 Hz, 8.0 Hz), 3.41 (1 H, dd, J = 14.3 Hz, 6.6 Hz), 3.77 (3 H, s), 4.46 (1 H, dd, J = 8.0 Hz, 6.6 Hz), 7.20 (1 H, s), 7.26 (2 H, d, J = 8.5 Hz), 7.35 (1 H, d, J = 8.5 Hz), 7.52 (1 H, dd, J = 8.5 Hz, 2.2 Hz), 7.78-7.81 (3 H, m), 10.71 (1 H, bs) (CDCl3) G-6 H F H 3.11-3.39 (2 H, m), 5.23-5.44 (1 H, m), 7.46 (2 H, d, J = 8.2 Hz), 7.72 (1 H, d, J = 8.2 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.2 Hz, 2.1 Hz), 8.09 (2 H, d, J = 8.2 Hz), 8.22 (1 H, d, J = 2.1 Hz), 13.45 (1 H, bs) -
TABLE 23 Com- pound No. R10 R1 R2 R5 1H-NMR (DMSO d-6) G-7 H F Et 1.20 (3 H, t, J = 7.1 Hz), 3.14-3.39 (2 H, m), 4.17 (2 H, q, J = 7.1 Hz), 5.36-5.56 (1 H, m), 7.45 (2 H, d, J = 8.5 Hz), 7.72 (1 H, d, J = 8.2 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.2 Hz, 1.9 Hz), 8.08 (2 H, d, J = 8.2 Hz), 8.22 (1 H, d, J = 1.9 Hz), 12.78 (1 H, bs) G-8 Me Cl H 1.39 (3 H, d, J = 7.1 Hz), 3.41-3.49 (1 H, m), 4.78 (1 H, d, J = 8.5 Hz), 7.52 (2 H, d, J = 8.5 Hz), 7.72 (1 H, d, J = 8.5 Hz), 7.92 (1 H, s), 7.95 (1 H, dd, J = 8.5 Hz, 1.9 Hz), 8.09 (2 H, d, J = 8.2 Hz), 8.22 (1 H, d, J = 1.9 Hz), 12.76 (1 H, bs) -
TABLE 24 Com- pound No. R10 Z R1 R2 R5 1H-NMR (DMSO d-6) H-1 H H Et (CDCl3) 10.10 (bs, 1 H), 8.06 (s, 1 H), 7.91 (d, 1 H, J = 8.0 Hz), 7.89 (d, 1 H, J = 2.0 Hz), 7.72 (d, 1 H, J = 8.0 Hz), 7.69 (d, 1 H, J = 16.0 Hz), 7.61 (d, 1 H, J = 8.5, 2.0 Hz), 7.53 (t, 1 H, J = 8.0 Hz), 7.43 (d, 1 H, J = 8.5 Hz), 7.23 (s, 1 H), 6.51 (d, 1 H, J = 16.0 Hz), 4.30 (q, 2 H, J = 7.0 Hz),1.35 (t, 3 H, J = 7.0 Hz) H-2 H H H 12.90 (s, 1 H), 12.50 (s, 1 H), 8.57 (s, 1 H), 8.23 (d, 1 H, J = 2.0 Hz), 8.10 (d, 1 H, J = 8.0 Hz), 7.96 (dd, 1 H, J = 8.5, 2.0 Hz), 7.94 (s, 1 H), 7.92 (d, 1 H, J = 8.0 Hz), 7.73 (d, 1 H, J = 8.0 Hz), 7.68 (d, 1 H, J = 16.0 Hz), 7.62 (t, 1 H, J = 8.0 Hz), 6.76 (d, 1 H, J = 16.0 Hz) H-3 H H Me 2.22 (3 H, s), 2.42 (3 H, s), 3.85 (3 H, s), 6.37 (1 H, d, J = 15.9 Hz), 7.10 (1 H, s), 7.18 (1 H, s), 7.25 (1 H, s), 7.31 (1 H, d, J = 8.5 Hz), 7.40 (1 H, dd, J = 8.5 Hz, 1.9 Hz), 7.63 (1 H, d, J = 1.9 Hz), 7.82 (1 H, d, J = 15.9 Hz), 11.30 (1 H, bs) (CDCl3) H-4 H H H 2.41 (6 H, s), 6.55 (1 H, d, J = 15.9 Hz), 7.53 (1 H, s), 7.69 (1 H, s), 7.72 (1 H, d, J = 8.4 Hz), 7.79 (1 H, d, J = 15.9 Hz), 7.73 (1 H, dd, J = 8.4 Hz, 1.9 Hz), 8.18 (1 H, d, J = 1.9 Hz), 12.70 (1 H, s) H-5 H Cl Et 1.42 (3 H, t, J = 6.9 Hz), 2.16 (3 H, s), 2.43 (3 H, s), 4.39 (q, 2 H, J = 6.9 Hz), 7.17 (1 H, s), 7.19 (1 H, s), 7.26 (1 H, s), 7.34 (1 H, d, J = 8.7 Hz), 7.45 (1 H, dd, J = 8.7 Hz, 2.1 Hz), 7.47 (1 H, s), 7.69 (1 H, d, J = 2.1 Hz), 7.91 (1 H, s), 11.09 (1 H, s) (CDCl3) H-6 H Cl H 2.31 (3 H, s), 2.42 (3 H, s), 7.56 (1 H, s), 7.57 (1 H, s), 7.72 (1 H, d, J = 8.5 Hz), 7.91-7.94 (2 H, m), 8.04 (1 H, s), 8.18 (1 H, d, J = 1.9 Hz), 12.71 (1 H, s) -
TABLE 25 Com- pound No. R10 Z R1 R2 R5 1H-NMR (DMSO d-6) H-7 H Cl H 7.73 (d, 1 H, J = 8.6 Hz), 7.95 (dd, 1 H, J = 8.6, 1.8 Hz), 7.97 (s, 1 H), 8.03 (s, 1 H), 8.04-8.10 (m, 2 H), 8.17 (t, 1 H, J = 7.7 Hz), 8.02 (d, 1 H, J = 1.8 Hz), 13.01 (s, 1 H), 14.09 (s, 1 H) H-8 H Cl H 7.55 (t, 1 H, J = 7.7 Hz), 7.78 (m, 1 H), 7.79 (d, 1 H, J = 2.7 Hz), 7.86 (d, 1 H, J = 4.5 Hz), 8.32 (s, 1 H), 8.35 (d, 1 H, J = 4.5 Hz), 8.39 (t, 1 H, J = 7.7 Hz), 13.18 (s, 1 H), 13.87 (br, 1 H) -
TABLE 26 Com- pound No. R10 Y R1 R2 R5 1H-NMR (DMSO d-6) I-1 —NHCH2— H Me Et (CDCl3) 7.91 (d, 1 H, J = 1.9 Hz), 7.67 (d, 1 H, J = 1.3 Hz), 7.62 (dd, 1 H, J = 8.3, 1.9 Hz), 7.43 (d, 1 H, J = 8.3 Hz), 7.41 (s, 4 H), 6.73 (s, 1 H), 5.57 (m, 1 H), 4.57 (d, 2 H, J = 5.8 Hz), 4.27 (q, 2 H, J = 7.1 Hz), 2.11 (d, 3 H, J = 1.3 Hz), 1.35 (t, 3 H, J = 7.1 Hz) I-2 —NHCH2— H Me H 12.50 (bs, 1 H), 8.29 (t, 1 H, J = 5.5 Hz), 8.03 (d, 1 H, J = 2.0 Hz), 7.80 (dd, 1 H, J = 8.5, 2.0 Hz), 7.61 (d, 1 H, J = 8.5 Hz, 7.57 (s, 1 H), 7.45 (s, 4 H), 7.30 (s, 1 H), 4.54 (d, 2 H, J = 5.5 Hz), 2.02 (d, 3 H, J = 0.5 Hz) I-3 —NHCOCH2— H Me Et (CDCl3) 8.82 (bs, 1 H), 7.88 (d, 1 H, J = 2.0 Hz), 7.68 (s, 1 H), 7.58 (dd, 1 H, J = 8.0, 2.0 Hz), 7.45 (d, 2 H, J = 8.2 Hz), 7.44 (d, 1 H, J = 8.5 Hz), 7.35 (d, 1 H, J = 8.2 Hz), 7.15 (s, 1 H), 4.29 (q, 2 H, J = 7.0 Hz), 3.85 (s, 2 H), 2.14 (d, 3 H, J = 1.4 Hz), 1.36 (t, 3 H, J = 7.0 Hz) I-4 —NHCOCH3— H Me H 12.60 (bs, 1 H), 12.50 (bs, 1 H), 8.14 (d, 1 H, J = 2.0 Hz), 7.88 (dd, 1 H, J = 8.5, 2.0 Hz), 7.84 (s, 1 H), 7.70 (d, 1 H, J = 8.5 Hz), 7.85 (s, 1 H), 7.45 (d, 2 H, J = 8.5 Hz), 7.40 (d, 2 H, J = 8.5 Hz), 3.84 (s, 2 H), 2.03 (d, 3 H, J = 1.5 Hz) I-5 —NHSO2— H Me Et (CDCl3) 1.35 (t, 3 H, J = 7.2 Hz), 2.06 (d, 3 H, J = 1.5 Hz), 4.27 (q, 2 H, J = 7.2 Hz), 6.64 (s, 1 H), 7.35 (dd, 1 H, J = 8.2, 2.1 Hz), 7.42 (d, 2 H, J = 8.2 Hz), 7.44 (d, 1 H, J = 8.2 Hz), 7.58 (d, 1 H, J = 2.1 Hz), 7.62 (s, 1 H), 7.98 (d, 2 H, J = 8.2 Hz). I-6 —NHSO2— H Me H (CDCl3 + CD3OD) 2.09 (d, 3 H, J = 1.5 Hz), 6.66 (s, 1 H), 7.40 (dd, 1 H, J = 8.2, 2.4 Hz), 7.49 (d, 2 H, J = 8.5 Hz), 7.52 (d, 1 H, J = 8.2 Hz), 7.66 (d, 1 H, J = 2.4 Hz), 7.69 (s, 1 H), 7.97 (d, 2 H, J = 8.5 Hz). -
- To a suspension of methoxy-methoxycarbonylmethyl-triphenylphosphonium chloride (152 mg) and 2-(4-formylbenzoylamino)-4-(3,4-dichlorophenyl)thiazole (57 mg) in methylene chloride (3 ml) was added triethylamine (38 mg), and the reaction mixture was stirred at room temperature for overnight. The mixture was concentrated, purified by silica gel column chromatography to obtain compound (A-15) 30 mg.
- Melting point: 203˜205° C.
- 1H-NMR (CDCl3) δ ppm: 3.85 (s, 3H), 3.89 (s, 3H), 6.96 (s, 1H), 7.22 (s, 1H), 7.46 (dd, 1H, J= 8.2, 1.9 Hz), 7.63 (d, 1H, J= 8.2 Hz) 7.86 (d, 2H, J= 8.6 Hz), 7.92 (d, 1H, J= 1.9 Hz), 7.94 (d, 2H, J= 8.6 Hz), 9.82 (brs, 1H).
- A solution of (E)-3-(4-iodophenyl)-2-methylacrylic acid ethyl ester (200 mg), dichlorobis(triphenylphosphine)palladium (II) (22 mg), 2-amino-4-(4′-chlorophenyl)-1H-imidazole (277 mg), and triethylamine (0.27 ml) in DMF (7 ml) was stirred under carbon monooxide atmosphere at 90° C. for 15 min. The reaction mixture was cooled, poured into water. The precipitated crystals were filtered, recrystallized with DMF to obtain compound (J-3) 117 mg as light yellow crystals.
- To a solution of ethyl ester of compound (A-53) (300 mg) in acetonitrile/tetrahydrofuran (1/1, 80 ml), was added 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bistetrafluoroborate (50% on alumina 1.24 g), was stirred at 80° C. for 30 min. Alumina was filtered off, the filtrate was concentrated under reduced pressure, and added chloroform. The insoluble materials was filtered off again, and the filtrate was concentrated. The residue was purified by preparative TLC plate to obtain fluoro derivative 20 mg as yellow crystals. The obtained ester derivative was solvolized in a manner similar to preparing compound (A-2) to obtain compound (J-16).
- Compound (J-1) to (J-2), (J-4) to (J-15), and (J-17) were synthesized in a manner similar to Example 4 and 5. Their physical data of compound were shown in Tables 27 to 28.
-
TABLE 27 Com- pound No. X R1 R2 R5 1H-NMR (DMSO d-6) J-1 H Cl Et 1.33 (3 H, t, J = 7.2 Hz), 4.32 (2 H, q, J = 7.2 Hz), 6.13 (1 H, s), 7.24 (1 H, t, J = 7.5 Hz), 7.46 (2 H, t, J = 8.1 Hz), 7.76 (2 H, d, J = 7.8 Hz), 7.98-8.12 (5 H, m), 11.02 (1 H, s), 11.89 (1 H, s) J-2 H Cl H 6.13 (1 H, s), 7.24 (1 H, t, J = 7.2 Hz), 7.46 (2 H, t, J = 8.1 Hz), 7.75 (2 H, d, J = 8.4 Hz), 7.96-8.12 (5 H, m), 11.01 (1 H, s), 11.86 (1 H, s), 13.80 (1 H, bs) J-3 H Me Et 12.07 (bs, 1 H), 11.74 (bs, 1 H), 8.13 (d, 2 H, J = 8.5 Hz), 7.79 (d, 2 H, J = 8.5 Hz), 7.67 (s, 1 H), 7.63 (d, 2 H, J = 8.5 Hz), 7.44 (s, 1 H), 7.40 (d, 2 H, J = 8.5 Hz), 4.22 (q, 2 H, J = 7.0 Hz), 2.09 (d, 3 H, J = 1.2 Hz), 1.29 (t, 3 H, J = 7.0 Hz) J-4 H Me H 12.10 (bs, 3 H), 8.12 (d, 2 H, J = 8.5 Hz), 7.80 (d, 2 H, J = 8.5 Hz), 7.65 (s, 1 H), 7.62 (d, 2 H, J = 8.5 Hz), 7.45 (s, 1 H), 7.40 (d, 2 H, J = 8.5 Hz), 2.07 (d, 3 H, J = 1.5 Hz) J-5 H Me Et 14.00 (bs, 1 H), 12.20 (bs, 1 H), 8.10-8.20 (m, 3 H), 7.95 (dd, 1 H, J = 8.2, 1.9 Hz), 7.77 (d, 1 H, J = 8.2 Hz), 7.60-7.70 (m, 3 H), 4.23 (q, 2 H, J = 7.0 Hz), 2.10 (s, 3 H), 1.29 (t, 3 H, J = 7.0 Hz) J-6 H Me H 13.95 (bs, 1 H), 12.69 (bs, 1 H), 12.22 (bs, 1 H), 8.10-8.18 (m, 3 H), 7.95 (dd, 1 H, J = 8.2, 2.0 Hz), 7.77 (d, 1 H, J = 8.2 Hz), 7.61- 7.68 (m, 3 H), 2.07 (d, 3 H, J = 1.2 Hz) J-7 H Me Et 13.24 (bs, 1 H), 8.20 (d, 2 H, J = 8.2 Hz), 7.96-8.04 (m, 2 H), 7.64-7.70 (m, 3 H), 7.52- 7.60 (m, 3 H), 4.23 (q, 2 H, J = 7.0 Hz), 2.10 (d, 3 H, J = 1.4 Hz), 1.29 (t, 3 H, J = 7.0 Hz) J-8 H Me Et 13.72 (bs, 1 H), 8.20-8.30 (m, 4 H), 7.66- 7.74 (m, 3 H), 7.50-7.58 (m, 3 H), 4.23 (q, 2 H, J = 7.0 Hz), 2.10 (s, 3 H), 1.30 (t, 3 H, J = 7.0 Hz) J-9 H Me Et 10.50 (s, 1 H), 8.06 (d, 2 H, J = 8.2 Hz), 7.79 (d, 2 H, J = 7.1 Hz), 7.62-7.70 (m, 3 H), 7.41 (t, 2 H, J = 7.5 Hz), 7.30 (t, 1 H, J = 7.5 Hz), 6.74 (s, 1 H), 4.23 (q, 2 H, J = 7.1 Hz), 3.77 (s, 3 H), 2.09 (d, 3 H, J = 1.1 Hz), 1.29 (t, 3 H, J = 7.1 Hz) -
TABLE 28 Com- pound No. X R1 R2 R5 1H-NMR (DMSO d-6) J-10 H Me H 12.64 (bs, 1 H), 7.99 (d, 2 H, J = 8.2 Hz), 7.72 (d, 2 H, J = 8.5 Hz), 7.66 (s, 1 H), 7.28- 7.38 (m, 5 H), 6.95 (s, .1 H), 2.07 (d, 3 H, J = 1.2 Hz) J-11 H Cl H 2.31 (3 H, d, J = 1.9 Hz), 7.18-7.24 (1 H, m), 7.35-7.42 (1 H, m), 7.56-7.64 (1 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.04 (1 H, s), 8.18 (2 H, d, J = 8.5 Hz), 12.79 (1 H, bs) J-12 H Cl H 2.35 (3 H, d, J = 1.6 Hz), 7.51-7.56 (1 H, m), 7.84-7.92 (1 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.04 (1 H, s), 8.19 (2 H, d, J = 8.5 Hz), 12.83 (1 H, s), 13.84 (1 H, bs) J-13 H Cl H 2.53 (3 H, s), 7.44 (1 H, t, J = 7.9 Hz), 7.55- 7.59 (1 H, m), 7.69-7.72 (1 H, m), 7.92 (1 H, t, J = 1.8 Hz), 8.02 (2 H, d, J = 8.5 Hz), 8.04 (1 H, s), 8.19 (2 H, d, J = 8.5 Hz), 12.76 (1 H, bs), 13.80 (1 H, bs) J-14 H Cl H 2.56 (3 H, s), 7.72-7.74 (2 H, m), 8.00-8.06 (5 H, m), 8.20 (2 H, d, J = 8.5 Hz), 12.77 (1 H, s), 13.75 (1 H, bs) J-15 H Cl H 0.86-0.90 (3 H, m), 1.33-1.35 (4 H, m), 1.48-1.58 (2 H, m), 2.64 (2 H, t, J = 7.5 Hz), 2.98 (4 H, s), 7.08-7.09 (1 H, m), 7.20 (1 H, t, J = 7.6 Hz), 7.63-7.66 (1 H, m), 8.03 (2 H, d, J = 8.5 Hz), 8.05 (1 H, s), 8.20 (2 H, d, J = 8.5 Hz), 12.81 (1 H, s), 13.79 (1 H, bs) J-16 H Cl H 13.80 (bs, 1 H), 13.20 (s, 1 H), 8.20 (d, 2 H, J = 8.5 Hz), 8.06 (s, 1 H), 8.04 (d, 2 H, J = 8.0 Hz), 7.75 (m, 1 H), 7.68 (m, 1 H), 7.42 (dd, 1 H, J = 8.2, 7.6 Hz), 7.26 (d, 1 H, J = 7.6 Hz), 2.65 (t, 2 H, J = 7.8 Hz), 1.50-1.70 (m, 2 H), 1.20-1.40 (m, 2 H), 0.92 (t, 3 H, J = 7.3 Hz) J-17 H Cl H 13.88 (bs, 1 H), 13.01 (s, 1 H), 8.10-8.24 (m, 4 H), 8.00-8.08 (m, 3 H), 7.74-7.80 (m, 2 H) -
- A solution of compound (11) (1.1 g), compound (12) (760 mg), potassium carbonate (1.44 g), tetrakistriphenylphosphinepalladium (250 mg) in DMF was stirred at 110°G for 2 h. The reaction solution was poured into ethyl acetate, and the mixture was washed with water four times and brine, dried over magnesium sulfate. The solvent was concentrated, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=2/3) to obtain compound (13) (870 mg) as a amorphous.
- 1H NMR (CDCl3, δ ppm): 4.06 (3H, s), 7.16 (1H, s), 7.28-7.50 (10H, m), 7.72 (1H, dd, J= 4.8 Hz, 1.8 Hz), 7.75-7.80 (2H, m), 8.25-8.30 (2H, m), 8.40 (1H, d, J=2.1 Hz).
- A solution of compound (13) (870 mg) in formic acid (98-100%, 20 ml) was stirred at 50° C. for 3 h. The reaction solution was concentrated, toluene was added to the residue, and concentrated again. The obtained residue was washed with isopropyl ether to obtain compound (4) (473 mg) as white crystals.
- 1H NMR(CDCl3, δ ppm): 3.93 (3H, s), 7.97-8.02 (2H, m), 8.04 (1H, dd, J= 7.8 Hz, 1.8 Hz), 8.07-8.12 (2H, m), 8.35 (1H, d, J= 1.5 Hz), 8.82 (1H, d. J= 4.8 Hz).
- Compound (K-14) was synthesized form compound (4) as starting material in a manner similar to Step 4 of Example 1. Its physical data was shown in Table 29.
- Compound (K-15) was synthesized form compound (K-14) as starting material in a manner similar to Step 5 of Example 1. Its physical data was shown in Table 29.
- A solution of compound (K-15) (100 mg), diphenylphosphoroazide (55 μl), triethylamine (351 μl), and tert-butanol (1 ml) in DMF (15 ml) was stirred at 100° C. for 1 h. The reaction solution was poured into ethyl acetate, THF was added according to necessity when the precipitate was produced, and the mixture was washed with water two times, sodium bicarbonate aqueous solution and brine, dried over magnesium sulfate. The solvent was concentrated, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/1) to obtain compound (K-18) (60 mg) as white crystals.
- Compound (K-16) to (K-17), and (K-19) were synthesized in a manner similar to Example 6 and compound (K-1) to (K-13) in a manner similar to Example 1. Their physical date were shown in Table 29 to 31.
-
TABLE 29 Com- pound No. R10 Y W 1H-NMR (DMSO d-6) K-1 —CONHMe 2.80 (3 H, d, J = 4.5 Hz), 7.00 (1 H, d, J = 15.8 Hz), 7.70-7.81 (4 H, m), 7.89-7.93 (4 H, m),. 8.16 (1 H, d, J = 2.0 Hz), 8.53 (1 H, q, J = 4.5 Hz), 12.62 (1 H, bs) K-2 —CONHMe 2.81 (3 H, d, J = 4.4 Hz), 7.02 (1 H, d, J = 15.8 Hz), 7.47-7.56 (1 H, m), 7.71-7.81 (5 H, m),. 7.90- 7.97 (3 H, m), 8.54 (1 H, q, J = 4.5 Hz), 12.60 (1 H, bs) K-3 —COOMe 3.88 (3 H, s), 7.03 (1 H, d, J = 15.9 Hz), 7.71 (1 H, d, J = 8.2 Hz), 7.76-7.83 (3 H, m), 7.89-7.92 (2 H, m), 8.03 (2 H, d, J = 8.2 Hz), 8.15 (1 H, d, J = 1.8 Hz), 12.66 (1 H, bs) K-4 —CONHMe 2.17 (3 H, d, J = 1.1 Hz), 2.80 (3 H, d, J = 4.5 Hz), 7.58 (2 H, d, J = 8.3 Hz), 7.62 (1 H, bs), 7.72 (1 H, d, J = 8.4 Hz), 7.89-7.95 (4 H, m), 8.20 (1 H, d, J = 2.0 Hz), 8.53 (1 H, q, J = 4.5 Hz), 12.46 (1 H, bs) K-5 —CONHMe 2.79 (3 H, d, J = 4.5 Hz), 7.16 (1 H, d, J = 24.2 Hz), 7.64 (2 H, d, J = 8.3 Hz), 7.71 (1 H, d, J = 8.5 Hz),. 7.81-7.83 (m, 2 H), 7.90-7.97 (m, 2 H), 8.18 (1 H, d, J = 1.7 Hz), 8.49 (1 H, q, J = 4.5 Hz), 13.01 (1 H, bs) K-6 —COOH 7.11 (1 H, d, J = 15.8 Hz), 7.69- 7.82 (4 H, m), 7.89-7.93 (2 H, m),. 8.02 (2 H, d, J = 8.1 Hz), 8.16 (1 H, d, J = 1.6 Hz), 12.72 (1 H, bs) K-7 —COOMe 2.59 (2 H, t, J = 7.5 Hz), 3.04 (2 H, t, J = 7.5 Hz), 3.91 (3 H, s), 7.14- 7.17 (3 H, m), 7.43 (2 H, d, J = 8.7 Hz), 7.58 (1 H, dd, J = 8.7 Hz, 2.0 Hz), 7.87 (1 H, d, J = 2.0 Hz), 7.94 (2 H, d, J = 8.7 Hz), 9.87 (1 H, s) (CDCl3) -
TABLE 30 Com- pound No. R10 Y W 1H-NMR (DMSO d-6) K-8 —COOH 2.82 (2 H, t, J = 7.2 Hz), 3.02 (2 H, t, J = 7.2 Hz), 7.38 (2 H, d, J = 8.5 Hz), 7.68 (1 H, d, J = 8.4 Hz), 7.83-7.89 (4 H, m), 8.12 (1 H, d, J = 2.0 Hz), 12.33 (1 H, s), 12.82 (1 H, s) K-9 —SO2NH(t-Bu) (CDCl3) 1.26 (s, 9 H), 2.25 (d, 3 H, J = 1.5 Hz), 4.61 (s, 1 H), 7.21 (s, 1 H), 7.45 (d, 2 H, J = 8.5 Hz), 7.47 (d, 1 H, J = 8.2 Hz), 7.60 (brs, 1 H), 7.63 (dd, 1 H, J = 8.2, 1.8 Hz), 7.94 (d, 1 H, J = 1.8 Hz), 7.95 (d, 2 H, J = 8.5 Hz), 9.58 (brs, 1 H). K-10 —SO2NH2 2.14 (d, 3 H, J = 1.5 Hz), 7.42 (brs, 2 H), 7.59 (brs, 1 H), 7.65 (d, 2 H, J = 8.2 Hz), 7.69 (d, 1 H, J = 8.2 Hz), 7.86 (s, 1 H), 7.87 (d, 2 H, J = 8.2 Hz), 7.91 (dd, 1 H, J = 8.2, 2.1 Hz), 8.18 (d, 1 H, J = 2.1 Hz), 12.47 (brs, 1 H). K-11 —SO2NH(t-Bu) 1.11 (s, 9 H), 7.03 (d, 1 H, J = 16.2 Hz), 7.65 (s, 1 H), 7.67 (d, 1 H, J = 8.5 Hz), 7.80 (d, 1 H, J = 16.2 Hz), 7.81 (d, 2 H, J = 8.5 Hz), 7.89- 7.93 (m, 4 H), 8.17 (d, 1 H, J = 1.8 Hz), 12.67 (s, 1 H). K-12 —SO2NH2 7.03 (d, 1 H, J = 16.0 Hz), 7.47 (2 H, s), 7.72 (d, 1 H, J = 8.5 Hz), 7.81 (d, 1 H, J = 16.0 Hz), 7.83 (d, 2 H, J = 8.4 Hz), 7.89 (d, 2 H, J = 8.4 Hz), 7.91 (s, 1 H), 7.91 (dd, 1 H, J = 8.5, 2.1 Hz), 8.17 (d, 2 H, J = 2.1 Hz), 12.67 (s, 1 H). K-13 —SO3H 6.94 (d, 1 H, J = 15.8 Hz), 7.60 (d, 2 H, J = 8.2 Hz), 7.67 (d, 2 H, J = 8.2 Hz), 7.72 (d, 1 H, J = 8.2 Hz), 7.74 (d, 1 H, J = 15.8 Hz), 7.89 (s, 1 H), 7.91 (dd, 1 H, J = 8.2, 1.9 Hz), 8.16 (d, 1 H, J = 1.9 Hz), 12.57 (brs, 1 H). K-14 —NHCO— 3.94 (3 H, s), 7.72 (1 H, d, J = 8.7 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 8.4 Hz, 1.8 Hz), 8.04-8.10 (3 H, m), 8.22 (1 H, d, J = 2.4 Hz), 8.30 (2 H, d, J = 8.4 Hz), 8.39 (1 H, d, J = 1.2 Hz), 12.93 (1 H, s) K-15 —NHCO— 7.71 (1 H, d, J = 8.4 Hz), 7.82 (1 H, bs), 7.89 (1 H, s), 7.93-8.01 (3 H, m), 8.22 (1 H, d, J = 2.1 Hz), 8.26-8.34 (3 H, m), 8.65 (1 H, bs) -
TABLE 31 Com- pound No. R10 Y W 1H-NMR (DMSO d-6) K-16 —NHCO— 3.53 (3 H, s), 5.26 (s, 1 H), 7.10 (1 H, ddd, J = 8.2 Hz, 2.5 Hz, 0.9 Hz), 7.21 (1 H, s), 7.22-7.28 (2 H, m), 7.36-7.40 (2 H, m), 7.55 (1 H, dd, J = 8.4 Hz, 2.0 Hz), 7.63 (2 H, d, J = 8.4 Hz), 7.83 (1 H, d, J = 2.0 Hz), 7.93 (2 H, d, J = 8.4 Hz), 10.86 (1 H, bs) (CDCl3) K-17 —NHCO— 6.82-6.86 (1 H, m), 7.12-7.13 (1 H, m), 7.17-7.20 (1 H, m), 7.28- 7.37 (1 H, m), 7.73 (1 H, d, J = 8.2 Hz), 7.89 (2 H, d, J = 8.5 Hz), 7.93 (1 H, s), 7.95 (1 H, dd, J = 8.2 Hz, 2.0 Hz), 8.21 (2 H, d, J = 8.5 Hz), 8.23 (1 H, d, J = 2.0 Hz), 9.62 (1 H, s), 12.83 (1 H, s) K-18 —NHCO— 6.06 (2 H, s), 6.79 (1 H, s), 6.87 (1 H, d, J = 4.8 Hz), 7.73 (1 H, d, J = 8.4 Hz), 7.82 (2 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.96 (1 H, dd, J = 8.1 Hz, 1.5 Hz), 8.02 (1 H, d, J = 5.1 Hz), 8.21-8.27 (3 H, m), 12.88 (1 H, s) K-19 —NHCO— 3.06 (2 H, s), 7.28 (1 H, dt, 7.2 Hz, 2.1 Hz), 7.45-7.57 (3 H, m), 7.73 (1 H, d, J = 8.1 Hz), 7.81 (2 H, d, J = 8.4 Hz), 7.93 (1 H, s), 7.96 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 8.21- 8.27 (3 H, m), 9.88 (1 H, bs), 12.84 (1 H, bs) -
- A solution of compound (15) (6.3 g), compound (16) (2.0 ml), triethylamine (6.3 ml), tetrakistriphenylphosphinepalladium (870 mg), and copper (I) iodide (290 mg) in DMF (70 ml) was stirred at 90° C. for 4 h. The reaction solution was poured into ethyl acetate, and the mixture was washed with water four times and brine, dried over magnesium sulfate. The solvent was concentrated, the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/4) to obtain compound (17) (2.25 g) as a amorphous.
- 1H NMR (CDCl3, δ ppm): 3.81 (3H, s), 7.06 (1H, s), 7.28-7.42 (6H, m), 7.51-7.55 (4H, m), 7.85 (2H, d, J= 8.7 Hz), 8.17 (2H, d, J= 8.7 Hz).
- A solution of compound (17) (180 mg) and formic acid (98-100%, 4 ml) in THF (4 ml) was stirred at room temperature for 18 h. The reaction solution was concentrated, toluene was added to the residue, and concentrated again. The obtained residue was washed with isopropyl ether to obtain compound (18) (95 mg) as white needles.
- 1H NMR (CDCl3, δ ppm): 3.80 (3H, s), 7.79 (2H, d, J= 8.1 Hz), 8.00 (2H, d, J=8.1 Hz), 13.33 (1H, bs).
- Compound (L-1) was synthesized form compound (4) as starting material in a manner similar to Step 4 of Example 1. Its physical data was shown in Table 32.
- Compound (L-2) was synthesized form compound (L-1) as starting material in a manner similar to Step 5 of Example 1. Its physical data was shown in Table 32.
- Compound (L-3) to (L-4) were synthesized in a manner similar to Example. Their physical date were shown in Table 32.
-
TABLE 32 Com- pound No. R10 Z R5 1H-NMR (DMSO d-6) L-1 Me 3.82 (3 H, s), 7.72 (1 H, s), 7.85 (2 H, d, J = 8.7 Hz), 7.94 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 7.94 (1 H, s), 8.16-8.22 (3 H, m), 12.97 (1 H, s) L-2 H 7.72 (1 H, d, J = 8.4 Hz), 7.81 (2 H, d, J = 8.4 Hz), 7.95 (1 H, dd, J = 8.4 Hz, 2.1 Hz), 7.94 (1 H, s), 8.18 (2 H, d, J = 8.4 Hz), 8.21 (1 H, d, J = 2.1 Hz), 12.96 (1 H, s) L-3 Me 3.80 (3 H, s), 4.01 (3 H, s), 7.70-7.74 (3 H, m), 7.88 (1 H, s), 7.92-7.96 (2 H, m), 8.21 (1 H, d, J = 1.8 Hz), 12.99 (1 H, s) L-4 H 4.01 (3 H, s), 7.70-7.74 (3 H, m), 7.88 (1 H, s), 7.93-7.97 (2 H, m), 8.22 (1 H, d, J = 2.1 Hz), 12.98 (1 H, s), 13.75 (1 H, bs) - The below mentioned compounds were synthesized in a manner similar to above described method.
- (Compound No., Ra, Rb, Rc, Rd, Re(M-1, H, H, H, H, H), (M-2, H, H, H, H, Cl), (M-3, H, H, H, H, F), (M-4, H, H, H, H, CF3), (M-5, H, H, H, H, Br), (M-6, H, H, H, H, CH3), (M-7, H, H, H, F, H), (M-8, H, H, H, F, Cl), (M-9, H, H, H, F, F), (M-10, H, H, H, F, CF3), (M-11, H, H, hi, F, Br), (M-12, H, H, H, F, CH3), (M-13, H, H, H, Cl, H), (M-14, MeO, H, H, Cl, Cl), (M-15, H, H, H, Cl, F), (M-16, H, H, H, Cl, CF3), (M-17, H, H, H, Cl, Br), (M-18, H, H, H, Cl, CH3), (M-19, H, H, H, CH3, H), (M-20, H, H, H, CH3, Cl), (M-21, H, H, H, CH3, F), (M-22, H, H, H, CH3, CF3, (M-23, H, H, H, CH3, Br), (M-24, H, H, H, CH3, CH3), (M-25, H, H, H, Et, H), (M-26, H, H, H, Et, Cl), (M-27, H, H, H, Et, F), (M-28, H, H, H, Et, CF3), (M-29, H, H, H, Et, Br), (M-30, H, H, H, Et, CH3), (M-31, H, H, H, n-Pr, H), (M-32, H, H, H, n-Pr, Cl), (M-33, H, H, H, n-Pr, F), (M-34, H, H, H, n-Pr, CF3), (M-35, H, H, H, n-Pr, Br), (M-36, H, H, H, n-Pr, CH3), (M-37, H, H, H, c-Pr, H), (M-38, H, H, H, c-Pr, Cl), (M-39, H, H, H, c-Pr, F), (M-40, H, H, H, c-Pr, CF3), (M-41, H, H, H, c-Pr, Br), (M-42, H, H, H, c-Pr, CH3), (M-43, H, H, H, i-Pr, H), (M-44, H, H, H, i-Pr, Cl), (M-45, H, H, H, i-Pr, F), (M-46, H, H, H, i-Pr, CF3), (M-47, H, H, H, i-Pr, Br), (M-48, H, H, H, i-Pr, CH3), (M-49, H, H, H, n-Bu, H), (M-50, H, H, H, n-Bu, Cl), (M-51, H, H, H, n-Bu, F), (M-52, H, H, H, n-Bu, CF3), (M-53, H, H, H, n-Bu, Br), (M-54, H, H, H, n-Bu, CH3), (M-55, H, H, H, i-Bu, H), (M-56, H, H, H, i-Bu, Cl), (M-57, H, H, H, i-Bu, F), (M-58, H, H, H, i-Bu, CF3), (M-69, H, H, H, i-Bu, Br), (M-60, H, H, H, i-Bu, CH3), (M-61, H, H, H, sec-Bu, H), (M-62, H, H, H, sec-Bu, Cl), (M-63, H, H, H, sec-Bu, F), (M-64, H, H, H, sec-Bu, CF3), (M-65, H, H, H, sec-Bu, Br), (M-66, H, H, H, sec-Bu, CH3), (M-67, H, H, H, n-Pen, H), (M-68, H, H, H, n-Pen, Cl), (M-69, H, H, H, n-Pen, F), (M-70, H, H, H, n-Pen, CF3), (M-71, H, H, H, n-Pen, Br), (M-72, H, H, H, n-Pen, CH3), (M-73, H, H, H, c-Pen, H), (M-74, H, H, H, c-Pen, Cl), (M-75, H, H, H, c-Pen, F), (M-76, H, H, H, c-Pen, CF3), (M-77, H, H, H, c-Pen, Br), (M-78, H, H, H, c-Pen, CH3), (M-79, H, H, H, n-Hex, H), (M-80, H, H, H, n-Hex, Cl), (M-81, H, H, H, n-Hex, F), (M-82, H, H, H, n-Hex, CF3), (M-83, H, H, H, n-Hex, Br), (M-84, H, H, H, n-Hex, CH3), (M-85, H, H, H, c-Hex, H), (M-86, H, H, H, c-Hex, Cl), (M-87, H, H, H, c-Hex, F), (M-88, H, H, H, c-Hex, CF3), (M-89, H, H, H, c-Hex, Br), (M-90, H, H, H, c-Hex, CH3), (M-91, H, H, H, OH, H), (M-92, H, H, H, OH, Cl), (M-93, H, H, H, OH, F), (M-94, H, H, H, OH, CF3), (M-95, H, H, H, OH, Br), (M-96, H, H, H, OH, CH3), (M-97, H, H, H, EtO, H), (M-98, H, H, H, EtO, Cl), (M-99, H, H, H, EtO, F), (M-100, H, H, H, EtO, CF3), (M-101, H, H, H, EtO, Br), (M-102, H, H, H, EtO, CH3), (M-103, H, H, H, n-PrO, H), (M-104, H, H, H, n-PrO, Cl), (M-105, H, H, H, n-PrO, F), (M-106, H, H, H, n-PrO, CF3), (M-107, H, H, H, n-PrO, Br), (M-108, H, H, H, n-PrO, CH3), (M-109, H, H, H, PhO, H), (M-110, H, H, H, PhO, Cl), (M-111, H, H, H, PhO, F), (M-112, H, H, H, PhO, CF3), (M-113, H, H, H, PhO, Br), (M-114, H, H, H, PhO, CH3), (M-115, H, H, H, BnO, H), (M-116, H, H, H, BnO, Cl), (M-117, H, H, H, BnO, F), (M-118, H, H, H, BnO, CF3), (M-119, H, H, H, BnO, Br), (M-120, H, H, H, BnO, CH3), (M-121, H, H, H, PhCH2CH2O, H), (M-122, H, H, H, PhCH2CH2O, Cl), (M-123, H, H, H, PhCH2CH2O, F), (M-124, H, H, H, PhCH2CH2O, CF3), (M-125, H, H, H, PhCH2CH2O, Br), (M-126, H, H, H, PhCH2CH2O, CH3), (M-127, H, H, H, CF3O, H), (M-128, H, H, H, CF3O, Cl), (M-129, H, H, H, CF3O, F), (M-130, H, H, H, CF3O, CF3), (M-131, H, H, H, CF3O, Br), (M-132, H, H, H, CF3O, CH3), (M-133, H, H, H, Ph, H), (M-134, H, H, H, Ph, Cl), (M-136, H, H, H, Ph, F), (M-136, H, H, H, Ph, CF3), (M-137, H, H, H, Ph, Br), (M-138, H, H, H, Ph, CH3), (M-139, H, H, H, 4-F-Ph, H), (M-140, H, H, H, 4-F-Ph, Cl), (M-141, H, H, H, 4-F-Ph, F), (M-142, H, H, H, 4-F-Ph, CF3), (M-143, H, H, H, 4-F-Ph, Br), (M-144, H, H, H, 4-F-Ph, CH3), (M-145, H, H, H, 4-CF3-Ph, H), (M-146, H, H, H, 4-CF3-Ph, Cl), (M-147, H, H, H, 4-CF3-Ph, F), (M-148, H, H, H, 4-CF3-Ph, CF3), (M-149, H, H, H, 4-CF3-Ph, Br), (M-150, H, H, H, 4-CF3-Ph, CH3), (M-151, H, H, H, 4-(Me)2N-Ph, H), (M-152, H, H, H, 4-(Me)2N-Ph, Cl), (M-153, H, H, H, 4-(Me)2N-Ph, F), (M-154, H, H, H, 4, (Me)2N-Ph, CF3), (M-165, H, H, H, 4-(Me)2N-Ph, Br), (M-156, H, H, H, 4-(Me)2N-Ph, CH2), (M-157, H, H, H, 4-OH-Ph, H), (M-158, H, H, H, 4-OH-Ph, Cl), (M-159, H, H, H, 4-OH-Ph, F), (M-160, H, H, H, 4-OH-Ph, CF3), (M-161, H, H, H, 4-OH-Ph, Br), (M-162, H, H, H, 4-OH-Ph, CH3), (M-163, H, H, H, 3,4-di-F-Ph, H), (M-164, H, H, H, 3,4-di-F-Ph, Cl), (M-165, H, H, H, 3,4-di-F-Ph, F), (M-168, H, H, H, 3,4-di-F-Ph, CF3), (M-167, H, H, H, 3,4-di-F-Ph, Br), (M-168, H, H, H, 3,4-di-F-Ph, CH3), (M-169, H, H, H, 4-COOH-Ph, H), (M-170, H, H, H, 4-COOH-Ph, Cl), (M-171, H, H, H, 4-COOH-Ph, F), (M-172, H, H, H, 4-COOH-Ph, CF3), (M-173, H, H, H, 4-COOH-Ph, Br), (M-174, H, H, H, 4-COOH-Ph, CH3), (M-175, H, H, H, Bn, H), (M-176, H, H, H, Bn, Cl), (M-177, H, H, H, Bn, F), (M-178, H, H, H, Bn, CF3), (M-179, H, H, H, Bn, Br), (M-180, H, H, H, Bn, CH3), (M-181, H, H, H, 4-F-Bn, H), (M-182, H, H, H, 4-F-Bn, Cl), (M-183, H, H, H, 4-F-Bn, F), (M-184, H, H, H, 4-F-Bn, CF3), (M-185, H, H, H, 4-F-Bn, Br), (M-186, H, H, H, 4-F-Bn, CH3), (M-187, H, H, H, 2-Py, H), (M-188, H, H, H, 2-Py, Cl), (M-189, H, H, H, 2-Py, F), (M-190, H, H, H, 2-Py, CF3), M-191, H, H, H, 2-Py, Br), (M-192, H, H, H, 2-Py, CH3), (M-193, H, H, H, 3-Py, H), (M-194, H, H, H, 3-Py, Cl), (M-195, H, H, H, 3-Py, F), (M-196, H, H, H, 3-Py, CF3), (M-197, H, H, H, 3-Py, Br), (M-198, H, H, H, 3-Py, CH3), (M-199, H, H, H, 4-Py, H), (M-200, H, H, H, 4-Py, Cl), (M-201, H, H, H, 4-Py, F), (M-202, H, H, H, 4-Py, CF3), (M-203, H, H, H, 4-Py, Br), (M-204, H, H, H, 4-Py, CH3), (M-205, H, H, H, 2-Th, H), (M-206, H, H, H, 2-Th, Cl), (M-207, H, H, H, 2-Th, F), (M-208, H, H, H, 2-Th, CF3), (M-209, H, H, H, 2-Th, Br), (M-210, H, H, H, 2-Th, CH3), (M-211, H, H, H, 3-Th, H), (M-212, H, H, H, 3-Th, Cl), (M-213, H, H, H, 3-Th, F), (M-214, H, H, H, 3-Th, CF3), (M-215, H, H, H, 3-Th, Br), (M-216, H, H, H, 3-Th, CH3), (M-217, H, H, H, pyrrazol-2-yl, H), (M-218, H, H, H, pyrrazol-2-yl, Cl), (M-219, H, H, H, pyrrazol-2-yl, F), (M-220, 11, H, H, pyrrazol-2-yl, CF3), (M-221, H, H, H, pyrrazol-2-yl, Br), (M-222, H, H, H, pyrrazol-2-yl, CH3), (M-223, H, H, H, pyrrazol-3-yl, H), (M-224, H, H, H, pyrrazol-3-yl, Cl), (M-225, H, H, H, pyrrazol-3-yl, F), (M-226, H, H, H, pyrrazol-3-yl, CF3), (M-227, H, H, H, pyrrazol-3-yl, Br), (M-228, H, H, H, pyrrazol-3-yl, CH3), (M-229, H, H, H, pyrimidin-2-yl, H), (M-230, H, H, H, pyrimidin-2-yl, Cl), (M-231, H, H, H, pyrimidin-2-yl, F), (M-232, H, H, H, pyrimidin-2-yl, CF3), (M-233, H, H, H, pyrimidin-2-yl, Br), (M-234, H, H, H, pyrimidin-2-yl, CH3), (M-235, H, H, H, pyrimidin-4-yl, H), (M-236, H, H, H, pyrimidin-4-yl, Cl), (M-237, H, H, H, pyridine-4-yl, F), (M-238, H, H, H, pyrimidin-4-yl, CF3), (M-239, H, H, H, pyrimidin-4-yl, Br), (M-240, H, H, H, pyrimidin-4-yl, CH3), (M-241, H, H, H, pyrimidin-5-yl, H), (M-242, H, H, H, pyrimidin-5-yl, Cl), (M-243, H, H, H, pyrimidin-5-yl, F), (M-244, H, H, H, pyrimidin-5-yl, CF3), (M-245, H, H, H, pyrimidin-5-yl, Br), (M-246, H, H, H, pyrimidin-5-yl, CH3), (M-247, H, H, H, HOOCCH2CH2CH2, H), (M-248, H, H, H, HOOCCH2CH2CH2, Cl), (M-249, H, H, H, HOOCCH2CH2CH2, F), (M-250, H, H, H, HOOCCH2CH2CH2, CF3), (M-251, H, H, H, HOOCCH2CH2CH2, Br), (M-252, H, H, H, HOOCCH2CH2CH2, CH3), (M-253, H, H, H, HOOCCH2CH2CH2CH2, H), (M-254, H, H, H, HOOCCH2CH2CH2CH2, Cl), (M-255, H, H, H, HOOCCH2CH2CH2CH2, F), (M-256, H, H, H, HOOCCH2CH2CH2CH2, CF3), (M-257, H, H, H, HOOCCH2CH2CH2CH2, Br), (M-258, H, H, H, HOOCCH2CH2CH2CH2, CH3), (M-259, H, H, H, (Me)2NCOCH2CH2CH2CH2, H), (M-260, H, H, H, (Me)2NCOCH2CH2CH2CH2(Cl), (M-261, H, H, H, (Me)2NCOCH2CH2CH2CH2, F), (M-262, H, H, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-263, H, H, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-264, H, H, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-265, H, H, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-266, H, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-267, H, H, H, (Me)3NCOCH2CH2CH2CH2CH2, F), (M-268, H, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-269, H, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-270, H, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-271, H, H, H, MeOCH2, H), (M-272, H, H, H, MeOCH2, Cl), (M-273, H, H, H, MeOCH2, F), (M-274, H, H, H, MeOCH2, CF3), (M-275, H, H, H, MeOCH2, Br), (M-276, H, H, H, MeOCH2, CH3), (M-277, H, H, H, EtOCH2, H), (M-278, H, H, H, EtOCH2, Cl), (M-279, H, H, H, EtOCH2, F), (M-280, H, H, H, EtOCH2, CF3), (M-281, H, H, H, EtOCH2, Br), (M-282, H, H, H, EtOCH2, CH3), (M-283, H, H, H, EtOCH2CH2, H), (M-284, H, H, H, EtOCH2CH2, Cl), (M-285, H, H, H, EtOCH2CH2, F), (M-286, H, H, H, EtOCH2CH2, CF3), (M-287, H, H, H, EtOCH2CH2, Br), (M-288, H, H, H, EtOCH2CH2, CH3), (M-289, H, H, H, MeOCH2CH2OCH2CH2, H), (M-290, H, H, H, MeOCH2CH2OCH2CH2, Cl), (M-291, H, H, H, MeOCH2CH2OCH2CH2, F), (M-292, H, H, H, MeOCH2CH2OCH2CH2, CF3), (M-293, H, H, H, MeOCH2CH2OCH2CH2, Br), (M-294, H, H, H, MeOCH2CH2OCH2CH2, CH3), (M-295, H, H, H, MeOCH2CH2, H), (M-296, H, H, H, MeOCH2CH2, Cl), (M-297, H, H, H, MeOCH2CH2, F), (M-298, H, H, H, MeOCH2CH2, CF3), (M-299, H, H, H, MeOCH2CH2, Br), (M-300, H, H, H, MeOCH2CH2, CH3), (M-301, H, H, H, HOCH2, H), (M-302, H, H, H, HOCH2, Cl), (M-303, H, H, H, HOCH2, F), (M-304, H, H, H, HOCH2, CF3), (M-305, H, H, H, HOCH2, Br), (M-306, H, H, H, HOCH2, CH3), (M-307, H, H, H, HOCH2CH2, H), (M-308, H, H, H, HOCH2CH2, Cl), (M-309, H, H, H, HOCH2CH2, F), (M-310, H, H, H, HOCH2CH2, CF3), (M-311, H, H, H, HOCH2CH2, Br), (M-312, H, H, H, HOCH2CH2, CH3), (M-313, H, H, H, HOCH2CH2CH2, H), (M-314, H, H, H, HOCH2CH2CH2, Cl), (M-315, H, H, H, HOCH2CH2CH2, F), (M-316, H, H, H, HOCH2CH2CH2, CF3), (M-317, H, H, H, HOCH2CH2CH2, Br), (M-318, H, H, H, HOCH2CH2CH2, CH3), (M-319, H, H, H, HOCH2CH2CH2CH2, H), (M-320, H, H, H, HOCH2CH2CH2CH2, Cl), (M-321, H, H, H, HOCH2CH2CH2CH2, F), (M-322, H, H, H, HOCH2CH2CH2CH2, CF3), (M-323, H, H, H, HOCH2CH2CH2CH2, Br), (M-324, H, H, H, HOCH2CH2CH2CH2, CH3), (M-325, H, H, H, HOCH2CH2CH2CH2, H), (M-326, H, H, H, HOCH2CH2CH2CH2CH2, Cl), (M-327, H, H, H, HOCH2CH2CH2CH2CH2, F), (M-328, H, H, H, HOCH2CH2CH2CH2CH2, CF3), (M-329, H, H, H, HOCH2CH2CH2CH2CH2, Br), (M-330, H, H, H, HOCH2CH2CH2CH2CH2, CH3), (M-331, H, H, H, HOCH2CH2OCH2CH2, H), (M-332, H, H, H, HOCH2CH2OCH3CH2, Cl), (M-333, H, H, H, HOCH2CH2CH2CH2, F), (M-334, H, H, H, HOCH2CH2CH2CH2, CF3), (M-335, H, H, H, HOCH2CH2OCH2CH2, Br), (M-336, H, H, H, HOCH2CH2OCH2CH2, CH3), (M-337, H, H, H, (Me)2N, H), (M-338, H, H, H, (Me)2N, Cl), (M-339, H, H, H, (Me)2N, F), (M-340, H, H, H, (Me)2N, CF3), (M-341, H, H, H, (Me)2N, Br), (M-342, H, H, H, (Me)2N, CH3), (M-343, H, H, H, piperidin-4-yl-methyl, H), (M-344, H, H, H, piperidin-4-yl-methyl, Cl), (M-345, H, H, H, piperidin-4-yl-methyl, F), (M-346, H, H, H, piperidin-4-yl-methyl, CF3), (M-347, H, H, H, piperidin-4-yl-methyl, Br), (M-348, H, H, H, piperidin-4-yl-methyl, CH3), (M-349, H, H, H, cyclohexylmethyl, H), (M-350, H, H, H, cyclohexylmethyl, Cl), (M-351, H, H, H, cyclohexylmethyl, F), (M-352, H, H, H, cyclohexylmethyl, CF3), (M-353, H, H, H, cyclohexylmethyl, Br), (M-354, H, H, H, cyclohexylmethyl, CH3), (M-355, H, H, F, H, H), (M-356, H, H, F, H, Cl), (M-357, H, H, F, H, F), (M-358, H, H, F, H, CF3), (M-359, H, H, F, H, Br), (M-360, H, H, F, H, CH3), (M-361, H, H, F, F, H), (M-362, H, H, F, F, Cl), (M-363, H, H, F, F, F), (M-364, H, H, F, F, CF3), (M-365, H, H, F, F, Br), (M-366, H, H, F, F, CH3), (M-367, H, H, F, Cl, H), (M-368, H, H, F, Cl, Cl), (M-369, H, H, F, Cl, F), (M-370, H, H, F, Cl, CF3), (M-371, H, H, F, Cl, Br), (M-372, H, H, F, Cl, CH3), (M-373, H, H, F, CH3, H), (M-374, H, H, F, CH3, Cl), (M-375, H, H, F, CH3, F), (M-376, H, H, F, CH3, CF3), (M-377, H, H, F, CH3, Br), (M-378, H, H, F, CH3, CH3), (M-379, H, H, F, Et, H), (M-380, H, H, F, Et, Cl), (M-381, H, H, F, Et, F), (M-382, H, H, F, Et, CF3), (M-383, H, H, F, Et, Br), (M-384, H, H, F, Et, CH3), (M-385, H, H, F, n-Pr, H), (M-386, H, H, F, n-Pr, Cl), (M-387, H, H, F, n-Pr, F), (M-388, H, H, F, n-Pr, CF3), (M-389, H, H, F, n-Pr, Br), (M-390, H, H, F, n-Pr, CH3), (M-391, H, H, F, c-Pr, H), (M-392, H, H, F, c-Pr, Cl), (M-393, H, H, F, c-Pr, F), (M-394, H, H, F, c-Pr, CF3), (M-395, H, H, F, c-Pr, Br), (M-396, H, H, F, i-Pr, CH3), (M-397, H, H, F, i-Pr, H), (M-398, H, H, F, i-Pr, Cl), (M-399, H, H, F, i-Pr, F), (M-400, H, H, F, i-Pr, CF3), (M-401, H, H, F, i-Pr, Br), (M-402, H, H, F, i-Pr, CH3), (M-403, H, H, F, n-Bu, H), (M-404, H, H, F, n-Bu, Cl), (M-405, H, H, F, n-Bu, F), (M-406, H, H, F, n-Bu, CF3), (M-407, H, H, F, n-Bu, Br), (M-408, H, H, F, n-Bu, CH3), (M-409, H, H, F, i-Bu, H), (M-410, H, H, F, i-Bu, Cl), (M-411, H, H, F, i-Bu, F), (M-412, H, H, F, i-Bu, CF3), (M-413, H, H, F, i-Bu, Br), (M-414, H, H, F, i-Bu, CH3), (M-415, H, H, F, sec-Bu, H), (M-416, H, H, F, sec-Bu, Cl), (M-417, H, H, F, sec-Bu, F), (M-418, H, H, F, sec-Bu, CF3), (M-419, H, H, F, sec-Bu, Br), (M-420, H, H, F, sec-Bu, CH3), (M-421, H, H, F, n-Pen, H), (M-422, H, H, F, n-Pen, Cl), (M-423, H, H, F, n-Pen, F), (M-424, H, H, F, n-Pen, CF3), (M-425, H, H, F, n-Pen, Br), (M-426, H, H, F, n-Pen, CH3), (M-427, H, H, F, c-Pen, H), (M-428, H, H, F, c-Pen, Cl), (M-429, H, H, F, c-Pen, F), (M-430, H, H, F, c-Pen, CF3), (M-431, H, H, F, c-Pen, Br), (M-432, H, H, F, c-Pen, CH3), (M-433, H, H, F, n-Hex, H), (M-434, H, H, F, n-Hex, Cl), (M-435, H, H, F, n-Hex, F), (M-436, H, H, F, n-Hex, CF3), (M-437, H, H, F, n-Hex, Br), (M-438, H, H, F, n-Hex, CH3), (M-439, H, H, F, c-Hex, H), (M-440, H, H, F, c-Hex, Cl), (M-441, H, H, F, c-Hex, F), (M-442, H, H, F, c-Hex, CF3), (M-443, H, H, F, c-Hex, Br), (M-444, H, H, F, c-Hex, CH3), (M-445, H, H, F, OH, H), (M-446, U, H, F, OH, Cl), (M-447, H, H, F, OH, F), (M-448, H, H, F, OH, CF3), (M-449, H, H, F, OH, Br), (M-450, H, H, F, OH, CH3), (M-451, H, H, F, EtO, H), (M-452, H, H, F, EtO, Cl), (M-453, H, H, F, EtO, F), (M-454, H, H, F, EtO, CF3), (M-455, H, H, F, EtO, Br), (M-456, H, H, F, EtO, CH3), (M-457, H, H, F, n-PrO, H), (M-458, H, H, F, n-PrO, Cl), (M-459, H, H, F, n-PrO, F), (M-460, H, H, F, n-PrO, CF3), (M-461, H, H, F, n-PrO, Br), (M-462, H, H, F, n-PrO, CH3), (M-463, H, H, F, PhO, H), (M-464, H, H, F, PhO, Cl), (M-465, H, H, F, PhO, F), (M-466, H, H, F, PhO, CF3), (M-467, H, H, F, PhO, Br), (M-468, H, H, F, PhO, CH3), (M-469, H, H, F, BnO, H), (M-470, H, H, F, BnO, Cl), (M-471, H, H, F, BnO, F), (M-472, H, H, F, BnO, CF3), (M-473, H, H, F, BnO, Br), (M-474, H, H, F, BnO, CH3), (M-475, H, H, F, PhCH2CH2O, H), (M-476, H, H, F, PhCH2CH2O, Cl), (M-477, H, H, F, PhCH2CH2O, F), (M-478, H, H, F, PhCH2CH2O, CF3), (M-479, H, H, F, PhCH2CH2O, Br), (M-480, H, H, F, PhCH2CH2O, CH3), (M-481, H, H, F, CF3O, H), (M-482, H, H, F, CF3O, Cl), (M-483, H, H, F, CF3O, F), (M-484, H, H, F, CF3O, CF3), (M-485, H, H, F, CF3O, Br), (M-486, H, H, F, CF3O, CH3), (M-487, H, H, F, Ph, H), (M-488, H, H, F, Ph, Cl), (M-489, H, H, F, Ph, F), (M-490, H, H, F, Ph, CF3), (M-491, H, H, F, Ph, Br), (M-492, H, H, F, Ph, CH3), (M-493, H, H, F, 4-F-Ph, H), (M-494, H, H, F, 4-F-Ph, Cl), (M-495, H, H, F, 4-F-Ph, F), (M-496, H, H, F, 4-F-Ph, CF3), (M-497, H, H, F, 4-F-Ph, Br), (M-498, H, H, F, 4-F-Ph, CH3), (M-499, H, H, F, 4-CF3-Ph, H), (M-500, H, H, F, 4-CF3-Ph, Cl), (M-501, H, H, F, 4-CF3-Ph, F), (M-502, H, H, F, 4-CF3-Ph, CF3), (M-503, H, H, F, 4-CF3-Ph, Br), (M-504, H, H, F, 4-CF3-Ph, CH3), (M-505, H, H, F, 4-(Me)2N-Ph, H), (M-506, H, H, F, 4-(Me)2N-Ph, Cl), (M-507, H, H, F, 4-(Me)2N-Ph, F), (M-508, H, H, F, 4-(Me)2N-Ph, CF3), (M-509, H, H, F, 4-(Me)2N-Ph, Br), (M-510, H, H, F, 4-(Me)2N-Ph, CH3), (M-511, H, H, F, 4-OH-Ph, H), (M-512, H, H, F, 4-OH-Ph, Cl), (M-513, H, H, F, 4-OH-Ph, F), (M-514, H, H, F, 4-OH-Ph, CF3), (M-515, H, H, F, 4-OH-Ph, Br), (M-516, H, H, F, 4-OH-Ph, CH3), (M-517, H, H, F, 3,4-di-F-Ph, H), (M-518, H, H, F, 3,4-di-F-Ph, Cl), (M-519, H, H, F, 3,4-di-F-Ph, F), (M-520, H, H, F, 3,4-di-F-Ph, CF3), (M-521, H, H, F, 3,4-di-F-Ph, Br), (M-522, H, H, F, 3,4-di-F-Ph, CH3), (M-523, H, H, F, 4-COOH-Ph, H), (M-524, H, H, F, 4-COOH-Ph, Cl), (M-525, H, H, F, 4-COOH-Ph, F), (M-526, H, H, F, 4-COOH-Ph, CF3), (M-527, H, H, F, 4-COOH-Ph, Br), (M-528, H, H, F, 4-COOH-Ph, CH3), (M-529, H, H, F, Bn, H), (M-530, H, H, F, Bn, Cl), (M-531, H, H, F, Bn, F), (M-532, H, H, F, Bn, CF3), (M-533, H, H, F, Bn, Br), (M-534, H, H, F, Bn, CH3), (M-535, H, H, F, 4-F-Bn, H), (M-536, H, H, F, 4-F-Bn, Cl), (M-537, H, H, F, 4-F-Bn, F), (M-538, H, H, F, 4-F-Bn, CF3), (M-539, H, H, F, 4-F-Bn, Br), (M-540, H, H, F, 4-F-Bn, CH3), (M-541, H, H, F, 2-Py, H), (M-542, H, H, F, 2-Py, Cl), (M-543, H, H, F, 2-Py, F), (M-544, H, H, F, 2-Py, CF3), (M-545, H, H, F, 2-Py, Br), (M-546, H, H, F, 2-Py, CH3), (M-547, H, H, F, 3-Py, H), (M-548, H, H, F, 3-Py, Cl), (M-549, H, H, F, 3-Py, F), (M-550, H, H, F, 3-Py, CF3), (M-551, H, H, F, 3-Py, Br), (M-552, H, H, F, 3-Py, CH3), (M-553, H, H, F, 4-Py, H), (M-554, H, H, F, 4-Py, Cl), (M-555, H, H, F, 4-Py, F), (M-556, H, H, F, 4-Py, CF3), (M-557, H, H, F, 4-Py, Br), (M-558, H, H, F, 4-Py, CH3), (M-559, H, H, F, 2-Th, H), (M-560, H, H, F, 2-Th, Cl), (M-561, H, H, F, 2-Th, F), (M-562, H, H, F, 2-Th, CF3), (M-563, H, H, F, 2-Th, Br), (M-564, H, H, F, 2-Th, CH3), (M-565, H, H, F, 3-Th, H), (M-566, H, H, F, 3-Th, Cl), (M-567, H, H, F, 3-Th, F), (M-568, H, H, F, 3-Th, CF3), (M-569, H, H, F, 3-Th, Br), (M-570, H, H, F, 3-Th, CH3), (M-571, H, H, F, pyrrazol-2-yl, H), (M-572, H, H, F, pyrrazol-2-yl, Cl), (M-573, H, H, F, pyrrazol-2-yl, F), (M-574, H, H, F, pyrrazol-2-yl, CF3), (M-575, H, H, F, pyrrazol-2-yl, Br), (M-576, H, H, F, pyrrazol-2-yl, CH3), (M-577, H, H, F, pyrrazol-3-yl, H), (M-578, H, H, F, pyrrazol-3-yl, Cl), (M-579, H, H, F, pyrrazol-3-yl, F), (M-580, H, H, F, pyrrazol-3-yl, CF3), (M-581, H, H, F, pyrrazol-3-yl, Br), (M-582, H, H, F, pyrrazol-3-yl, CH3), (M-583, H, H, F, pyrimidine-2-yl, H), (M-584, H, H, F, pyrimidin-2-yl, Cl), (M-585, H, H, F, pyrimidin-2-yl, F), (M-586, H, H, F, pyrimidin-2-yl, CF3), (M-587, H, H, F, pyrimidin-2-yl, Br), (M-588, H, H, F, pyrimidin-2-yl, CH3), (M-589, H, H, F, pyrimidin-4-yl, H), (M-590, H, H, F, pyrimidin-4-yl, Cl), (M-591, H, H, F, pyrimidin-4-yl, F), (M-592, H, H, F, pyrimidin-4-yl, CF3), (M-593, H, H, F, pyrimidin-4-yl, Br), (M-594, H, H, F, pyrimidin-4-yl, CH3), (M-595, H, H, F, pyrimidin-5-yl, H), (M-596, H, H, F, pyrimidin-5-yl, Cl), (M-597, H, H, F, pyrimidin-5-yl, F), (M-598, H, H, F, pyrimidin-5-yl, CF3), (M-599, H, H, F, pyrimidin-5-yl, Br), (M-600, H, H, F, pyrimidin-5-yl, CH3), (M-601, H, H, F, HOOCCH2CH2CH2, H), (M-602, H, H, F, HOOCCH2CH2CH2, Cl), (M-603, H, H, F, HOOCCH2CH2CH2, F), (M-604, H, H, F, HOOCCH2CH2CH2, CF3), (M-605, H, H, F, HOOCCH2CH2CH2, Br), (M-606, H, H, F, HOOCCH2CH2CH2, CH3), (M-607, H, H, F, HOOCCH2CH2CH2CH2, H), (M-608, H, H, F, HOOCCH2CH2CH2CH2, Cl), (M-609, H, H, F, HOOCCH2CH2CH2CH2, F), (M-610, H, H, F, HOOCCH2CH2CH2CH2, CF3), (M-611, H, H, F, HOOCCH2CH2CH2CH2, Br), (M-612, H, H, F, HOOCCH2CH2CH2CH2, CH3), (M-613, H, H, F, (Me)2NCOCH2CH2CH2CH2, H), (M-614, H, H, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-615, H, H, F, (Me)2NCOCH2CH2CH2CH2, F), (M-616, H, H, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-617, H, H, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-618, H, H, F, (Me)2NCOCH2CHaCH2CH2, CH2), (M-619, H, H, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-620, H, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-621, H, H, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-622, H, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-623, H, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-624, H, H, F, (Me)3NCOCH2CH2CH2CH2CH2, CH2), (M-625, H, H, F, MeOCH2, H), (M-626, H, H, F, MeOCH2, Cl), (M-627, H, H, F, MeOCH2, F), (M-628, H, H, F, MeOCH2, CF3), (M-629, H, H, F, MeOCH2, Br), (M-630, H, H, F, MeOCH2, CH3), (M-631, H, H, F, EtOCH2, H), (M-632, H, H, F, EtOCH2, Cl), (M-633, H, H, F, EtOCH2, F), (M-634, H, H, F, EtOCH2, CF3), (M-635, H, H, F, EtOCH2, Br), (M-636, H, Ft, F, EtOCH2, CH3), (M-637, H, H, F, EtOCH2CH2, H), (M-638, H, H, F, EtOCH2CH2, Cl), (M-639, H, H, F, EtOCH2CH2, F), (M-640, H, H, F, EtOCH2CH2, CF3), (M-641, H, H, F, EtOCH2CH2, Br), (M-642, H, H, F, EtOCH2CH2, CH3), (M-643, H, H, F, MeOCH2CH2OCH2CH2, H), (M-644, H, H, F, MeOCH2CH2OCH2CH2, Cl), (M-645, H, H, F, MeOCH2CH2OCH2CH2, F), (M-646, H, H, F, MeOCH2CH2OCH2CH2, CF3), (M-647, H, H, F, MeOCH2CH2OCH2CH2, Br), (M-648, H, H, F, MeOCH2CH2OCH2CH2, CH3), (M-649, H, H, F, MeOCH2CH2, H), (M-650, H, H, F, MeOCH2CH2, Cl), (M-651, H, H, F, MeOCH2CH2, F), (M-652, H, H, F, MeOCH2CH2, CF3), (M-653, H, H, F, MeOCH2CH2, Br), (M-654, H, H, F, MeOCH2CH2, CH3), (M-655, H, H, F, HOCH2, H), (M-656, H, H, F, HOCH2, Cl), (M-657, H, H, F, HOC Ha, F), (M-658, H, H, F, HOCH2, CF3), (M-659, H, H, F, HOCH2, Br), (M-660, H, H, F, HOCH2, CH3), (M-661, H, H, F, HOCH2CH2, H), (M-662, H, H, F, HOCH2CH2, Cl), (M-663, H, H, F, HOCH2CH2, F), (M-664, H, H, F, HOCH2CH2, CF3), (M-665, H, H, F, HOCH2CH2, Br), (M-666, H, H, F, HOCH2CH2, CH3), (M-667, H, H, F, HOCH2CH2CH2, H), (M-668, H, H, F, HOCH2CH2CH2, Cl), (M-669, H, H, F, HOCH2CH2CH2, F), (M-670, H, H, F, HOCH2CH2CH3, CF3), (M-671, H, H, F, HOCH2CH2CH2, Br), (M-672, H, H, F, HOCH2CH2CH2, CH3), (M-673, H, H, F, HOCH2CH2CH2CH2, H), (M-674, H, H, F, HOCH2CH2CH2CH2, Cl), (M-675, H, H, F, HOCH2CH2CH2CH2, F), (M-676, H, H, F, HOCH2CH2CH2CH2, CF3), (M-677, H, H, F, HOCH2CH2CH2CH2, Br), (M-678, H, H, F, HOCH2CH2CH2CH2, CH3), (M-679, H, H, F, HOCH2CH2CH2CH2CH2, H), (M-680, H, H, F, HOCH2CH2CH2CH2CH2, Cl), (M-681, H, H, F, HOCH2CH2CH2CH2CH2, F), (M-682, H, H, F, HOCH2CH2CH2CH2CH2, CF3), (M-683, H, H, F, HOCH2CH2CH2CH2CH2, Br), (M-684, H, H, F, HOCH2CH2CH2CH2CH2, CH3), (M-685, H, H, F, HOCH2CH2OCH3CH2, H), (M-686, H, H, F, HOCH2CH2OCH2CH2, Cl), (M-687, H, H, F, HOCH2CH2OCH2CH2, F), (M-688, H, H, F, HOCH2CH2OCH2CH2, CF3), (M-689, H, H, F, HOCH2CH2OCH2CH2, Br), (M-690, H, H, F, HOCH2CH2OCH2CH2, CH3), (M-691, H, H, F, (Me)2N, H), (M-692, H, H, F, (Me)2N, Cl), (M-693, H, H, F, (Me)2N, F), (M-694, H, H, F, (Me)2N, CF3), (M-695, H, H, F, (Me)2N, Br), (M-696, H, H, F, (Me)2N, CH3), (M-697, H, H, F, piperidin-4-ylmethyl, H), (M-698, H, H, F, piperidin-4-yl-methyl, Cl), (M-699, H, H, F, piperidin-4-yl-methyl, F), (M-700, H, H, F, piperidin-4-yl-methyl, CF3), (M-701, H, H, F, piperidin-4-yl-methyl, Br), (M-702, H, H, F, piperidin-4-yl-methyl, CH3), (M-703, H, H, F, cyclohexylmethyl, H), (M-704, H, H, F, cyclohexylmethyl, Cl), (M-705, H, H, F, cyclohexylmethyl, F), (M-706, H, H, F, cyclohexylmethyl, CF3), (M-707, H, H, F, cyclohexylmethyl, Br), (M-708, H, H, F, cyclohexylmethyl, CH3), (M-709, H, H, Cl, H, H), (M-710, H, H, Cl, H, Cl), (M-711, H, H, Cl, H, F), (M-712, H, H, Cl, H, CF3), (M-713, H, H, Cl, H, Br), (M-714, H, H, Cl, H, CH3), (M-715, H, H, Cl, F, H), (M-716, H, H, Cl, F, Cl), (M-717, H, H, Cl, F, F), (M-718, H, H, Cl, F, CF3), (M-719, H, H, Cl, F, Br), (M-720, H, H, Cl, F, CH3), (M-721, H, H, Cl, Cl, H), (M-722, H, H, Cl, Cl, Cl), (M-723, H, H, Cl, Cl, F), (M-724, H, H, Cl, Cl, CF3), (M-725, H, H, Cl, Cl, Br), (M-726, H, H, Cl, Cl, CH3), (M-727, H, H, H, CH3H), (M-728, H, H, Cl, CH3, Cl), (M-729, H, H, Cl, CH3, F), (M-730, H, H, Cl, CH3, CF3), (M-731, H, H, Cl, CH3, Br), (M-732, H, H, Cl, CH3, CH3), (M-733, H, H, Cl, Et, H), (M-734, H, H, Cl, Et, Cl), (M-735, H, H, Cl, Et, F), (M-736, H, H, Cl, Et, CF3), (M-737, H, H, Cl, Et, Br), (M-738, H, H, Cl, Et, CH3), (M-739, H, H, Cl, n-Pr, H), (M-740, H, H, Cl, n-Pr, Cl), (M-741, H, H, Cl, n-Pr, F), (M-742, H, H, Cl, n-Pr, CF3), (M-743, H, H, Cl, n-Pr, Br), (M-744, H, H, Cl, n-Pr, CH3), (M-745, H, H, Cl, c-Pr, H), (M-746, H, H, Cl, c-Pr, Cl), (M-747, H, H, Cl, c-Pr, F), (M-748, H, H, Cl, c-Pr, CF3), (M-749, H, H, Cl, c-Pr, Br), (M-750, H, H, Cl, c-Pr, CH3), (M-751, H, H, Cl, i-Pr, H), (M-752, H, H, Cl, i-Pr, Cl), (M-753, H, H, Cl, i-Pr, F), (M-754, H, H, Cl, i-Pr, CF3), (M-755, H, H, Cl, i-Pr, Br), (M-756, H, H, Cl, i-Pr, CH3), (M-757, H, H, Cl, n-Bu, H), (M-758, H, H, Cl, n-Bu, Cl), (M-759, H, H, Cl, n-Bu, F), (M-760, H, H, Cl, n-Bu, CF3), (M-761, H, H, Cl, n-Bu, Br), (M-762, H, H, Cl, n-Bu, CH3), (M-763, H, H, Cl, i-Bu, H), (M-764, H, H, Cl, i-Bu, Cl), (M-765, H, H, Cl, i-Bu, F), (M-766, H, H, Cl, i-Bu, CF3), (M-767, H, H, Cl, i-Bu, Br), (M-768, H, H, Cl, i-Bu, CH3), (M-769, H, H, Cl, sec-Bu, H), (M-770, H, H, Cl, sec-Bu, Cl), (M-771, H, H, Cl, sec-Bu, F), (M-772, H, H, Cl, sec-Bu, CF3), (M-773, H, H, Cl, sec-Bu, Br), (M-774, H, H, Cl, sec-Bu, CH3), (M-775, H, H, Cl, n-Pen, H), (M-776, H, H, Cl, n-Pen, Cl), (M-777, H, H, Cl, n-Pen, F), (M-778, H, H, Cl, n-Pen, CF3), (M-779, H, H, Cl, n-Pen, Br), (M-780, H, H, Cl, n-Pen, CH3), (M-781, H, H, Cl, c-Pen, H), (M-782, H, H, Cl, c-Pen, Cl), (M-783, H, H, Cl, c-Pen, F), (M-784, H, H, Cl, c-Pen, CF3), (M-785, H, H, Cl, c-Pen, Br), (M-786, H, H, Cl, c-Pen, CH3), (M-787, H, H, Cl, n-Hex, H), (M-788, H, H, Cl, n-Hex, Cl), (M-789, H, H, Cl, n-Hex, F), (M-790, H, H, Cl, n-Hex, CF3), (M-791, H, H, Cl, n-Hex, Br), (M-792, H, H, Cl, n-Hex, CH3), (M-793, H, H, Cl, c-Hex, H), (M-794, H, H, Cl, c-Hex, Cl), (M-795, H, H, Cl, c-Hex, F), (M-796, H, H, Cl, c-Hex, CF3), (M-797, H, H, Cl, c-Hex, Br), (M-798, H, H, Cl, c-Hex, CH3), (M-799, H, H, Cl, OH, H), (M-800, H, H, Cl, OH, Cl), (M-801, H, H, Cl, OH, F), (M-802, H, H, Cl, OH, CF3), (M-803, H, H, Cl, OH, Br), (M-804, H, H, Cl, OH, CH3), (M-805, H, H, Cl, EtO, H), (M-806, H, H, Cl, EtO, Cl), (M-807, H, H, Cl, EtO, P), (M-808, H, H, Cl, EtO, CF3), (M-809, H, H, Cl, EtO, Br), (M-810, H, H, Cl, EtO, CH3), (M-811, H, H, Cl, n-PrO, H), (M-812, H, H, Cl, n-PrO, Cl), (M-813, H, H, Cl, n-PrO, F), (M-814, H, H, Cl, n-PrO, CF3), (M-815, H, H, Cl, n-PrO, Br), (M-816, H, H, Cl, n-PrO, CH3), (M-817, H, H, Cl, PhO, H), (M-818, H, H, Cl, PhO, Cl), (M-819, H, H, Cl, PhO, F), (M-820, H, H, Cl, PhO, CF3), (M-821, H, H, Cl, PhO, Br), (M-822, H, H, Cl, PhO, CH3), (M-823, H, H, Cl, BnO, H), (M-824, H, H, Cl, BnO, Cl), (M-825, H, H, Cl, BnO, F), (M-826, H, H, Cl, BnO, CF3), (M-827, H, H, Cl, BnO, Br), (M-828, H, H, Cl, BnO, CH3), (M-829, H, H, Cl, PhCH2CH2O, H), (M-830, H, H, Cl, PhCH2CH2O, Cl), (M-831, H, H, Cl, PhCH2CH2O, F), (M-832, H, H, Cl, PhCH2CH2O, CF3), (M-833, H, H, Cl, PhCH2CH2O, Br), (M-834, H, H, Cl, PhCH2CH2O, CH3), (M-835, H, H, Cl, CF3O, H), (M-836, H, H, Cl, CF3O, Cl), (M-837, H, H, Cl, CF3O, F), (M-838, H, H, Cl, CF3O, CF3), (M-839, H, H, Cl, CF3O, Br), (M-840, H, H, Cl, CF3O, CH3), (M-841, H, H, Cl, Ph, H), (M-842, H, H, Cl, Ph, Cl), (M-843, H, H, Cl, Ph, F), (M-844, H, H, Cl, Ph, CF3), (M-845, H, H, Cl, Ph, Br), (M-846, H, H, Cl, Ph, CH3), (M-847, H, H, Cl, 4-F-Ph, H), (M-848, H, H, Cl, 4-F-Ph, Cl), (M-849, H, H, Cl, 4-F-Ph, F), (M-850, H, H, Cl, 4-F-Ph, CF3), (M-851, H, H, Cl, 4-F-Ph, Br), (M-852, H, H, Cl, 4-F-Ph, CH3), (M-853, H, H, Cl, 4-CF3-Ph, H), (M-854, H, H, Cl, 4-CF3-Ph, Cl), (M-855, H, H, Cl, 4-CF3-Ph, F), (M-856, H, H, Cl, 4-CF3-Ph, CF3), (M-857, H, H, Cl, 4-CF3-Ph, Br), (M-858, H, H, Cl, 4-CF3-Ph, CH3), (M-859, H, H, Cl, 4-(Me)2N-Ph, H), (M-860, H, H, Cl, 4-(Me)2N-Ph, Cl), (M-861, H, H, Cl, 4-(Me)2N-Ph, F), (M-862, H, H, Cl, 4-(Me)2N-Ph, CF3), (M-863, H, H, Cl, 4-(Me)2N-Ph, Br), (M-864, H, H, Cl, 4-(Me)2N-Ph, CH3), (M-865, H, H, Cl, 4-OH-Ph, H), (M-866, H, H, Cl, 4-OH-Ph, Cl), (M-867, H, H, Cl, 4-OH-Ph, F), (M-868, H, H, Cl, 4-OH-Ph, CF3), (M-869, H, H, Cl, 4-OH-Ph, Br), (M-870, H, H, Cl, 4-OH-Ph, CH3), (M-871, H, H, Cl, 3,4-di-F-Ph, H), (M-872, H, H, Cl, 3,4-di-F-Ph, Cl), (M-873, H, H, Cl, 3,4-di-F-Ph, F), (M-874, H, H, Cl, 3,4-di-F-Ph, CF3), (M-875, H, H, Cl, 3,4-di-F-Ph, Br), (M-876, H, H, Cl, 3,4-di-F-Ph, CH3), (M-877, H, H, Cl, 4-COOH-Ph, H), (M-878, H, H, Cl, 4-COOH-Ph, Cl), (M-879, H, H, Cl, 4-COOH-Ph, F), (M-880, H, H, Cl, 4-COOH-Ph, CF3), (M-881, H, H, Cl, 4-COOH-Ph, Br), (M-882, H, H, Cl, 4-COOH-Ph, CH3), (M-883, H, H, Cl, Bn, H), (M-884, H, H, Cl, Bn, Cl), (M-885, H, H, Cl, Bn, F), (M-886, H, H, Cl, Bn, CF3), (M-887, H, H, Cl, Bn, Br), (M-888, H, H, CL, Bn, CH3), (M-889, H, H, Cl, 4-F-Bn, H), (M-890, H, H, Cl, 4-F-Bn, Cl), (M-891, H, H, Cl, 4-F-Bu, F), (M-892, H, H, Cl, 4-F-Bn, CF3), (M-893, H, H, Cl, 4-F-Bn, Br), (M-894, H, H, Cl, 4-F-Bn, CH3), (M-895, H, H, Cl, 2-Py, H), (M-896, H, H, Cl, 2-Py, Cl), (M-897, H, H, Cl, 2-Py, F), (M-898, H, H, Cl, 2-Py, CF3), (M-899, H, H, Cl, 2-Py, Br), (M-900, H, H, Cl, 2-Py, CH3), (M-901, H, H, Cl, 3-Py, H), (M-902, H, H, Cl, 3-Py, Cl), (M-903, H, H, Cl, 3-Py, F), (M-904, H, H, Cl, 3-Py, CF3), (M-905, H, H, Cl, 3-Py, Br), (M-906, H, H, Cl, 3-Py, CH3), (M-907, H, H, Cl, 4-Py, H), (M-908, H, H, Cl, 4-Py, Cl), (M-909, H, H, Cl, 4-Py, F), (M-910, H, H, Cl, 4-Py, CF3), (M-911, H, H, Cl, 4-Py, Br), (M-912, H, H, Cl, 4-Py, CH3), (M-913, H, H, Cl, 2-Th, H), (M-914, H, H, Cl, 2-Th, Cl), (M-915, H, H, Cl, 2-Th, F), (M-916, H, H, Cl, 2-Th, CF3), (M-917, H, H, Cl, 2-Th, Br), (M-918, H, H, Cl, 2-Th, CH3), (M-919, H, H, Cl, 3-Th, H), (M-920, H, H, Cl, 3-Th, Cl), (M-921, H, H, Cl, 3-Th, F), (M-922, H, H, Cl, 3-Th, CF3), (M-923, H, H, Cl, 3-Th, Br), (M-924, H, H, Cl, 3-Th, CH3), (M-925, H, H, Cl, pyrrazol, 2-yl, H), (M-926, H, H, Cl, pyrrazol-2-yl, Cl), (M-927, H, H, Cl, pyrrazol-2-yl, F), (M-928, H, H, Cl, pyrrazol-2-yl, CF3), (M-929, H, H, Cl, pyrrazol-2-yl, Br), (M-930, H, H, Cl, pyrrazol-2-yl, CH3), (M-931, H, H, Cl, pyrrazol-3-yl, H), (M-932, H, H, Cl, pyrrazol-3-yl, Cl), (M-933, H, H, Cl, pyrrazol-3-yl, F), (M-934, H, H, Cl, pyrrazol-2-yl, CF3), (M-935, H, H, Cl, pyrrazol-3-yl, Br), (M-936, H, H, Cl, pyrrazol-3-yl, CH3), (M-937, H, H, Cl, pyrimidin-2-yl, H), (M-938, H, H, Cl, pyrimidin-2-yl, Cl), (M-939, H, H, Cl, pyrimidin-2-yl, F), (M-940, H, H, Cl, pyrimidin-2-yl, CF3), (M-941, H, H, Cl, pyrimidin-2-yl, Br), (M-942, H, H, Cl, pyrimidin-2-yl, CH2), (M-943, H, H, Cl, pyrimidin-4-yl, H), (M-944, H, H, Cl, pyrimidin-4-yl, Cl), (M-945, H, H, Cl, pyrimidin-4-yl, F), (M-946, H, H, Cl, pyrimidin-4-yl, CF3), (M-947, H, H, Cl, pyrimidin-4-yl, Br), (M-948, H, H, Cl, pyrimidin-4-yl, CH3), (M-949, H, H, Cl, pyrimidin-5-yl, H), (M-950, H, H, Cl, pyrimidin-5-yl, Cl), (M-951, H, H, Cl, pyrimidin-5-yl, F), (M-952, H, H, Cl, pyrimidin-5-yl, CF3), (M-953, H, H, Cl, pyrimidin-5-yl, Br), (M-954, H, H, Cl, pyrimidin-5-yl, CH3), (M-955, H, H, Cl, HOOCCH2CH2CH2, H), (M-956, H, H, Cl, HOOCCH2CH2CH2, Cl), (M-957, H, H, Cl, HOOCCH2CH2CH2, F), (M-958, H, H, Cl, HOOCCH2CH2CH2, CF3), (M-959, H, H, Cl, HOOCCH2CH2CH2, Br), (M-960, H, H, Cl, HOOCCH2CH2CH2, CH3), (M-961, H, H, Cl, HOOCCH2CH2CH2CH2, H), (M-962, H, H, Cl, HOOCCH2CH2CH2CH2, Cl), (M-963, H, H, Cl, HOOCCH2CH2CH2CH2, F), (M-964, H, H, Cl, HOOCCH2CH2CH2CH2, CF3), (M-965, H, H, Cl, HOOCCH2CH2CH2CH2, Br), (M-966, H, H, Cl, HOOCCH2CH2CH2CH2, CH3), (M-967, H, H, Cl, (Me)2NCOCH3CH2CH2CF2, H), (M-968, H, H, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-969, H, H, Cl, (Me)2NCOCH3CH2CH2CH2, F), (M-970, H, H, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-971, H, H, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-972, H, H, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-973, H, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-974, H, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-975, H, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-976, H, H, Cl, (Me2NCOC)2CH2CH2CH2CH2, CF3), (M-977, H, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-978, H, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-979, H, H, Cl, MeOCH2, H), (M-980, H, H, Cl, MeOCH2, Cl), (M-981, H, H, Cl, MeOCH2, F), (M-982, H, H, Cl, MeOCH2, CF3), (M-983, H, H, Cl, MeOCH2, Br), (M-984, H, H, Cl, MeOCH2, CH2), (M-985, H, H, Cl, EtOCH2, H), (M-986, H, H, Cl, EtOCH2, Cl), (M-987, H, H, Cl, EtOCH2, F), (M-988, H, H, Cl, EtOCH2, CF3), (M-989, H, H, Cl, EtOCH2, Br), (M-990, H, H, Cl, EtOCH2, CH3), (M-991, H, H, Cl, EtOCH2CH2, H), (M-992, H, H, Cl, EtOCH2CH2, Cl), (M-993, H, H, Cl, EtOCH2CH2, F), (M-994, H, H, Cl, EtOCH2CH2, CF3), (M-995, H, H, Cl, EtOCH2CH2, Br), (M-996, H, H, Cl, EtOCH2CH2, CH3), (M-997, H, H, Cl, MeOCH2CH2OCH2CH2, H), (M-998, H, H, Cl, MeOCH2CH2OCH2CH2, Cl), (M-999, H, H, Cl, MeOCH2CH2OCH2CH2, F), (M-1000, H, H, Cl, MeOCH2CH2OCH2CH2, CF3), (M-1001, H, H, Cl, MeOCH2CH2OCH2CH2, Br), (M-1002, H, H, Cl, MeOCH2CH2OCH2CH2, CH3), (M-1003, H, H, Cl, MeOCH2CH2, H), (M-1004, H, H, Cl, MeOCH2CH2, Cl), (M-1005, H, H, Cl, MeOCH2CH2, F), (M-1006, H, H, Cl, MeOCH2CH2, CF3), (M-1007, H, H, Cl, MeOCH2CH2, Br), (M-1008, H, H, Cl, MeOCH2CH2, CH2), (M-1009, H, H, Cl, HOCH2, H), (M-1010, H, H, Cl, HOCH2, Cl), (M-1011, H, H, Cl, HOCH2, F), (M-1012, H, H, Cl, HOCH2, CF3), (M-1013, H, H, Cl, HOCH2, Br), (M-1014, H, H, Cl, HOCH2, CH3), (M-1015, H, H, Cl, HOCH2CH2, H), (M-1016, H, H, Cl, HOCH2CH2, Cl), (M-1017, H, H, Cl, HOCH2CH2, F), (M-1018, H, H, Cl, HOCH2CH2, CF3), (M-1019, H, H, Cl, HOCH2CH2, Br), (M-1020, H, H, Cl, HOCH2CH2, CH3), (M-1021, H, H, Cl, HOCH2CH2CH2, H), (M-1022, H, H, Cl, HOCH2CH2CH2, Cl), (M-1023, H, H, Cl, HOCH2CH2CH2, F), (M-1024, H, H, Cl, HOCH2CH2CH2, CF3), (M-1025, H, H, Cl, HOCH2CH2CH2, Br), (M-1026, H, H, Cl, HOCH2CH2CH2, CH2), (M-1027, H, H, Cl, HOCH2CH2CH2CH2, H), (M-1028, H, H, Cl, HOCH2CH2CH2CH2, Cl), (M-1029, H, H, Cl, HOCH2CH2CH2CH2, F), (M-1030, H, H, Cl, HOCH2CH2CH2CH2, CF3), (M-1031, H, H, Cl, HOCH2CH2CH2CH2, Br), (M-1032, H, H, Cl, HOCH2CH2CH2CH2, CH3), (M-1033, H, H, Cl, HOCH2CH2CH2CH2CH2, H), (M-1034, H, H, Cl, HOCH2CH2CH2CH2CH2, Cl), (M-1035, H, H, Cl, HOCH2CH2CH2CH2CH2, F), (M-1036, H, H, Cl, HOCH2CH2CH2CH2CH2, CF3), (M-1037, H, H, Cl, HOCH2CH2CH2CH2CH2, Br), (M-1038, H, H, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-1039, H, H, Cl, HOCH2CH2OCH2CH2, H), (M-1040, H, H, Cl, HOCH2CH2OCH2CH2, Cl), (M-1041, H, H, Cl, HOCH2CH2OCH2CH2, F), (M-1042, H, H, Cl, HOCH2CH2OCH2CH2, CF3), (M-1043, H, H, Cl, HOCH2CH2OCH2CH2, Br) (M-1044, H, H, Cl, HOCH2CH2OCH2CH2, CH3), (M-1045, H, H, Cl, (Me)2N, H), (M-1046, H, H, Cl, (Me)2N, Cl), (M-1047, H, H, Cl, (Me)3N, F), (M-1048, H, H, Cl, (Me)2N, CF3), (M-1049, H, H, Cl, (Me)2N, Br), (M-1050, H, H, Cl, (Me)2N, CH3), (M-1051, H, H, Cl, piperidin-4-yl-methyl, H), (M-1052, H, H, Cl, piperidin-4-yl-methyl, Cl), (M-1053, H, H, Cl, piperidin-4-yl-methyl, F), (M-1054, H, H, Cl, piperidin-4-yl-methyl, CF3), (M-1055, H, H, Cl, piperidin-4-yl-methyl, Br), (M-1056, H, H, Cl, piperidin-4-yl-methyl, CH3), (M-1057, H, H, Cl, cyclohexylmethyl, H), (M-1058, H, H, Cl, cyclohexylmethyl, Cl), (M-1059, H, H, Cl, cyclohexylmethyl, F), (M-1060, H, H, Cl, cyclohexylmethyl, CF3), (M-1061, H, H, Cl, cyclohexylmethyl, Br), (M-1062, H, H, Cl, cyclohexylmethyl, CH3), (M-1063, H, F, H, H, H), (M-1064, H, F, H, H, Cl), (M-1065, H, F, H, H, F), (M-1066, H, F, H, H, CF3), (M-1067, H, F, H, H, Br), (M-1068, H, F, H, H, CH3), (M-1069, H, F, H, F, H), (M-1070, H, F, H, F, Cl), (M-1071, H, F, H, F, F), (M-1072, H, F, H, F, CF3), (M-1073, H, F, H, F, Br), (M-1074, H, F, H, F, CH3), (M-1075, H, F, H, Cl, H), (M-1076, H, F, H, Cl, Cl), (M-1077, H, F, H, Cl, F), (M-1078, H, F, H, Cl, CF3), (M-1079, H, F, H, Cl, Br), (M-1080, H, F, H, Cl, CH2), (M-1081, H, F, H, CH2, H), (M-1082, H, F, H, CH2, Cl), (M-1083, H, F, H, CH2, F), (M-1084, H, F, H, CH2, CF3), (M-1085, H, F, H, CH2, Br), (M-1086, H, F, H, CH3, CH3), (M-1087, H, F, H, Et, H), (M-1088, H, F, H, Et, Cl), (M-1089, H, F, H, Et, F), (M-1090, H, F, H, Et, CF3), (M-1091, H, F, H, Et, Br), (M-1092, H, F, H, Et, CH3), (M-1093, H, F, H, n-Pr, H), (M-1094, H, F, H, n-Pr, Cl), (M-1095, H, F, H, n-Pr, F), (M-1096, H, F, H, n-Pr, CF3), (M-1097, H, F, H, n-Pr, Br), (M-1098, H, F, H, n-Pr, CH3), (M-1099, H, F, H, c-Pr, H), (M-1100, H, F, H, c-Pr, Cl), (M-1101, H, F, H, c-Pr, F), (M-1102, H, F, H, c-Pr, CF3), (M-1103, H, F, H, c-Pr, Br), (M-1104, H, F, H, c-Pr, CH3), (M-1105, H, F, H, i-Pr, H), (M-1106, H, F, H, i-Pr, Cl), (M-1107, H, F, H, i-Pr, F), (M-1108, H, F, H, i-Pr, CF3), (M-1109, H, F, H, i-Pr, Br), (M-1110, H, F, H, i-Pr, CH3), (M-1111, H, F, H, n-Bu, H), (M-1112, H, F, H, n-Bu, Cl), (M-1113, H, F, H, n-Bu, F), (M-1114, H, F, H, n-Bu, CF3), (M-1115, H, F, H, n-Bu, Br), (M-1116, H, F, H, n-Bu, CH3), (M-1117, H, F, H, i-Bu, H), (M-1118, H, F, H, i-Bu, Cl), (M-1119, H, F, H, i-Bu, F), (M-1120, H, F, H, i-Bu, CF3), (M-1121, H, F, H, i-Bu, Br), (M-1122, H, F, H, i-Bu, CH3), (M-1123, H, F, H, sec-Bu, H), (M-1124, H, F, H, sec-Bu, Cl), (M-1125, H, F, H, sec-Bu, F), (M-1126, H, F, H, sec-Bu, CF3), (M-1127, H, F, H, sec-Bu, Br), (M-1128, H, F, H, sec-Bu, CH3), (M-1129, H, F, H, n-Pen, H), (M-1130, B, F, H, n-Pen, Cl), (M-1131, H, F, H, n-Pen, F), (M-1132, H, F, H, n-Pen, CF3), (M-1133, H, F, H, n-Pen, Br), (M-1134, H, F, H, n-Pen, CH2), (M-1135, H, F, H, c-Pen, H), (M-1136, H, F, H, c-Pen, Cl), (M-1137, H, F, H, c-Pen, F), (M-1138, H, F, H, c-Pen, CF3), (M-1139, H, F, H, c-Pen, Br), (M-1140, H, F, H, c-Pen, CH3), (M-1141, H, F, H, n-Hex, H), (M-1142, H, F, H, n-Hex, Cl), (M-1143, H, F, H, n-Hex, F), (M-1144, H, F, H, n-Hex, CF3), (M-1145, H, F, H, n-Hex, Br), (M-1146, H, F, H, n-Hex, CH3), (M-1147, H, F, H, c-Hex, H), (M-1148, H, F, H, c-Hex, Cl), (M-1149, H, F, H, c-Hex, F), (M-1150, H, F, H, c-Hex, CF3), (M-1151, H, F, H, c-Hex, Br), (M-1152, H, F, H, c-Hex, CH2), (M-1153, H, F, H, OH, H), (M-1154, H, F, H, OH, Cl), (M-1155, H, F, H, OH, F), (M-1156, H, F, H, OH, CF3), (M-1157, H, F, H, OH, Br), (M-1158, H, F, H, OH, CH3), (M-1159, H, F, H, EtO, H), (M-1160, H, F, H, EtO, Cl), (M-1161, H, F, H, EtO, F), (M-1162, H, F, H, EtO, CF3), (M-1163, H, F, H, EtO, Br), (M-1164, H, F, H, EtO, CH3), (M-1165, H, F, H, n-PrO, H), (M-1166, H, F, H, n-PrO, Cl), (M-1167, H, F, H, n-PrO, F), (M-1168, H, F, H, n-PrO, CF3), (M-1169, H, F, H, n-PrO, Br), (M-1170, H, F, H, n-PrO, CH2), (M-1171, H, F, H, PhO, H), (M-1172, H, F, H, PhO, Cl), (M-1173, H, F, H, PhO, F), (M-1174, H, F, H, PhO, CF3), (M-1175, H, F, H, PhO, Br), (M-1176, H, F, H, PhO, CH3), (M-1177, H, F, H, BnO, H), (M-1178, H, F, H, BnO, Cl), (M-1179, H, F, H, BnO, F), (M-1180, H, F, H, BnO, CF3), (M-1181, H, F, H, BnO, Br), (M-1182, H, F, H, BnO, CH2), (M-1183, H, F, H, PhCH2CH2O, H), (M-1184, H, F, H, PhCH2CH2O, Cl), (M-1185, H, F, H, PhCH2CH2O, F), (M-1186, H, F, H, PhCH2CH2O, CF3), (M-1187, H, F, H, PhCH2CH2O, Br), (M-1188, H, F, H, PhCH2CH2O, CH3), (M-1189, H, F, H, CF3O, H), (M-1190, H, F, H, CF3, Cl), (M-1191, H, F, H, CF3O, F), (M-1192, H, F, H, CF3O, CF3), (M-1193, H, F, H, CF3O, Br), (M-1194, H, F, H, CF3O, CH3), (M-1195, H, F, H, Ph, H, (M-1196, H, F, H, Ph, Cl), (M-1197, H, F, H, Ph, F), (M-1198, H, F, H, Ph, CF3), (M-1199, H, F, H, Ph, Br), (M-1200, H, F, H, Ph, CH3), (M-1201, H, F, H, 4-F-Ph, H), (M-1202, H, F, H, 4-F-Ph, Cl), (M-1203, H, F, H, 4-F-Ph, F), (M-1204, H, F, H, 4-F-Ph, CF3), (M-1205, H, F, H, 4-F-Ph, Br), (M-1206, H, F, H, 4-F-Ph, CH3), (M-1207, H, F, H, 4-CF2-Ph, H), (M-1208, H, F, H, 4-CF3-Ph, Cl), (M-1209, H, F, H, 4-CF2-Ph, F), (M-1210, H, F, H, 4-CF3-Ph, CF3), (M-1211, H, F, H, 4-CF3-Ph, Br), (M-1212, H, F, H, 4-CF3-Ph, CH3), (M-1213, H, F, H, 4-(Me)2N-Ph, H), (M-1214, H, F, H, 4-(Me)2N-Ph, Cl), (M-1215, H, F, H, 4-(Me)2N-Ph, F), (M-1216, H, F, H, 4-(Me)2N-Ph, CF3), (M-1217, H, F, H, 4-(Me)2N-Ph, Br), (M-1218, H, F, H, 4-(Me)2N-Ph, CH3), (M-1219, H, F, H, 4-OH-Ph, H), (M-1220, H, F, H, 4-OH-Ph, Cl), (M-1221, H, F, H, 4-OH-Ph, F), (M-1222, H, F, H, 4-OH-Ph, CF3), (M-1223, H, F, H, 4-OH-Ph, Br), (M-1224, H, F, H, 4-OH-Ph, CH3), (M-1225, H, F, H, 3,4-di-F-Ph, H), (M-1226, H, F, H, 3,4-di-F-Ph, Cl), (M-1227, H, F, H, 3,4-di-F-Ph, F), (M-1228, H, F, H, 3,4-di-F-Ph, CF3), (M-1229, H, F, H, 3,4-di-F-Ph, Br), (M-1230, H, F, H, 3,4-di-F-Ph, CH3), (M-1231, H, F, H, 4-COOH-Ph, H), (M-1232, H, F, H, 4-COOH-Ph, Cl), (M-1233, H, F, H, 4-COOH-Ph, F), (M-1234, H, F, H, 4-COOH-Ph, CF3), (M-1235, H, F, H, 4-COOH-Ph, Br), (M-1236, H, F, H, 4-COOH-Ph, CH3), (M-1237, H, F, H, Bn, H), (M-1238, H, F, H, Bn, Cl), (M-1239, H, F, H, Bn, F), (M-1240, H, F, H, Bn, CF3), (M-1241, H, F, H, Bn, Br), (M-1242, H, F, H, Bn, CH3), (M-1243, H, F, H, 4-F-Bn, H), (M-1244, H, F, H, 4-F-Bn, Cl), (M-1245, H, F, H, 4-F-Bn, F), (M-1246, H, F, H, 4-F-Bn, CF3), (M-1247, H, F, H, 4-F-Bn, Br), (M-1248, H, F, H, 4-F-Bn, CH3), (M-1249, H, F, H, 2-Py, H), (M-1250, H, F, H, 2-Ph, Cl), (M-1251, H, F, H, 2-Py, F), (M-1252, H, F, H, 2-Py, CF3), (M-1253, H, F, H, 2-Py, Br), (M-1254, H, F, H, 2-Py, CH3), (M-1255, H, F, H, 3-Py, H), (M-1256, H, F, H, 3-Py, Cl), (M-1257, H, F, H, 3-Py, F), (M-1258, H, F, H, 3-Py, CF3), (M-1259, H, F, H, 3-Py, Br), (M-1260, H, F, H, 3-Py, CH3), (M-1261, H, F, H, 4-Py, H), (M-1262, H, F, H, 4-Py, Cl), (M-1263, H, F, H, 4-Py, F), (M-1264, H, F, H, 4-Py, CF3), (M-1265, H, F, H, 4-Py, Br), (M-1266, H, F, H, 4-Py, CH3), (M-1267, H, F, H, 2-Th, H), (M-1268, H, F, H, 2-Th, Cl), (M-1269, H, F, H, 2-Th, F), (M-1270, H, F, H, 2-Th, CF3), (M-1271, H, F, H, 2-Th, Br), (M-1272, H, F, H, 2-Th, CH3), (M-1273, H, F, H, 3-Th, H), (M-1274, H, F, H, 3-Th, Cl), (M-1275, H, F, H, 3-Th, F), (M-1276, H, F, H, 3-Th, CF3), (M-1277, H, F, H, 3-Th, Br), (M-1278, H, F, H, 3-Th, CH3), (M-1279, H, F, H, pyrrazol-2-yl, H), (M-1280, H, F, H, pyrrazol-2-yl, Cl), (M-1281, H, F, H, pyrrazol-2-yl, F), (M-1282, H, F, H, pyrrazol-2-yl, CF3), (M-1283, H, F, H, pyrrazol-2-yl, Br), (M-1284, H, F, H, pyrrazol-2-yl, CH3), (M-1285, H, F, H, pyrrazol-3-yl, H), (M-1286, H, F, H, pyrrazol-3-yl, Cl), (M-1287, H, F, H, pyrrazol-3-yl, F), (M-1288, H, F, H, pyrrazol-3-yl, CF3), (M-1289, H, F, H, pyrrazol-3-yl, Br), (M-1290, H, F, H, pyrrazol-3-yl, CH3), (M-1291, H, F, H, pyrimidin, 2-yl, H), (M-1292, H, F, H, pyrimidin-2-yl, Cl), (M-1293, H, F, H, pyrimidin-2-yl, F), (M-1294, H, F, H, pyrimidin-2-yl, CF3), (M-1295, H, F, H, pyrimidin-2-yl, Br), (M-1296, H, F, H, pyrimidin-2-yl, CH3), (M-1297, H, F, H, pyrimidin-4-yl, H), (M-1298, H, F, H, pyrimidin-4-yl, Cl), (M-1299, H, F, H, pyrimidin-4-yl, F), (M-1300, H, F, H, pyrimidin-4-yl, CF3), (M-1301, H, F, H, pyrimidin-4-yl, Br), (M-1302, H, F, H, pyrimidin-4-yl, CH3), (M-1303, H, F, H, pyrimidin-5-yl, H), (M-1304, H, F, H, pyrimidin-5-yl, Cl), (M-1305, H, F, H, pyrimidin-5-yl, F), (M-1306, H, F, H, pyrimidin-5-yl, CF3), (M-1307, H, F, H, pyrimidin-5-yl, Br), (M-1308, H, F, H, pyrimidin-5-yl, CH3), (M-1309, H, F, H, HOOCCH2CH2CH3, H), (M-1310, H, F, H, HOOCCH2CH2CH2, Cl), (M-1311, H, F, H, HOOCCH2CH2CH2, F), (M-1312, H, F, H, HOOCCH2CH2CH2, CF3), (M-1313, H, F, H, HOOCCH2CH2CH2, Br), (M-1314, H, F, H, HOOCCH2CH2CH2, CH2), (M-1315, H, F, H, HOOCCH2CH2CH2CH2, H), (M-1316, H, F, H, HOOCCH2CH2CH2CH2, Cl), (M-1317, H, F, H, HOOCCH2CH2CH2CH2, F), (M-1318, H, F, H, HOOCCH2CH2CH2CH2, CF3), (M-1319, H, F, H, HOOCCH2CH2CH2CH2, Br), (M-1320, H, F, H, HOOCCH2CH2CH2CH2, CH3), (M-1321, H, F, H, (Me)2NCOCH2CH2CH2CH2, H), (M-1322, H, F, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-1323, H, F, H, (Me)3NCOCH2CH2CH2CH2, F), (M-1324, H, F, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-1325, H, F, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-1326, H, F, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-1327, H, F, H, (Me2NCOCH2CH2CH2CH2CH2, H), (M-1328, H, F, H, (Me)2NCOCH3CH2CH2CH2CH2, Cl), (M-1329, H, F, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-1330, H, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-1331, H, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-1332, H, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-1333, H, F, H, MeOCH2, H), (M-1334, H, F, H, MeOCH2, Cl), (M-1335, H, F, H, MeOCH2, F), (M-1336, H, F, H, MeOCH2, CF3), (M-1337, H, F, H, MeOCH2, Br), (M-1338, H, F, H, MeOCH2, CH3), (M-1339, H, F, H, EtOCH2, H), (M-1340, H, F, H, EtOCH2, Cl), (M-1341, H, F, H, EtOCH2, F), (M-1342, H, F, H, EtOCH2, CF3), (M-1343, H, F, H, EtOCH2, Br), (M-1344, H, F, H, EtOCH2, CH3), (M-1345, H, F, H, EtOCH2CH2, H), (M-1346, H, F, H, EtOCH2CH2, Cl), (M-1347, H, F, H, EtOCH2CH2, F), (M-1348, H, F, H, EtOCH2CH2, CF3), (M-1349, H, F, H, EtOCH2CH2, Br), (M-1350, H, F, H, EtOCH2CH2, CH3), (M-1351, H, F, H, MeOCH2CH2OCH2CH2, H), (M-1352, H, F, H, MeOCH2CH2OCH2CH2, Cl), (M-1353, H, F, H, MeOCH2CH2OCH2CH2, F), (M-1354, H, F, H, MeOCH2CH2OCH2CH2, CF3), (M-1355, H, F, H, MeOCH2CH2OCH2CH2, Br), (M-1356, H, F, H, MeOCH2CH2OCH1CH2, CH3), (M-1357, H, F, H, MeOCH2CH2, H), (M-1358, H, F, H, MeOCH2CH2, Cl), (M-1359, H, F, H, MeOCH2CH2, F), (M-1360, H, F, H, MeOCH2CH2, CF3), (M-1361, H, F, H, MeOCH2CH2, Br), (M-1362, H, F, H, MeOCH2CH2, CH3), (M-1363, H, F, H, HOCH2, H), (M-1364, H, F, H, HOCH2, Cl), (M-1365, H, F, H, HOCH2, F), (M-1366, H, F, H, HOCH2, CF3), (M-1367, H, F, H, HOCH2, Br), (M-1368, H, F, H, HOCH2, CH3), (M-1369, H, F, H, HOCH2CH2, H), (M-1370, H, F, H, HOCH2CH2, Cl), (M-1371, H, F, H, HOCH2CH2, F), (M-1372, H, F, H, HOCH2CH2, CF3), (M-1373, H, F, H, HOCH2CH2, Br), (M-1374, H, F, H, HOCH2CH2, CH3), (M-1375, H, F, H, HOCH2CH2CH2, H), (M-1376, H, F, H, HOCH2CH2CH2, Cl), (M-1377, H, F, H, HOCH2CH2CH2, F), (M-1378, H, F, H, HOCH2CH2CH2, CF3), (M-1379, H, F, H, HOCH2CH2CH2, Br), (M-1380, H, F, H, HOCH2CH2CH2, CH3), (M-1381, H, F, H, HOCH2CH2CH2CH2, H), (M-1382, H, F, H, HOCH2CH2CH2CH2, Cl), (M-1383, H, F, H, HOCH2CH2CH2CH2, F), (M-1384, H, F, H, HOCH2CH2CH2CH2, CF3), (M-1385, H, F, H, HOCH2CH2CH2CH2, Br), (M-1386, H, F, H, HOCH2CH2CH2CH2, CH2), (M-1387, H, F, H, HOCH2CH2CH2CH2CF3, H), (M-1388, H, F, H, HOCH2CH2CH2CH2CH2, Cl), (M-1389, H, F, H, HOCH2CH2CH2CH2CH2, F), (M-1390, H, F, H, HOCH2CH2CH2CH2CH2, CF3), (M-1391, H, F, H, HOCH2CH2CH2CH2CH2, Br), (M-1392, H, F, H, HOCH2CH2CH2CH2CH2, CH3), (M-1393, H, F, H, HOCH2CH2OCH2CH2, H), (M-1394, H, F, H, HOCH2CH2OCH2CH2, Cl), (M-1395, H, F, H, HOCH2CH2OCH2CH2, F), (M-1396, H, F, H, HOCH2CH2OCH2CH2, CF3), (M-1397, H, F, H, HOCH2CH2OCH2CH2, Br), (M-1398, H, F, H, HOCH2CH2OCH2CH2, CH3), (M-1399, H, F, H, (Me)2N, H), (M-1400, H, F, H, (Me)2N, Cl), (M-1401, H, F, H, (Me)2N, F), (M-1402, H, F, H, (Me)2N, CF3), (M-1403, H, F, H, (Me)2N, Br), (M-1404, H, F, H, (Me)2N, CH3), (M-1405, H, F, H, piperidin-4-yl-methyl, H), (M-1406, H, F, H, piperidin-4-yl-methyl, Cl), (M-1407, H, F, H, piperidin-4-yl-methyl, F), (M-1408, H, F, H, piperidin-4-yl-methyl, CF3), (M-1409, H, F, H, piperidin-4-yl-methyl, Br), (M-1410, H, F, H, piperidin-4-yl-methyl, CH3), (M-1411, H, F, H, cyclohexylmethyl, H), (M-1412, H, F, H, cyclohexylmethyl, Cl), (M-1413, H, F, H, cyclohexylmethyl, F), (M-1414, H, F, H, cyclohexylmethyl, CF3), (M-1415, H, F, H, cyclohexylmethyl, Br), (M-1416, H, F, H, cyclohexylmethyl, CH3), (M-1417, H, F, F, H, H), (M-1418, H, F, F, H, Cl), (M-1419, H, F, F, H, F), (M-1420, H, F, F, H, CF3), (M-1421, H, F, F, H, Br), (M-1422, H, F, F, H, CH3), (M-1423, H, F, F, F, H), (M-1424, H, F, F, F, Cl), (M-1425, H, F, F, F, F), (M-1426, H, F, F, F, CF3), (M-1427, H, F, F, F, Br), (M-1428, H, F, F, F, CH3), (M-1429, H, F, F, Cl, H), (M-1430, H, F, F, Cl, Cl), (M-1431, H, F, F, Cl, F), (M-1432, H, F, F, Cl, CF3), (M-1433, H, F, F, Cl, Br), (M-1434, H, F, F, Cl, CH3), (M-1435, H, F, F, CH3, H), (M-1436, H, F, F, CH3, Cl), (M-1437, H, F, F, CH3, F), (M-1438, H, F, F, CH3, CF3), (M-1439, H, F, F, CH3, Br), (M-1440, H, F, F, CH3, CH3), (M-1441, H, F, F, Et, H), (M-1442, H, F, F, Et, Cl), (M-1443, H, F, F, Et, F), (M-1444, H, F, F, Et, CF3), (M-1445, H, F, F, Et, Br), (M-1446, H, F, F, Et, CH3), (M-1447, H, F, F, n-Pr, H), (M-1448, H, F, F, n-Pr, Cl), (M-1449, H, F, F, n-Pr, F), (M-1450, H, F, F, n-Pr, CF3), (M-1451, H, F, F, n-Pr, Br), (M-1452, H, F, F, n-Pr, CH3), (M-1453, H, F, F, c-Pr, H), (M-1454, H, F, F, c-Pr, Cl), (M-1455, H, F, F, c-Pr, F), (M-1456, H, F, F, c-Pr, CF3), (M-1457, H, F, F, c-Pr, Br), (M-1458, H, F, F, c-Pr, CH3), (M-1459, H, F, F, i-Pr, H), (M-1460, H, F, F, i-Pr, Cl), (M-1461, H, F, F, i-Pr, F), (M-1462, H, F, F, i-Pr, CF3), (M-1463, H, F, F, i-Pr, Br), (M-1464, H, F, F, i-Pr, CH3), (M-1465, H, F, F, n-Bu, H), (M-1466, H, F, F, n-Bu, Cl), (M-1467, H, F, F, n-Bu, F), (M-1468, H, F, F, n-Bu, CF3), (M-1469, H, F, F, n-Bu, Br), (M-1470, H, F, F, n-Bu, CH3), (M-1471, H, F, F, i-Bu, H), (M-1472, H, F, F, i-Bu, Cl), (M-1473, H, F, F, i-Bu, F), (M-1474, H, F, F, i-Bu, CF3), (M-1475, H, F, F, i-Bu, Be), (M-1476, H, F, F, i-Bu, CH3), (M-1477, H, F, F, sec-Bu, H), (M-1478, H, F, F, sec-Bu, Cl), (M-1479, H, F, F, sec-Bu, F), (M-1480, H, F, F, sec-Bu, CF3), (M-1481, H, F, F, sec-Bu, Br), (M-1482, H, F, F, sec-Bu, CH3), (M-1483, H, F, F, n-Pen, H), (M-1484, H, F, F, n-Pen, Cl), (M-1485, H, F, F, n-Pen, F), (M-1486, H, F, F, n-Pen, CF3), (M-1487, H, F, F, n-Pen, Br), (M-1488, H, F, F, n-Pen, CH3), (M-1489, H, F, F, c-Pen, H), (M-1490, H, F, F, c-Pen, Cl), (M-1491, H, F, F, c-Pen, F), (M-1492, H, F, F, c-Pen, CF3), (M-1493, H, F, F, c-Pen, Br), (M-1494, H, F, F, c-Pen, CH3), (M-1495, H, F, F, n-Hex, H), (M-1496, H, F, F, n-Hex, Cl), (M-1497, H, F, F, n-Hex, F), (M-1498, H, F, F, n-Hex, CF3), (M-1499, H, F, F, n-Hex, Br), (M-1500, H, F, F, n-Hex, CH3), (M-1501, H, F, F, c-Hex, H), (M-1502, H, F, F, c-Hex, Cl), (M-1503, H, F, F, c-Hex, F), (M-1504, H, F, F, c-Hex, CF3), (M-1505, H, F, F, c-Hex, Br), (M-1506, H, F, F, c-Hex, CH3), (M-1507, H, F, F, OH, H), (M-1508, H, F, F, OH, Cl), (M-1509, H, F, F, OH, F), (M-1510, H, F, F, OH, CF3), (M-1511, H, F, F, OH, Br), (M-1512, H, F, F, OH, CH3), (M-1513, H, F, F, EtO, H), (M-1514, H, F, F, EtO, Cl), (M-1515, H, F, F, EtO, F), (M-1516, H, F, F, EtO, CF3), (M-1517, H, F, F, EtO, Br), (M-1518, H, F, F, EtO, CH3), (M-1519, H, F, F, n-PrO, H), (M-1520, H, F, F, n-PrO, Cl), (M-1521, H, F, F, n-PrO, F), (M-1522, H, F, F, n-PrO, CF3), (M-1523, H, F, F, n-PrO, Br), (M-1524, H, F, F, n-PrO, CH3), (M-1525, H, F, F, PhO, H), (M-1526, H, F, F, PhO, Cl), (M-1527, H, F, F, PhO, F), (M-1528, H, F, F, PhO, CF3), (M-1529, H, F, F, PhO, Br), (M-1530, H, F, F, PhO, CH3), (M-1531, H, F, F, BnO, H), (M-1532, H, F, F, BnO, Cl), (M-1533, H, F, F, BnO, F), (M-1534, H, F, F, BnO, CF3), (M-1535, H, F, F, BnO, Br), (M-1536, H, F, F, BnO, CH3), (M-1537, H, F, F, PhCH2CH2O, H), (M-1538, H, F, F, PhCH2CH2O, Cl), (M-1539, H, F, F, PhCH2CH3O, F), (M-1540, H, F, F, PhCH2CH2O, CF3), (M-1541, H, F, F, PhCH2CH2O, Br), (M-1542, H, F, F, PhCH2CH2O, CH3), (M-1543, H, F, F, CF3O, H), (M-1544, H, F, F, CF3O, Cl), (M-1545, H, F, F, CF3O, F), (M-1546, H, F, F, CF3O, CF3), (M-1547, H, F, F, CF3O, Br), (M-1548, H, F, F, CF3O, CH3), (M-1549, H, F, F, Ph, H), (M-1550, H, F, F, Ph, Cl), (M-1551, H, F, F, Ph, F), (M-1552, H, F, F, Ph, CF3), (M-1553, H, F, F, Ph, Br), (M-1554, H, F, F, Ph, CH3), (M-1555, H, F, F, 4-F-Ph, H), (M-1556, H, F, F, 4-F-Ph, Cl), (M-1557, H, F, F, 4-F-Ph, F), (M-1558, H, F, F, 4-F-Ph, CF3), (M-1559, H, F, F, 4-F-Ph, Br), (M-1560, H, F, F, 4-F-Ph, CH3), (M-1561, H, F, F, 4-CF2-Ph, H), (M-1562, H, F, F, 4-CF2-Ph, Cl), (M-1563, H, F, F, 4-CF2, Ph, F), (M-1564, H, F, F, 4-CF3-Ph, CF3), (M-1565, H, F, F, 4-CF2-Ph, Br), (M-1566, H, F, F, 4-CF3-Ph, CH3), (M-1567, H, F, F, 4-(Me)2N-Ph, H), (M-1568, H, F, F, 4-(Me)2N-Ph, Cl), (M-1569, H, F, F, 4-(Me)2N-Ph, F), (M-1570, H, F, F, 4-(Me)2N-Ph, CF3), (M-1571, H, F, F, 4-(Me)2N-Ph, Br), (M-1572, H, F, F, 4-(Me)2N-Ph, CH3), (M-1573, H, F, F, 4-OH-Ph, H), (M-1574, H, F, F, 4-OH-Ph, Cl), (M-1575, H, F, F, 4-OH-Ph, F), (M-1576, H, F, F, 4-OH-Ph, CF3), (M-1577, H, F, F, 4-OH-Ph, Br), (M-1578, H, F, F, 4-OH-Ph, CH3), (M-1579, H, F, F, 3,4-di-F-Ph, H), (M-1580, H, F, F, 3,4-di-F-Ph, Cl), (M-1581, H, F, F, 3,4-di-F-Ph, F), (M-1582, H, F, F, 3,4-di-F-Ph, CF3), (M-1583, H, F, F, 3,4-di-F-Ph, Br), (M-1584, H, F, F, 3,4-di-F-Ph, CH3), (M-1585, H, F, F, 4-COOH-Ph, H), (M-1586, H, F, F, 4-COOH-Ph, Cl), (M-1587, H, F, F, 4-COOH-Ph, F), (M-1588, H, F, F, 4-COOH-Ph, CF3), (M-1589, H, F, F, 4-COOH-Ph, Br), (M-1590, H, F, F, 4-COOH-Ph, CH3), (M-1591, H, F, F, Bn, H), (M-1592, H, F, F, Bn, Cl), (M-1593, H, F, F, Bn, F), (M-1594, H, F, F, Bn, CF3), (M-1595, H, F, F, Bn, Br), (M-1596, H, F, F, Bn, CH3), (M-1597, H, F, F, 4-F-Bn, H), (M-1598, H, F, F, 4-F-Bn, Cl), (M-1599, H, F, F, 4-F-Bn, F), (M-1600, H, F, F, 4-F-Bn, CF3), (M-1601, H, F, F, 4-F-Bn, Br), (M-1602, H, F, F, 4-F-Bn, CH3), (M-1603, H, F, F, 2-Py, H), (M-1604, H, F, F, 2-Py, Cl), (M-1605, H, F, F, 2-Py, F), (M-1606, H, F, F, 2-Py, CF3), (M-1607, H, F, F, 2-Py, Br), (M-1608, H, F, F, 2-Py, CH3), (M-1609, H, F, F, 3-Py, H), (M-1610, H, F, F, 3-Py, Cl), (M-1611, H, F, F, 3-Py, F), (M-1612, H, F, F, 3-Py, CF3), (M-1613, H, F, F, 3-Py, Br), (M-1614, H, F, F, 3-Py, CH3), (M-1615, H, F, F, 4-Py, H), (M-1616, H, F, F, 4-Py, Cl), (M-1617, H, F, F, 4-Py, F), (M-1618, H, F, F, 4-Py, CF3), (M-1619, H, F, F, 4-Py, Br), (M-1620, H, F, F, 4-Py, CH3), (M-1621, H, F, F, 2-Th, H), (M-1622, H, F, F, 2-Th, Cl), (M-1623, B, F, F, 2-Th, F), (M-1624, H, F, F, 2-Th, CF3), (M-1625, H, F, F, 2-Th, Br), (M-1626, H, F, F, 2-Th, CH3), (M-1627, H, F, F, 3-Th, H), (M-1628, H, F, F, 3-Th, Cl), (M-1629, H, F, F, 3-Th, F), (M-1630, H, F, F, 3-Th, CF3), (M-1631, H, F, F, 3-Th, Br), (M-1632, H, F, F, 3-Th, CH3), (M-1633, H, F, F, pyrrazol-2-yl, H), (M-1634, H, F, F, pyrrazol-2-yl, Cl), (M-1635, H, F, F, pyrrazol-2-yl, F), (M-1636, H, F, F, pyrrazol-2-yl, CF3), (M-1637, H, F, F, pyrrazol-2-yl, Br), (M-1638, H, F, F, pyrrazol-2-yl, CH3), (M-1639, H, F, F, pyrrazol-3-yl, H), (M-1640, H, F, F, pyrrazol-3-yl, Cl), (M-1641, H, F, F, pyrrazol-3-yl, F), (M-1642, H, F, F, pyrrazol-3-yl, CF3), (M-1643, H, F, F, pyrrazol-3-yl, Br), (M-1644, H, F, F, pyrrazol-3-yl, CH3), (M-1645, H, F, F, pyrimidin-2-yl, H), (M-1646, H, F, F, pyrimidin-2-yl, Cl), (M-1647, H, F, F, pyrimidin-2-yl, F), (M-1648, H, F, F, pyrimidin-2-yl, CF3), (M-1649, H, F, F, pyrimidin-2-yl, Br), (M-1650, H, F, F, pyrimidin-2-yl, CH3), (M-1651, H, F, F, pyrimidin-4-yl, H), (M-1652, H, F, F, pyrimidin-4-yl, Cl), (M-1653, H, F, F, pyrimidin-4-yl, F), (M-1654, H, F, F, pyrimidin-4-yl, CF3), (M-1655, H, F, F, pyrimidin-4-yl, Br), (M-1656, H, F, F, pyrimidin-4-yl, CH3), (M-1657, H, F, F, pyrimidin-5-yl, H), (M-1658, H, F, F, pyrimidin-5-yl, Cl), (M-1659, H, F, F, pyrimidin-5-yl, F), (M-1660, H, F, F, pyrimidin-5-yl, CF3), (M-1661, H, F, F, pyrimidin-5-yl, Br), (M-1662, H, F, F, pyrimidin-5-yl, CH3), (M-1663, H, F, F, HOOCCH2CH2CH2, H), (M-1664, H, F, F, HOOCCH2CH2CH2, Cl), (M-1665, H, F, F, HOOCCH2CH2CH2, F), (M-1666, H, F, F, HOOCCH2CH2CH2, CF3), (M-1667, H, F, F, HOOCCH2CH2CH2, Br), (M-1668, H, F, F, HOOCCH2CH2CH2, CH3), (M-1669, H, F, F, HOOCCH2CH2CH2CH2, H), (M-1670, H, F, F, HOOCCH2CH2CH2CH2, Cl), (M-1671, H, F, F, HOOCCH2CH2CH2CH2, F), (M-1672, H, F, F, HOOCCH2CH2CH2CH2, CF3), (M-1673, H, F, F, HOOCCH2CH2CH2CH2, Br), (M-1674, H, F, F, HOOCCH2CH2CH2CH2, CH3), (M-1675, H, F, F, (Me)2NCOCH2CH2CH2CH2, H), (M-1676, H, F, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-1677, H, F, F, (Me)2NCOCH2CH2CH2CH2, F), (M-1678, H, F, F, (Me)3NCOCH2CH2CH2CH2, CF3), (M-1679, H, F, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-1680, H, F, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-1681, H, F, F, (Me)3NCOCH2CH2CH2CH2CH2, H), (M-1682, H, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-1683, H, F, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-1684, H, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-1685, H, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-1686, H, F, F, (Me)2NCOCH2CH2CH2CH2CH3, CH3), (M-1687, H, F, F, MeOCH2, H), (M-1688, H, F, F, MeOCH2, Cl), (M-1689, H, F, F, MeOCH2, F), (M-1690, H, F, F, MeOCH2, CF3), (M-1691, H, F, F, MeOCH2, Br), (M-1692, H, F, F, MeOCH2, CH3), (M-1693, H, F, F, EtOCH2, H), (M-1694, H, F, F, EtOCH2, Cl), (M-1695, H, F, F, EtOCH2, F), (M-1696, H, F, F, EtOCH2, CF3), (M-1697, H, F, F, EtOCH2, Br), (M-1698, H, F, F, EtOCH2, CH3), (M-1699, H, F, F, EtOCH2CH2, H), (M-1700, H, F, F, EtOCH2CH2, Cl), (M-1701, H, F, F, EtOCH2CH2, F), (M-1702, H, F, F, EtOCH2CH2, CF3), (M-1703, H, F, F, EtOCH2CH2, Br), (M-1704, H, F, F, EtOCH2CH2, CH3), (M-1705, H, F, F, MeOCH2CH2OCH2CH2, H), (M-1706, H, F, F, MeOCH2—CH2OCH2CH2, Cl), (M-1707, H, F, F, MeOCH2CH2OCH2CH2, F), (M-1708, H, F, F, MeOCH2CH2OCH2CH2, CF3), (M-1709, H, F, F, MeOCH2CH2OCH2CH2, Br), (M-1710, H, F, F, MeOCH2CH2OCH2CH2, CH3), (M-1711, H, F, F, MeOCH2CH2, H), (M-1712, H, F, F, MeOCH2CH2, Cl), (M-1713, H, F, F, MeOCH2CH2, F), (M-1714, H, F, F, MeOCH2CH2, CF3), (M-1715, H, F, F, MeOCH2CH2, Br), (M-1716, H, F, F, MeOCH2CH2, CH3), (M-1717, H, F, F, HOCH2, H), (M-1718, H, F, F, HOCH2, Cl), (M-1719, H, F, F, HOCH2, F), (M-1720, H, F, F, HOCH2, CF3), (M-1721, H, F, F, HOCH2, Br), (M-1722, H, F, F, HOCH2, CH3), (M-1723, H, F, F, HOCH1CH2, H), (M-1724, H, F, F, HOCH2CH2, Cl), (M-1725, H, F, F, HOCH2CH2, F), (M-1726, H, F, F, HOCH2CH2, CF3), (M-1727, H, F, F, HOCH2CH2, Br), (M-1728, H, F, F, HOCH2CH2, CH3), (M-1729, H, F, F, HOCH2CH2CH2, H), (M-1730, H, F, F, HOCH2CH2CH2, Cl), (M-1731, H, F, F, HOCH2CH2CH2, F), (M-1732, H, F, F, HOCH2CH2CH2, CF3), (M-1733, H, F, F, HOCH2CH2CH2, Br), (M-1734, H, F, F, HOCH2CH2CH2, CH3), (M-1735, H, F, F, HOCH2CH2CH2CH2, H), (M-1736, H, F, F, HOCH2CH2CH2CH2, Cl), (M-1737, H, F, F, HOCH2CH2CH2CH2, F), (M-1738, H, F, F, HOCH2CH2CH2CH2, CF3), (M-1739, H, F, F, HOCH2CH2CH2CH2, Br), (M-1740, H, F, F, HOCH2CH2CH2CH2, CH3), (M-1741, H, F, F, HOCH2CH2CH2CH2CH2, H), (M-1742, H, F, F, HOCH2CH2CH2CH2CH2, Cl), (M-1743, H, F, F, HOCH2CH2CH2CH2CH2, F), (M-1744, H, F, F, HOCH2CH2CH2CH2CH2, CF3), (M-1745, H, F, F, HOCH2CH2CH2CH2CH2Br), (M-1746, H, F, F, HOCH2CH2CH2CH2CH2, CH3), (M-1747, H, F, F, HOCH2CH2OCH2CH2, H), (M-1748, H, F, F, HOCH2CH2OCH2CH2, Cl), (M-1749, H, F, F, HOCH2CH3OCH2CH2, F), (M-1750, H, F, F, HOCH2CH2OCH2CH2, CF3), (M-1751, H, F, F, HOCH2CH2CH2CH2, Br), (M-1752, H, F, F, HOCH2CH2OCH2CH2, CH3), (M-1753, H, F, F, (Me)2N, H), (M-1754, H, F, F, (Me)2N, Cl), (M-1755, H, F, F, (Me)2N, F), (M-1756, H, F, F, (Me)2N, CF3), (M-1757, H, F, F, (Me)2N, Br), (M-1758, H, F, F, (Me)2N, CH2) (M-1759, H, F, F, piperidin-4-yl-methyl, H), (M-1760, H, F, F, piperidin-4-yl-methyl, Cl), (M-1761, H, F, F, piperidin-4-yl-methyl, F), (M-1762, H, F, F, piperidin-4-yl-methyl, CF3), (M-1763, H, F, F, piperidin-4-yl-methyl, Br), (M-1764, H, F, F, piperidin-4-yl-methyl, CH3), (M-1765, H, F, F, cyclohexylmethyl, H), (M-1766, H, F, F, cyclohexylmethyl, Cl), (M-1767, H, F, F, cyclohexylmethyl, F), (M-1768, H, F, F, cyclohexylmethyl, CF3), (M-1769, H, F, F, cyclohexylmethyl, Br), (M-1770, H, F, F, cyclohexylmethyl, CH3), (M-1771, H, F, Cl, H, H), (M-1772, H, F, Cl, H, Cl), (M-1773, H, F, Cl, H, F), (M-1774, H, F, Cl, H, CF3), (M-1775, H, F, Cl, H, Br), (M-1776, H, F, Cl, H, CH3), (M-1777, H, F, Cl, F, H), (M-1778, H, F, Cl, F, Cl), (M-1779, H, F, Cl, F, F), (M-1780, H, F, Cl, F, CF3), (M-1781, H, F, Cl, F, Br), (M-1782, H, F, Cl, F, CH3), (M-1783, H, F, Cl, Cl, H), (M-1784, H, F, Cl, Cl, Cl), (M-1785, H, F, Cl, Cl, F), (M-1786, H, F, Cl, Cl, CF3), (M-1787, H, F, Cl, Cl, Br), (M-1788, H, F, Cl, Cl, CH3), (M-1789, H, F, Cl, CH3, H), (M-1790, H, F, Cl, CH3, Cl), (M-1791, H, F, Cl, CH3, F), (M-1792, H, F, Cl, CH3, CF3), (M-1793, H, F, Cl, CH3, Br), (M-1794, H, F, Cl, CH3, CH3), (M-1795, H, F, Cl, Et, H), (M-1796, H, F, Cl, Et, Cl), (M-1797, H, F, Cl, Et, F), (M-1798, H, F, Cl, Et, CF3), (M-1799, H, F, Cl, Et, Br), (M-1800, H, F, Cl, Et, CH3), (M-1801, H, F, Cl, n-Pr, H), (M-1802, H, F, Cl, n-Pr, Cl), (M-1803, H, F, Cl, n-Pr, F), (M-1804, H, F, Cl, n-Pr, CF3), (M-1805, H, F, Cl, n-Pr, Br), (M-1806, H, F, Cl, n-Pr, CH3), (M-1807, H, F, Cl, c-Pr, H), (M-1808, H, F, Cl, c-Pr, Cl), (M-1809, H, F, Cl, c-Pr, F), (M-1810, H, F, Cl, c-Pr, CF3), (M-1811, H, F, Cl, c-Pr, Br), (M-1812, H, F, Cl, c-Pr, CF3), (M-1813, H, F, Cl, i-Pr, H), (M-1814, H, F, Cl, i-Pr, Cl), (M-1815, H, F, Cl, i-Pr, F), (M-1816, H, F, Cl, i-Pr, CF3), (M-1817, H, F, Cl, i-Pr, Br), (M-1818, H, F, Cl, i-Pr, CH3), (M-1819, H, F, Cl, n-Bu, H), (M-1820, H, F, Cl, n-Bu, Cl), (M-1821, H, F, Cl, n-Bu, F), (M-1822, H, F, Cl, n-Bu, CF3), (M-1823, H, F, Cl, n-Bu, Br), (M-1824, H, F, Cl, n-Bu, CH3), (M-1825, H, F, Cl, i-Bu, H), (M-1826, H, F, Cl, i-Bu, Cl), (M-1827, H, F, Cl, i-Bu, F), (M-1828, H, F, Cl, i-Bu, CF3), (M-1829, H, F, Cl, i-Bu, Br), (M-1830, H, F, Cl, i-Bu, CH3), (M-1831, H, F, Cl, sec-Bu, H), (M-1832, H, F, Cl, sec-Bu, Cl), (M-1833, H, F, Cl, sec-Bu, F), (M-1834, H, F, Cl, sec-Bu, CF3), (M-1835, H, F, Cl, sec-Bu, Br), (M-1836, H, F, Cl, sec-Bu, CH3), (M-1837, H, F, Cl, n-Pen, H), (M-1838, H, F, Cl, n-Pen, Cl), (M-1839, H, F, Cl, n-Pen, F), (M-1840, H, F, Cl, n-Pen, CF3), (M-1841, H, F, Cl, n-Pen, Br), (M-1842, H, F, Cl, n-Pen, CH3), (M-1843, H, F, Cl, c-Pen, H), (M-1844, H, F, Cl, c-Pen, Cl), (M-1845, H, F, Cl, c-Pen, F), (M-1846, H, F, Cl, c-Pen, CF3), (M-1847, H, F, Cl, c-Pen, Br), (M-1848, H, F, Cl, c-Pen, CH3), (M-1849, H, F, Cl, n-Hex, H), (M-1850, H, F, Cl, n-Hex, Cl), (M-1851, H, F, Cl, n-Hex, F), (M-1852, H, F, Cl, n-Hex, CF3), (M-1853, H, F, Cl, n-Hex, Br), (M-1854, H, F, Cl, n-Hex, CH3), (M-1855, H, F, Cl, c-Hex, H), (M-1856, H, F, Cl, c-Hex, Cl), (M-1857, H, F, Cl, c-Hex, F), (M-1858, H, F, Cl, c-Hex, CF3), (M-1859, H, F, Cl, c-Hex, Br), (M-1860, H, F, Cl, c-Hex, CH3), (M-1861, H, F, Cl, OH, H), (M-1862, H, F, Cl, OH, Cl), (M-1863, H, F, Cl, OH, F), (M-1864, H, F, Cl, OH, CF3), (M-1865, H, F, Cl, OH, Br), (M-1866, H, F, Cl, OH, CH3), (M-1867, H, F, Cl, EtO, H), (M-1868, H, F, Cl, EtO, Cl), (M-1869, H, F, Cl, EtO, F), (M-1870, H, F, Cl, EtO, CF3), (M-1871, H, F, Cl, EtO, Br), (M-1872, H, F, Cl, EtO, CH3), (M-1873, H, F, Cl, n-PrO, H), (M-1874, H, F, Cl, n-PrO, Cl), (M-1875, H, F, Cl, n-PrO, F), (M-1876, H, F, Cl, n-PrO, CF3), (M-1877, H, F, Cl, n-PrO, Br), (M-1878, H, F, Cl, n-PrO, CH3), (M-1879, H, F, Cl, PhO, H), (M-1880, H, F, Cl, PhO, Cl), (M-1881, H, F, Cl, PhO, F), (M-1882, H, F, Cl, PhO, CF3), (M-1883, H, F, Cl, PhO, Br), (M-1884, H, F, Cl, PhO, CH3), (M-1885, H, F, Cl, BnO, H), (M-1886, H, F, Cl, BnO, Cl), (M-1887, H, F, Cl, BnO, F), (M-1888, H, F, Cl, BnO, CF3), (M-1889, H, F, Cl, BnO, Br), (M-1890, H, F, Cl, BnO, CH3), (M-1891, H, F, Cl, PhCH2CH2O, H), (M-1892, H, F, Cl, PhCH2CH2O, Cl), (M-1893, H, F, Cl, PhCH2CH2O, F), (M-1894, H, F, Cl, PhCH2CH2O, CF3), (M-1895, H, F, Cl, PhCH2CH2O, Br), (M-1896, H, F, Cl, PhCH2CH2O, CH3), (M-1897, H, F, Cl, CF3O, H), (M-1898, H, F, Cl, CF3O, Cl), (M-1899, H, F, Cl, CF3O, F), (M-1900, H, F, Cl, CF3O, CF3), (M-1901, H, F, Cl, CF3O, Br), (M-1902, H, F Cl, CF3O, CH3), (M-1903, H, F, Cl, Ph, H), (M-1904, H, F, Cl, Ph, Cl), (M-1905, H, F, Cl, Ph, F), (M-1906, H, F, Cl, Ph, CF3), (M-1907, H, F, Cl, Ph, Br), (M-1908, H, F, Cl, Ph, CH3), (M-1909, H, F, Cl, 4-F-Ph, H), (M-1910, H, F, Cl, 4-F-Ph, Cl), (M-1911, H, F, Cl, 4-F-Ph, F), (M-1912, H, F, Cl, 4-F-Ph, CF3), (M-1913, H, F, Cl, 4-F-Ph, Br), (M-1914, H, F, Cl, 4-F-Ph, CH3), (M-1915, H, F, Cl, 4-CF3-Ph, H), (M-1916, H, F, Cl, 4-CF3-Ph, Cl), (M-1917, H, F, Cl, 4-CF3-Ph, F), (M-1918, H, F, Cl, 4-CF3-Ph, CF3), (M-1919, H, F, Cl, 4-CF3-Ph, Br), (M-1920, H, F, Cl, 4-CF3-Ph, CH3), (M-1921, H, F, Cl, 4-(Me)2N-Ph, H), (M-1922, H, F, Cl, 4-(Me)2N-Ph, Cl), (M-1923, H, F, Cl, 4-(Me)2N-Ph, F), (M-1924, H, F, Cl, 4-(Me)2N-Ph, CF3), (M-1925, H, F, Cl, 4-(Me)2N-Ph, Br), (M-1926, H, F, Cl, 4-(Me)2N-Ph, CH3), (M-1927, H, F, Cl, 4-OH-Ph, H), (M-1928, H, F, Cl, 4-OH-Ph, Cl), (M-1929, H, F, Cl, 4-OH-Ph, F), (M-1930, H, F, Cl, 4-OH-Ph, CF3), (M-1931, H, F, Cl, 4-OH-Ph, Br), (M-1932, H, F, Cl, 4-OH-Ph, CH3), (M-1933, H, F, Cl, 3,4-di-F-Ph, H), (M-1934, H, F, Cl, 3,4-di-F-Ph, Cl), (M-1935, H, F, Cl, 3,4-di-F-Ph, F), (M-1936, H, F, Cl, 3,4-di-F-Ph, CF3), (M-1937, H, F, Cl, 3,4-di-F-Ph, Br), (M-1938, H, F, Cl, 3,4-di-F-Ph, CH3), (M-1939, H, F, Cl, 4-COOH-Ph, H), (M-1940, H, F, Cl, 4-COOH-Ph, Cl), (M-1941, H, F, Cl, 4-COOH-Ph, F), (M-1942, H, F, Cl, 4-COOH-Ph, CF3), (M-1943, H, F, Cl, 4-COOH-Ph, Br), (M-1944, H, F, Cl, 4-COOH-Ph, CH3), (M-1945, H, F, Cl, Bn, H), (M-1946, H, F, Cl, Bn, Cl), (M-1947, H, F, Cl, Bn, F), (M-1948, H, F, Cl, Bn, CF3), (M-1949, H, F, Cl, Bn, Br), (M-1950, H, F, Cl, Bn, CH3), (M-1951, H, F, Cl, 4-F-Bn, H), (M-1952, H, F, Cl, 4-F-Bn, Cl), (M-1953, H, F, Cl, 4-F-Bn, F), (M-1954, H, F, Cl, 4-F-Bn, CF3), (M-1955, H, F, Cl, 4-F-Bn, Br), (M-1956, H, F, Cl, 4-F-Bn, CH3), (M-1957, H, F, Cl, 2-Py, H), (M-1958, H, F, Cl, 2-Py, Cl), (M-1959, H, F, Cl, 2-Py, F), (M-1960, H, F, Cl, 2-Py, CF3), (M-1961, H, F, Cl, 2-Py, Br), (M-1962, H, F, Cl, 2-Py, CH3), (M-1963, H, F, Cl, 3-Py, H), (M-1964, H, F, Cl, 3-Py, Cl), (M-1965, H, F, Cl, 3-Py, F), (M-1966, H, F, Cl, 3-Py, CF3), (M-1967, H, F, Cl, 3-Py, Br), (M-1968, H, F, Cl, 3-Py, CH3), (M-1969, H, F, Cl, 4-Py, H), (M-1970, H, F, Cl, 4-Py, Cl), (M-1971, H, F, Cl, 4-Py, F), (M-1972, H, F, Cl, 4-Py, CF3), (M-1973, H, F, Cl, 4-Py, Br), (M-1974, H, F, Cl, 4-Py, CH3), (M-1975, H, F, Cl, 2-Th, H), (M-1976, H, F, Cl, 2-Th, Cl), (M-1977, H, F, Cl, 2-Th, F), (M-1978, H, F, Cl, 2-Th, CF3), (M-1979, H, F, Cl, 2-Th, Br), (M-1980, H, F, Cl, 2-Th, CH3), (M-1981, H, F, Cl, 3-Th, H), (M-1982, H, F, Cl, 3-Th, Cl), (M-1983, H, F, Cl, 3-Th, F), (M-1984, H, F, Cl, 3-Th, CF3), (M-1985, H, F, Cl, 3-Th, Br), (M-1986, H, F, Cl, 3-Th, CH3), (M-1987, H, F, Cl, pyrrazol-2-yl, H), (M-1988, H, F, Cl, pyrrazol-2-yl, Cl), (M-1989, H, F, Cl, pyrrazol-2-yl, F), (M-1990, H, F, Cl, pyrrazol-2-yl, CF3), (M-1991, H, F, Cl, pyrrazol-2-yl, Br), (M-1992, H, F, Cl, pyrrazol-2-yl, CH3), (M-1993, H, F, Cl, pyrrazol-3-yl, H), (M-1994, H, F, Cl, pyrrazol-3-yl, Cl), (M-1995, H, F, Cl, pyrrazol-3-yl, F), (M-1996, H, F, Cl, pyrrazol-3-yl, CF3), (M-1997, H, F, Cl, pyrrazol-3-yl, Br), (M-1998, H, F, Cl, pyrrazol-3-yl, CH3), (M-1999, H, F, Cl, pyrimidin-2-yl, H), (M-2000, H, F, Cl, pyrimidin-2-yl, Cl), (M-2001, H, F, Cl, pyrimidin-2-yl, F), (M-2002, H, F, Cl, pyrimidin-2-yl, CF3), (M-2003, H, F, Cl, pyrimidin-2-yl, Br), (M-2004, H, F, Cl, pyrimidin-2-yl, CH3), (M-2005, H, F, Cl, pyrimidin-4-yl, H), (M-2006, H, F, Cl, pyrimidin-4-yl, Cl), (M-2007, H, F, Cl, pyrimidin-4-yl, F), (M-2008, H, F, Cl, pyrimidin-4-yl, CF3), (M-2009, H, F, Cl, pyrimidin-4-yl, Br), (M-2010, H, F, Cl, pyrimidin-4-yl, CH3), (M-2011, H, F, Cl, pyrimidin-5-yl, H), (M-2012, H, F, Cl, pyrimidin-5-yl, Cl), (M-2013, H, F, Cl, pyrimidin-5-yl, F), (M-2014, H, F, Cl, pyrimidin-5-yl, CF3), (M-2015, H, F, Cl, pyrimidin-5-yl, Br), (M-2016, H, F, Cl, pyrimidin-5-yl, CH3), (M-2017, H, F, Cl, HOOCCH2CH2CH2, H), (M-2018, H, F, Cl, HOOCCH2CH2CH2, Cl), (M-2019, H, F, Cl, HOOCCH2CH2CH2, F), (M-2020, H, F, Cl, HOOCCH2CH2CH2, CF3), (M-2021, H, H, Cl, HOOCCH2CH2CH2, Br), (M-2022, H, F, Cl, HOOCCH2CH2CH2, CH3), (M-2023, H, F, Cl, HOOCCH2CH2CH2CH2, H), (M-2024, H, F, Cl, HOOCCH2CH2CH2CH2, Cl), (M-2025, H, F, Cl, HOOCCH2CH2CH2CH2, F), (M-2026, H, F, Cl, HOOCCH2CH2CH2CH2, CF3), (M-2027, H, F, Cl, HOOCCH2CH2CH2CH2, Br), (M-2028, H, F, Cl, HOOCCH2CH2CH2CH2, CH3), (M-2029, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-2030, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-2031, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-2032, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-2033, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-2034, H, F, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-2035, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2H), (M-2036, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-2037, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-2038, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2CF3), (M-2039, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-2040, H, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2CH3), (M-2041, H, F, Cl, MeOCH2, H), (M-2042, H, F, Cl, MeOCH2, Cl), (M-2043, H, F, Cl, MeOCH2, F), (M-2044, H, F, Cl, MeOCH2, CF3), (M-2045, H, F, Cl, MeOCH2, Br), (M-2046, H, F, Cl, MeOCH2, CH3), (M-2047, H, F, Cl, EtOCH2, H), (M-2048, H, F, Cl, EtOCH2, Cl), (M-2049, H, F, Cl, EtOCH2, F), (M-2050, H, F, Cl, EtOCH2, CF3), (M-2051, H, F, Cl, EtOCH2, Br), (M-2052, H, F, Cl, EtOCH2, CH3), (M-2053, H, F, Cl, EtOCH2CH2, H), (M-2054, H, F, Cl, EtOCH2CH2, Cl), (M-2055, H, F, Cl, EtOCH2CH2, F), (M-2056, H, F, Cl, EtOCH2CH2, CF3), (M-2057, H, F, Cl, EtOCH2CH2, Br), (M-2058, H, F, Cl, EtOCH2CH2, CH3), (M-2059, H, F, Cl, MeOCH2CH2OCH2CH2, H), (M-2060, H, F, Cl, MeOCH2CH2CH2CH2, Cl), (M-2061, H, F, Cl, MeOCH2CH2OCH2CH2, F), (M-2062, H, F, Cl, MeOCH2CH2OCH2CH2, CF3), (M-2063, H, F, Cl, MeOCH2CH2OCH2CH2, Br), (M-2064, H, F, Cl, MeOCH2CH2OCH2CH2, CH3), (M-2065, H, F, Cl, MeOCH2CH2, H), (M-2066, H, F, Cl, MeOCH2CH2, Cl), (M-2067, H, F, Cl, MeOCH2CH2, F), (M-2068, H, F, Cl, MeOCH2CH2, CF3), (M-2069, H, F, Cl, MeOCH2CH2, Br), (M-2070, H, F, Cl, MeOCH2CH2, CH3), (M-2071, H, F, Cl, HOCH2, H), (M-2072, H, F, Cl, HOCH2, Cl), (M-2073, H, F, Cl, HOCH2, F), (M-2074, H, F, Cl, HOCH2, CF3), (M-2075, H, F, Cl, HOCH2, Br), (M-2076, H, F, Cl, HOCH2, CH3), (M-2077, H, F, Cl, HOCH2CH2, H), (M-2078, H, F, Cl, HOCH2CH2, Cl), (M-2079, H, F, Cl, HOCH2CH2, F), (M-2080, H, F, Cl, HOCH2CH2, CF3), (M-2081, H, F, Cl, HOCH2CH2, Br), (M-2082, H, F, Cl, HOCH2CH2, CH3), (M-2083, H, F, Cl, HOCH2CH2CH2, H), (M-2084, H, F, Cl, HOCH2CH2CH2, Cl), (M-2085, H, F, Cl, HOCH2CH2CH2, F), (M-2086, H, F, Cl, HOCH2CH2CH2, CF3), (M-2087, H, F, Cl, HOCH2CH2CH2, Br), (M-2088, H, F, Cl, HOCH2CH2CH2, CH3), (M-2089, H, F, Cl, HOCH2CH2CH2CH2, H), (M-2090, H, F, Cl, HOCH2CH2CH2CH2, Cl), (M-2091, H, F, Cl, HOCH2CH2CH2CH2, F), (M-2092, H, F, Cl, HOCH2CH2CH2CH2, CF3), (M-2093, H, F, Cl, HOCH2CH2CH2CH2, Br), (M-2094, H, F, Cl, HOCH2CH2CH2CH2, CH3), (M-2095, H, F, Cl, HOCH2CH2CH2CH2CH2H), (M-2096, H, F, Cl, HOCH2CH2CH2CH2CH2Cl), (M-2097, H, F, Cl, HOCH2CH2CH2CH2CH2, F), (M-2098, H, F, Cl, HOCH2CH2CH2CH2CH2CF3), (M-2099, H, F, Cl, HOCH2CH2CH2CH2CH2Br), (M-2100, H, F, Cl, HOCH2CH2CH2CH2CH2CH3), (M-2101, H, F, Cl, HOCH2CH2OCH2CH2, H), (M-2102, H, F, Cl, HOCH2CH2OCH2CH2, Cl), (M-2103, H, F, Cl, HOCH2CH2OCH2CH2, F), (M-2104, H, F, Cl, HOCH2CH2OCH2CH2, CF3), (M-2105, H, F, Cl, HOCH2CH2OCH2CH2, Br), (M-2106, H, F, Cl, HOCH2CH2OCH2CH2, CH3), (M-2107, H, F, Cl, (Me)2N, H), (M-2108, H, F, Cl, (Me)2N, Cl), (M-2109, H, F, Cl, (Me)2N, F), (M-2110, H, F, Cl, (Me)2N, CF3), (M-2111, H, F, Cl, (Me)2N, Br), (M-2112, H, F, Cl, (Me)2N, CH3), (M-2113, H, F, Cl, piperidin-4-yl-methyl, H), (M-2114, H, F, Cl, piperidin-4-yl-methyl, Cl), (M-2115, H, F, Cl, piperidin-4-yl-methyl, F), (M-2116, H, F, Cl, piperidin-4-yl-methyl, CF3), (M-2117, H, F, Cl, piperidin-4-yl-methyl, Br), (M-2118, H, F, Cl, piperidin, 4-yl-methyl, CH3), (M-2119, H, F, Cl, cyclohexylmethyl, H), (M-2120, H, F, Cl, cyclohexylmethyl, Cl), (M-2121, H, F, Cl, cyclohexylmethyl, F), (M-2122, H, F, Cl, cyclohexylmethyl, CF3), (M-2123, H, F, Cl, cyclohexylmethyl, Br), (M-2124, H, F, Cl, cyclohexylmethyl, CH3), (M-2125, H, CH3, H, H, H), (M-2126, H, CH3, H, H, Cl), (M-2127, H, CH3, H, H, F), (M-2128, H, CH3, H, H, CF3), (M-2129, H, CH3, H, H, Br), (M-2130, H, CH3, H, H, CH3), (M-2131, H, CH3, H, F, H), (M-2132, H, CH3, H, F, Cl), (M-2133, H, CH3, H, F, F), (M-2134, H, CH3, H, F, CF3), (M-2135, H, CH3, H, F, Br), (M-2136, H, CH3, H, F, CH3), (M-2137, H, CH3, H, Cl, H), (M-2138, H, CH3, H, Cl, Cl), (M-2139, H, CH3, H, Cl, F), (M-2140, H, CH3, H, Cl, CF3), (M-2141, H, CH3, H, Cl, Br), (M-2142, H, CH3, H, Cl, CH3), (M-2143, H, CH3, H, CH3, H), (M-2144, H, CH3, H, CH3, Cl), (M-2145, H, CH3, H, CH3, F), (M-2146, H, CH3, H, CH3, CF3), (M-2147, H, CH3, H, CH3, Br), (M-2148, H, CH3, H, CH3, CH3), (M-2149, H, CH3, H, Et, H), (M-2150, H, CH3, H, Et, Cl), (M-2151, H, CH3, H, Et, F), (M-2152, H, CH3, H, Et, CF3), (M-2153, H, CH3, H, Et, Br), (M-2154, H, CH3, H, Et, CH3), (M-2155, H, CH3, H, n-Pr, H), (M-2156, H, CH3, H, n-Pr, Cl), (M-2357, H, CH3, H, n-Pr, F), (M-2158, H, CH3, H, n-Pr, CF3), (M-2159, H, CH3, H, n-Pr, Br), (M-2160, H, CH3, H, n-Pr, CH3), (M-2161, H, CH3, H, c-Pr, H), (M-2162, H, CH3, H, c-Pr, Cl), (M-2163, H, CH3, H, c-Pr, F), (M-2164, H, CH3, H, c-Pr, CF3), (M-2165, H, CH3, H, c-Pr, Br), (M-2166, H, CH3, H, c-Pr, CH3), (M-2167, H, CH3, H, i-Pr, H), (M-2168, H, CH3, H, i-Pr, Cl), (M-2169, H, CH3, H, i-Pr, F), (M-2170, H, CH3, H, i-Pr, CF3), (M-2171, H, CH3, H, i-Pr, Br), (M-2172, H, CH3, H, i-Pr, CH3), (M-2173, H, CH3, H, n-Bu, H), (M-2174, H, CH3, H, n-Bu, Cl), (M-2175, H, CH3, H, n-Bu, F), (M-2176, H, CH3, H, n-Bu, CF3), (M-2177, H, CH3, H, n-Bu, Br), (M-2178, H, CH3, H, n-Bu, CH3), (M-2179, H, CH3H, i-Bu, H), (M-2180, H, CH3, H, i-Bu, Cl), (M-2181, H, CH3, H, i-Bu, F), (M-2182, H, CH3, H, i-Bu, CF3), (M-2183, H, CH3, H, i-Bu, Br), (M-2184, H, CH3, H, i-Bu, CH3), (M-2185, H, CH3, H, sec-Bu, H), (M-2186, H, CH3, H, sec-Bu, Cl), (M-2187, H, CH3, H, sec-Bu, F), (M-2188, H, CH3, H, sec-Bu, CF3), (M-2189, H, CH3, H, sec-Bu, Br), (M-2190, H, CH3, H, sec-Bu, CH3), (M-2191, H, CH3, H, n-Pen, H), (M-2192, H, CH3, H, n-Pen, Cl), (M-2193, H, CH3, H, n-Pen, F), (M-2194, H, CH3, H, n-Pen, CF3), (M-2195, H, CH3, H, n-Pen, Br), (M-2196, H, CH3, H, n-Pen, CH3), (M-2197, H, CH2, H, c-Pen, H), (M-2198, H, CH3, H, c-Pen, Cl), (M-2199, H, CH3, H, c-Pen, F), (M-2200, H, CH3, H, c-Pen, CF3), (M-2201, H, CH3, H, c-Pen, Br), (M-2202, H, CH3, H, c-Pen, CH3), (M-2203, H, CH3, H, n-Hex, H), (M-2204, H, CH3, H, n-Hex, Cl), (M-2205, H, CH3, H, n-Hex, F), (M-2206, H, CH3, H, n-Hex, CF3), (M-2207, H, CH3, H, n-Hex, Br), (M-2208, H, CH3, H, n-Hex, CH3), (M-2209, H, CH3, H, c-Hex, H), (M-2210, H, CH3, H, c-Hex, Cl), (M-2211, H, CH3, H, c-Hex, F), (M-2212, H, CH3, H, c-Hex, CF3), (M-2213, H, CH3, H, c-Hex, Br), (M-2214, H, CH3, H, c-Hex, CH3), (M-2215, H, CH3, H, OH, H), (M-2216, H, CH3, H, OH, Cl), (M-2217, H, CH3, H, OH, F), (M-2218, H, CH3, H, OH, CF3), (M-2219, H, CH3, H, OH, Br), (M-2220, H, CH3, H, OH, CH3), (M-2221, H, CH3, H, EtO, H), (M-2222, H, CH3, H, EtO, Cl), (M-2223, H, CH3, H, EtO, F), (M-2224, H, CH3, H, EtO, CF3), (M-2225, H, CH3, H, EtO, Br), (M-2226, H, CH3, H, EtO, CH3), (M-2227, H, CH3, H, n-PrO, H), (M-2228, H, CH3, H, n-PrO, Cl), (M-2229, H, CH3, H, n-PrO, F), (M-2230, H, CH3, H, n-PrO, CF3), (M-2231, H, CH3, H, n-PrO, Br), (M-2232, H, CH3, H, n-PrO, CH3), (M-2233, H, CH3, H, PhO, H), (M-2234, H, CH3, H, PhO, Cl), (M-2235, H, CH3, H, PhO, F), (M-2236, H, CH3, H, PhO, CF3), (M-2237, H, CH3, H, PhO, Br), (M-2238, H, CH3, H, PhO, CH3), (M-2239, H, CH3, H, BnO, H), (M-2240, H, CH3, H, BnO, Cl), (M-2241, H, CH3, H, BnO, F), (M-2242, H, CH3, H, BnO, CF3), (M-2243, H, CH3, H, BnO, Br), (M-2244, H, CH3, H, BnO, CH3), (M-2245, H, CH3, H, PhCH2CH2O, H), (M-2246, H, CH3, H, PhCH2CH30, Cl), (M-2247, H, CH3, H, PhCH2CH2O, F), (M-2248, H, CH3, H, PhCH2CH2O, CF3), (M-2249, H, CH3, H, PhCH2CH2O, Br), (M-2250, H, CH3, H, PhCH2CH2O, CH3), (M-2251, H, CH3, H, CF3O, H), (M-2252, H, CH3, H, CF3O, Cl), (M-2253, H, CH3, H, CF3O, F), (M-2254, H, CH3, H, CF3O, CF3), (M-2255, H, CH3, H, CF3O, Br), (M-2256, H, CH3, H, CF3O, CH3), (M-2257, H, CH3, H, Ph, H), (M-2258, H, CH3, H, Ph, Cl), (M-2259, H, CH3, H, Ph, F), (M-2260, H, CH3, H, Ph, CF3), (M-2261, H, CH3, H, Ph, Br), (M-2262, H, CH3, H, Ph, CH3), (M-2263, H, CH3, H, 4-F-Ph, H), (M-2264, H, CH3, H, 4-F-Ph, Cl), (M-2265, H, CH3(H, 4-F-Ph, F), (M-2266, H, CH3, H, 4-F-Ph, CF3), (M-2267, H, CH3, H, 4-F-Ph, Br), (M-2268, H, CH3, H, 4-F-Ph, CH3), (M-2269, H, CH3, H, 4-CF3-Ph, H), (M-2270, H, CH3, H, 4-CF3-Ph, Cl), (M-2271, H, CH3, H, 4-CF3-Ph, F), (M-2272, H, CH3, H, 4-CF3-Ph, CF3), (M-2273, H, CH3, H, 4-CF3-Ph, Br), (M-2274, H, CH3, H, 4-CF3-Ph, CH3), (M-2275, H, CH3, H, 4-(Me)2N-Ph, H), (M-2276, H, CH3, H, 4-(Me)2N-Ph, Cl), (M-2277, H, CH3, H, 4-(Me)2N-Ph, F), (M-2278, H, CH3, H, 4-(Me)2N-Ph, CF3), (M-2279, H, CH3, H, 4-(Me)2N-Ph, Br), (M-2280, H, CH3, H, 4-(Me)2N-Ph, CH3), (M-2281, H, CH3, H, 4-OH-Ph, H), (M-2282, H, CH3, H, 4-OH-Ph, Cl), (M-2283, H, CH3, H, 4-OH-Ph, F), (M-2284, H, CH3, H, 4-OH-Ph, CF3), (M-2285, H, CH3, H, 4-OH-Ph, Br), (M-2286, H, CH3, H, 4-OH-Ph, CH3), (M-2287, H, CH3, H, 3,4-di-F-Ph, H), (M-2288, H, CH3, H, 3,4-di-F-Ph, Cl), (M-2289, H, CH3, H, 3,4-di-F-Ph, F), (M-2290, H, CH3, H, 3,4-di-F-Ph, CF3), (M-2291, H, CH3, H, 3,4-di-F-Ph, Br), (M-2292, H, CH3, H, 3,4-di-F-Ph, CH3), (M-2293, H, CH3, H, 4-COOH-Ph, H), (M-2294, H, CH3, H, 4-COOH-Ph, Cl), (M-2295, H, CH3, H, 4-COOH-Ph, F), (M-2296, H, CH3, H, 4-COOH-Ph, CF3), (M-2297, H, CH3, H, 4-COOH-Ph, Br), (M-2298, H, CH3, H, 4-COOH-Ph, CH3), (M-2299, H, CH3, H, Bn, H), (M-2300, H, CH3, H, Bn, Cl), (M-2301, H, CH3, H, Bn, F), (M-2302, H, CH3, H, Bn, CF3), (M-2303, H, CH3, H, Bn, Br), (M-2304, H, CH3, H, Bn, CH3), (M-2305, H, CH3, H, 4-F-Bn, H), (M-2306, H, CH3, H, 4-F-Bn, Cl), (M-2307, H, CH3, H, 4-F-Bn, F), (M-2308, H, CH3, H, 4-F-Bn, CF3), (M-2309, H, CH3, H, 4-F-Bn, Br), (M-2310, H, CH3, H, 4-F-Bn, CH3), (M-2311, H, CH3, H, 2-Py, H), (M-2312, H, CH3, H, 2-Py, Cl), (M-2313, H, CH3, H, 2-Py, F), (M-2314, H, CH3, H, 2-Py, CF3), (M-2315, H, CH3, H, 2-Py, Br), (M-2316, H, CH3, H, 2-Py, CH3), (M-2317, H, CH3, H, 3-Py, H), (M-2318, H, CH3, H, 3-Py, Cl), (M-2319, H, CH3, H, 3-Py, F), (M-2320, H, CH3, H, 3-Py, CF3), (M-2321, H, CH3, H, 3-Py, Br), (M-2322, H, CH3, H, 3-Py, CH3), (M-2323, H, CH3, H, 4-Py, H), (M-2324, H, CH3, H, 4-Py, Cl), (M-2325, H, CH3, H, 4-Py, F), (M-2326, H, CH3, H, 4-Py, CF3), (M-2327, H, CH3, H, 4-Py, Br), (M-2328, H, CH3, H, 4-Py, CH3), (M-2329, H, CH3, H, 2-Th, H), (M-2330, H, CH3, H, 2-Th, Cl), (M-2331, H, CH3, H, 2-Th, F), (M-2332, H, CH3, H, 2-Th, CF3), (M-2333, H, CH3, H, 2-Th, Br), (M-2334, H, CH3, H, 2-Th, CH3), (M-2335, H, CH3, H, 3-Th, H), (M-2336, H, CH3, H, 3-Th, Cl), (M-2337, H, CH3, H, 3-Th, F), (M-2338, H, CH3, H, 3-Th, CF3), (M-2339, H, CH3, H, 3-Th, Br), (M-2340, H, CH3, H, 3-Th, CH3), (M-2341, H, CH3, H, pyrrazol-2-yl, H), (M-2342, H, CH3, H, pyrrazol-2-yl, Cl), (M-2343, H, CH3, H, pyrrazol-2-yl, F), (M-2344, H, CH3, H, pyrrazol-2-yl, CF3), (M-2345, H, CH3, H, pyrrazol-2-yl, Br), (M-2346, H, CH3, H, pyrrazol-2-yl, CH3), (M-2347, H, CH3, H, pyrrazol-3-yl, H), (M-2348, H, CH3, H, pyrrazol-3-yl, Cl), (M-2349, H, CH3, H, pyrrazol-3-yl, F), (M-2350, H, CH3, H, pyrrazol-3-yl, CF3), (M-2351, H, CH3, H, pyrrazol-3-yl, Br), (M-2352, H, CH3, H, pyrrazol-3-yl, CH3), (M-2353, H, CH3, H, pyrimidin-2-yl, H), (M-2354, H, CH3, H, pyrimidin-2-yl, Cl), (M-2355, H, CH3, H, pyrimidin-2-yl, F), (M-2356, H, CH3, H, pyrimidin-2-yl, CF3), (M-2357, H, CH3, H, pyrimidin-2-yl, Br), (M-2358, H, CH3, H, pyrimidin-2-yl, CH3), (M-2359, H, CH3, H, pyrimidin-4-yl, H), (M-2360, H, CH3, H, pyrimidin-4-yl, Cl), (M-2361, H, CH3, H, pyrimidin-4-yl, F), (M-2362, H, CH3, H, pyrimidin-4-yl, CF3), (M-2363, H, CH3, H, pyrimidin-4-yl, Br), (M-2364, H, CH3, H, pyrimidin-4-yl, CH3), (M-2365, H, CH3, H, pyrimidin-5-yl, H), (M-2366, H, CH3, H, pyrimidin-5-yl, Cl), (M-2367, H, CH3, H, pyrimidin-5-yl, F), (M-2368, H, CH3, H, pyrimidin-5-yl, CF3), (M-2369, H, CH3, H, pyrimidin-5-yl, Br), (M-2370, H, CH3, H, pyrimidin-5-yl, CH3), (M-2371, H, CH3, H, HOOCCH2CH2CH2, H), (M-2372, H, CH3, H, HOOCCH2CH2CH2, Cl), (M-2373, H, CH3, H, HOOCCH2CH2CH2, F), (M-2374, H, CH3, H, HOOCCH2CH2CH2, CF3), (M-2375, H, CH3, H, HOOCCH2CH2CH2, Br), (M-2376, H, CH3, H, HOOCCH2CH2CH2, CH3), (M-2377, H, CH3, H, HOOCCH2CH2CH2CH2, H), (M-2378, H, CH3, H, HOOCCH2CH2CH2CH2, Cl), (M-2379, H, CH3, H, HOOCCH2CH2CH2CH2, F), (M-2380, H, CH3, H, HOOCCH2CH2CH2CH2, CF3), (M-2381, H, CH3, H, HOOCCH2CH2CH2CH2, Br), (M-2382, H, CH3, H, HOOCCH2CH2CH2CH2, CH3), (M-2383, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, H), (M-2384, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-2385, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, F), (M-2386, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-2387, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-2388, H, CH3, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-2389, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-2390, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-2391, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-2392, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-2393, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-2394, H, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-2395, H, CH3, H, MeOCH2, H), (M-2396, H, CH3, H, MeOCH2, Cl), (M-2397, H, CH3, H, MeOCH2, F), (M-2398, H, CH3, H, MeOCH2, CF3), (M-2399, H, CH3, H, MeOCH2, Br), (M-2400, H, CH3, H, MeOCH2, CH3), (M-2401, H, CH3, H, EtOCH2, H), (M-2402, H, CH3, H, EtOCH2, Cl), (M-2403, H, CH3, H, EtOCH2, F), (M-2404, H, CH3, H, EtOCH2, CF3), (M-2405, H, CH3, H, EtOCH2, Br), (M-2406, H, CH3, H, EtOCH2, CH3), (M-2407, H, CH3, H, EtOCH2CH2, H), (M-2408, H, CH3, H, EtOCH2CH2, Cl), (M-2409, H, CH3, H, EtOCH2CH2, F), (M-2410, H, CH3, H, EtOCH2CH2, CF3), (M-2411, H, CH3, H, EtOCH2CH2, Br), (M-2412, H, CH3, H, EtOCH2CH2, CH3), (M-2413, H, CH3, H, MeOCH2CH2OCH2CH2, H), (M-2414, H, CH3, H, MeOCH2CH2OCH2CH2, Cl), (M-2415, H, CH3, H, MeOCH2CH2OCH2CH2, F), (M-2416, H, CH3, H, MeOCH2CH2OCH2CH2, CF3), (M-2417, H, CH3, H, MeOCH2CH2OCH3, Br), (M-2418, H, CH3, H, MeOCH2CH2OCH2CH2, CH3), (M-2419, H, CH3, H, MeOCH2CH2, H), (M-2420, H, CH3, H, MeOCH2CH2, Cl), (M-2421, H, CH3, H, MeOCH2CH2, F), (M-2422, H, CH3, H, MeOCH2CH2, CF3), (M-2423, H, CH3, H, MeOCH2CH2, Br), (M-2424, H, CH3, H, MeOCH2CH2, CH3), (M-2425, H, CH3, H, HOCH2, H), (M-2426, H, CH3, H, HOCH2, Cl), (M-2427, H, CH3, H, HOCH2, F), (M-2428, H, CH3, H, HOCH2, CF3), (M-2429, H, CH3, H, HOCH2, Br), (M-2430, H, CH3, H, HOCH2, CH3), (M-2431, H, CH3, H, HOCH2CH2, H), (M-2432, H, CH3, H, HOCH2CH2, Cl), (M-2433, H, CH3, H, HOCH2CH2, F), (M-2434, H, CH3, H, HOCH2CH2, CF3), (M-2435, H, CH3, H, HOCH2CH2, Br), (M-2436, H, CH3, H, HOCH2CH2, CH3), (M-2437, H, CH3, H, HOCH2CH2CH2, H), (M-2438, H, CH3, H, HOCH2CH2CH2, Cl), (M-2439, H, CH3, H, HOCH2CH2CH2, F), (M-2440, H, CH3, H, HOCH2CH2CH2, CF3), (M-2441, H, CH3, H, HOCH2CH2CH2, Br), (M-2442, H, CH3, H, HOCH2CH2CH2, CH3), (M-2443, H, CH3, H, HOCH2CH2CH2CH2, H), (M-2444, H, CH3, H, HOCH2CH2CH2CH2, Cl), (M-2445, H, CH3, H, HOCH2CH2CH2CH2, F), (M-2446, H, CH3, H, HOCH2CH2CH2CH2, CF3), (M-2447, H, CH3, H, HOCH2CH2CH2CH2, Br), (M-2448, H, CH3, H, HOCH2CH2CH2CH2, CH3), (M-2449, H, CH3, H, HOCH2CH2CH2CH2CH2H), (M-2450, H, CH3, H, HOCH2CH2CH2CH2CH2Cl), (M-2451, H, CH3, H, HOCH2CH2CH2CH2CH2, F), (M-2452, H, CH3, H, HOCH2CH2CH2CH2CH2CF3), (M-2453, H, CH3, H, HOCH2CH2CH2CH2CH2Br), (M-2454, H, CH3, H, HOCH2CH2CH2CH2CH2, CH3), (M-2455, H, CH3, H, HOCH2CH2OCH2CH2, H), (M-2456, H, CH3, H, HOCH2CH2OCH2CH2, Cl), (M-2457, H, CH3, H, HOCH2CH2OCH2CH2, F), (M-2458, H, CH3, H, HOCH2CH2OCH2CH2, CF3), (M-2459, H, CH3, H, HOCH2CH2OCH2CH2, Br), (M-2460, H, CH3, H, HOCH2CH2OCH2CH2, CH3), (M-2461, H, CH3, H, (Me)2N, H), (M-2462, H, CH3, H, (Me)2N, Cl), (M-2463, H, CH3, H, (Me)2N, F), (M-2464, H, CH3, H, (Me)2N, CF3), (M-2465, H, CH3, H, (Me)2N, Br), (M-2466, H, CH3, H, (Me)2N, CH3), (M-2467, H, CH3, H, piperidin-4-yl-methyl, H), (M-2468, H, CH3, H, piperidin-4-yl-methyl, Cl), (M-2469, H, CH3, H, piperidin-4-yl-methyl, F), (M-2470, H, CH3, H, piperidin-4-yl-methyl, CF3), (M-2471, H, CH3, H, piperidin-4-yl-methyl, Br), (M-2472, H, CH3, H, piperidin-4-yl-methyl, CH3), (M-2473, H, CH3, H, cyclohexylmethyl, H), (M-2474, H, CH3, H, cyclohexylmethyl, Cl), (M-2475, H, CH3, H, cyclohexylmethyl, F), (M-2476, H, CH3, H, cyclohexylmethyl, CF3), (M-2477, H, CH3, H, cyclohexylmethyl, Br), (M-2478, H, CH3, H, cyclohexylmethyl, CH3), (M-2479, H, CH3, F, H, H), (M-2480, H, CH3, F, H, Cl), (M-2481, H, CH3, F, H, F), (M-2482, H, CH3, F, H, CF3), (M-2483, H, CH3, F, H, Br), (M-2484, H, CH3, F, H, CH3), (M-2485, H, CH3, F, F, H), (M-2486, H, CH3, F, F, Cl), (M-2487, H, CH3, F, F, F), (M-2488, H, CH3, F, F, CF3), (M-2489, H, CH3, F, F, Br), (M-2490, H, CH3, F, F, CH3), (M-2491, H, CH3, F, Cl, H), (M-2492, H, CH3, F, Cl, Cl), (M-2493, H, CH3, F, Cl, F), (M-2494, H, CH3, F, Cl, CF3), (M-2495, H, CH3, F, Cl, Br), (M-2496, H, CH3, F, Cl, CH3), (M-2497, H, CH3, F, CH3, H), (M-2498, H, CH3, F, CH3, Cl), (M-2499, H, CH3, F, CH3, F), (M-2500, H, CH3, F, CH3, CF3), (M-2501, H, CH3, F, CH3, Br), (M-2502, H, CH3, F, CH3, CH3), (M-2503, H, CH3, F, Et, H), (M-2504, H, CH3, F, Et, Cl), (M-2505, H, CH3, F, Et, F), (M-2506, H, CH3, F, Et, CF3), (M-2507, H, CH3, F, Et, Br), (M-2508, H, CH3, F, Et, CH3), (M-2509, H, CH3, F, n-Pr, H), (M-2510, H, CH3, F, n-Pr, Cl), (M-2511, H, CH3, F, n-Pr, F), (M-2512, H, CH3, F, n-Pr, CF3), (M-2513, H, CH3, F, n-Pr, Br), (M-2514, H, CH3, F, n-Pr, CH3), (M-2515, H, CH3, F, c-Pr, H), (M-2516, H, CH3, F, c-Pr, Cl), (M-2517, H, CH3, F, c-Pr, F), (M-2518, H, CH3, F, c-Pr, CF3), (M-2519, H, CH3, F, c-Pr, Br), (M-2520, H, CH3, F, c-Pr, CH3), (M-2521, H, CH3, F, i-Pr, H), (M-2522, H, CH3, F, i-Pr, Cl), (M-2523, H, CH3, F, i-Pr, F), (M-2524, H, CH3, F, i-Pr, CF3), (M-2525, H, CH3, F, i-Pr, Br), (M-2526, H, CH3, F, i-Pr, CH3), (M-2527, H, CH3, F, n-Bu, H), (M-2528, H, CH3, F, n-Bu, Cl), (M-2529, H, CH3, F, n-Bu, F), (M-2530, H, CH3, F, n-Bu, CF3), (M-2531, H, CH3, F, n-Bu, Br), (M-2532, H, CH3, F, n-Bu, CH3), (M-2533, H, CH3, F, i-Bu, H), (M-2534, H, CH3, F, i-Bu, Cl), (M-2535, H, CH3, F, i-Bu, F), (M-2536, H, CH3, F, i-Bu, CF3), (M-2537, H, CH3, F, i-Bu, Br), (M-2538, H, CH3, F, i-Bu, CH3), (M-2539, H, CH3, F, sec-Bu, H), (M-2540, H, CH3, F, sec-Bu, Cl), (M-2541, H, CH3, F, sec-Bu, F), (M-2542, H, CH3, F, sec-Bu, CF3), (M-2543, H, CH3, F, sec-Bu, Br), (M-2544, H, CH3, F, sec-Bu, CH3), (M-2545, H, CH3, F, n-Pen, H), (M-2546, H, CH3, F, n-Pen, Cl), (M-2547, H, CH3, F, n-Pen, F), (M-2548, H, CH3, F, n-Pen, CF3), (M-2549, H, CH3, F, n-Pen, Br), (M-2550, H, CH3, F, n-Pen, CH3), (M-2551, H, CH3, F, c-Pen, H), (M-2552, H, CH3, F, c-Pen, Cl), (M-2553, H, CH3, F, c-Pen, F), (M-2554, H, CH3, F, c-Pen, CF3), (M-2555, H, CH3, F, c-Pen, Br), (M-2556, H, CH3, F, c-Pen, CH3), (M-2557, H, CH3, F, n-Hex, H), (M-2558, H, CH3, F, n-Hex, Cl), (M-2559, H, CH3, F, n-Hex, F), (M-2560, H, CH3, F, n-Hex, CF3), (M-2561, H, CH3, F, n-Hex, Br), (M-2562, H, CH3, F, n-Hex, CH3), (M-2563, H, CH3, F, c-Hex, H), (M-2564, H, CH3, F, c-Hex, Cl), (M-2565, H, CH3, F, c-Hex, F), (M-2566, H, CH3, F, c-Hex, CF3), (M-2567, H, CH3, F, c-Hex, Br), (M-2568, H, CH3, F, c-Hex, CH3), (M-2569, H, CH3, F, OH, H), (M-2570, H, CH3, F, OH, Cl), (M-2571, H, CH3, F, OH, F), (M-2572, H, CH3, F, OH, CF3), (M-2573, H, CH3, F, OH, Br), (M-2574, H, CH3, F, OH, CH3), (M-2575, H, CH3, F, EtO, H), (M-2576, H, CH3, F, EtO, Cl), (M-2577, H, CH3, F, EtO, F), (M-2578, H, CH3, F, EtO, CF3), (M-2579, H, CH3, F, EtO, Br), (M-2580, H, CH3, F, EtO, CH3), (M-2581, H, CH3, F, n-PrO, H), (M-2582, H, CH3, F, n-PrO, Cl), (M-2583, H, CH3, F, n-PrO, F), (M-2584, H, CH3, F, n-PrO, CF3), (M-2585, H, CH3, F, n-PrO, Br), (M-2586, H, CH3, F, n-PrO, CH3), (M-2587, H, CH3, F, PhO, H), (M-2588, H, CH3, F, PhO, Cl), (M-2589, H, CH3, F, PhO, F), (M-2590, H, CH3, F, PhO, CF3), (M-2591, H, CH3, F, PhO, Br), (M-2592, H, CH3, F, PhO, CH3), (M-2593, H, CH3, F, BnO, H), (M-2594, H, CH3, F, BnO, Cl), (M-2595, H, CH3, F, BnO, F), (M-2596, H, CH3, F, BnO, CF3), (M-2597, H, CH3, F, BnO, Br), (M-2598, H, CH3, F, BnO, CH3), (M-2599, H, CH3, F, PhCH2CH2O, H), (M-2600, H, CH3, F, PhCH2CH2O, Cl), (M-2601, H, CH3, F, PhCH2CH2O, F), (M-2602, H, CH3, F, PhCH2CH2O, CF3), (M-2603, H, CH3, F, PhCH2CH2O, Br), (M-2604, H, CH3, F, PhCH2CH2O, CH3), (M-2605, H, CH3, F, CF3O, H), (M-2606, H, CH3, F, CF3O, Cl), (M-2607, H, CH3, F, CF3O, F), (M-2608, H, CH3, F, CF3O, CF3), (M-2609, H, CH3, F, CF3O, Br), (M-2610, H, CH3, F, CF3O, CH3), (M-2611, H, CH3, F, Ph, H), (M-2612, H, CH3, F, Ph, Cl), (M-2613, H, CH3, F, Ph, F), (M-2614, H, CH3, F, Ph, CF3), (M-2615, H, CH3, F, Ph, Br), (M-2616, H, CH3, F, Ph, CH3), (M-2617, H, CH3, F, 4-F-Ph, H), (M-2618, H, CH3, F, 4-F-Ph, Cl), (M-2619, H, CH3, F, 4-F-Ph, F), (M-2620, H, CH3, F, 4-F-Ph, CF3), (M-2621, H, CH3, F, 4-F-Ph, Br), (M-2622, H, CH3, F, 4-F-Ph, CH3), (M-2623, H, CH3, F, 4-CF3-Ph, H), (M-2624, H, CH3, F, 4-CF3-Ph, Cl), (M-2625, H, CH3, F, 4-CF3-Ph, F), (M-2626, H, CH3, F, 4-CF3-Ph, CF3), (M-2627, H, CH3, F, 4-CF3-Ph, Br), (M-2628, H, CH3, F, 4-CF3-Ph, CH3), (M-2629, H, CH3, F, 4-(Me)2N-Ph, H), (M-2630, H, CH3, F, 4-(Me)3N-Ph, Cl), (M-2631, H, CH3, F, 4-(Me)2N-Ph, F), (M-2632, H, CH3, F, 4-(Me)2N-Ph, CF3), (M-2633, H, CH3, F, 4-(Me)2N-Ph, Br), (M-2634, H, CH3, F, 4-(Me)2N-Ph, CH3), (M-2635, H, CH3, F, 4-OH-Ph, H), (M-2636, H, CH3, F, 4-OH-Ph, Cl), (M-2637, H, CH3, F, 4-OH-Ph, F), (M-2638, H, CH3, F, 4-OH-Ph, CF3), (M-2639, H, CH3, F, 4-OH-Ph, Br), (M-2640, H, CH3, F, 4-OH-Ph, CH3), (M-2641, H, CH3, F, 3,4-di-F-Ph, H), (M-2642, H, CH3, F, 3,4-di-F-Ph, Cl), (M-2643, H, CH3, F, 3,4-di-F-Ph, F), (M-2644, H, CH3, F, 3,4-di-F-Ph, CF3), (M-2645, H, CH3, F, 3,4-di-F-Ph, Br), (M-2646, H, CH3, F, 3,4-di-F-Ph, CH3), (M-2647, H, CH3, F, 4-COOH-Ph, H), (M-2648, H, CH3, F, 4-COOH-Ph, Cl), (M-2649, H, CH3, F, 4-COOH-Ph, F), (M-2650, H, CH3, F, 4-COOH-Ph, CF3), (M-2651, H, CH3, F, 4-COOH-Ph, Br), (M-2652, H, CH3, F, 4-COOH-Ph, CH3), (M-2653, H, CH3, F, Bn, H), (M-2654, H, CH31 F, Bn, Cl), (M-2655, H, CH3F, Bn, F), (M-2656, H, CH3, F, Bn, CF3), (M-2657, H, CH3, F, Bn, Br), (M-2658, H, CH3, F, Bn, CH3), (M-2659, H, CH3, F, 4-F-Bn, H), (M-2660, H, CH3, F, 4-F-Bn, Cl), (M-2661, H, CH3, F, 4-F-Bn, F), (M-2662, H, CH3, F, 4-F-Bn, CF3), (M-2663, H, CH3, F, 4-F-Bn, Br), (M-2664, H, CH3, F, 4-F-Bn, CH3), (M-2665, H, CH3, F, 2-Py, H), (M-2666, H, CH3, F, 2-Py, Cl), (M-2667, H, CH3, F, 2-Py, F), (M-2668, H, CH3, F, 2-Py, CF3), (M-2669, H, CH3, F, 2-Py, Br), (M-2670, H, CH3, F, 2-Py, CH3), (M-2671, H, CH3, F, 3-Py, H), (M-2672, H, CH3, F, 3-Py, Cl), (M-2673, H, CH3, F, 3-Py, F), (M-2674, H, CH3, F, 3-Py, CF3), (M-2675, H, CH3, F, 3-Py, Br), (M-2676, H, CH3, F, 3-Py, CH3), (M-2677, H, CH3, F, 4-Py, H), (M-2678, H, CH3, F, 4-Py, Cl), (M-2679, H, CH3, F, 4-Py, F), (M-2680, H, CH3, F, 4-Py, CF3), (M-2681, H, CH3, F, 4-Py, Br), (M-2682, H, CH3, F, 4-Py, CH3), (M-2683, H, CH3, F, 2-Th, H), (M-2684, H, CH3, F, 2-Th, Cl), (M-2685, H, CH3, F, 2-Th, F), (M-2686, H, CH3, F, 2-Th, CF3), (M-2687, H, CH3, F, 2-Th, Br), (M-2688, H, CH3, F, 2-Th, CH3), (M-2689, H, CH3, F, 3-Th, H), (M-2690, H, CH3, F, 3-Th, Cl), (M-2691, H, CH3, F, 3-Th, F), (M-2692, H, CH3, F, 3-Th, CF3), (M-2693, H, CH3, F, 3-Th, Br), (M-2694, H, CH3, F, 3-Th, CH3), (M-2695, H, CH3, F, pyrrazol-2-yl, H), (M-2696, H, CH3, F, pyrrazol-2-yl, Cl), (M-2697, H, CH3, F, pyrazolyl, F), (M-2698, H, CH3, F, pyrrazol-2-yl, CF3), (M-2699, H, CH3, F, pyrrazol-2-yl, Br), (M-2700, H, CH3, F, pyrrazol-2-yl, CH3), (M-2701, H, CH3, F, pyrrazol-3-yl, H), (M-2702, H, CH3, F, pyrrazol-3-yl, Cl), (M-2703, H, CH3, F, pyrrazol-3-yl, F), (M-2704, H, CH3, F, pyrrazol-3-yl, CF3), (M-2705, H, CH3, F, pyrrazol-3-yl, Br), (M-2706, H, CH3, F, pyrazol-3-yl, CH3), (M-2707, H, CH3, F, pyrimidin-2-yl, H), (M-2708, H, CH3, F, pyrimidin-2-yl, Cl), (M-2709, H, CH3, F, pyrimidin-2-yl, F), (M-2710, H, CH3, F, pyrimidin-2-yl, CF3), (M-2711, H, CH3, F, pyrimidin-2-yl, Br), (M-2712, H, CH3, F, pyrimidin-2-yl, CH3), (M-2713, H, CH3, F, pyrimidin-4-yl, H), (M-2714, H, CH3, F, pyrimidin-4-yl, Cl), (M-2715, H, CH3, F, pyrimidin-4-yl, F), (M-2716, H, CH3, F, pyrimidin-4-yl, CF3), (M-2717, H, CH3, F, pyrimidin-4-yl, Br), (M-2718, H, CH3, F, pyrimidin-4-yl, CH3), (M-2719, H, CH3, F, pyrimidin-5-yl, H), (M-2720, H, CH3, F, pyrimidin-5-yl, Cl), (M-2721, H, CH3, F, pyrimidin-5-yl, F), (M-2722, H, CH3, F, pyrimidin-5-yl, CF3), (M-2723, H, CH3, F, pyrimidin-5-yl, Br), (M-2724, H, CH3, F, pyrimidin-5-yl, CH3), (M-2725, H, CH3, F, HOOCCH2CH2CH2H), (M-2726, H, CH3, F, HOOCCH2CH2CH2, Cl), (M-2727, H, CH3, F, HOOCCH2CH2CH2, F), (M-2728, H, CH3, F, HOOCCH2CH2CH2, CF3), (M-2729, H, CH3, F, HOOCCH2CH2CH2Br), (M-2730, H, CH3, F, HOOCCH2CH2CH2CH3), (M-2731, H, CH3, F, HOOCCH2CH2CH2CH2, H), (M-2732, H, CH3, F, HOOCCH2CH2CH2CH2, Cl), (M-2733, H, CH3, F, HOOCCH2CH2CH2CH2, F), (M-2734, H, CH3, F, HOOCCH2CH2CH2CH2, CF3), (M-2735, H, CH3, F, HOOCCH2CH2CH2CH2, Br), (M-2736, H, CH3, F, HOOCCH2CH2CH2CH2, CH3), (M-2737, H, CH3, F, (Me)2NCOCH2CH2CH2CH2, H), (M-2738, H, CH3, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-2739, H, CH3, F, (Me)2NCOCH2CH2CH2CH2, F), (M-2740, H, CH3, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-2741, H, CH3, F, (Me)2NCOCH3CH2CH2CH2, Br), (M-2742, H, CH3, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-2743, H, CH3, F, (Me)3NCOCH2CH2CH2CH2CH2, H), (M-2744, H, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-2745, H, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-2746, H, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-2747, H, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-2748, H, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-2749, H, CH3, F, MeOCH2, H), (M-2750, H, CH3, F, MeOCH2, Cl), (M-2751, H, CH3, F, MeOCH2, F), (M-2752, H, CH3, F, MeOCH2, CF3), (M-2753, H, CH3, F, MeOCH2, Br), (M-2754, H, CH3, F, MeOCH2, CH3), (M-2755, H, CH3, F, EtOCH2, H), (M-2756, H, CH3, F, EtOCH2, Cl), (M-2757, H, CH3, F, EtOCH2, F), (M-2758, H, CH3, F, EtOCH2, CF3), (M-2759, H, CH3, F, EtOCH2, Br), (M-2760, H, CH3, F, EtOCH2, CH3), (M-2761, H, CH3, F, EtOCH2CH2, H), (M-2762, H, CH3, F, EtOCH2CH2, Cl), (M-2763, H, CH3, F, EtOCH2CH2, F), (M-2764, H, CH3, F, EtOCH2CH2, CH3), (M-2765, H, CH3, F, EtOCH2CH2, Br), (M-2766, H, CH3, F, EtOCH2CH2, CH3), (M-2767, H, CH3, F, MeOCH2CH2OCH2CH2, H), (M-2768, H, CH3, F, MeOCH2CH2OCH2CH2, Cl), (M-2769, H, CH3, F, MeOCH2CH2OCH2CH2, F), (M-2770, H, CH3, F, MeOCH2CH2OCH2CH2, CF3), (M-2771, H, CH3, F, MeOCH2CH2OCH2CH2, Br), (M-2772, H, CH3, F, MeOCH2CH2OCH2CH2, CH3), (M-2773, H, CH3, F, MeOCH2CH2, H), (M-2774, H, CH3, F, MeOCH2CH2, Cl), (M-2775, H, CH3, F, MeOCH2CH2, F), (M-2776, H, CH3, F, MeOCH2CH2, CF3), (M-2777, H, CH3, F, MeOCH2CH2, Br), (M-2778, H, CH3, F, MeOCH2CH2, CH3), (M-2779, H, CH3, F, HOCH2, H), (M-2780, H, CH3, F, HOCH2, Cl), (M-2781, H, CH3, F, HOCH2, F), (M-2782, H, CH3, F, HOCH2, CF3), (M-2783, H, CH3, F, HOCH2, Br), (M-2784, H, CH3, F, HOCH2, CH3), (M-2785, H, CH3, F, HOCH2CH3, H), (M-2786, H, CH3, F, HOCH2CH2, Cl), (M-2787, H, CH3, F, HOCH2CH2, F), (M-2788, H, CH3, F, HOCH2CH2, CF3), (M-2789, H, CH3, F, HOCH2CH2, Br), (M-2790, H, CH3, F, HOCH2CH2, CH3), (M-2791, H, CH3, F, HOCH2CH2CH2, H), (M-2792, H, CH3, F, HOCH2CH2CH2, Cl), (M-2793, H, CH3, F, HOCH2CH2CH2, F), (M-2794, H, CH3, F, HOCH2CH2CH2, CF3), (M-2795, H, CH3, F, HOCH2CH2CH2, Br), (M-2796, H, CH3, F, HOCH2CH2CH2, CH3), (M-2797, H, CH3, F, HOCH2CH2CH2CH2, H), (M-2798, H, CH3, F, HOCH2CH2CH2CH2, Cl), (M-2799, H, CH3, F, HOCH2CH2CH2CH2, F), (M-2800, H, CH3, F, HOCH2CH2CH2CH2, CF3), (M-2801, H, CH3, F, HOCH2CH2CH2CH2, Br), (M-2802, H, CH3, F, HOCH2CH2CH2CH2, CH3), (M-2803, H, CH3, F, HOCH2CH2CH2CH2CH2, H), (M-2804, H, CH3, F, HOCH2CH2CH2CH2CH2Cl), (M-2805, H, CH3, F, HOCH2CH2CH2CH2CH2, F), (M-2806, H, CH3, F, HOCH2CH2CH2CH2CH2, CF3), (M-2807, H, CH3, F, HOCH2CH2CH2CH2CH2, Br), (M-2808, H, CH3, F, HOCH2CH2CH2CH2CH2CH3), (M-2809, H, CH3, F, HOCH2CH2OCH2CH2, H), (M-2810, H, CH3, F, HOCH2CH2OCH2CH2, Cl), (M-2811, H, CH3, F, HOCH2CH2OCH2CH2, F), (M-2812, H, CH3, F, HOCH2CH2OCH2CH2, CF3), (M-2813, H, CH3, F, HOCH2CH2OCH2CH2, Br), (M-2814, H, CH3, F, HOCH2CH2OCH2CH2, CH3), (M-2815, H, CH3, F, (Me)2N, H), (M-2816, H, CH3, F, (Me)2N, Cl), (M-2817, H, CH3, F, (Me)2N, F), (M-2818, H, CH3, F, (Me)2N, CF3), (M-2819, H, CH3, F, (Me)2N, Br), (M-2820, H, CH3, F, (Me)2N, CH3), (M-2821, H, CH3, F, piperidin-4-yl-methyl, H), (M-2822, H, CH3, F, piperidin-4-yl-methyl, Cl), (M-2823, H, CH3, F, piperidin-4-yl-methyl, F), (M-2824, H, CH3, F, piperidin-4-yl-methyl, CF3), (M-2825, H, CH3, F, piperidin-4-yl-methyl, Br), (M-2826, H, CH3, F, piperidin-4-yl-methyl, CH3), (M-2827, H, CH3, F, cyclohexylmethyl, H), (M-2828, H, CH3, F, cyclohexylmethyl, Cl), (M-2829, H, CH3, F, cyclohexylmethyl, F), (M-2830, H, CH3, F, cyclohexylmethyl, CF3), (M-2831, H, CH3, F, cyclohexylmethyl, Br), (M-2832, H, CH3, F, cyclohexylmethyl, CH3), (M-2833, H, CH3, Cl, H, H), (M-2834, H, CH3, Cl, H, Cl), (M-2835, H, CH3, Cl, H, F), (M-2836, H, CH3, Cl, H, CF3), (M-2837, H, CH3, Cl, H, Br), (M-2838, H, CH3, Cl, H, CH3), (M-2839, H, CH3, Cl, F, H), (M-2840, H, CH3, Cl, F, Cl), (M-2841, H, CH3, Cl, F, F), (M-2842, H, CH3, Cl, F, CF3), (M-2843, H, CH3, Cl, F, Br), (M-2844, H, CH3, Cl, F, CH3), (M-2845, H, CH3, Cl, Cl, H), (M-2846, H, CH3, Cl, Cl, Cl), (M-2847, H, CH3, Cl, Cl, F), (M-2848, H, CH3, Cl, Cl, CF3), (M-2849, H, CH3, Cl, Cl, Br), (M-2850, H, CH3, Cl, Cl, CH3), (M-2851, H, CH3, Cl, CH3, H), (M-2852, H, CH3, Cl, CH3, Cl), (M-2853, H, CH3, Cl, CH3, F), (M-2854, H, CH3, Cl, CH3, CF3), (M-2855, H, CH3, Cl, CH3, Br), (M-2856, H, CH3, Cl, CH3, CH3), (M-2857, H, CH3, Cl, Et, H), (M-2858, H, CH3, Cl, Et, Cl), (M-2859, H, CH3, Cl, Et, F), (M-2860, H, CH3, Cl, Et, CF3), (M-2861, H, CH3, Cl, Et, Br), (M-2862, H, CH3, Cl, Et, CH3), (M-2863, H, CH3, Cl, n-Pr, H), (M-2864, H, CH3, Cl, n-Pr, Cl), (M-2865, H, CH3, Cl, n-Pr, F), (M-2866, H, CH3, Cl, n-Pr, CF3), (M-2867, H, CH3, Cl, n-Pr, Br), (M-2868, H, CH3, Cl, n-Pr, CH3), (M-2869, H, CH3, Cl, c-Pr, H), (M-2870, H, CH3, Cl, c-Pr, Cl), (M-2871, H, CH3, Cl, c-Pr, F), (M-2872, H, CH3, Cl, c-Pr, CF3), (M-2873, H, CH3, Cl, c-Pr, Br), (M-2874, H, CH3, Cl, c-Pr, CH3), (M-2875, H, CH3, Cl, i-Pr, H), (M-2876, H, CH3, Cl, i-Pr, Cl), (M-2877, H, CH3, Cl, i-Pr, F), (M-2878, H, CH3, Cl, i-Pr, CF3), (M-2879, H, CH3, Cl, i-Pr, Br), (M-2880, H, CH3, Cl, i-Pr, CH3), (M-2881, H, CH3, Cl, n-Bu, H), (M-2882, H, CH3, Cl, n-Bu, Cl), (M-2883, H, CH3, Cl, n-Bu, F), (M-2884, H, CH3, Cl, n-Bu, CF3), (M-2885, H, CH3, Cl, n-Bu, Br), (M-2886, H, CH3, Cl, n-Bu, CH3), (M-2887, H, CH3, Cl, i-Bu, H), (M-2888, H, CH3, Cl, i-Bu, Cl), (M-2889, H, CH3, Cl, i-Bu, F), (M-2890, H, CH3, Cl, i-Bu, CF3), (M-2891, H, CH3, Cl, i-Bu, Br), (M-2892, H, CH3, Cl, i-Bu, CH3), (M-2893, H, CH3, Cl, sec-Bu, H), (M-2894, H, CH3, Cl, sec-Bu, Cl), (M-2895, H, CH3, Cl, sec-Bu, F), (M-2896, H, CH3, Cl, sec-Bu, CF3), (M-2897, H, CH3, Cl, sec-Bu, Br), (M-2898, H, CH3, Cl, sec-Bu, CH3), (M-2899, H, CH3, Cl, n-Pen, H), (M-2900, H, CH3, Cl, n-Pen, Cl), (M-2901, H, CH3, Cl, n-Pen, F), (M-2902, H, CH3, Cl, n-Pen, CF3), (M-2903, H, CH3, Cl, n-Pen, Br), (M-2904, H, CH3, Cl, n-Pen, CH3), (M-2905, H, CH3, Cl, c-Pen, H), (M-2906, H, CH3, Cl, c-Pen, Cl), (M-2907, H, CH3, Cl, c-Pen, F), (M-2908, H, CH3, Cl, c-Pen, CF3), (M-2909, H, CH3, Cl, c-Pen, Br), (M-2910, H, CH3, Cl, c-Pen, CH3), (M-2911, H, CH3, Cl, n-Hex, H), (M-2912, H, CH3, Cl, n-Hex, Cl), (M-2913, H, CH3, Cl, n-Hex, F), (M-2914, H, CH3, Cl, n-Hex, CF3), (M-2915, H, CH3, Cl, n-Hex, Br), (M-2916, H, CH3, Cl, n-Hex, CH3), (M-2917, H, CH3, Cl, c-Hex, H), (M-2918, H, CH3, Cl, c-Hex, Cl), (M-2919, H, CH3, Cl, c-Hex, F), (M-2920, H, CH3, Cl, c-Hex, CF3), (M-2921, H, CH3, Cl, c-Hex, Br), (M-2922, H, CH3, Cl, c-Hex, CH3), (M-2923, H, CH3, Cl, OH, H), (M-2924, H, CH3, Cl, OH, Cl), (M-2925, H, CH3, Cl, OH, F), (M-2926, H, CH3, Cl, OH, CF3), (M-2927, H, CH3, Cl, OH, Br), (M-2928, H, CH3, Cl, OH, CH3), (M-2929, H, CH3, Cl, EtO, H), (M-2930, H, CH3, Cl, EtO, Cl), (M-2931, H, CH3, Cl, EtO, F), (M-2932, H, CH3, Cl, EtO, CF3), (M-2933, H, CH3, Cl, EtO, Br), (M-2934, H, CH3, Cl, EtO, CH3), (M-2935, H, CH3, Cl, n-PrO, H), (M-2936, H, CH3, Cl, n-PrO, Cl), (M-2937, H, CH3, Cl, n-PrO, F), (M-2938, H, CH3, Cl, n-PrO, CF3), (M-2939, H, CH3, Cl, n-PrO, Br), (M-2940, H, CH3, Cl, n-PrO, CH3), (M-2941, H, CH3, Cl, PhO, H), (M-2942, H, CH3, Cl, PhO, Cl), (M-2943, H, CH3, Cl, PhO, F), (M-2944, H, CH3, Cl, PhO, CF3), (M-2945, H, CH3, Cl, PhO, Br), (M-2946, H, CH3, Cl, PhO, CH3), (M-2947, H, CH3, Cl, BnO, H), (M-2948, H, CH3, Cl, BnO, Cl), (M-2949, H, CH3, Cl, BnO, F), (M-2950, H, CH3, Cl, BnO, CF3), (M-2951, H, CH3, Cl, BnO, Br), (M-2952, H, CH3, Cl, BnO, CH3), (M-2953, H, CH3, Cl, PhCH2CH2O, H), (M-2954, H, CH3, Cl, PhCH2CH2O, Cl), (M-2955, H, CH3, Cl, PhCH2CH2O, F), (M-2956, H, CH3, Cl, PhCH2CH2O, CF3), (M-2957, H, CH3, Cl, PhCH2CH2O, Br), (M-2958, H, CH3, Cl, PhCH2CH2O, CH3), (M-2959, H, CH3, Cl, CF3O, H), (M-2960, H, CH3, Cl, CF3O, Cl), (M-2961, H, CH3, Cl, CF3O, F), (M-2962, H, CH3, Cl, CF3O, CF3), (M-2963, H, CH3, Cl, CF3O, Br), (M-2964, H, CH3, Cl, CF3O, CH3), (M-2965, H, CH3, Cl, Ph, H), (M-2966, H, CH3, Cl, Ph, Cl), (M-2967, H, CH3, Cl, Ph, F), (M-2968, H, CH3, Cl, Ph, CF3), (M-2969, H, CH3, Cl, Ph, Br), (M-2970, H, CH3, Cl, Ph, CH3), (M-2971, H, CH3, Cl, 4-F-Ph, H), (M-2972, H, CH3, Cl, 4-F-Ph, Cl), (M-2973, H, CH3, Cl, 4-F-Ph, F), (M-2974, H, CH3, Cl, 4-F-Ph, CF3), (M-2975, H, CH3, Cl, 4-F-Ph, Br), (M-2976, H, CH3, Cl, 4-F-Ph, CH3), (M-2977, H, CH3, Cl, 4-CF3-Ph, H), (M-2978, H, CH3, Cl, 4-CF3-Ph, Cl), (M-2979, H, CH3, Cl, 4-CF3-Ph, F), (M-2980, H, CH3, Cl, 4-CF3-Ph, CF3), (M-2981, H, CH3, Cl, 4-CF3-Ph, Br), (M-2982, H, CH3, Cl, 4-CF3-Ph, CH3), (M-2983, H, CH3, Cl, 4-(Me)2N-Ph, H), (M-2984, H, CH3, Cl, 4-(Me)2N-Ph, Cl), (M-2985, H, CH3, Cl, 4-(Me)2N-Ph, F), (M-2986, H, CH3, Cl, 4-(Me)2N-Ph, CF3), (M-2987, H, CH3, Cl, 4-(Me)2N-Ph, Br), (M-2988, H, CH3, Cl, 4-(Me)2N-Ph, CH3), (M-2989, H, CH3, Cl, 4-OH-Ph, H), (M-2990, H, CH3, Cl, 4-OH-Ph, Cl), (M-2991, H, CH3, Cl, 4-OH-Ph, F), (M-2992, H, CH3, Cl, 4-OH-Ph, CF3), (M-2993, H, CH3, Cl, 4-OH-Ph, Br), (M-2994, H, CH3, Cl, 4-OH-Ph, CH3), (M-2995, H, CH3, Cl, 3,4-di-F-Ph, H), (M-2996, H, CH3, Cl, 3,4-di-F-Ph, Cl), (M-2997, H, CH3, Cl, 3,4-di-F-Ph, F), (M-2998, H, CH3, Cl, 3,4-di-F-Ph, CF3), (M-2999, H, CH3, Cl, 3,4-di-F-Ph, Br), (M-3000, H, CH3, Cl, 3,4-di-F-Ph, CH3), (M-3001, H, CH3, Cl, 4-COOH-Ph, H), (M-3002, H, CH3, Cl, 4-COOH-Ph, Cl), (M-3003, H, CH3, Cl, 4-COOH-Ph, F), (M-3004, H, CH3, Cl, 4-COOH-Ph, CF3), (M-3005, H, CH3, Cl, 4-COOH-Ph, Br), (M-3006, H, CH3, Cl, 4-COOH-Ph, CH3), (M-3007, H, CH3, Cl, Bn, H), (M-3008, H, CH3, Cl, Bn, Cl), (M-3009, H, CH3, Cl, Bn, F), (M-3010, H, CH3, Cl, Bn, CF3), (M-3011, H, CH3, Cl, Bn, Br), (M-3012, H, CH3, Cl, Bn, CH3), (M-3013, H, CH3, Cl, 4-F-Bn, H), (M-3014, H, CH3, Cl, 4-F-Bn, Cl), (M-3015, H, CH3, Cl, 4-F-Bn, F), (M-3016, H, CH3, Cl, 4-F-Bn, CF3), (M-3017, H, CH3, Cl, 4-F-Bn, Br), (M-3018, H, CH3, Cl, 4-F-Bn, CH3), (M-3019, H, CH3, Cl, 2-Py, H), (M-3020, H, CH3, Cl, 2-Py, Cl), (M-3021, H, CH3, Cl, 2-Py, F), (M-3022, H, CH3, Cl, 2-Py, CF3), (M-3023, H, CH3, Cl, 2-Py, Br), (M-3024, H, CH3, Cl, 2-Py, CH3), (M-3025, H, CH3, Cl, 3-Py, H), (M-3026, H, CH3, Cl, 3-Py, Cl), (M-3027, H, CH3, Cl, 3-Py, F), (M-3028, H, CH3, Cl, 3-Py, CF3), (M-3029, H, CH3, Cl, 3-Py, Br), (M-3030, H, CH3, Cl, 3-Py, CH3), (M-3031, H, CH3, Cl, 4-Py, H), (M-3032, H, CH3, Cl, 4-Py, Cl), (M-3033, H, CH3, Cl, 4-Py, F), (M-3034, H, CH3, Cl, 4-Py, CF3), (M-3035, H, CH3, Cl, 4-Py, Br), (M-3036, H, CH3, Cl, 4-Py, CH3), (M-3037, H, CH3, Cl, 2-Th, H), (M-3038, H, CH3, Cl, 2-Th, Cl), (M-3039, H, CH3, Cl, 2-Th, F), (M-3040, H, CH3, Cl, 2-Th, CF3), (M-3041, H, CH3, Cl, 2-Th, Br), (M-3042, H, CH3, Cl, 2-Th, CH3), (M-3043, H, CH3, Cl, 3-Th, H), (M-3044, H, CH3, Cl, 3-Th, Cl), (M-3045, H, CH3, Cl, 3-Th, F), (M-3046, H, CH3, Cl, 3-Th, CF3), (M-3047, H, CH3, Cl, 3-Th, Br), (M-3048, H, CH3, Cl, 3-Th, CH3), (M-3049, H, CH3, Cl, pyrrazol-2-yl, H), (M-3050, H, CH3, Cl, pyrrazol-2-yl, Cl), (M-3051, H, CH3, Cl, pyrrazol-2-yl, F), (M-3052, H, CH3, Cl, pyrrazol-2-yl, CF3), (M-3053, H, CH3, Cl, pyrrazol-2-yl, Br), (M-3054, H, CH3, Cl, pyrrazol-2-yl, CH3), (M-3055, H, CH3, Cl, pyrrazol-3-yl, H), (M-3056, H, CH3, Cl, pyrrazol-3-yl, Cl), (M-3057, H, CH3, Cl, pyrrazol-3-yl, F), (M-3058, H, CH3, Cl, pyrrazol-3-yl, CF3), (M-3059, H, CH3, Cl, pyrrazol-3-yl, Br), (M-3060, H, CH3, Cl, pyrrazol-3-yl, CH3), (M-3061, H, CH3, Cl, pyrimidin-2-yl, H), (M-3062, H, CH3, Cl, pyrimidin-2-yl, Cl), (M-3063, H, CH3, Cl, pyrimidin-2-yl, F), (M-3064, H, CH3, Cl, pyrimidin-2-yl, CF3), (M-3065, H, CH3, Cl, pyrimidin-2-yl, Br), (M-3066, H, CH3, Cl, pyrimidin-2-yl, CH3), (M-3067, H, CH3, Cl, pyrimidin-4-yl, H), (M-3068, H, CH3, Cl, pyrimidin-4-yl, Cl), (M-3069, H, CH3, Cl, pyrimidin-4-yl, F), (M-3070, H, CH3, Cl, pyrimidin-4-yl, CF3), (M-3071, H, CH3, Cl, pyrimidin-4-yl, Br), (M-3072, H, CH3, Cl, pyrimidin-4-yl, CH3), (M-3073, H, CH3, Cl, pyrimidin-5-yl, H), (M-3074, H, CH3, Cl, pyrimidin-4-yl, Cl), (M-3075, H, CH3, Cl, pyrimidin-5-yl, F), (M-3076, H, CH3, Cl, pyrimidin-5-yl, CF3), (M-3077, H, CH3, Cl, pyrimidin-5-yl, Br), (M-3078, H, CH3, Cl, pyrimidin-5-yl, CH3), (M-3079, H, CH3, Cl, HOOCCH2CH2CH2, H), (M-3080, H, CH3, Cl, HOOCCH2CH2CH2, Cl), (M-3081, H, CH3, Cl, HOOCCH2CH2CH2, F), (M-3082, H, CH3, Cl, HOOCCH2CH2CH2, CF3), (M-3083, H, CH3, Cl, HOOCCH2CH2CH2, Br), (M-3084, H, CH3, Cl, HOOCCH2CH2CH2, CH3), (M-3085, H, CH3, Cl, HOOCCH2CH2CH2CH2, H), (M-3086, H, CH3, Cl, HOOCCH2CH2CH2CH2, Cl), (M-3087, H, CH3, Cl, HOOCCH2CH2CH2CH2, F), (M-3088, H, CH3, Cl, HOOCCH2CH2CH2CH2, CF3), (M-3089, H, CH3, Cl, HOOCCH2CH2CH2CH2, Br), (M-3090, H, CH3, Cl, HOOCCH2CH2CH2CH2, CH3), (M-3091, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-3092, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-3093, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-3094, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-3095, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-3096, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-3097, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-3098, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-3099, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-3100, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-3101, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2Br), (M-3102, H, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-3103, H, CH3, Cl, MeOCH2, H), (M-3104, H, CH3, Cl, MeOCH2, Cl), (M-3105, H, CH3, Cl, MeOCH2, F), (M-3106, H, CH3, Cl, MeOCH2, CF3), (M-3107, H, CH3, Cl, MeOCH2, Br), (M-3108, H, CH3, Cl, MeOCH2, CH3), (M-3109, H, CH3, Cl, EtOCH2, H), (M-3110, H, CH3, Cl, EtOCH2, Cl), (M-3111, H, CH3, Cl, EtOCH2, F), (M-3112, H, CH3, Cl, EtOCH2, CF3), (M-3113, H, CH3, Cl, EtOCH2, Br), (M-3114, H, CH3, Cl, EtOCH2, CH3), (M-3115, H, CH3, Cl, EtOCH2CH2, H), (M-3116, H, CH3, Cl, EtOCH2CH2, Cl), (M-3117, H, CH3, Cl, EtOCH2CH2, F), (M-3118, H, CH3, Cl, EtOCH2CH2, CF3), (M-3119, H, CH3, Cl, EtOCH2CH2, Br), (M-3120, H, CH3, Cl, EtOCH2CH2, CH3), (M-3121, H, CH3, Cl, MeOCH2CH2OCH2, H), (M-3122, H, CH3, Cl, MeOCH2CH2OCH2CH2, Cl), (M-3123, H, CH3, Cl, MeOCH2CH2OCH2CH2, F), (M-3124, H, CH3, Cl, MeOCH2CH2OCH2CH3, CF3), (M-3125, H, CH3, Cl, MeOCH2CH2OCH2CH2, Br), (M-3126, H, CH3, Cl, MeOCH2CH2OCH2CH2, CH3), (M-3127, H, CH3, Cl, MeOCH2CH2, H), (M-3128, H, CH3, Cl, MeOCH2CH2, Cl), (M-3129, H, CH3, Cl, MeOCH2CH2, F), (M-3130, H, CH3, Cl, MeOCH2CH2, CF3), (M-3131, H, CH3, Cl, MeOCH2CH2, Br), (M-3132, H, CH3, Cl, MeOCH2CH2, CH3), (M-3133, H, CH3, Cl, HOCH2, H), (M-3134, H, CH3, Cl, HOCH2, Cl), (M-3135, H, CH3, Cl, HOCH2, F), (M-3136, H, CH3, Cl, HOCH2, CF3), (M-3137, H, CH3, Cl, HOCH2, Br), (M-3138, H, CH3, Cl, HOCH2, CH3), (M-3139, H, CH3, Cl, HOCH2CH2, H), (M-3140, H, CH3, Cl, HOCH2CH2, Cl), (M-3141, H, CH3, Cl, HOCH2CH2, F), (M-3142, H, CH3, Cl, HOCH2CH2, CF3), (M-3143, H, CH3, Cl, HOCH2CH2, Br), (M-3144, H, CH3, Cl, HOCH2CH2, CH3), (M-3145, H, CH3, Cl, HOCH2CH2CH2H), (M-3146, H, CH3, Cl, HOCH2CH2CH2, Cl), (M-3147, H, CH3, Cl, HOCH2CH2CH2, F), (M-3148, H, CH3, Cl, HOCH2CH2CH2, CF3), (M-3149, H, CH3, Cl, HOCH2CH2CH2, Br), (M-3150, H, CH3, Cl, HOCH2CH2CH2, CH3), (M-3151, H, CH3, Cl, HOCH2CH2CH2CH2, H), (M-3152, H, CH3, Cl, HOCH2CH2CH2CH2, Cl), (M-3153, H, CH3, Cl, HOCH2CH2CH2CH2, F), (M-3154, H, CH3, Cl, HOCH2CH2CH2CH2, CF3), (M-3155, H, CH3, Cl, HOCH2CH2CH2CH2, Br), (M-3156, H, CH3, Cl, HOCH2CH2CH2CH2, CH3), (M-3157, H, CH3, Cl, HOCH2CH2CH2CH2CH2H), (M-3158, H, CH3, Cl, HOCH2CH2CH2CH2CH2Cl), (M-3159, H, CH3, Cl, HOCH2CH2CH2CH2CH2, F), (M-3160, H, CH3, Cl, HOCH2CH2CH2CH2CH2CF3), (M-3161, H, CH3, Cl, HOCH2CH2CH2CH2CH2Br), (M-3162, H, CH3, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-3163, H, CH3, Cl, HOCH2CH2OCH2CH2, H), (M-3164, H, CH3, Cl, HOCH2CH2OCH2CH2, Cl), (M-3165, H, CH3, Cl, HOCH2CH2OCH2CH2, F), (M-3106, H, CH3, Cl, HOCH2CH2OCH2CH2, CF3), (M-3167, H, CH3, Cl, HOCH2CH2OCH2CH2, Br), (M-3168, H, CH3, Cl, HOCH2CH2OCH2CH2, CH3), (M-3169, H, CH3, Cl, (Me)2N, H), (M-3170, H, CH3, Cl, (Me)2N, Cl), (M-3171, H, CH3, Cl, (Me)2N, F), (M-3172, H, CH3, Cl, (Me)2N, CF3), (M-3173, H, CH3, Cl, (Me)2N, Br), (M-3174, H, CH3, Cl, (Me)2N, CH3), (M-3175, H, CH3, Cl, piperidin-4-yl-methyl, H), (M-3176, H, CH3, Cl, piperidin-4-yl-methyl, Cl), (M-3177, H, CH3, Cl, piperidin-4-yl-methyl, F), (M-3178, H, CH3, Cl, piperidin-4-yl-methyl, CF3), (M-3179, H, CH3, Cl, piperidin-4-yl-methyl, Br), (M-3180, H, CH3, Cl, piperidin-4-yl-methyl, CH3), (M-3181, H, CH3, Cl, cyclohexylmethyl, H), (M-3182, H, CH3, Cl, cyclohexylmethyl, Cl), (M-3183, H, CH3, Cl, cyclohexylmethyl, F), (M-3184, H, CH3, Cl, cyclohexylmethyl, CF3), (M-3185, H, CH3, Cl, cyclohexylmethyl, Br), (M-3186, H, CH3, Cl, cyclohexylmethyl, CH3), (M-3187, F, H, H, H, H), (M-3188, F, H, H, H, Cl), (M-3189, MeO, F, H, H, CF3), (M-3190, MeO, F, F, H, CF3), (M-3191, F, H, H, H, Br), (M-3192, F, H, H, H, CH3), (M-3193, F, H, H, F, H), (M-3194, F, H, H, F, Cl), (M-3195, F, H, H, F, F), (M-3196, F, H, H, F, CF3), (M-3197, F, H, H, F, Br), (M-3198, F, H, H, F, CH3), (M-3199, F, H, H, Cl, H), (M-3200, MeO, F, H, H, n-Pr), (M-3201, F, H, H, Cl, F), (M-3202, F, H, H, Cl, CF3), (M-3203, F, H, H, Cl, Br), (M-3204, F, H, H, Cl, CH3), (M-3205, F, H, H, CH3, H), (M-3206, F, H, H, CH3, Cl), (M-3207, F, H, H, CH3, F), (M-3208, F, H, H, CH3, CF3), (M-3209, F, H, H, CH3, Br), (M-3210, F, H, H, CH3, CH3), (M-3211, F, H, H, Et, H), (M-3212, F, H, H, Et, Cl), (M-3213, F, H, H, Et, F), (M-3214, F, H, H, Et, CF3), (M-3215, F, H, H, Et, Br), (M-3216, F, H, H, Et, CH3), (M-3217, F, H, H, n-Pr, H), (M-3218, F, H, H, n-Pr, Cl), (M-3219, F, H, H, n-Pr, F), (M-3220, F, H, H, n-Pr, CF3), (M-3221, F, H, H, n-Pr, Br), (M-3222, F, H, H, n-Pr, CH3), (M-3223, F, H, H, c-Pr, H), (M-3224, F, H, H, c-Pr, Cl), (M-3225, F, H, H, c-Pr, F), (M-3226, F, H, H, c-Pr, CF3), (M-3227, F, H, H, c-Pr, Br), (M-3228, F, H, H, c-Pr, CH3), (M-3229, F, H, H, i-Pr, H), (M-3230, F, H, H, i-Pr, Cl), (M-3231, F, H, H, i-Pr, F), (M-3232, F, H, H, i-Pr, CF3), (M-3233, F, H, H, i-Pr, Br), (M-3234, F, H, H, i-Pr, CH3), (M-3235, F, H, H, n-Bu, H), (M-3236, F, H, H, n-Bu, Cl), (M-3237, F, H, H, n-Bu, F), (M-3238, F, H, H, n-Bu, CF3), (M-3239, F, H, H, n-Bu, Br), (M-3240, F, H, H, n-Bu, CH3), (M-3241, F, H, H, i-Bu, H), (M-3242, F, H, H, i-Bu, Cl), (M-3243, F, H, H, i-Bu, F), (M-3244, F, H, H, i-Bu, CF3), (M-3245, F, H, H, i-Bu, Br), (M-3246, F, H, H, i-Bu, CH3), (M-3247, F, H, H, sec-Bu, H), (M-3248, F, H, H, sec-Bu, Cl), (M-3249, F, H, H, sec-Bu, F), (M-3250, F, H, H, sec-Bu, CF3), (M-3251, F, H, H, sec-Bu, Br), (M-3252, F, H, H, sec-Bu, CH3), (M-3253, F, H, H, n-Pen, H), (M-3254, F, H, H, n-Pen, Cl), (M-3255, F, H, H, n-Pen, F), (M-3256, F, H, H, n-Pen, CF3), (M-3257, F, H, H, n-Pen, Br), (M-3258, F, H, H, n-Pen, CH3), (M-3259, F, H, H, c-Pen, H), (M-3260, F, H, H, c-Pen, Cl), (M-3261, F, H, H, c-Pen, F), (M-3262, F, H, H, c-Pen, CF3), (M-3263, F, H, H, c-Pen, Br), (M-3264, F, H, H, c-Pen, CH3), (M-3265, F, H, H, n-Hex, H), (M-3266, F, H, H, n-Hex, Cl), (M-3267, F, H, H, n-Hex, F), (M-3268, F, H, H, n-Hex, CF3), (M-3269, F, H, H, n-Hex, Br), (M-3270, F, H, H, n-Hex, CH3), (M-3271, F, H, H, c-Hex, H), (M-3272, F, H, H, c-Hex, Cl), (M-3273, F, H, H, c-Hex, F), (M-3274, F, H, H, c-Hex, CF3), (M-3275, F, H, H, c-Hex, Br), (M-3276, F, H, H, c-Hex, CH3), (M-3277, F, H, H, OH, H), (M-3278, F, H, H, OH, Cl), (M-3279, F, H, H, OH, F), (M-3280, F, H, H, OH, CF3), (M-3281, F, H, H, OH, Br), (M-3282, F, H, H, OH, CH3), (M-3283, F, H, H, EtO, H), (M-3284, F, H, H, EtO, Cl), (M-3285, F, H, H, EtO, F), (M-3286, F, H, H, EtO, CF3), (M-3287, F, H, H, EtO, Br), (M-3288, F, H, H, EtO, CH3), (M-3289, F, H, H, n-PrO, H), (M-3290, F, H, H, n-PrO, Cl), (M-3291, F, H, H, n-PrO, F), (M-3292, F, H, H, n-PrO, CF3), (M-3293, F, H, H, n-PrO, Br), (M-3294, F, H, H, n-PrO, CH3), (M-3295, F, H, H, PhO, H), (M-3296, F, H, H, PhO, Cl), (M-3297, F, H, H, PhO, F), (M-3298, F, H, H, PhO, CF3), (M-3299, F, H, H, PhO, Br), (M-3300, F, H, H, PhO, CH3), (M-3301, F, H, H, BnO, H), (M-3302, F, H, H, BnO, Cl), (M-3303, F, H, H, BnO, F), (M-3304, F, H, H, BnO, CF3), (M-3305, F, H, H, BnO, Br), (M-3306, F, H, H, BnO, CH3), (M-3307, F, H, H, PhCH2CH2O, H), (M-3308, F, H, H, PhCH2CH2O, Cl), (M-3309, F, H, H, PhCH2CH2O, F), (M-3310, F, H, H, PhCH2CH2O, CF3), (M-3311, F, H, H, PhCH2CH2O, Br), (M-3312, F, H, H, PhCH2CH2O, CH3), (M-3313, MeO, H, H, CF3O, CH3), (M-3314, F, H, H, CF3O, Cl), (M-3315, F, H, H, CF3O, F), (M-3316, F, H, H, CF3O, CF3), (M-3317, F, H, H, CF3O, Br), (M-3318, F, H, H, CF3O, CH3), (M-3319, F, H, H, Ph, H), (M-3320, F, H, H, Ph, Cl), (M-3321, F, H, H, Ph, F), (M-3322, F, H, H, Ph, CF3), (M-3323, F, H, H, Ph, Br), (M-3324, F, H, H, Ph, CH3), (M-3325, F, H, H, 4-F-Ph, H), (M-3326, F, H, H, 4-F-Ph, Cl), (M-3327, F, H, H, 4-F-Ph, F), (M-3328, F, H, H, 4-F-Ph, CF3), (M-3329, F, H, H, 4-F-Ph, Br), (M-3330, F, H, H, 4-F-Ph, CH3), (M-3331, F, H, H, 4-CF3-Ph, H), (M-3332, F, H, H, 4-CF3-Ph, Cl), (M-3333, F, H, H, 4-CF3-Ph, F), (M-3334, F, H, H, 4-CF3-Ph, CF3), (M-3335, F, H, H, 4-CF3-Ph, Br), (M-3336, F, H, H, 4-CF3-Ph, CH3), (M-3337, F, H, H, 4-(Me)2N-Ph, H), (M-3338, F, H, H, 4-(Me)2N-Ph, Cl), (M-3339, F, H, H, 4-(Me)2N-Ph, F), (M-3340, F, H, H, 4-(Me)2N-Ph, CF3), (M-3341, F, H, H, 4-(Me)2N-Ph, Br), (M-3342, F, H, H, 4-(Me)3N-Ph, CH3), (M-3343, F, H, H, 4-OH-Ph, H), (M-3344, F, H, H, 4-OH-Ph, Cl), (M-3345, F, H, H, 4-OH-Ph, F), (M-3346, F, H, H, 4-OH-Ph, CF3), (M-3347, F, H, H, 4-OH-Ph, Br), (M-3348, F, H, H, 4-OH-Ph, CH3), (M-3349, F, H, H, 3,4-di-F-Ph, H), (M-3350, F, H, H, 3,4-di-F-Ph, Cl), (M-3351, F, H, H, 3,4-di-F-Ph, F), (M-3352, F, H, H, 3,4-di-F-Ph, CF3), (M-3353, F, H, H, 3,4-di-F-Ph, Br), (M-3354, F, H, H, 3,4-di-F-Ph, CH3), (M-3355, F, H, H, 4-COOH-Ph, H), (M-3356, F, H, H, 4-COOH-Ph, Cl), (M-3357, F, H, H, 4-COOH-Ph, F), (M-3358, F, H, H, 4-COOH-Ph, CF3), (M-3359, F, H, H, 4-COOH-Ph, Br), (M-3360, F, H, H, 4-COOH-Ph, CH3), (M-3361, F, H, H, Bo, H), (M-3362, F, H, H, Bn, Cl), (M-3363, F, H, H, Bn, F), (M-3364, F, H, H, Bn, CF3), (M-3365, F, H, H, Bu, Br), (M-3366, F, H, H, Bn, CH3), (M-3367, F, H, H, 4-F-Bn, H), (M-3368, F, H, H, 4-F-Bn, Cl), (M-3369, F, H, H, 4-F-Bn, F), (M-3370, F, H, H, 4-F-Bn, CF3), (M-3371, F, H, H, 4-F-Bn, Br), (M-3372, F, H, H, 4-F-Bn, CH3), (M-3373, F, H, H, 2-Py, H), (M-3374, F, H, H, 2-Py, Cl), (M-3375, F, H, H, 2-Py, F), (M-3376, F, H, H, 2-Py, CF3), (M-3377, F, H, H, 2-Py, Br), (M-3378, F, H, H, 2-Py, CH3), (M-3379, F, H, H, 3-Py, H), (M-3380, F, H, H, 3-Py, Cl), (M-3381, F, H, H, 3-Py, F), (M-3382, F, H, H, 3-Py, CF3), (M-3383, F, H, H, 3-Py, Br), (M-3384, F, H, H, 3-Py, CH3), (M-3385, F, H, H, 4-Py, H), (M-3386, F, H, H, 4-Py, Cl), (M-3387, F, H, H, 4-Py, F), (M-3388, F, H, H, 4-Py, CF3), (M-3389, F, H, H, 4-Py, Br), (M-3390, F, H, H, 4-Py, CH3), (M-3391, F, H, H, 2-Th, H), (M-3392, F, H, H, 2-Th, Cl), (M-3393, F, H, H, 2-Th, F), (M-3394, F, H, H, 2-Th, CF3), (M-3395, F, H, H, 2-Th, Br), (M-3396, F, H, H, 2-Th, CH3), (M-3397, F, H, H, 3-Th, H), (M-3398, F, H, H, 3-Th, Cl), (M-3399, F, H, H, 3-Th, F), (M-3400, F, H, H, 3-Th, CF3), (M-3401, F, H, H, 3-Th, Br), (M-3402, F, H, H, 3-Th, CH3), (M-3403, F, H, H, pyrrazol-2-yl, H), (M-3404, F, H, H, pyrrazol-2-yl, Cl), (M-3405, F, H, H, pyrrazol-2-yl, F), (M-3406, F, H, H, pyrrazol-2-yl, CF3), (M-3407, F, H, H, pyrrazol-2-yl, Br), (M-3408, F, H, H, pyrrazol-2-yl, CH3), (M-3409, F, H, H, pyrrazol-3-yl, H), (M-3410, F, H, H, pyrrazol-3-yl, Cl), (M-3411, F, H, H, pyrrazol-3-yl, F), (M-3412, F, H, H, pyrrazol-3-yl, CF3), (M-3413, F, H, H, pyrrazol-3-yl, Br), (M-3414, F, H, H, pyrrazol-3-yl, CH3), (M-3415, F, H, H, pyrimidin-2-yl, H), (M-3416, F, H, H, pyrimidin-2-yl, Cl), (M-3417, F, H, H, pyrimidin-2-yl, F), (M-3418, F, H, H, pyrimidin-2-yl, CF3), (M-3419, F, H, H, pyrimidin-2-yl, Br), (M-3420, F, H, H, pyrimidin-2-yl, CH3), (M-3421, F, H, H, pyrimidin-4-yl, H), (M-3422, F, H, H, pyrimidin-4-yl, Cl), (M-3423, F, H, H, pyrimidin-4-yl, F), (M-3424, F, H, H, pyrimidin-4-yl, CF3), (M-3425, F, H, H, pyrimidin-4-yl, Br), (M-3426, F, H, H, pyrimidin-4-yl, CH3), (M-3427, F, H, H, pyrimidin-5-yl, PT), (M-3428, F, H, H, pyrimidin-5-yl, Cl), (M-3429, F, H, H, pyrimidin-5-yl, F), (M-3430, F, H, H, pyrimidin-5-yl, CF3), (M-3431, F, H, H, pyrimidin-5-yl, Br), (M-3432, F, H, H, pyrimidin-5-yl, CH3), (M-3433, F, H, H, HOOCCH2CH2CH2, H), (M-3434, F, H, H, HOOCCH2CH2CH2, Cl), (M-3435, F, H, H, HOOCCH2CH2CH2, F), (M-3436, F, H, H, HOOCCH2CH2CH2, CF3), (M-3437, F, H, H, HOOCCH2CH2CH2Br), (M-3438, F, H, H, HOOCCH2CH2CH2CH3), (M-3439, F, H, H, HOOCCH2CH2CH2CH2, H), (M-3440, F, H, H, HOOCCH2CH2CH2CH2, Cl), (M-3441, F, H, H, HOOCCH2CH2CH2CH2, F), (M-3442, F, H, H, HOOCCH2CH2CH2CH2, CF3), (M-3443, F, H, H, HOOCCH2CH2CH2CH2, Br), (M-3444, F, H, H, HOOCCH2CH2CH2CH2, CH3), (M-3445, F, H, H, (Me)2NCOCH2CH2CH2CH2, H), (M-3446, F, H, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-3447, F, H, H, (Me)2NCOCH2CH2CH2CH2, F), (M-3448, F, H, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-3449, F, H, H, (Me)2NCOCH2CH2CH2CH2, (Br), (M-3450, F, H, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-3451, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-3452, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-3453, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-3454, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-3455, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-3456, F, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-3457, F, H, H, MeOCH2, H), (M-3458, F, H, H, MeOCH2, Cl), (M-3459, F, H, H, MeOCH2, F), (M-3460, F, H, H, MeOCH2, CF3), (M-3461, F, H, H, MeOCH2, Br), (M-3462, F, H, H, MeOCH2, CH3), (M-3463, F, H, H, EtOCH2, H), (M-3464, F, H, H, EtOCH2, Cl), (M-3465, F, H, H, EtOCH2, F), (M-3466, F, H, H, EtOCH2, CF3), (M-3467, F, H, H, EtOCH2, Br), (M-3468, F, H, H, EtOCH2, CH3), (M-3469, F, H, H, EtOCH2CH2, H), (M-3470, F, H, H, EtOCH2CH2, Cl), (M-3471, F, H, H, EtOCH2CH2, F), (M-3472, F, H, H, EtOCH2CH2, CF3), (M-3473, F, H, H, EtOCH2CH2, Br), (M-3474, F, H, H, EtOCH2CH2, CH3), (M-3475, F, H, H, MeOCH2CH2OCH2CH2, H), (M-3476, F, H, H, MeOCH2CH2OCH2CH2, Cl), (M-3477, F, H, H, MeOCH2CH2OCH2CH2, V), (M-3478, F, H, H, MeOCH2CH2OCH2CH2, CF3), (M-3479, F, H, H, MeOCH2CH2OCH2CH2, Br), (M-3480, F, H, H, MeOCH2CH2OCH2CH2, CH3), (M-3481, F, H, H, MeOCH2CH2, H), (M-3482, F, H, H, MeOCH2CH2, Cl), (M-3483, F, H, H, MeOCH2CH2, F), (M-3484, F, H, H, MeOCH2CH2, CF3), (M-3485, F, H, H, MeOCH2CH2, Br), (M-3486, F, H, H, MeOCH2CH2, CH3), (M-3487, F, H, H, HOCH2, H), (M-3488, F, H, H, HOCH2, Cl), (M-3489, F, H, H, HOCH2, F), (M-3490, F, H, H, HOCH2, CF3), (M-3491, F, H, H, HOCH2, Br), (M-3492, F, H, H, HOCH2, CH3), (M-3493, F, H, H, HOCH2CH2, H), (M-3494, F, H, H, HOCH2CH2, Cl), (M-3495, F, H, H, HOCH2CH2, F), (M-3496, F, H, H, HOCH2CH2, CF3), (M-3497, F, H, H, HOCH2CH2, Br), (M-3498, F, H, H, HOCH2CH2, CH3), (M-3499, F, H, H, HOCH2CH2CH2, H), (M-3500, F, H, H, HOCH2CH2CH2, Cl), (M-3501, F, H, H, HOCH2CH2CH2, F), (M-3502, F, H, H, HOCH2CH2CH2, CF3), (M-3503, F, H, H, HOCH2CH2CH2, Br), (M-3504, F, H, H, HOCH2CH2CH2, CH3), (M-3505, F, H, H, HOCH2CH2CH2CH2, H), (M-3506 F, H, H, HOCH2CH2CH2CH2, Cl), (M-3507, F, H, H, HOCH2CH2CH2CH2, F), (M-3508, F, H, H, HOCH2CH2CH2 CH2, CF3), (M-3509, F, H, B, HOCH2CH2CH2CH2, Br), (M-3510, F, H, H, HOCH2CH2CH2CH2, CH3), (M-3511, F, H, H, HOCH2CH2CH2CH2CH2, H), (M-3512, F, H, H, HOCH2CH2CH2CH2CH2, Cl), (M-3513, F, H, H, HOCH2CH2CH2CH2CH2, F), (M-3514, F, H, H, HOCH2CH2CH2CH2CH2, CF3), (M-3515, F, H, H, HOCH2CH2CH2CH2CH2, Br), (M-3516, F, H, H, HOCH2CH2CH2CH2CH2, CH3), (M-3517, F, H, H, HOCH2CH2OCH2CH2, H), (M-3518, F, H, H, HOCH2CH2OCH2CH2, Cl), (M-3519, F, H, H, HOCH2CH2OCH2CH2, F), (M-3520, F, H, H, HOCH2CH2OCH2CH2, CF3), (M-3521, F, H, H, HOCH2CH2OCH2CH2, Br), (M-3522, F, H, H, HOCH2CH2OCH2CH2, CH3), (M-3523, F, H, H, (Me)2N, H), (M-3524, F, H, H, (Me)2N, Cl), (M-3525, F, H, H, (Me)2N, F), (M-3526, F, H, H, (Me)2N, CF3), (M-3527, F, H, H, (Me)2N, Br), (M-3528, F, H, H, (Me)2N, CH3), (M-3529, F, H, H, piperidin-4-yl-methyl, H), (M-3530, F, H, H, piperidin-4-yl-methyl, Cl), (M-3531, F, H, H, piperidin-4-yl-methyl, F), (M-3532, F, H, H, piperidin-4-yl-methyl, CF3), (M-3533, F, H, H, piperidin-4-yl-methyl, Br), (M-3534, F, H, H, piperidin-4-yl-methyl, CH3), (M-3535, F, H, H, cyclohexylmethyl, H), (M-3536, F, H, H, cyclohexylmethyl, Cl), (M-3537, F, H, H, cyclohexylmethyl, F), (M-3538, F, H, H, cyclohexylmethyl, CF3), (M-3539, F, H, H, cyclohexylmethyl, Br), (M-3540, F, H, H, cyclohexylmethyl, CH3), (M-3541, F, H, F, H, H), (M-3542, F, H, F, H, Cl), (M-3543, F, H, F, H, F), (M-3544, F, H, F, H, CF3), (M-3545, F, H, F, H, Br), (M-3546, F, H, F, H, CH3), (M-3547, F, H, F, F, H), (M-3548, F, H, F, F, Cl), (M-3549, F, H, F, F, F), (M-3550, F, H, F, F, CF3), (M-3551, F, H, F, F, Br), (M-3552, F, H, F, F, CH3), (M-3553, F, H, F, Cl, H), (M-3554, F, H, F, Cl, Cl), (M-3555, F, H, F, Cl, F), (M-3556, F, H, F, Cl, CF3), (M-3557, F, H, F, Cl, Br), (M-3558, F, H, F, Cl, CH3), (M-3559, F, H, F, CH3, H), (M-3560, F, H, F, CH3, Cl), (M-3561, F, H, F, CH3, F), (M-3562, F, H, F, CH3, CF3), (M-3663, F, H, F, CH3, Br), (M-3564, F, H, F, CH3, CH3), (M-3565, F, H, F, Et, H), (M-3566, F, H, F, Et, Cl), (M-3567, F, H, F, Et, P), (M-3568, F, H, F, Et, CF3), (M-3569, F, H, F, Et, Br), (M-3570, F, H, F, Et, CH3), (M-3571, F, H, F, n-Pr, H), (M-3572, F, H, F, n-Pr, Cl), (M-3573, F, H, F, n-Pr, F), (M-3574, F, H, F, n-Pr, CF3), (M-3575, F, H, F, n-Pr, Br), (M-3576, F, H, F, n-Pr, CH3), (M-3577, F, H, F, c-Pr, H), (M-3578, F, H, F, c-Pr, Cl), (M-3579, F, H, F, c-Pr, F), (M-3580, F, H, F, c-Pr, CF3), (M-3581, F, H, F, c-Pr, Br), (M-3582, F, H, F, c-Pr, CH3), (M-3583, F, H, F, i-Pr, H), (M-3584, F, H, F, i-Pr, Cl), (M-3585, F, H, F, i-Pr, F), (M-3586, F, H, F, i-Pr, CF3), (M-3587, F, H, F, i-Pr, Br), (M-3588, F, H, F, i-Pr, CH3), (M-3589, F, H, F, n-Bu, H), (M-3590, F, H, F, n-Bu, Cl), (M-3591, F, H, F, n-Bu, F), (M-3592, F, H, F, n-Bu, CF3), (M-3593, F, H, F, n-Bu, Br), (M-3594, F, H, F, n-Bu, CH3), (M-3595, F, H, F, i-Bu, H), (M-3596, F, H, F, i-Bu, Cl), (M-3597, F, H, F, i-Bu, F), (M-3598, F, H, F, i-Bu, CF3), (M-3599, F, H, F, i-Bu, Br), (M-3600, F, H, F, i-Bu, CH3), (M-3601, F, H, F, sec-Bu, H), (M-3602, F, H, F, sec-Bu, Cl), (M-3603, F, H, F, sec-Bu, F), (M-3604, F, H, F, sec-Bu, CF3), (M-3605, F, H, F, sec-Bu, Br), (M-3606, F, H, F, sec-Bu, CH3), (M-3607, F, H, F, n-Pen, H), (M-3608, F, H, F, n-Pen, Cl), (M-3609, F, H, F, n-Pen, F), (M-3610, F, H, F, n-Pen, CF3), (M-3611, F, H, F, n-Pen, Br), (M-3612, F, H, F, n-Pen, CH3), (M-3613, F, H, F, c-Pen, H), (M-3614, F, H, F, c-Pen, Cl), (M-3615, F, H, F, c-Pen, F), (M-3616, F, H, F, c-Pen, CF3), (M-3617, F, H, F, c-Pen, Br), (M-3618, F, H, F, c-Pen, CH3), (M-3619, F, H, F, n-Hex, H), (M-3620, F, H, F, n-Hex, Cl), (M-3621, F, H, F, n-Hex, F), (M-3622, F, H, F, n-Hex, CF3), (M-3623, F, H, F, n-Hex, Br), (M-3624, F, H, F, n-Hex, CH3), (M-3625, F, H, F, c-Hex, H), (M-3626, F, H, F, c-Hex, Cl), (M-3627, F, H, F, c-Hex, F), (M-3628, F, H, F, c-Hex, CF3), (M-3629, F, H, F, c-Hex, Br), (M-3630, F, H, F, c-Hex, CH3), (M-3631, F, H, F, OH, H), (M-3632, F, H, F, OH, Cl), (M-3633, F, H, F, OH, F), (M-3634, F, H, F, OH, CF3), (M-3635, F, H, F, OH, Br), (M-3636, F, H, F, OH, CH3), (M-3637, F, H, F, EtO, H), (M-3638, F, H, F, EtO, Cl), (M-3639, F, H, F, EtO, F), (M-3640, F, H, F, EtO, CF3), (M-3641, F, H, F, EtO, Br), (M-3642, F, H, F, EtO, CH3), (M-3643, F, H, F, n-PrO, H), (M-3644, F, H, F, n-PrO, Cl), (M-3645, F, H, F, n-PrO, F), (M-3646, F, H, F, n-PrO, CF3), (M-3647, F, H, F, n-PrO, Br), (M-3648, F, H, P, n-PrO, CH3), (M-3649, F, H, F, PhO, H), (M-3650, F, H, F, PhO, Cl), (M-3651, F, H, F, PhO, F), (M-3652, F, H, F, PhO, CF3), (M-3653, F, H, F, PhO, Br), (M-3654, F, H, F, PhO, CH3), (M-3655, F, H, F, BnO, H), (M-3656, F, H, F, BnO, Cl), (M-3657, F, H, F, BnO, F), (M-3658, F, H, F, BnO, CF3), (M-3659, F, H, F, BnO, Br), (M-3660, F, H, F, BnO, CH3), (M-3661, F, H, F, PhCH2CH2O, H), (M-3662, F, H, F, PhCH2CH2O, Cl), (M-3663, F, H, F, PhCH2CH2O, F), (M-3664, F, H, F, PhCH2CH2O, CF3), (M-3665, F, H, F, PhCH2CH2O, Br), (M-3666, F, H, F, PhCH2CH2O, CH3), (M-3667, F, H, F, CF3O, H), (M-3668, F, H, F, CF3O, Cl), (M-3669, F, H, F, CF3O, F), (M-3670, F, H, F, CF3O, CF3), (M-3671, F, H, F, CF3O, Br), (M-3672, F, H, F, CF3O, CH3), (M-3673, F, H, F, Ph, H), (M-3674, F, H, F, Ph, Cl), (M-3675, F, H, F, Ph, F), (M-3676, F, H, F, Ph, CF3), (M-3677, F, H, F, Ph, Br), (M-3678, F, H, F, Ph, CH3), (M-3679, F, H, F, 4-F-Ph, H), (M-3680, F, H, F, 4-F-Ph, Cl), (M-3681, F, H, F, 4-F-Ph, F), (M-3682, F, H, F, 4-F-Ph, CF3), (M-3683, F, H, F, 4-F-Ph, Br), (M-3684, F, H, F, 4-F-Ph, CH3), (M-3685, F, H, F, 4-CF3-Ph, H), (M-3686, F, H, F, 4-CF3-Ph, Cl), (M-3687, F, H, F, 4-CF3-Ph, F), (M-3688, F, H, F, 4-CF3-Ph, CF3), (M-3689, F, H, F, 4-CF3-Ph, Br), (M-3690, F, H, F, 4-CF3-Ph, CH3), (M-3691, F, H, F, 4-(Me)2N-Ph, H), (M-3692, F, H, F, 4-(Me)2N-Ph, Cl), (M-3693, F, H, F, 4-(Me)2N-Ph, F), (M-3694, F, H, F, 4-(Me)2N-Ph, CF3), (M-3695, F, H, F, 4-(Me)2N-Ph, Br), (M-3696, F, H, F, 4-(Me)2N-Ph, CH3), (M-3697, F, H, F, 4-OH-Ph, H), (M-3698, F, H, F, 4-OH-Ph, Cl), (M-3699, F, H, F, 4-OH-Ph, F), (M-3700, F, H, F, 4-OH-Ph, CF3), (M-3701, F, H, F, 4-OH-Ph, Br), (M-3702, F, H, F, 4-OH-Ph, CH3), (M-3703, F, H, F, 3,4-di-F-Ph, H), (M-3704, F, H, F, 3,4-di-F-Ph, Cl), (M-3705, F, H, F, 3,4-di-F-Ph, F), (M-3706, F, H, F, 3,4-di-F-Ph, CF3), (M-3707, F, H, F, 3,4-di-F-Ph, Br), (M-3708, F, H, F, 3,4-di-F-Ph, CH3), (M-3709, F, H, F, 4-COOH-Ph, H), (M-3710, F, H, F, 4-COOH-Ph, Cl), (M-3711, F, H, F, 4-COOH-Ph, F), (M-3712, F, H, F, 4-COOH-Ph, CF3), (M-3713, F, H, F, 4-COOH-Ph, Br), (M-3714, F, H, F, 4-COOH-Ph, CH3), (M-3715, F, H, F, Bn, H), (M-3716, F, H, F, Bn, Cl), (M-3717, F, H, F, Bn, F), (M-3718, F, H, F, Bn, CF3), (M-3719, F, H, F, Bn, Br), (M-3720, F, H, F, Bn, CH3), (M-3721, F, H, F, 4-F-Bn, H), (M-3722, F, H, F, 4-F-Bn, Cl), (M-3723, F, H, F, 4-F-Bn, F), (M-3724, F, H, F, 4-F-Bn, CF3), (M-3725, F, H, F, 4-F-Bn, Br), (M-3726, F, H, F, 4-F-Bn, CH3), (M-3727, F, H, F, 2-Py, H), (M-3728, F, H, F, 2-Py, Cl), (M-3729, F, H, F, 2-Py, F), (M-3730, F, H, F, 2-Py, CF3), (M-3731, F, H, F, 2-Py, Br), (M-3732, F, H, F, 2-Py, CH3), (M-3733, F, H, F, 3-Py, H), (M-3734, F, H, F, 3-Py, Cl), (M-3735, F, H, F, 3-Py, F), (M-3736, F, H, F, 3-Py, CF3), (M-3737, F, H, F, 3-Py, Br), (M-3738, F, H, F, 3-Py, CH3), (M-3739, F, H, F, 4-Py, H), (M-3740, F, H, F, 4-Py, Cl), (M-3741, F, H, F, 4-Py, F), (M-3742, F, H, F, 4-Py, CF3), (M-3743, F, H, F, 4-Py, Br), (M-3744, F, H, F, 4-Py, CH3), (M-3745, F, H, F, 2-Th, H), (M-3746, F, H, F, 2-Th, Cl), (M-3747, F, H, F, 2-Th, F), (M-3748, F, H, F, 2-Th, CF3), (M-3749, F, H, F, 2-Th, Br), (M-3750, F, H, F, 2-Th, CH3), (M-3751, F, H, F, 3-Th, H), (M-3752, F, H, F, 3-Th, Cl), (M-3753, F, H, F, 3-Th, F), (M-3754, F, H, F, 3-Th, CF3), (M-3755, F, H, F, 3-Th, Br), (M-3756, F, H, F, 3-Th, CH3), (M-3757, F, H, F, pyrrazol-2-yl, H), (M-3758, F, H, F, pyrrazol-2-yl, Cl), (M-3759, F, H, F, pyrrazol-2-yl, F), (M-3760, F, H, F, pyrrazol-2-yl, CF3), (M-3761, F, H, F, pyrrazol-2-yl, Br), (M-3762, F, H, F, pyrrazol-2-yl, CH3), (M-3763, F, H, F, pyrrazol-3-yl, H), (M-3764, F, H, F, pyrrazol-3-yl, Cl), (M-3765, F, H, F, pyrrazol-3-yl, F), (M-3766, F, H, F, pyrrazol-3-yl, CF3), (M-3767, F, H, F, pyrrazol-3-yl, Br), (M-3768, F, H, F, pyrrazol-3-yl, CH3), (M-3769, F, H, F, pyrimidin-2-yl, H), (M-3770, F, H, F, pyrimidin-2-yl, Cl), (M-3771, F, H, F, pyrimidin-2-yl, F), (M-3772, F, h, F, pyrimidin-2-yl, CF3), (M-3773, F, H, F, pyrimidin-2-yl, Br), (M-3774, F, H, F, pyrimidin-2-yl, CH3), (M-3775, F, H, F, pyrimidin-4-yl, H), (M-3776, F, H, F, pyrimidin-4-yl, Cl), (M-3777, F, H, F, pyrimidin-4-yl, F), (M-3778, F, H, F, pyrimidin-4-yl, CF3), (M-3779, F, H, F, pyrimidin-4-yl, Br), (M-3780, F, H, F, pyrimidin-4-yl, CH3), (M-3781, F, H, F, pyrimidin-5-yl, h), (M-3782, F, H, F, pyrimidin-5-yl, Cl), (M-3783, F, H, F, pyrimidin-5-yl, F), (M-3784, F, H, F, pyrimidin-5-yl, CF3), (M-3785, F, H, F, pyrimidin-5-yl, Br), (M-3786, F, H, F, pyrimidin-5-yl, CH3), (M-3787, F, H, F, HOOCCH2CH2CH2, H), (M-3788, F, H, F, HOOCCH2CH2CH2, Cl), (M-3789, F, H, F, HOOCCH2CH2CH2, F), (M-3790, F, H, F, HOOCCH2CH2CH2, CF3), (M-3791, F, H, F, HOOCCH2CH2CH2, Br), (M-3792, F, H, F, HOOCCH2CH2CH2, CH3), (M-3793, F, H, F, HOOCCH2CH2CH2CH2, H), (M-3794, F, H, F, HOOCCH2CH2CH2CH2, Cl), (M-3795, F, H, F, HOOCCH2CH2CH2CH2, F), (M-3796, F, H, F, HOOCCH2CH2CH2CH2, CF3), (M-3797, F, H, F, HOOCCH2CH2CH2CH2, Br), (M-3798, F, H, F, HOOCCH2CH2CH2CH2, CH3), (M-3799, F, H, F, (Me)2NCOCH2CH2CH2CH2, H), (M-3800, F, H, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-3801, F, H, F, (Me)2NCOCH2CH2CH2CH2, F), (M-3802, F, H, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-3803, F, H, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-3804, F, H, F, (Me)2NCOCH2CH2CH2CH3, CH3), (M-3805, F, H, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-3806, F, H, F, (Me)2NCOCH2CH2CH2CH2CH2) Cl), (M-3807, F, h, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-3808, F, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-3809, F, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-3810, F, h, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-3811, F, H, F, MeOCH2, H), (M-3812, F, H, F, MeOCH2, Cl), (M-3813, F, H, F, MeOCH2, F), (M-3814, F, H, F, MeOCH2, CF3), (M-3815, F, H, F, MeOCH2, Br), (M-3816, F, H, F, MeOCH2, CH3), (M-3817, F, H, F, EtOCH2, H), (M-3818, F, H, F, EtOCH2, Cl), (M-3819, F, H, F, EtOCH2, F), (M-3820, F, H, F, EtOCH2, CF3), (M-3821, F, H, F, EtOCH2, Br), (M-3822, F, H, F, EtOCH2, CH3), (M-3823, F, H, F, EtOCH2CH2, H), (M-3824, F, H, F, EtOCH2CH2, Cl), (M-3825, F, H, F, EtOCH2CH2, F), (M-3826, F, H, F, EtOCH2CH2, CF3), (M-3827, F, H, F, EtOCH2CH2, Br), (M-3828, F, H, F, EtOCH2CH2, CH3), (M-3829, F, H, F, MeOCH2CH2OCH2CH2, H), (M-3830, F, H, F, MeOCH2CH2OCH2CH2, Cl), (M-3831, F, H, F, MeOCH2CH2OCH2CH2, F), (M-3832, F, H, F, MeOCH2CH2OCH2CH2, CF3), (M-3833, F, H, F, MeOCH2CH2OCH2CH2, Br), (M-3834, F, H, F, MeOCH2CH2OCH2CH2, CH3), (M-3835, F, H, F, MeOCH2CH2, H), (M-3836, F, H, F, MeOCH2CH2, Cl), (M-3837, F, H, F, MeOCH2CH2, F), (M-3838, F, H, F, MeOCH2CH2, CF3), (M-3839, F, H, F, MeOCH2CH2, Br), (M-3840, F, H, F, MeOCH2CH2, CH3), (M-3841, F, H, F, HOCH2, H), (M-3842, F, H, F, HOCH2, Cl), (M-3843, F, H, F, HOCH2, F), (M-3844, F, H, F, HOCH2, CF3), (M-3845, F, H, F, HOCH2, Br), (M-3846, F, H, F, HOCH2, CH3), (M-3847, F, H, F, HOCH2CH2, H), (M-3848, F, H, F, HOCH2CH2, Cl), (M-3849, F, H, F, HOCH2CH2, F), (M-3850, F, H, F, HOCH2CH2, CF3), (M-3851, F, H, F, HOCH2CH2, Br), (M-3852, F, H, F, HOCH2CH2, CH3), (M-3853, F, H, F, HOCH2CH2CH2, H), (M-3854, F, H, F, HOCH2CH2CH2, Cl), (M-3855, F, H, F, HOCH2CH2CH2, F), (M-3856, F, H, F, HOCH2CH2CH2, CF3), (M-3857, F, H, F, HOCH2CH2CH2, Br), (M-3858, F, H, F, HOCH2CH2CH2, CH3), (M-3859, F, H, F, HOCH2CH2CH2CH2, H), (M-3860, F, H, F, HOCH2CH2CH2CH2, Cl), (M-3861, F, H, F, HOCH2CH2CH2CH2, F), (M-3862, F, H, F, HOCH2CH2CH2CH2, CF3), (M-3863, F, H, F, HOCH2CH2CH2CH2, Br), (M-3864, F, H, F, HOCH2CH2CH2CH2, CH3), (M-3865, F, H, F, HOCH2CH2CH2CH2CH2, H), (M-3866, F, H, F, HOCH2CH2CH2CH2CH2Cl), (M-3867, F, H, F, HOCH2CH2CH2CH2CH2, F), (M-3868, F, H, F, HOCH2CH2CH2CH2CH2, CF3), (M-3869, F, H, F, HOCH2CH2CH2CH2CH3, Br), (M-3870, F, H, F, HOCH2CH2CH2CH2CH2, CH3), (M-3871, F, H, F, HOCH2CH2OCH2CH2, H), (M-3872, F, H, F, HOCH2CH2OCH2CH2, Cl), (M-3873, F, H, F, HOCH2CH2OCH2CH2, F), (M-3874, F, H, F, HOCH2CH2OCH2CH2, CF3), (M-3875, F, H, F, HOCH2CH2OCH2CH2, Br), (M-3876, F, H, F, HOCH2CH2OCH2CH2, CH3), (M-3877, F, H, F, (Me)2N, H), (M-3878, F, H, F, (Me)2N, Cl), (M-3879, F, H, F, (Me)2N, F), (M-3880, F, H, F, (Me)2N, CF3), (M-3881, F, H, F, (Me)2N, Br), (M-3882, F, H, F, (Me)2N, CH3), (M-3883, F, H, F, piperidin-4-yl-methyl, H), (M-3884, F, H, F, piperidin-4-yl-methyl, Cl), (M-3885, F, H, F, piperidin-4-yl-methyl, F), (M-3886, F, H, F, piperidin-4-yl-methyl, CF3), (M-3887, F, H, F, piperidin-4-yl-methyl, Br), (M-3888, F, H, F, piperidin-4-yl-methyl, CH3), (M-3889, F, H, F, cyclohexylmethyl, H), (M-3890, F, H, F, cyclohexylmethyl, Cl), (M-3891, F, H, F, cyclohexylmethyl, F), (M-3892, F, H, F, cyclohexylmethyl, CF3), (M-3893, F, H, F, cyclohexylmethyl, Br), (M-3894, F, H, F, cyclohexylmethyl, CH3), (M-3895, F, H, Cl, H, H), (M-3896, F, H, Cl, H, Cl), (M-3897, F, H, Cl, H, F), (M-3898, F, H, Cl, H, CF3), (M-3899, F, H, Cl, H, Br), (M-3900, F, H, Cl, H, CH3), (M-3901, F, H, Cl, F, H), (M-3902, F, H, Cl, F, Cl), (M-3903, F, H, Cl, F, F), (M-3904, F, H, Cl, F, CF3), (M-3905, F, H, Cl, F, Br), (M-3906, F, H, Cl, F, CH3), (M-3907, F, H, Cl, Cl, H), (M-3908, F, H, Cl, Cl, Cl), (M-3909, F, H, Cl, Cl, F), (M-3910, F, H, Cl, Cl, CF3), (M-3911, F, H, Cl, Cl, Br), (M-3912, F, H, Cl, Cl, CH3), (M-3913, F, H, Cl, CH3, H), (M-3914, F, H, Cl, CH3, Cl), (M-3915, F, H, Cl, CH3, F), (M-3916, F, H, Cl, CH3, CF3), (M-3917, F, H, Cl, CH3, Br), (M-3918, F, H, Cl, CH3, CH3), (M-3919, F, H, Cl, Et, H), (M-3920, F, H, Cl, Et, Cl), (M-3921, F, H, Cl, Et, F), (M-3922, F, H, Cl, Et, CF3), (M-3923, F, H, Cl, Et, Br), (M-3924, F, H, Cl, Et, CH3), (M-3925, F, H, Cl, n-Pr, H), (M-3926, F, H, Cl, n-Pr, Cl), (M-3927, F, H, Cl, n-Pr, F), (M-3928, F, H, Cl, n-Pr, CF3), (M-3929, F, H, Cl, n-Pr, Br), (M-3930, F, H, Cl, n-Pr, CH3), (M-3931, F, H, Cl, c-Pr, H), (M-3932, F, H, Cl, c-Pr, Cl), (M-3933, F, H, Cl, c-Pr, F), (M-3934, F, H, Cl, c-Pr, CF3), (M-3935, F, H, Cl, c-Pr, Br), (M-3936, F, H, Cl, c-Pr, CH3), (M-3937, F, H, Cl, i-Pr, H), (M-3938, F, H, Cl, i-Pr, Cl), (M-3939, F, H, Cl, i-Pr, F), (M-3940, F, H, Cl, i-Pr, CF3), (M-3941, F, H, Cl, i-Pr, Br), (M-3942, F, H, Cl, i-Pr, CH3), (M-3943, F, H, Cl, n-Bu, H), (M-3944, F, H, Cl, n-Bu, Cl), (M-3945, F, H, Cl, n-Bu, F), (M-3946, F, H, Cl, n-Bu, CF3), (M-3947, F, H, Cl, n-Bu, Br), (M-3948, F, H, Cl, n-Bu, CH3), (M-3949, F, H, Cl, i-Bu, H), (M-3950, F, H, Cl, i-Bu, Cl), (M-3951, F, H, Cl, i-Bu, F), (M-3952, F, H, Cl, i-Bu, CF3), (M-3953, F, H, Cl, i-Bu, Br), (M-3954, F, H, Cl, i-Bu, CH3), (M-3955, F, H, Cl, sec-Bu, H), (M-3956, F, H, Cl, sec-Bu, Cl), (M-3957, F, H, Cl, sec-Bu, F), (M-3958, F, H, Cl, sec-Bu, CF3), (M-3959, F, H, Cl, sec-Bu, Br), (M-3960, F, H, Cl, sec-Bu, CH3), (M-3961, F, H, Cl, n-Pen, H), (M-3962, F, H, Cl, n-Pen, Cl), (M-3963, F, H, Cl, n-Fen, F), (M-3964, F, H, Cl, n-Pen, CF3), (M-3965, F, H, Cl, n-Pen, Br), (M-3966, F, H, Cl, n-Pen, CH3), (M-3967, F, H, Cl, c-Pen, H), (M-3968, F, H, Cl, c-Pen, Cl), (M-3969, F, H, Cl, c-Pen, F), (M-3970, F, H, Cl, c-Pen, CF3), (M-3971, F, H, Cl, c-Pen, Br), (M-3972, F, H, Cl, c-Pen, CH3), (M-3973, F, H, Cl, n-Hex, H), (M-3974, F, H, Cl, n-Hex, Cl), (M-3975, F, H, Cl, n-Hex, F), (M-3976, F, H, Cl, n-Hex, CF3), (M-3977, F, H, Cl, n-Hex, Br), (M-3978, F, H, Cl, n-Hex, CH3), (M-3979, F, H, Cl, c-Hex, H), (M-3980, F, H, Cl, c-Hex, Cl), (M-3981, F, H, Cl, c-Hex, F), (M-3982, F, H, Cl, c-Hex, CF3), (M-3983, F, H, Cl, c-Hex, Br), (M-3984, F, H, Cl, c-Hex, CH3), (M-3985, F, H, Cl, OH, H), (M-3986, F, H, Cl, OH, Cl), (M-3987, F, H, Cl, OH, F), (M-3988, F, H, Cl, OH, CF3), (M-3989, F, H, Cl, OH, Br), (M-3990, F, H, Cl, OH, CH3), (M-3991, F, H, Cl, EtO, H), (M-3992, F, H, Cl, EtO, Cl), (M-3993, F, H, Cl, EtO, F), (M-3994, F, H, Cl, EtO, CF3), (M-3995, F, H, Cl, EtO, Br), (M-3996, F, H, Cl, EtO, CH3), (M-3997, F, H, Cl, n-PrO, H), (M-3998, F, H, Cl, n-PrO, Cl), (M-3999, F, H, Cl, n-PrO, F), (M-4000, F, H, Cl, n-PrO, CF3), (M-4001, F, H, Cl, n-PrO, Br), (M-4002, F, H, Cl, n-PrO, CH3), (M-4003, F, H, Cl, PhO, H), (M-4004, F, H, Cl, PhO, Cl), (M-4005, F, H, Cl, PhO, F), (M-4006, F, H, Cl, PhO, CF3), (M-4007, F, H, Cl, PhO, Br), (M-4008, F, H, Cl, PhO, CH3), (M-4009, F, H, Cl, BnO, H), (M-4010, F, H, Cl, BnO, Cl), (M-4011, F, H, Cl, BnO, F), (M-4012, F, H, Cl, BnO, CF3), (M-4013, F, H, Cl, BnO, Br), (M-4014, F, H, Cl, BnO, CH3), (M-4015, F, H, Cl, PhCH2CH2O, H), (M-4016, F, H, Cl, PhCH2CH2O, Cl), (M-4017, F, H, Cl, PhCH2CH2O, F), (M-4018, F, H, Cl, PhCH2CH2O, CF3), (M-4019, F, H, Cl, PhCH2CH2O, Br), (M-4020, F, H, Cl, PhCH2CH2O, CH3), (M-4021, F, H, Cl, CF3O, H), (M-4022, F, H, Cl, CF3O, Cl), (M-4023, F, H, CJ, CF3O, F), (M-4024, F, H, Cl, CF3O, CF3), (M-4025, F, H, Cl, CF3O, Br), (M-4026, F, H, Cl, CF3O, CH3), (M-4027, F, H, Cl, Ph, H), (M-4028, F, H, Cl, Ph, Cl), (M-4029, F, H, Cl, Ph, F), (M-4030, F, H, Cl, Ph, CF3), (M-4031, F, H, Cl, Ph, Br), (M-4032, F, H, Cl, Ph, CH3), (M-4033, F, H, Cl, 4-F-Ph, H), (M-4034, F, H, Cl, 4-F-Ph, Cl), (M-4035, F, H, Cl, 4-F-Ph, F), (M-4036, F, H, Cl, 4-F-Ph, CF3), (M-4037, F, H, Cl, 4-F-Ph, Br), (M-4038, F, H, Cl, 4-F-Ph, CH3), (M-4039, F, H, Cl, 4-CF3-Ph, H), (M-4040, F, H, Cl, 4-CF3-Ph, Cl), (M-4041, F, H, Cl, 4-CF3-Ph, F), (M-4042, F, H, Cl, 4-CF3-Ph, CF3), (M-4043, F, H, Cl, 4-CF3-Ph, Br), (M-4044, F, H, Cl, 4-CF3-Ph, CH3), (M-4045, F, H, Cl, 4-(Me)2N-Ph, H), (M-4046, F, H, Cl, 4-(Me)2N-Ph, Cl), (M-4047, F, H, Cl, 4-(Me)2N-Ph, F), (M-4048, F, H, Cl, 4-(Me)2N-Ph, CF3), (M-4049, F, H, Cl, 4-(Me)2N-Ph, Br), (M-4050, F, H, Cl, 4-(Me)2N-Ph, CH3), (M-4051, F, H, Cl, 4-OH-Ph, H), (M-4052, F, H, Cl, 4-OH-Ph, Cl), (M-4053, F, H, Cl, 4-OH-Ph, F), (M-4054, F, H, Cl, 4-OH-Ph, CF3), (M-4055, F, H, Cl, 4-OH-Ph, Br), (M-4056, F, H, Cl, 4-OH-Ph, CH3), (M-4057, F, H, Cl, 3,4-di-F-Ph, H), (M-4058, F, H, Cl, 3,4-di-F-Ph, Cl), (M-4059, F, H, Cl, 3,4-di-F-Ph, F), (M-4060, F, H, Cl, 3,4-di-F-Ph, CF3), (M-4061, F, H, Cl, 3,4-di-F-Ph, Br), (M-4062, F, H, Cl, 3,4-di-F-Ph, CH3), (M-4063, F, H, Cl, 4-COOH-Ph, H), (M-4064, F, H, Cl, 4-COOH-Ph, Cl), (M-4065, F, H, Cl, 4-COOH-Ph, F), (M-4066, F, H, Cl, 4-COOH-Ph, CF3), (M-4067, F, H, Cl, 4-COOH-Ph, Br), (M-4068, F, H, Cl, 4-COOH-Ph, CH3), (M-4069, F, H, Cl, Bn, H), (M-4070, F, H, Cl, Bn, Cl), (M-4071, F, H, Cl, Bn, F), (M-4072, F, H, Cl, Bn, CF3), (M-4073, F, H, Cl, Bn, Br), (M-4074, F, H, Cl, Bn, CH3), (M-4075, F, H, Cl, 4-F-Bn, H), (M-4076, F, hi, Cl, 4-F-Bn, Cl), (M-4077, F, H, Cl, 4-F-Bn, F), (M-4078, F, H, Cl, 4-F-Bn, CF3), (M-4079, F, H, Cl, 4-F-Bn, Br), (M-4080, F, H, Cl, 4-F-Bn, CH3), (M-4081, F, H, Cl, 2-Py, H), (M-4082, F, H, Cl, 2-Py, Cl), (M-4083, F, H, Cl, 2-Py, F), (M-4084, F, H, Cl, 2-Py, CF3), (M-4085, F, H, Cl, 2-Py, Br), (M-4086, F, H, Cl, 2-Py, CH3), (M-4087, F, H, Cl, 3-Py, H), (M-4088, F, H, Cl, 3-Py, Cl), (M-4089, F, H, Cl, 3-Py, F), (M-4090, F, H, Cl, 3-Py, CF3), (M-4091, F, H, Cl, 3-Py, Br), (M-4092, F, H, Cl, 3-Py, CH3), (M-4093, F, H, Cl, 4-Py, H), (M-4094, F, H, Cl, 4-Py, Cl), (M-4095, F, H, Cl, 4-Py, F), (M-4096, F, H, Cl, 4-Py, CF3), (M-4097, F, H, Cl, 4-Py, Br), (M-4098, F, H, Cl, 4-Py, CH3), (M-4099, F, H, Cl, 2-Th, H), (M-4100, F, H, Cl, 2-Th, Cl), (M-4101, F, H, Cl, 2-Th, F), (M-4102, F, H, Cl, 2-Th, CF3), (M-4103, F, H, Cl, 2-Th, Br), (M-4104, F, H, Cl, 2-Th, CH3), (M-4105, F, H, Cl, 3-Th, H), (M-4106, F, H, Cl, 3-Th, Cl), (M-4107, F, H, Cl, 3-Th, F), (M-4108, F, H, Cl, 3-Th, CF3), (M-4109, F, H, Cl, 3-Th, Br), (M-4110, F, H, Cl, 3-Th, CH3), (M-4111, F, H, Cl, pyrrazol-2-yl, H), (M-4112, F, H, Cl, pyrrazol-2-yl, Cl), (M-4113, F, H, Cl, pyrrazol-2-yl, F), (M-4114, F, H, Cl, pyrrazol-2-yl, CF3), (M-4115, F, H, Cl, pyrrazol-2-yl, Br), (M-4116, F, H, Cl, pyrrazol-2-yl, CH3), (M-4117, F, H, Cl, pyrrazol-3-yl, H), (M-4118, F, H, Cl, pyrrazol-3-yl, Cl), (M-4119, F, H, Cl, pyrrazol-3-yl, F), (M-4120, F, H, Cl, pyrrazol-3-yl, CF3), (M-4121, F, H, Cl, pyrrazol-3-yl, Br), (M-4122, F, H, Cl, pyrrazol-3-yl, CH3), (M-4123, F, H, Cl, pyrimidin-2-yl, H), (M-4124, F, H, Cl, pyrimidin-2-yl, Cl), (M-4125, F, H, Cl, pyrimidin-2-yl, F), (M-4126, F, H, Cl, pyrimidin-2-yl, CF3), (M-4127, F, H, Cl, pyrimidin-2-yl, Br), (M-4128, F, H, Cl, pyrimidin-2-yl, CH3), (M-4129, F, H, Cl, pyrimidin-4-yl, H), (M-4130, F, H, Cl, pyrimidin-4-yl, Cl), (M-4131, F, H, Cl, pyrimidin-4-yl, F), (M-4132, F, H, Cl, pyrimidin-4-yl, CF3), (M-4133, F, H, Cl, pyrimidin-4-yl, Br), (M-4134, F, H, Cl, pyrimidin-4-yl, CH3), (M-4135, F, H, Cl, pyrimidin-5-yl, H), (M-4136, F, H, Cl, pyrimidin-5-yl, Cl), (M-4137, F, H, Cl, pyrimidin-5-yl, F), (M-4138, F, H, Cl, pyrimidin-5-yl, CF3), (M-4139, F, H, Cl, pyrimidin-5-yl, Br), (M-4140, F, H, Cl, pyrimidin-5-yl, CH3), (M-4141, F, H, Cl, HOOCCH2CH2CH2, H), (M-4142, F, H, Cl, HOOCCH2CH2CH2, Cl), (M-4143, F, H, Cl, HOOCCH2CH2CH2, F), (M-4144, F, H, Cl, HOOCCH2CH2CH2, CF3), (M-4145, F, H, Cl, HOOCCH2CH2CH2, Br), (M-4146, F, H, Cl, HOOCCH2CH2CH2CH3), (M-4147, F, H, Cl, HOOCCH2CH2CH2CH2, H), (M-4148, F, H, Cl, HOOCCH2CH2CH2CH2, Cl), (M-4149, F, H, Cl, HOOCCH2CH2CH2CH2, F), (M-4150, F, H, Cl, HOOCCH2CH2CH2CH2, CF3), (M-4151, F, H, Cl, HOOCCH2CH2CH2CH2, Br), (M-4152, F, H, Cl, HOOCCH2CH2CH2CH2, CH3), (M-4153, F, H, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-4154, F, H, Cl, (Me)2NCOCH2CH2CH2CH3, Cl), (M-4155, F, H, Cl, (Me)3NCOCH2CH2CH2CH2, F), (M-4156, F, H, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-4157, F, H, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-4158, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH3), (M-4159, F, H, Cl, (Me)2NCOCH2CH2C2CH2CH2, H), (M-4160, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-4161, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-4162, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-4163, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-4164, F, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-4165, F, H, Cl, MeOCH2, H), (M-4166,
- F, H, Cl, MeOCH2, Cl), (M-4167, F, H, Cl, MeOCH2, F), (M-4168, F, H, Cl, MeOCH2, CF3), (M-4169, F, H, Cl, MeOCH2, Br), (M-4170, F, H, Cl, MeOCH2, CH3), (M-4171, F, H, Cl, EtOCH2, H), (M-4172, F, H, Cl, EtOCH2, Cl), (M-4173, F, H, Cl, EtOCH2, F), (M-4174, F, H, Cl, EtOCH2, CF3), (M-4175, F, H, Cl, EtOCH2, Br), (M-4176, F, H, Cl, EtOCH2, CH3), (M-4177, F, H, Cl, EtOCH2CH3, H), (M-4178, F, H, Cl, EtOCH2CH2, Cl), (M-4179, F, H, Cl, EtOCH2CH2, F), (M-4180, F, H, Cl, EtOCH2CH2, CF3), (M-4181, F, H, Cl, EtOCH2CH2, Br), (M-4182, F, H, Cl, EtOCH2CH2, CH3), (M-4183, F, H, Cl, MeOCH2CH2OCH2CH2, H), (M-4184, F, H, Cl, MeOCH2CH2OCH2CH2, Cl), (M-4185, F, H, Cl, MeOCH2CH2OCH2CH2, F), (M-4186, F, H, Cl, MeOCH2CH2OCH2CH2, CF3), (M-4187, F, H, Cl, MeOCH2CH2OCH2CH2, Br), (M-4188, F, H, Cl, MeOCH2CH2OCH2CH2, CH3), (M-4189, F, H, Cl, MeOCH2CH2, H), (M-4190, F, H, Cl, MeOCH2CH2, Cl), (M-4191, F, H, Cl, MeOCH2CH2, F), (M-4192, F, H, Cl, MeOCH2CH2, CF3), (M-4193, F, H, Cl, MeOCH2CH2, Br), (M-4194, F, H, Cl, MeOCH2CH2, CH3), (M-4195, F, H, Cl, HOCH2, H), (M-4196, F, H, Cl, HOCH2, Cl), (M-4197, F, H, Cl, HOCH2, F), (M-4198, F, H, Cl, HOCH2, CH3), (M-4199, F, H, Cl, HOCH2, Br), (M-4200, F, H, Cl, HOCH2, CH3), (M-4201, F, H, Cl, HOCH2CH2, H), (M-4202, F, H, Cl, HOCH2CH2, Cl), (M-4203, F, H, Cl, HOCH2CH2, F), (M-4204, F, H, Cl, HOCH2CH2, CF3), (M-4205, F, H, Cl, HOCH2CH2, Br), (M-4206, F, H, Cl, HOCH2CH2, CH3), (M-4207, F, H, Cl, HOCH2CH2CH2, H), (M-4208, F, H, Cl, HOCH2CH2CH2, Cl), (M-4209, F, H, Cl, HOCH2CH2CH2, F), (M-4210, F, H, Cl, HOCH2CH2CH2, CF3), (M-4211, F, H, Cl, HOCH2CH2CH2, Br), (M-4212, F, H, Cl, HOCH2CH2CH2, CH3), (M-4213, F, H, Cl, HOCH2CH2CH2CH2, H), (M-4214, F, H, Cl, HOCH2CH2CH2CH2, Cl), (M-4215, F, H, Cl, HOCH2CH2CH2CH2, F), (M-4216, F, H, Cl, HOCH2CH2CH2CH2, CF3), (M-4217, F, H, Cl, HOCH2CH2CH2CH2, Br), (M-4218, F, H, Cl, HOCH2CH2CH2CH2, CH3), (M-4219, F, H, Cl, HOCH2CH2CH2CH2CH2H), (M-4220, F, H, Cl, HOCH2CH2CH2CH2CH2Cl), (M-4221, F, H, Cl, HOCH2CH2CH2CH2CH2, F), (M-4222, F, H, Cl, HOCH2CH2CH2CH2CH2CF3), (M-4223, F, H, Cl, HOCH2CH2CH2CH2CH2Br), (M-4224, F, H, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-4225, F, H, Cl, HOCH2CH2OCH2CH2, H), (M-4226, F, H, Cl, HOCH2CH2OCH2CH2, Cl), (M-4227, F, H, Cl, HOCH2CH2OCH2CH2, F), (M-4228, F, H, Cl, HOCH2CH2OCH2CH2, CF3), (M-4229, F, H, Cl, HOCH2CH2OCH2CH2, Br), (M-4230, F, H, Cl, HOCH2CH2OCH2CH2, CH3), (M-4231, F, H, Cl, (Me)2N, H), (M-4232, F, H, Cl, (Me)2N, Cl), (M-4233, F, H, Cl, (Me)2N, F), (M-4234, F, H, Cl, (Me)2N, CF3), (M-4235, F, H, Cl, (Me)2N, Br), (M-4236, F, H, Cl, (Me)2N, CH3), (M-4237, F, H, Cl, piperidin-4-yl-methyl, H), (M-4238, F, H, Cl, piperidin-4-yl-methyl, Cl), (M-4239, F, H, Cl, piperidin-4-yl-methyl, F), (M-4240, F, H, Cl, piperidin-4-yl-methyl, CF3), (M-4241, F, H, Cl, piperidin-4-yl-methyl, Br), (M-4242, F, H, Cl, piperidin-4-yl-methyl, CH3), (M-4243, F, H, Cl, cyclohexylmethyl, H), (M-4244, F, H, Cl, cyclohexylmethyl, Cl), (M-4245, F, H, Cl, cyclohexylmethyl, F), (M-4246, F, H, Cl, cyclohexylmethyl, CF3), (M-4247, F, H, Cl, cyclohexylmethyl, Br), (M-4248, F, H, Cl, cyclohexylmethyl, CH3), (M-4249, F, F, H, H, H), (M-4250, F, F, H, H, Cl), (M-4251, F, F, H, H, F), (M-4252, F, F, H, H, CF3), (M-4253, F, F, H, H, Br), (M-4254, F, F, H, H, CH3), (M-4255, F, F, H, F, H), (M-4256, F, F, H, F, Cl), (M-4257, F, F, H, F, F), (M-4258, F, F, H, F, CF3), (M-4259, F, F, H, F, Br), (M-4260, F, F, H, F, CH3), (M-4261, F, F, H, Cl, H), (M-4262, F, F, H, Cl, Cl), (M-4263, F, F, H, Cl, F), (M-4264, F, F, H, Cl, CF3), (M-4265, F, F, H, Cl, Br), (M-4266, F, F, H, Cl, CH3), (M-4267, F, F, H, CH3, H), (M-4268, F, F, H, CH3, Cl), (M-4269, F, F, H, CH3, F), (M-4270, F, F, H, CH3, CF3), (M-4271, F, F, H, CH3, Br), (M-4272, F, F, H, CH3, CH3), (M-4273, F, F, H, Et, H), (M-4274, F, F, H, Et, Cl), (M-4275, F, F, H, Et, F), (M-4276, F, F, H, Et, CF3), (M-4277, F, F, H, Et, Br), (M-4278, F, F, H, Et, CH3), (M-4279, F, F, H, n-Pr, H), (M-4280, F, F, H, n-Pr, Cl), (M-4281, F, F, H, n-Pr, F), (M-4282, F, F, H, n-Pr, CF3), (M-4283, F, F, H, n-Pr, Br), (M-4284, F, F, H, n-Pr, CH3), (M-4285, F, F, H, c-Pr, H), (M-4286, F, F, H, c-Pr, Cl), (M-4287, F, F, H, c-Pr, F), (M-4288, F, F, H, c-Pr, CF3), (M-4289, F, F, H, c-Pr, Br), (M-4290, F, F, H, c-Pr, CH3), (M-4291, F, F, H, i-Pr, H), (M-4292, F, F, H, i-Pr, Cl), (M-4293, F, F, H, i-Pr, F), (M-4294, F, F, H, i-Pr, CF3), (M-4295, F, F, H, i-Pr, Br), (M-4296, F, F, H, i-Pr, CH3), (M-4297, F, F, H, n-Bu, H), (M-4298, F, F, H, n-Bu, Cl), (M-4299, F, F, H, n-Bu, F), (M-4300, F, F, H, n-Bu, CF3), (M-4301, F, F, H, n-Bu, Br), (M-4302, F, F, H, n-Bu, CH3), (M-4303, F, F, H, i-Bu, H), (M-4304, F, F, H, i-Bu, Cl), (M-4305, F, F, H, i-Bu, F), (M-4306, F, F, H, i-Bu, CF3), (M-4307, F, F, H, i-Bu, Br), (M-4308, F, F, H, i-Bu, CH3), (M-4309, F, F, H, sec-Bu, H), (M-4310, F, F, H, sec-Bu, Cl), (M-4311, F, F, H, sec-Bu, F), (M-4312, F, F, H, sec-Bu, CF3), (M-4313, F, F, H, sec-Bu, Br), (M-4314, F, F, H, sec-Bu, CH3), (M-4315, F, F, H, n-Pen, H), (M-4316, F, F, H, n-Pen, Cl), (M-4317, F, F, H, n-Pen, F), (M-4318, F, F, H, n-Pen, CF3), (M-4319, F, F, H, n-Pen, Br), (M-4320, F, F, H, n-Pen, CH3), (M-4321, F, F, H, c-Pen, H), (M-4322, F, F, H, c-Pen, Cl), (M-4323, F, F, H, c-Pen, F), (M-4324, F, F, H, c-Pen, CF3), (M-4325, F, F, H, c-Pen, Br), (M-4326, F, F, H, c-Pen, CH3), (M-4327, F, F, H, n-Hex, H), (M-4328, F, F, H, n-Hex, Cl), (M-4329, F, F, H, n-Hex, F), (M-4330, F, F, H, n-Hex, CF3), (M-4331, F, F, H, n-Hex, Br), (M-4332, F, F, H, n-Hex, CH3), (M-4333, F, F, H, c-Hex, H), (M-4334, F, F, H, c-Hex, Cl), (M-4335, F, F, H, c-Hex, F), (M-4336, F, F, H, C-Hex, CF3), (M-4337, F, F, H, c-Hex, Br), (M-4338, F, F, H, c-Hex, CH3), (M-4339, F, F, H, OH, H), (M-4340, F, F, H, OH, Cl), (M-4341, F, F, H, OH, F), (M-4342, F, F, H, OH, CF3), (M-4343, F, F, H, OH, Br), (M-4344, F, F, H, OH, CH3), (M-4345, F, F, H, EtO, H), (M-4346, F, F, H, EtO, Cl), (M-4347, F, F, H, EtO, F), (M-4348, F, F, H, EtO, CF3), (M-4349, F, F, H, EtO, Br), (M-4350, F, F, H, EtO, CH3), (M-4351, F, F, H, n-PrO, H), (M-4352, F, F, H, n-PrO, Cl), (M-4363, F, F, H, n-PrO, F), (M-4354, F, F, H, n-PrO, CF3), (M-4355, F, F, H, n-PrO, Br), (M-4356, F, F, H, n-PrO, CH3), (M-4357, F, F, H, PhO, H), (M-4358, F, F, H, PhO, Cl), (M-4359, F, F, H, PhO, F), (M-4360, F, F, H, PhO, CF3), (M-4361, F, F, H, PhO, Br), (M-4362, F, F, H, PhO, CH3), (M-4363, F, F, H, BnO, H), (M-4364, F, F, H, BnO, Cl), (M-4365, F, F, H, BnO, F), (M-4366, F, F, H, BnO, CF3), (M-4367, F, F, H, BnO, Br), (M-4368, F, F, H, BnO, CH3), (M-4369, F, F, H, PhCH2CH2O, H), (M-4370, F, F, H, PhCH2CH2, Cl), (M-4371, F, F, H, PhCH2CH2O, F), (M-4372, F, F, H, PhCH2CH2O, CF3), (M-4373, F, F, H, PhCH2CH2O, Br), (M-4374, F, F, H, PhCH2CH2O, CH3), (M-4375, F, F, H, CF3O, H), (M-4376, F, F, H, CF3O, Cl), (M-4377, F, P, H, CF3O, F), (M-4378, F, F, H, CF3O, CF3), (M-4379, F, F, H, CF3O, Br), (M-4380, F, F, H, CF3O, CH3), (M-4381, F, F, H, Ph, H), (M-4382, F, F, H, Ph, Cl), (M-4383, F, F, H, Ph, F), (M-4384, F, F, H, Ph, CF3), (M-4385, F, F, H, Ph, Br), (M-4386, F, F, H, Ph, CH3), (M-4387, F, F, H, 4-F-Ph, H), (M-4388, F, F, H, 4-F-Ph, Cl), (M-4389, F, F, H, 4-F-Ph, F), (M-4390, F, F, H, 4-F-Ph, CF3), (M-4391, F, F, H, 4-F-Ph, Br), (M-4392, F, F, H, 4-F-Ph, CH3), (M-4393, F, F, H, 4-CF3-Ph, H), (M-4394, F, F, H, 4-CF3-Ph, Cl), (M-4395, F, F, H, 4-CF3-Ph, F), (M-4396, F, F, H, 4-CF3-Ph, CF3), <M-4397, F, F, H, 4-CF3-Ph, Br), (M-4398, F, F, H, 4-CF3-Ph, CH3), (M-4399, F, F, H, 4-(Me)2N-Ph, H), (M-4400, F, F, H, 4-(Me)2N-Ph, Cl), (M-4401, F, F, H, 4-(Me)2N-Ph, F), (M-4402, F, F, H, 4-(Me)2N-Ph, CF3), (M-4403, F, F, H, 4-(Me)2N-Ph, Br), (M-4404, F, F, H, 4-(Me)2N-Ph, CH3), (M-4405, F, F, H, 4-OH-Ph, H), (M-4406, F, F, H, 4-OH-Ph, Cl), (M-4407, F, F, H, 4-OH-Ph, F), (M-4408, F, F, H, 4-OH-Ph, CF3), (M-4409, F, F, H, 4-OH-Ph, Br), (M-4410, F, F, H, 4-OH-Ph, CH3), (M-4411, F, F, H, 3,4-di-F-Ph, H), (M-4412, F, F, H, 3,4-di-F-Ph, Cl), (M-4413, F, F, H, 3,4-di-F-Ph, F), (M-4414, F, F, H, 3,4-di-F-Ph, CF3), (M-4415, F, F, H, 3,4-di-F-Ph, Br), (M-4416, F, F, H, 3,4-di-R-Ph, CH3), (M-4417, F, F, H, 4-COOH-Ph, H), (M-4418, F, F, H, 4-COOH-Ph, Cl), (M-4419, F, F, H, 4-COOH-Ph, F), (M-4420, F, F, H, 4-COOH-Ph, CF3), (M-4421, F, F, H, 4-COOH-Ph, Br), (M-4422, F, F, H, 4-COOH-Ph, CH3), (M-4423, F, F, H, Bn, H), (M-4424, F, F, H, Bn, Cl), (M-4425, F, F, H, Bn, F), (M-4426, F, F, H, Bn, CF3), (M-4427, F, F, H, Bn, Br), (M-4428, F, F, H, Bn, CH3), (M-4429, F, F, H, 4-F-Bn, H), (M-4430, F, F, H, 4-F-Bn, Cl), (M-4431, F, F, H, 4-F-Bn, F), (M-4432, F, F, H, 4-F-Bn, CF3), (M-4433, F, F, H, 4-F-Bn, Br), (M-4434, F, F, H, 4-F-Bn, CH3), (M-4435, F, F, H, 2-Py, H), (M-4436, F, F, H, 2-Py, Cl), (M-4437, F, F, H, 2-Py, F), (M-4438, F, F, H, 2-Py, CF3), (M-4439, F, F, H, 2-Py, Br), (M-4440, F, F, H, 2-Py, CH3), (M-4441, F, F, H, 3-Py, H), (M-4442, F, F, H, 3-Py, Cl), (M-4443, F, F, H, 3-Py, F), (M-4444, F, F, H, 3-Py, CF3), (M-4445, F, F, H, 3-Py, Br), (M-4446, F, F, H, 3-Py, CH3), (M-4447, F, F, H, 4-Py, H), (M-4448, F, F, H, 4-Py, Cl), (M-4449, F, F, H, 4-Py, F), (M-4450, F, F, H, 4-Py, CF3), (M-4451, F, F, H, 4-Py, Br), (M-4452, F, F, H, 4-Py, CH3), (M-4453, F, F, H, 2-Th, H), (M-4454, F, F, H, 2-Th, Cl), (M-4455, F, F, H, 2-Th, F), (M-4456, F, F, H, 2-Th, CF3), (M-4457, F, F, H, 2-Th, Br), (M-4458, F, F, H, 2-Th, CH3), (M-4459, F, F, H, 3-Th, H), (M-4460, F, F, H, 3-Th, Cl), (M-4461, F, F, H, 3-Th, F), (M-4462, F, F, H, 3-Th, CF3), (M-4463, F, F, H, 3-Th, Br), (M-4464, F, F, H, 3-Th, CH3), (M-4465, F, F, H, pyrrazol-2-yl, H), (M-4466, F, F, H, pyrrazol-2-yl, Cl), (M-4467, F, F, H, pyrrazol-2-yl, F), (M-4468, F, F, H, pyrrazol-2-yl, CF3), (M-4469, F, F, H, pyrrazol-2-yl, Br), (M-4470, F, F, H, pyrrazol-2-yl, CH3), (M-4471, F, F, H, pyrrazol-3-yl, H), (M-4472, F, F, H, pyrrazol-3-yl, Cl), (M-4473, F, F, H, pyrrazol-3-yl, F), (M-4474, F, F, H, pyrrazol-3-yl, CF3), (M-4475, F, F, H, pyrrazol-3-yl, Br), (M-4476, F, F, H, pyrrazol-3-yl, CH3), (M-4477, F, F, H, pyrimidin-2-yl, H), (M-4478, F, F, H, pyrimidin-2-yl, Cl), (M-4479, F, F, H, pyrimidin-2-yl, F), (M-4480, F, F, H, pyrimidin-2-yl, CF3), (M-4481, F, F, H, pyrimidin-2-yl, Br), (M-4482, F, F, H, pyrimidin-2-yl, CH3), (M-4483, F, F, H, pyrimidin-4-yl, H), (M-4484, F, F, H, pyrimidin-4-yl, Cl), (M-4485, F, F, H, pyrimidin-4-yl, F), (M-4486, F, F, H, pyrimidin-4-yl, CF3), (M-4487, F, F, H, pyrimidin-4-yl, Br), (M-4488, F, F, H, pyrimidin-4-yl, CH3), (M-4489, F, F, H, pyrimidin-5-yl, H), (M-4490, F, F, H, pyrimidin-5-yl, Cl), (M-4491, F, F, H, pyrimidin-5-yl, F), (M-4492, F, F, H, pyrimidin-5-yl, CF3), (M-4493, F, F, H, pyrimidin-5-yl, Br), (M-4494, F, F, H, pyrimidin-5-yl, CH3), (M-4495, F, F, H, HOOCCH2CH2CH2H), (M-4496, F, F, H, HOOCCH2CH2CH2Cl), (M-4497, F, F, H, HOOCCH2CH2CH2, F), (M-4498, F, F, H, HOOCCH2CH2CH2CF3), (M-4499, F, F, H, HOOCCH2CH2CH2Br), (M-4500, F, F, H, HOOCCH2CH2CH2CH3), (M-4501, F, F, H, HOOCCH2CH2CH2CH2, H), (M-4502, F, F, H, HOOCCH2CH2CH2CH2, Cl), (M-4503, F, F, H, HOOCCH2CH2CH2CH2, F), (M-4504, F, F, H, HOOCCH2CH2CH2CH2, CF3), (M-4505, F, F, H, HOOCCH2CH2CH2CH2, Br), (M-4506, F, F, H, HOOCCH2CH2CH2CH2, CH3), (M-4507, F, F, H, (Me)2NCOCH2CH2CH2CH2, H), (M-4508, F, F, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-4509, F, F, H, (Me)2NCOCH2CH2CH2CH2, F), (M-4510, F, F, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-4511, F, F, H, (Me)2NCOCH2CH2CH2, CH2, Br), (M-4512, F, F, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-4513, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-4514, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-4515, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-4516, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-4517, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-4518, F, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-4519, F, F, H, MeOCH2, H), (M-4520, F, F, H, MeOCH2, Cl), (M-4521, F, F, H, MeOCH2, F), (M-4522, F, F, H, MeOCH2, CF3), (M-4523, F, F, H, MeOCH2, Br), (M-4524, F, F, H, MeOCH2, CH3), (M-4525, F, F, H, EtOCH2, H), (M-4526, F, F, H, EtOCH2, Cl), (M-4527, F, F, H, EtOCH2, F), (M-4528, F, F, H, EtOCH2, CF3), (M-4529, F, F, H, EtOCH2, Br), (M-4530, F, F, H, EtOCH2, CH3), (M-4531, F, F, H, EtOCH2CH2, H), (M-4532, F, F, H, EtOCH2CH2, Cl), (M-4533, F, F, H, EtOCH2CH2, F), (M-4534, F, F, H, EtOCH2CH2, CF3), (M-4535, F, F, H, EtOCH2CH2, Br), (M-4536, F, F, H, EtOCH2CH2, CH3), (M-4537, F, F, H, MeOCH2CH2OCH2CH2, H), (M-4538, F, F, H, MeOCH2CH2OCH2CH2, Cl), (M-4539, F, F, H, MeOCH2CH2OCH2CH2, F), (M-4540, F, F, H, MeOCH2CH2OCH2CH2, CF3), (M-4541, F, F, H, MeOCH2CH2OCH2CH2, Br), (M-4542, F, F, H, MeOCH2CH2OCH2CH2, CH3), (M-4543, F, F, H, MeOCH2CH2, H), (M-4544, F, F, H, MeOCH2CH2, Cl), (M-4545, F, F, H, MeOCH2CH2, F), (M-4546, F, F, H, MeOCH2CH2, CF3), (M-4547, F, F, H, MeOCH2CH2, Br), (M-4548, F, F, H, MeOCH2CH2, CH3), (M-4549, F, F, H, HOCH2, H), (M-4550, F, F, H, HOCH2, Cl), (M-4551, F, F, H, HOCH2, F), (M-4552, F, F, H, HOCH2, CF3), (M-4553, F, F, H, HOCH2, Br), (M-4554, F, F, H, HOCH2, CH3), (M-4555, F, F, H, HOCH2CH2, H), (M-4556, F, F, H, HOCH2CH2, Cl), (M-4557, F, F, H, HOCH2CH2, F), (M-4558, F, F, H, HOCH2CH2, CF3), (M-4559, F, F, H, HOCH2CH2, Br), (M-4560, F, F, H, HOCH2CH2, CH3), (M-4561, F, F, H, HOCH2CH2CH2, H), (M-4562, F, F, H, HOCH2CH2CH2, Cl), (M-4563, F, F, H, HOCH2CH2CH2, F), (M-4564, F, F, H, HOCH2CH2CH2, CF3), (M-4565, F, F, H, HOCH2CH2CH2, Br), (M-4566, F, F, Pt, HOCH2CH2CH2, CH3), (M-4567, F, F, H, HOCH2CH2CH2CH2, H), (M-4568, F, F, H, HOCH2CH2CH2CH2, Cl), (M-4569, F, F, H, HOCH2CH2CH2CH2, F), (M-4570, F, F, H, HOCH2CH2CH2CH2, CF3), (M-4571, F, F, H, HOCH2CH2CH2CH2, Br), (M-4572, F, F, H, HOCH2CH2CH2CH2, CH3), (M-4573, F, F, H, HOCH2CH2CH2CH2CH2H), (M-4574, F, F, H, HOCH2CH2CH2CH2CH2, Cl), (M-4575, F, F, H, HOCH2CH2CH2CH2CH2, F), (M-4576, F, F, H, HOCH2CH2CH2CH2CH2, CF3), (M-4577, F, F, H, HOCH2CH2CH2CH2CH2Br), (M-4578, F, F, H, HOCH2CH2CH2CH2CH2, CH3), (M-4579, F, F, H, HOCH2CH2OCH2CH2, H), (M-4580, F, F, H, HOCH2CH2OCH2CH2, Cl), (M-4581, F, F, H, HOCH2CH2OCH2CH2, F), (M-4582, F, F, H, HOCH2CH2OCH2CH2, CF3), (M-4583, F, F, H, HOCH2CH2OCH2CH2, Br), (M-4584, F, F, H, HOCH2CH2OCH2CH2, CH3), (M-4585, F, F, H, (Me)2N, H), (M-4586, F, F, H, (Me)2N, Cl), (M-4587, F, F, H, (Me)2N, F), (M-4588, F, F, H, (Me)2N, CF3), (M-4589, F, F, H, (Me)2N, Br), (M-4590, F, F, H, (Me)2N, CH3), (M-4591, F, F, H, piperidin-4-yl-methyl, H), (M-4592, F, F, H, piperidin-4-yl-methyl, Cl), (M-4593, F, F, H, piperidin-4-yl-methyl, F), (M-4594, F, F, H, piperidin-4-yl-methyl, CF3), (M-4595, F, F, B, piperidin-4-yl-methyl, Br), (M-4596, F, F, H, piperidin-4-yl-methyl, CH3), (M-4597, F, F, H, cyclohexylmethyl, H), (M-4598, F, F, H, cyclohexylmethyl, Cl), (M-4599, F, F, H, cyclohexylmethyl, F), (M-4600, F, F, H, cyclohexylmethyl, CF3), (M-4601, F, F, H, cyclohexylmethyl, Br), (M-4602, F, F, H, cyclohexylmethyl, CH3), (M-4603, F, F, F, H, H), (M-4604, F, F, F, H, Cl), (M-4605, F, F, F, H, F), (M-4606, F, F, F, H, CF3), (M-4607, F, F, F, H, Br), (M-4608, F, F, F, H, CH3), (M-4609, F, F, F, F, H), (M-4610, F, F, F, F, Cl), (M-4611, F, F, F, F, F), (M-4612, F, F, F, F, CF3), (M-4613, F, F, F, F, Br), (M-4614, F, F, F, F, CH3), (M-4615, F, F, F, Cl, H), (M-4616, F, F, F, Cl, Cl), (M-4617, F, F, F, Cl, F), (M-4618, F, F, F, Cl, CF3), (M-4619, F, F, F, Cl, Br), (M-4620, F, F, F, Cl, CH3), (M-4621, F, F, F, CH3, H), (M-4622, F, F, F, CH3, Cl), (M-4623, F, F, F, CH3, F), (M-4624, F, F, F, CH3, CF3), (M-4625, F, F, F, CH3, Br), (M-4626, F, F, F, CH3, CH3), (M-4627, F, F, F, Et, H), (M-4628, F, F, F, Et, Cl), (M-4629, F, F, F, Et, F), (M-4630, F, F, F, Et, CF3), (M-4631, F, F, F, Et, Br), (M-4632, F, F, F, Et, CH3), (M-4633, F, F, F, n-Pr, H), (M-4634, F, F, F, n-Pr, Cl), (M-4635, F, F, F, n-Pr, F), (M-4636, F, F, F, n-Pr, CF3), (M-4637, F, F, F, n-Pr, Br), (M-4638, F, F, F, n-Pr, CH3), (M-4639, F, F, F, c-Pr, H), (M-4640, F, F, F, c-Pr, Cl), (M-4641, F, F, F, c-Pr, F), (M-4642, F, F, F, c-Pr, CF3), (M-4643, F, F, F, c-Pr, Br), (M-4644, F, F, F, c-Pr, CH3), (M-4645, F, F, F, i-Pr, H), (M-4646, F, F, F, i-Pr, Cl), (M-4647, F, F, F, i-Pr, F), (M-4648, F, F, F, i-Pr, CF3), (M-4649, F, F, F, i-Pr, Br), (M-4650, F, F, F, i-Pr, CH3), (M-4651, F, F, F, n-Bu, H), (M-4652, F, F, F, n-Bu, Cl), (M-4653, F, F, F, n-Bu, F), (M-4654, F, F, F, n-Bu, CF3), (M-4655, F, F, F, n-Bu, Br), (M-4656, F, F, F, n-Bu, CH3), (M-4657, F, F, F, i-Bu, H), (M-4658, F, F, F, i-Bu, Cl), (M-4659, F, F, F, i-Bu, F), (M-4660, F, F, F, i-Bu, CF3), (M-4661, F, F, F, i-Bu, Br), (M-4662, F, F, F, i-Bu, CH3), (M-4663, F, F, F, sec-Bu, H), (M-4664, F, F, F, sec-Bu, Cl), (M-4665, F, F, F, sec-Bu, F), (M-4666, F, F, F, sec-Bu, CF3), (M-4667, F, F, F, sec-Bu, Br), (M-4668, F, F, F, sec-Bu, CH3), (M-4669, F, F, F, n-Pen, H), (M-4670, F, F, F, n-Pen, Cl), (M-4671, F, F, F, n-Pen, F), (M-4672, F, F, F, n-Pen, CF3), (M-4673, F, F, F, n-Pen, Br), (M-4674, F, F, F, n-Pen, CH3), (M-4675, F, F, F, c-Pen, H), (M-4676, F, F, F, c-Pen, Cl), (M-4677, F, F, F, c-Pen, F), (M-4678, F, F, F, c-Pen, CF3), (M-4679, F, F, F, c-Pen, Br), (M-4680, F, F, F, c-Pen, CH3), (M-4681, F, F, F, n-Hex, H), (M-4682, F, F, F, n-Hex, Cl), (M-4683, F, F, F, n-Hex, F), (M-4684, F, F, F, n-Hex, CF3), (M-4685, F, F, F, n-Hex, Br), (M-4686, F, F, F, n-Hex, CH3), (M-4687, F, F, F, c-Hex, H), (M-4688, F, F, F, c-Hex, Cl), (M-4689, F, F, F, c-Hex, F), (M-4690, F, F, F, c-Hex, CF3), (M-4691, F, F, F, c-Hex, Br), (M-4692, F, F, F, c-Hex, CH3), (M-4693, F, F, F, OH, H), (M-4694, F, F, F, OH, Cl), (M-4695, F, F, F, OH, F), (M-4696, F, F, F, OH, CF3), (M-4697, F, F, F, OH, Br), (M-4698, F, F, F, OH, CH3), (M-4699, F, F, F, EtO, H), (M-4700, F, F, F, EtO, Cl), (M-4701, F, F, F, EtO, F), (M-4702, F, F, F, EtO, CF3), (M-4703, F, F, F, EtO, Br), (M-4704, F, F, F, EtO, CH3), (M-4705, F, F, F, n-PrO, H), (M-4706, F, F, F, n-PrO, Cl), (M-4707, F, F, F, n-PrO, F), (M-4708, F, F, F, n-PrO, CF3), (M-4709, F, F, F, n-PrO, Br), (M-4710, F, F, F, n-PrO, CH3), (M-4711, F, F, F, PhO, H), (M-4712, F, F, F, PhO, Cl), (M-4713, F, F, F, PhO, F), (M-4714, F, F, F, PhO, CF3), (M-4715, F, F, F, PhO, Br), (M-4716, F, F, F, PhO, CH3), (M-4717, F, F, F, BnO, H), (M-4718, F, F, F, BnO, Cl), (M-4719, F, F, F, BnO, F), (M-4720, F, F, F, BnO, CF3), (M-4721, F, F, F, BnO, Br), (M-4722, F, F, F, BnO, CH3), (M-4723, F, F, F, PhCH2CH2O, H), (M-4724, F, F, F, PhCH2CH2O, Cl), (M-4725, F, F, F, PhCH2CH2O, F), (M-4726, F, F, F, PhCH2CH2O, CF3), (M-4727, F, F, F, PhCH2CH2O, Br), (M-4728, F, F, F, PhCH2CH2O, CH3), (M-4729, F, F, F, CF3O, H), (M-4730, F, F, F, CF3O, Cl), (M-4731, F, F, F, CF3O, F), (M-4732, F, F, F, CF3O, CF3), (M-4733, F, F, F, CF3O, Br), (M-4734, F, F, F, CF3O, CH3), (M-4735, F, F, F, Ph, H), (M-4736, F, F, F, Ph, Cl), (M-4737, F, F, F, Ph, F), (M-4738, F, F, F, Ph, CF3), (M-4739, F, F, F, Ph, Br), (M-4740, F, F, F, Ph, CH3), (M-4741, F, F, F, 4-F-Ph, H), (M-4742, F, F, F, 4-F-Ph, Cl), (M-4743, F, F, F, 4-F-Ph, F), (M-4744, F, F, F, 4-F-Ph, CF3), (M-4745, F, F, F, 4-F-Ph, Br), (M-4746, F, F, F, 4-F-Ph, CH3), (M-4747, F, F, F, 4-CF3-Ph, H), (M-4748, F, F, F, 4-CF3-Ph, Cl), (M-4749, F, F, F, 4-CF3-Ph, F), (M-4750, F, F, F, 4-CF3-Ph, CF3), (M-4751, F, F, F, 4-CF3-Ph, Br), (M-4752, F, F, F, 4-CF3-Ph, CH3), (M-4753, F, F, F, 4-(Me)2N-Ph, H), (M-4754, F, F, F, 4-(Me)2N-Ph, Cl), (M-4755, F, F, F, 4-(Me)2N-Ph, F), (M-4756, F, F, F, 4-(Me)2N-Ph, CF3), (M-4757, F, F, F, 4-(Me)2N-Ph, Br), (M-4758, F, F, F, 4-(Me)2N-Ph, CH3), (M-4759, F, F, F, 4-OH-Ph, H), (M-4760, F, F, F, 4-OH-Ph, Cl), (M-4761, F, F, F, 4-OH-Ph, F), (M-4762, F, F, F, 4-OH-Ph, CF3), (M-4763, F, F, F, 4-OH-Ph, Br), (M-4764, F, F, F, 4-OH-Ph, CH3), (M-4765, F, F, F, 3,4-di-F-Ph, H), (M-4766, F, F, F, 3,4-di-F-Ph, Cl), (M-4767, F, F, F, 3,4-di-F-Ph, F), (M-4768, F, F, F, 3,4-di-F-Ph, CF3), (M-4769, F, F, F, 3,4-di-F-Ph, Br), (M-4770, F, F, F, 3,4-di-F-Ph, CH3), (M-4771, F, F, F, 4-COOH-Ph, H), (M-4772, F, F, F, 4-COOH-Ph, Cl), (M-4773, F, F, F, 4-COOH-Ph, F), (M-4774, F, F, F, 4-COOH-Ph, CF3), (M-4775, F, F, F, 4-COOH-Ph, Br), (M-4776, F, F, F, 4-COOH-Ph, CH3), (M-4777, F, F, F, Bn, H), (M-4778, F, F, F, Bn, Cl), (M-4779, F, F, F, Bn, F), (M-4780, F, F, F, Bn, CF3), (M-4781, F, F, F, Bn, Br), (M-4782, F, F, F, Bn, CH3), (M-4783, F, F, F, 4-F-Bn, H), (M-4784, F, F, F, 4-F-Bn, Cl), (M-4785, F, F, F, 4-F-Bn, F), (M-4786, F, F, F, 4-F-Bn, CF3), (M-4787, F, F, F, 4-F-Bn, Br), (M-4788, F, F, F, 4-F-Bn, CH3), (M-4789, F, F, F, 2-Py, H), (M-4790, F, F, F, 2-Py, Cl), (M-4791, F, F, F, 2-Py, F), (M-4792, F, F, F, 2-Py, CF3), (M-4793, F, F, F, 2-Py, Br), (M-4794, F, F, F, 2-Py, CH3), (M-4795, F, F, F, 3-Py, H), (M-4796, F, F, F, 3-Py, Cl), (M-4797, F, F, F, 3-Py, F), (M-4798, F, F, F, 3-Py, CF3), (M-4799, F, F, F, 3-Py, Br), (M-4800, F, F, F, 3-Py, CH3), (M-4801, F, F, F, 4-Py, H), (M-4802, F, F, F, 4-Py, Cl), (M-4803, F, F, F, 4-Py, F), (M-4804, F, F, F, 4-Py, CF3), (M-4805, F, F, F, 4-Py, Br), (M-4806, F, F, F, 4-Py, CH3), (M-4807, F, F, F, 2-Th, H), (M-4808, F, F, F, 2-Th, Cl), (M-4809, F, F, F, 2-Th, F), (M-4810, F, F, F, 2-Th, CF3), (M-4811, F, F, F, 2-Th, Br), (M-4812, F, F, F, 2-Th, CH3), (M-4813, F, F, F, 3-Th, H), (M-4814, F, F, F, 3-Th, Cl), (M-4815, F, F, F, 3-Th, F), (M-4816, F, F, F, 3-Th, CF3), (M-4817, F, F, F, 3-Th, Br), (M-4818, F, F, F, 3-Th, CH3), (M-4819, F, F, F, pyrrazol-2-yl, H), (M-4820, F, F, F, pyrrazol-2-yl, Cl), (M-4821, F, F, F, pyrrazol-2-yl, F), (M-4822, F, F, F, pyrrazol-2-yl, CF3), (M-4823, F, F, F, pyrrazol-2-yl, Br), (M-4824, F, F, F, pyrrazol-2-yl, CH3), (M-4825, F, F, F, pyrrazol-3-yl, H), (M-4826, F, F, F, pyrrazol-3-yl, Cl), (M-4827, F, F, F, pyrrazol-3-yl, F), (M-4828, F, F, F, pyrrazol-3-yl, CF3), (M-4829, F, F, F, pyrrazol-3-yl, Br), (M-4830, F, F, F, pyrrazol-3-yl, CH3), (M-4831, F, F, F, pyrimidin-2-yl, H), (M-4832, F, F, F, pyrimidin-2-yl, Cl), (M-4833, F, F, F, pyrimidin-2-yl, F), (M-4834, F, F, F, pyrimidin-2-yl, CF3), (M-4835, F, F, F, pyrimidin-2-yl, Br), (M-4836, F, F, F, pyrimidin-2-yl, CH3), (M-4837, F, F, F, pyrimidin-4-yl, H), (M-4838, F, F, F, pyrimidin-4-yl, Cl), (M-4839, F, F, F, pyrimidin-4-yl, F), (M-4840, F, F, F, pyrimidin-4-yl, CF3), (M-4841, F, F, F, pyrimidin-4-yl, Br), (M-4842, F, F, F, pyrimidin-4-yl, CH3), (M-4843, F, F, F, pyrimidin-5-yl, H), (M-4844, F, F, F, pyrimidin-5-yl, Cl), (M-4845, F, F, F, pyrimidin-5-yl, F), (M-4846, F, F, F, pyrimidin-5-yl, CF3), (M-4847, F, F, F, pyrimidin-5-yl, Br), (M-4848, F, F, F, pyrimidin-5-yl, CH3), (M-4849, F, F, F, HOOCCH2CH2CH2, H), (M-4850, F, F, F, HOOCCH2CH2CH2, Cl), (M-4851, F, F, F, HOOCCH2CH2CH2, F), (M-4852, F, F, F, HOOCCH2CH2CH2, CF3), (M-4853, F, F, F, HOOCCH2CH2CH2, Br), (M-4854, F, F, F, HOOCCH2CH2CH2, CH3), (M-4855, F, F, F, HOOCCH2CH2CH2CH2, H), (M-4856, F, F, F, HOOCCH2CH2CH2CH2, Cl), (M-4857, F, F, F, HOOCCH2CH2CH2CH2, F), (M-4858, F, F, F, HOOCCH2CH2CH2CH2, CF3), (M-4859, F, F, F, HOOCCH2CH2CH2CH2, Br), (M-4860, F, F, F, HOOCCH2CH2CH2CH2, CH3), (M-4861, F, F, F, (Me)2NCOCH2CH2CH2CH2, H), (M-4862, F, F, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-4863, F, F, F, (Me)2NCOCH2CH2CH2CH2, F), (M-4864, F, F, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-4865, F, F, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-4866, F, F, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-4867, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-4868, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-4869, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-4870, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-4871, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-4872, F, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-4873, F, F, F, MeOCH2, H), (M-4874, F, F, F, MeOCH2, Cl), (M-4875, F, F, F, MeOCH2, F), (M-4876, F, F, F, MeOCH2, CF3), (M-4877, F, F, F, MeOCH2, Br), (M-4878, F, F, F, MeOCH2, CH3), (M-4879, F, F, F, EtOCH2, H), (M-4880, F, F, F, EtOCH2, Cl), (M-4881, F, F, F, EtOCH2, F), (M-4882, F, F, F, EtOCH2, CF3), (M-4883, F, F, F, EtOCH2, Br), (M-4884, F, F, F, EtOCH2, CH3), (M-4885, F, F, F, EtOCH2CH2, H), (M-4886, F, F, F, EtOCH2CH2, Cl), (M-4887, F, F, F, EtOCH2CH2, F), (M-4888, F, F, F, EtOCH2CH2, CF3), (M-4889, F, F, F, EtOCH2CH2, Br), (M-4890, F, F, F, EtOCH2CH2, CH3), (M-4891, F, F, F, MeOCH2CH2OCH2CH2, H), (M-4892, F, F, F, MeOCH2CH2OCH2CH2, Cl), (M-4893, F, F, F, MeOCH2CH2OCH2CH2, F), (M-4894, F, F, F, MeOCH2CH2OCH2CH2, CF3), (M-4895, F, F, F, MeOCH2CH2OCH2CH2, Br), (M-4896, F, F, F, MeOCH2CH2OCH2CH2, CH3), (M-4897, F, F, F, MeOCH2CH2, H), (M-4898, F, F, F, MeOCH2CH2, Cl), (M-4899, F, F, F, MeOCH2CH2, F), (M-4900, F, F, F, MeOCH2CH2, CF3), (M-4901, F, F, F, MeOCH2CH2, Br), (M-4902, F, F, F, MeOCH2CH2, CH3), (M-4903, F, F, F, HOCH2, H), (M-4904, F, F, F, HOCH2, Cl), (M-4905, F, F, F, HOCH2, F), (M-4906, F, F, F, HOCH2, CF3), (M-4907, F, F, F, HOCH2, Br), (M-4908, F, F, F, HOCH2, CH3), (M-4909, F, F, F, HOCH2CH2, H), (M-4910, F, F, F, HOCH2CH2, Cl), (M-4911, F, F, F, HOCH2CH2, F), (M-4912, F, F, F, HOCH2CH2, CF3), (M-4913, F, F, F, HOCH2CH2, Br), (M-4914, F, F, F, HOCH2CH2, CH3), (M-4915, F, F, F, HOCH2CH2CH2, H), (M-4916, F, F, F, HOCH2CH2CH2, Cl), (M-4917, F, F, F, HOCH2CH2CH2, F), (M-4918, F, F, F, HOCH2CH2CH2, CF3), (M-4919, F, F, F, HOCH2CH2CH2, Br), (M-4920, F, F, F, HOCH2CH2CH2, CH3), (M-4921, F, F, F, HOCH2CH2CH2CH2, H), (M-4922, F, F, F, HOCH2CH2CH2CH2, Cl), (M-4923, F, F, F, HOCH2CH2CH2CH2, F), (M-4924, F, F, F, HOCH2CH2CH2CH2, CF3), (M-4925, F, F, F, HOCH2CH2CH2CH2, Br), (M-4926, F, F, F, HOCH2CH2CH2CH2, CH3), (M-4927, F, F, F, HOCH2CH2CH2CH2CH2H), (M-4928, F, F, F, HOCH2CH2CH2CH2CH2Cl), (M-4929, F, F, F, HOCH2CH2CH2CH2CH2, F), (M-4930, F, F, F, HOCH2CH2CH2CH2CH2CF3), (M-4931, F, F, F, HOCH2CH2CH2CH2CH2Br), (M-4932, F, F, F, HOCH2CH2CH2CH2CH2CH3), (M-4933, F, F, F, HOCH2CH2OCH2CH2, H), (M-4934, F, F, F, HOCH2CH2OCH2CH2, Cl), (M-4935, F, F, F, HOCH2CH2OCH2CH2, F), (M-4936, F, F, F, HOCH2CH2OCH2CH2, CF3), (M-4937, F, F, F, HOCH2CH2OCH2CH2, Br), (M-4938, F, F, F, HOCH2CH2OCH2CH2, CH3), (M-4939, F, F, F, (Me)2N, H), (M-4940, F, F, F, (Me)2N, Cl), (M-4941, F, F, F, (Me)2N, F), (M-4942, F, F, F, (Me)2N, CF3), (M-4943, F, F, F, (Me)2N, Br), (M-4944, F, F, F, (Me)2N, CH3), (M-4945, F, F, F, piperidin-4-yl-methyl, H), (M-4946, F, F, F, piperidin-4-yl-methyl, Cl), (M-4947, F, F, F, piperidin-4-yl-methyl, F), (M-4948, F, F, F, piperidin-4-yl-methyl, CF3), (M-4949, F, F, F, piperidin-4-yl-methyl, Br), (M-4950, F, F, F, piperidin-4-yl-methyl, CH3), (M-4951, F, F, F, cyclohexylmethyl, H), (M-4952, F, F, F, cyclohexylmethyl, Cl), (M-4953, F, F, F, cyclohexylmethyl, F), (M-4954, F, F, F, cyclohexylmethyl, CF3), (M-4955, F, F, F, cyclohexylmethyl, Br), (M-4956, F, F, F, cyclohexylmethyl, CH3), (M-4957, F, F, Cl, H, H), (M-4958, F, F, Cl, H, Cl), (M-4959, F, F, Cl, H, F), (M-4960, F, F, Cl, H, CF3), (M-4961, F, F, Cl, H, Br), (M-4962, F, F, Cl, H, CH3), (M-4963, F, F, Cl, F, H), (M-4964, F, F, Cl, F, Cl), (M-4965, F, F, Cl, F, F), (M-4966, F, F, Cl, F, CF3), (M-4967, F, F, Cl, F, Br), (M-4968, F, F, Cl, F, CH3), (M-4969, F, F, Cl, Cl, H), (M-4970, F, F, Cl, Cl, Cl), (M-4971, F, F, Cl, Cl, F), (M-4972, F, F, Cl, Cl, CF3), (M-4973, F, F, Cl, Cl, Br), (M-4974, F, F, Cl, Cl, CH3), (M-4975, F, F, Cl, CH3, H), (M-4976, F, F, Cl, CH3, Cl), (M-4977, F, F, Cl, CH3, F), (M-4978, F, F, Cl, CH3, CF3), (M-4979, F, F, Cl, CH3, Br), (M-4980, F, F, Cl, CH3, CH3), (M-4981, F, F, Cl, Et, H), (M-4982, F, F, Cl, Et, Cl), (M-4983, F, F, Cl, Et, F), (M-4984, F, F, Cl, Et, CF3), (M-4985, F, F, Cl, Et, Br), (M-4986, F, F, Cl, Et, CH3), (M-4987, F, F, Cl, Q-Pr, H), (M-4988, F, F, Cl, n-Pr, Cl), (M-4989, F, F, Cl, n-Pr, F), (M-4990, F, F, Cl, n-Pr, CF3), (M-4991, F, F, Cl, n-Pr, Br), (M-4992, F, F, Cl, n-Pr, CH3), (M-4993, F, F, Cl, c-Pr, H), (M-4994, F, F, Cl, c-Pr, Cl), (M-4995, F, F, Cl, c-Pr, F), (M-4996, F, F, Cl, c-Pr, CF3), (M-4997, F, F, Cl, c-Pr, Br), (M-4998, F, F, Cl, c-Pr, CH3), (M-4999, F, F, Cl, i-Pr, H), (M-5000, F, F, Cl, i-Pr, Cl), (M-5001, F, F, Cl, i-Pr, F), (M-5002, F, F, Cl, i-Pr, CF3), (M-5003, F, F, Cl, i-Pr, Br), (M-5004, F, F, Cl, i-Pr, CH3), (M-5005, F, F, Cl, n-Bu, H), (M-5006, F, F, Cl, n-Bu, Cl), (M-5007, F, F, Cl, n-Bu, F), (M-5008, F, F, Cl, n-Bu, CF3), (M-5009, F, F, Cl, n-Bu, Br), (M-5010, F, F, Cl, n-Bu, CH3), (M-5011, F, F, Cl, i-Bu, H), (M-5012, F, F, Cl, i-Bu, Cl), (M-5013, F, F, Cl, i-Bu, F), (M-5014, F, F, Cl, i-Bu, CF3), (M-5015, F, F, Cl, i-Bu, Br), (M-5016, F, F, Cl, i-Bu, CH3), (M-5017, F, F, Cl, sec-Bu, H), (M-5018, F, F, Cl, sec-Bu, Cl), (M-5019, F, F, Cl, sec-Bu, F), (M-5020, F, F, Cl, sec-Bu, CF3), (M-5021, F, F, Cl, sec-Bu, Br), (M-5022, F, F, Cl, sec-Bu, CH3), (M-5023, F, F, Cl, n-Pen, H), (M-5024, F, F, Cl, n-Pen, Cl), (M-5025, F, F, Cl, n-Pen, F), (M-5026, F, F, Cl, n-Pen, CF3), (M-5027, F, F, Cl, n-Pen, Br), (M-5028, F, F, Cl, n-Pen, CH3), (M-5029, F, F, Cl, c-Pen, H), (M-5030, F, F, Cl, c-Pen, Cl), (M-5031, F, F, Cl, c-Pen, F), (M-5032, F, F, Cl, c-Pen, CF3), (M-5033, F, F, Cl, c-Pen, Br), (M-5034, F, F, Cl, c-Pen, CH3), (M-5035, F, F, Cl, n-Hex, H), (M-5036, F, F, Cl, n-Hex, Cl), (M-5037, F, F, Cl, n-Hex, F), (M-5038, F, F, Cl, n-Hex, CF3), (M-5039, F, F, Cl, n-Hex, Br), (M-5040, F, F, Cl, n-Hex, CH3), (M-5041, F, F, Cl, c-Hex, H), (M-5042, F, F, Cl, c-Hex, Cl), (M-5043, F, F, Cl, c-Hex, F), (M-5044, F, F, Cl, c-Hex, CF3), (M-5045, F, F, Cl, c-Hex, Br), (M-5046, F, F, Cl, c-Hex, CH3), (M-5047, F, F, Cl, OH, H), (M-5048, F, F, Cl, OH, Cl), (M-5049, F, F, Cl, OH, F), (M-5050, F, F, Cl, OH, CF3), (M-5051, F, F, Cl, OH, Br), (M-5052, F, F, Cl, OH, CH3), (M-5053, F, F, Cl, EtO, H), (M-5054, F, F, Cl, EtO, Cl), (M-5055, F, F, Cl, EtO, F), (M-5056, F, F, Cl, EtO, CF3), (M-5057, F, F, Cl, EtO, Br), (M-5058, F, F, Cl, EtO, CH3), (M-5059, F, F, Cl, n-PrO, H), (M-5060, F, F, Cl, n-PrO, Cl), (M-5061, F, F, Cl, n-PrO, F), (M-5062, F, F, Cl, n-PrO, CF3), (M-5063, F, F, Cl, n-PrO, Br), (M-5064, F, F, Cl, n-PrO, CH3), (M-5065, F, F, Cl, PhO, H), (M-5066, F, F, Cl, PhO, Cl), (M-5067, F, F, Cl, PhO, F), (M-5068, F, F, Cl, PhO, CF3), (M-5069, F, F, Cl, PhO, Br), (M-5070, F, F, Cl, PhO, CH3), (M-5071, F, F, Cl, BnO, H), (M-5072, F, F, Cl, BnO, Cl), (M-5073, F, F, Cl, BnO, F), (M-5074, F, F, Cl, BnO, CF3), (M-5075, F, F, Cl, BnO, Br), (M-5076, F, F, Cl, BnO, CH3), (M-5077, F, F, Cl, PhCH2CH2O, H), (M-5078, F, F, Cl, PhCH2CH2O, Cl), (M-5079, F, F, Cl, PhCH2CH2O, F), (M-5080, F, F, Cl, PhCH2CH2O, CF3), (M-5081, F, F, Cl, PhCH2CH2O, Br), (M-5082, F, F, Cl, PhCH2CH2O, CH3), (M-5083, F, F, Cl, CF3O, H), (M-5084, F, F, Cl, CF3O, Cl), (M-5085, F, F, Cl, CF3O, F), (M-5086, F, F, Cl, CF3O, CF3), (M-5087, F, F, Cl, CF3O, Br), (M-5088, F, F, Cl, CF3O, CH3), (M-5089, F, F, Cl, Ph, H), (M-5090, F, F, Cl, Ph, Cl), (M-5091, F, F, Cl, Ph, F), (M-5092, F, F, Cl, Ph, CF3), (M-5093, F, F, Cl, Ph, Br), (M-5094, F, F, Cl, Ph, CH3), (M-5095, F, F, Cl, 4-F-Ph, H), (M-5096, F, F, Cl, 4-F-Ph, Cl), (M-5097, F, F, Cl, 4-F-Ph, F, (M-5098, F, F, Cl, 4-F-Ph, CF3), (M-5099, F, F, Cl, 4-F-Ph, Br), (M-5100, F, F, Cl, 4-F-Ph, CH3), (M-5101, F, F, Cl, 4-CF3-Ph, H), (M-5102, F, F, Cl, 4-CF3-Ph, Cl), (M-5103, F, F, Cl, 4-CF3-Ph, F), (M-5104, F, F, Cl, 4-CF3-Ph, CF3), (M-5105, F, F, Cl, 4-CF3-Ph, Br), (M-5106, F, F, Cl, 4-CF3-Ph, CH3), (M-5107, F, F, Cl, 4-(Me)2N-Ph, H), (M-5108, F, F, Cl, 4-<Me)2N-Ph, Cl), (M-5109, F, F, Cl, 4-(Me)2N-Ph, F), (M-5110, F, F, Cl, 4-(Me)2N-Ph, CF3), (M-5111, F, F, Cl, 4-(Me)2N-Ph, Br), (M-5112, F, F, Cl, 4-(Me)2N-Ph, CH3), (M-5113, F, F, Cl, 4-OH-Ph, H), (M-5114, F, F, Cl, 4-OH-Ph, Cl), (M-5115, F, F, Cl, 4-OH-Ph, F), (M-5116, F, F, Cl, 4-OH-Ph, CF3), (M-5117, F, F, Cl, 4-OH-Ph, Br), (M-5118, F, F, Cl, 4-OH-Ph, CH3), (M-5119, F, F, Cl, 3,4-di-F-Ph, H), (M-5120, F, F, Cl, 3,4-di-F-Ph, Cl), (M-5121, F, F, Cl, 3,4-di-F-Ph, F), (M-5122, F, F, Cl, 3,4-di-F-Ph, CF3), (M-5123, F, F, Cl, 3,4-di-F-Ph, Br), (M-5124, F, F, Cl, 3,4-di-F-Ph, CH3), (M-6125, F, F, Cl, 4-COOH-Ph, H), (M-5126, F, F, Cl, 4-COOH-Ph, Cl), (M-5127, F, F, Cl, 4-COOH-Ph, F), (M-5128, F, F, Cl, 4-COOH-Ph, CF3), (M-5129, F, F, Cl, 4-COOH-Ph, Br), (M-5130, F, F, Cl, 4-COOH-Ph, CH3), (M-5131, F, F, Cl, Bn, H), (M-5132, F, F, Cl, Bn, Cl), (M-5133, F, F, Cl, Bn, F), (M-5134, F, F, Cl, Bn, CF3), (M-5135, F, F, Cl, Bn, Br), (M-5136, F, F, Cl, Bn, CH3), (M-5137, F, F, Cl, 4-F-Bn, H), (M-5138, F, F, Cl, 4-F-Bn, Cl), (M-5139, F, F, Cl, 4-F-Bn, F), (M-5140, F, F, Cl, 4-F-Bn, CF3), (M-5141, F, F, Cl, 4-F-Bn, Br), (M-5142, F, F, Cl, 4-F-Bn, CH3), (M-5143, F, F, Cl, 2-Py, H), (M-5144, F, F, Cl, 2-Py, Cl), (M-5145, F, F, Cl, 2-Py, F), (M-5146, F, F, Cl, 2-Py, CF3), (M-5147, F, F, Cl, 2-Py, Br), (M-5148, F, F, Cl, 2-Py, CH3), (M-5149, F, F, Cl, 3-Py, H), (M-5150, F, F, Cl, 3-Py, Cl), (M-5151, F, F, Cl, 3-Py, F), (M-5152, F, F, Cl, 3-Py, CF3), (M-5153, F, F, Cl, 3-Py, Br), (M-5154, F, F, Cl, 3-Py, CH3), (M-5155, F, F, Cl, 4-Py, H), (M-5156, F, F, Cl, 4-Py, Cl), (M-5157, F, F, Cl, 4-Py, F), (M-5158, F, F, Cl, 4-Py, CF3), (M-5159, F, F, Cl, 4-Py, Br), (M-5160, F, F, Cl, 4-Py, CH3), (M-5161, F, F, Cl, 2-Th, H), (M-5162, F, F, Cl, 2-Th, Cl), (M-5163, F, F, Cl, 2-Th, F), (M-5164, F, F, Cl, 2-Th, CF3), (M-5165, F, F, Cl, 2-Th, Br), (M-5166, F, F, Cl, 2-Th, CH3), (M-5167, F, F, Cl, 3-Th, H), (M-5168, F, F, Cl, 3-Th, Cl), (M-5169, F, F, Cl, 3-Th, F), (M-6170, F, F, Cl, 3-Th, CF3), (M-5171, F, F, Cl, 3-Th, Br), (M-5172, F, F, Cl, 3-Th, CH3), (M-5173, F, F, Cl, pyrrazol-2-yl, H), (M-5174, F, F, Cl, pyrrazol-2-yl, Cl), (M-5175, F, F, Cl, pyrrazol-2-yl, F), (M-5176, F, F, Cl, pyrrazol-2-yl, CF3), (M-5177, F, F, Cl, pyrrazol-2-yl, Br), (M-5178, F, F, Cl, pyrrazol-2-yl, CH3), (M-5179, F, F, Cl, pyrrazol-3-yl, H), (M-5180, F, F, Cl, pyrrazol-3-yl, Cl), (M-5181, F, F, Cl, pyrrazol-3-yl, F), (M-5182, F, F, Cl, pyrrazol-3-yl, CF3), (M-5183, F, F, Cl, pyrrazol-3-yl, Br), (M-5184, F, F, Cl, pyrrazol-3-yl, CH3), (M-5185, F, F, Cl, pyrimidin-2-yl, H), (M-5186, F, F, Cl, pyrimidin-2-yl, Cl), (M-5187, F, F, Cl, pyrimidin-2-yl, F), (M-5188, F, F, Cl, pyrimidin-2-yl, CF3), (M-5189, F, F, Cl, pyrimidin-2-yl, Br), (M-5190, F, F, Cl, pyrimidin-2-yl, CH3), (M-5191, F, F, Cl, pyrimidin-4-yl, H), (M-5192, F, F, Cl, pyrimidin-4-yl, Cl), (M-5193, F, F, Cl, pyrimidin-4-yl, F), (M-5194, F, F, Cl, pyrimidin-4-yl, CF3), (M-5195, F, F, Cl, pyrimidin-4-yl, Br), (M-5196, F, F, Cl, pyrimidin-4-yl, CH3), (M-5197, F, F, Cl, pyrimidin-5-yl, H), (M-5198, F, F, Cl, pyrimidin-5-yl, Cl), (M-5199, F, F, Cl, pyrimidin-5-yl, F), (M-5200, F, F, Cl, pyrimidin-5-yl, CF3), (M-5201, F, F, Cl, pyrimidin-5-yl, Br), (M-5202, F, F, Cl, pyrimidin-5-yl, CH3), (M-5203, F, F, Cl, HOOCCH2CH2CH2, H), (M-5204, F, F, Cl, HOOCCH2CH2CH2, Cl), (M-5205, F, F, Cl, HOOCCH2CH2CH2, F), (M-5206, F, F, Cl, HOOCCH2CH2CH2, CF3), (M-5207, F, F, Cl, HOOCCH2CH2CH2, Br), (M-5208, F, F, Cl, HOOCCH2CH2CH2, CH3), (M-5209, F, F, Cl, HOOCCH2CH26H2CH2, H), (M-5210, F, F, Cl, HOOCCH2CH2CH2CH2, Cl), (M-5211, F, F, Cl, HOOCCH2CH2CH2CH2, F), (M-5212, F, F, Cl, HOOCCH2CH2CH2CH2, CF3), (M-5213, F, F, Cl, HOOCCH2CH2CH2CH2, Br), (M-5214, F, F, Cl, HOOCCH2CH2CH2CH2, CH3), (M-5215, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-5216, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-5217, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-5218, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-5219, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-5220, F, F, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-5221, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-5222, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-5223, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-5224, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2CF3), (M-5225, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-5226, F, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-5227, F, F, Cl, MeOCH2, H), (M-5228, F, F, Cl, MeOCH2, Cl), (M-5229, F, F, Cl, MeOCH2, F), (M-5230, F, F, Cl, MeOCH2, CF3), (M-5231, F, F, Cl, MeOCH2, Br), (M-5232, F, F, Cl, MeOCH2, CH3), (M-5233, F, F, Cl, EtOCH2, H), (M-5234, F, F, Cl, EtOCH2, Cl), (M-5235, F, F, Cl, EtOCH2, F), (M-5236, F, F, Cl, EtOCH2, CF3), (M-5237, F, F, Cl, EtOCH2, Br), (M-5238, F, F, Cl, EtOCH2, CH3), (M-5239, F, F, Cl, EtOCH2CH2, H), (M-5240, F, F, Cl, EtOCH2CH2, Cl), (M-5241, F, F, Cl, EtOCH2CH2, F), (M-5242, F, F, Cl, EtOCH2CH2, CF3), (M-5243, F, F, Cl, EtOCH2CH2, Br), (M-5244, F, F, Cl, EtOCH2CH2, CH3), (M-5245, F, F, Cl, MeOCH2CH2OCH2CH2, H), (M-5246, F, F, Cl, MeOCH2CH2OCH2CH2, Cl), (M-5247, F, F, Cl, MeOCH2CH2OCH2CH2, F), (M-5248, F, F, Cl, MeOCH2CH2OCH2CH2, CF3), (M-5249, F, F, Cl, MeOCH2CH2OCH2CH2, Br), (M-5250, F, F, Cl, MeOCH2CH2OCH2CH2, CH3), (M-5251, F, F, Cl, MeOCH2CH2, H), (M-5252, F, F, Cl, MeOCH2CH2, Cl), (M-5253, F, F, Cl, MeOCH2CH2, F), (M-5254, F, F, Cl, MeOCH2CH2, CF3), (M-5255, F, F, Cl, MeOCH2CH2, Br), (M-5256, F, F, Cl, MeOCH2CH2, CH3), (M-5257, F, F, Cl, HOCH2, H), (M-5258, F, F, Cl, HOCH2, Cl), (M-5259, F, F, Cl, HOCH2, F), (M-5260, F, F, Cl, HOCH2, CF3), (M-5261, F, F, Cl, HOCH2, Br), (M-5262, F, F, Cl, HOCH2, CH3), (M-5263, F, F, Cl, HOCH2CH2, H), (M-5264, F, F, Cl, HOCH2CH2, Cl), (M-5265, F, F, Cl, HOCH2CH2, F), (M-5266, F, F, Cl, HOCH2CH2, CF3), (M-5267, F, F, Cl, HOCH2CH2, Br), (M-5268, F, F, Cl, HOCH2CH2, CH3), (M-5269, F, F, Cl, HOCH2CH2CH2, H), (M-5270, F, F, Cl, HOCH2CH2CH2, Cl), (M-5271, F, F, Cl HOCH2CH2CH2, F), (M-5272, F, F, Cl, HOCH2CH2CH2, CF3), (M-5273, F, F, Cl, HOCH2CH2CH2, Br), (M-5274, F, F, Cl, HOCH2CH2CH2, CH3), (M-5275, F, F, Cl, HOCH2CH2CH2CH2, H), (M-5276, F, F, Cl, HOCH2CH2CH2CH2, Cl), (M-5277, F, F, Cl, HOCH2CH2CH2CH2, F), (M-5278, F, F, Cl, HOCH2CH2CH2CH2, CF3), (M-5279, F, F, Cl, HOCH2CH2CH2CH2, Br), (M-5280, F, F, Cl, HOCH2CH1CH2CH2, CH3), (M-5281, F, F, Cl, HOCH2CH2CH2CH2CH2, H), (M-5282, F, F, Cl, HOCH2CH2CH2CH2CH2, Cl), (M-5283, F, F, Cl, HOCH2CH2CH2CH2CH2, F), (M-5284, F, F, Cl, HOCH2CH2CH2CH2CH2CF3), (M-5285, F, F, Cl, HOCH2CH2CH2CH2CH2Br), (M-5286, F, F, Cl, HOCH2CH2CH2CH2CH2CH3), (M-5287, F, F, Cl, HOCH2CH2OCH2CH2, H), (M-5288, F, F, Cl, HOCH2CH2OCH2CH2, Cl), (M-5289, F, F, Cl, HOCH2CH2OCH2CH2, F), (M-5290, F, F, Cl, HOCH2CH2OCH2CH2, CF3), (M-5291, F, F, Cl, HOCH2CH2OCH2CH2, Br), (M-5292, F, F, Cl, HOCH2CH2OCH2CH2, CH3), (M-5293, F, F, Cl, (Me)2N, H), (M-5294, F, F, Cl, (Me)2N, Cl), (M-5295, F, F, Cl, (Me)2N, F), (M-5296, F, F, Cl, (Me)2N, CF3), (M-5297, F, F, Cl, (Me)3N, Br), (M-5298, F, F, Cl, (Me)2N, CH3), (M-5299, F, F, Cl, piperidin-4-yl-methyl, H), (M-5300, F, F, Cl, piperidin-4-yl-methyl, Cl), (M-5301, F, F, Cl, piperidin-4-yl-methyl, F), (M-5302, F, F, Cl, piperidin-4-yl-methyl, CF3), (M-5303, F, F, Cl, piperidin-4-yl-methyl, Br), (M-5304, F, F, Cl, piperidin-4-yl-methyl, CH3), (M-5305, F, F, Cl, cyclohexylmethyl, H), (M-5306, F, F, Cl, cyclohexylmethyl, Cl), (M-5307, F, F, Cl, cyclohexylmethyl, F), (M-5308, F, F, Cl, cyclohexylmethyl, CF3), (M-5309, F, F, Cl, cyclohexylmethyl, Br), (M-5310, F, F, Cl, cyclohexylmethyl, CH3), (M-53H, F, CH3, H, H, H), (M-5312, F, CH3, H, H, Cl), (M-5313, F, CH3, H, H, F), (M-5314, F, CH3, H, H, CF3), (M-5315, F, CH3, H, H, Br), (M-5316, F, CH3, H, H, CH3), (M-5317, F, CH3, H, F, H), (M-5318, F, CH3, H, F, Cl), (M-5319, F, CH3, H, F, F), (M-5320, F, CH3, H, F, CF3), (M-5321, F, CH3, H, F, Br), (M-5322, F, CH3, H, F, CH3), (M-5323, F, CH3, H, Cl, H), (M-5324, F, CH3, H, Cl, Cl), (M-5325, F, CH3, H, Cl, F), (M-5326, F, CH3, H, Cl, CF3), (M-5327, F, CH3, H, Cl, Br), (M-5328, F, CH3, H, Cl, CH3), (M-5329, F, CH3, H, CH3, H), (M-5330, F, CH3, H, CH3, Cl), (M-5331, F, CH3, H, CH3, F), (M-5332, F, CH3, H, CH3, CF3), (M-5333, F, CH3, H, CH3, Br), (M-5334, F, CH3, H, CH3, CH3), (M-5335, F, CH3, H, Et, H), (M-5336, F, CH3, H, Et, Cl), (M-5337, F, CH3, H, Et, F), (M-5338, F, CH3, H, Et, CF3), (M-5339, F, CH3, H, Et, Br), (M-5340, F, CH3, H, Et, CH3), (M-5341, F, CH3, H, n-Pr, H), (M-5342, F, CH3, H, n-Pr, Cl), (M-5343, F, CH3, H, n-Pr, F), (M-5344, P, CH3, H, n-Pr, CF3), (M-5345, F, CH3, H, n-Pr, Br), (M-5346, F, CH3, H, n-Pr, CH3), (M-5347, F, CH3, H, c-Pr, H), (M-5348, F, CH3, H, c-Pr, Cl), (M-5349, F, CH3, H, c-Pr, F), (M-5350, F, CH3, H, c-Pr, CF3), (M-5351, F, CH3, H, c-Pr, Br), (M-5352, F, CH3, H, c-Pr, CH3), (M-5353, F, CH3, H, i-Pr, H), (M-5354, F, CH3, H, i-Pr, Cl), (M-5355, F, CH3, H, i-Pr, F), (M-5356, F, CH3, H, i-Pr, CF3), (M-5357, F, CH3, H, i-Pr, Br), (M-5358, F, CH3, H, i-Pr, CH3), (M-5359, F, CH3, H, n-Bu, H), (M-5360, F, CH3, H, n-Bu, Cl), (M-5361, F, CH3, H, n-Bu, F), (M-5362, F, CH3, H, n-Bu, CF3), (M-5363, F, CH3, H, n-Bu, Br), (M-5364, F, CH3, H, n-Bu, CH3), (M-5365, F, CH3, H, i-Bu, H), (M-5366, F, CH3, H, i-Bu, Cl), (M-5367, F, CH3, H, i-Bu, F), (M-5368, F, CH3, H, i-Bu, CF3), (M-5369, F, CH3, H, i-Bu, Br), (M-5370, F, CH3, H, i-Bu, CH3), (M-5371, F, CH3, H, sec-Bu, H), (M-5372, F, CH3, H, sec-Bu, Cl), (M-5373, F, CH3, H, sec-Bu, F), (M-5374, F, CH3, H, sec-Bu, CF3), (M-5375, F, CH3, H, sec-Bu, Br), (M-5376, F, CH3, H, sec-Bu, CH3), (M-5377, F, CH3, H, n-Pen, H), (M-5378, F, CH3, H, n-Pen, Cl), (M-5379, F, CH3, H, n-Pen, F), (M-5380, F, CH3, H, n-Pen, CF3), (M-5381, F, CH3, H, n-Pen, Br), (M-5382, F, CH3, H, n-Pen, CH3), (M-5383, F, CH3, H, c-Pen, H), (M-5384, F, CH3, H, c-Pen, Cl), (M-5385, F, CH3, H, c-Pen, F), (M-5386, F, CH3, H, c-Pen, CF3), (M-5387, F, CH3, H, c-Pen, Br), (M-5388, F, CH3, H, c-Pen, CH3), (M-5389, F, CH3, H, n-Hex, H), (M-5390, F, CH3, H, n-Hex, Cl), (M-5391, F, CH3, H, n-Hex, F), (M-5392, F, CH3, H, n-Hex, CF3), (M-5393, F, CH3, H, n-Hex, Br), (M-5394, F, CH3, H, n-Hex, CH3), (M-5395, F, CH3, H, c-Hex, H), (M-5396, F, CH3, H, c-Hex, Cl), (M-5397, F, CH3, H, c-Hex, F), (M-5398, F, CH3, H, c-Hex, CF3), (M-5399, F, CH3, H, c-Hex, Br), (M-5400, F, CH3, H, c-Hex, CH3), (M-5401, F, CH3, H, OH, H), (M-5402, F, CH3, H, OH, Cl), (M-5403, F, CH3, H, OH, F), (M-5404, F, CH3, H, OH, CF3), (M-5405, F, CH3, H, OH, Br), (M-5406, F, CH3, H, OH, CH3), (M-5407, F, CH3, H, EtO, H), (M-5408, F, CH3, H, EtO, Cl), (M-5409, F, CH3, H, EtO, F), (M-5410, F, CH3, H, EtO, CF3), (M-5411, F, CH3, H, EtO, Br), (M-5412, F, CH3, H, EtO, CH3), (M-5413, F, CH3, H, n-PrO, H), (M-5414, F, CH3, H, n-PrO, Cl), (M-5415, F, CH3, H, n-PrO, F), (M-5416, F, CH3, H, n-PrO, CF3), (M-5417, F, CH3, H, n-PrO, Br), (M-5418, F, CH3, H, n-PrO, CH3), (M-5419, F, CH3, H, PhO, H), (M-5420, F, CH3, H, PhO, Cl), (M-5421, F, CH3, H, PhO, F), (M-5422, F, CH3, H, PhO, CF3), (M-5423, F, CH3, H, PhO, Br), (M-5424, F, CH3, H, PhO, CH3), (M-5425, F, CH3, H, BnO, H), (M-5426, F, CH3, H, BnO, Cl), (M-5427, F, CH3, H, BnO, F), (M-5428, F, CH3, H, BnO, CF3), (M-5429, F, CH3, H, BnO, Br), (M-5430, F, CH3, H, BnO, CH3), (M-5431, F, CH3, H, PhCH2CH2O, H), (M-5432, F, CH3, H, PhCH2CH2O, Cl), (M-5433, F, CH3, H, PhCH2CH2O, F), (M-5434, F, CH3, H, PhCH2CH2O, CF3), (M-5435, F, CH3, H, PhCH2CH2O, Br), (M-5436, F, CH3, H, PhCH2CH2O, CH3), (M-5437, F, CH3, H, CF3O, H), (M-5438, F, CH3, H, CF3O, Cl), (M-5439, F, CH3, H, CF3O, F), (M-5440, F, CH3, H, CF3O, CF3), (M-5441, F, CH3, H, CF3O, Br), (M-5442, F, CH3, H, CF3O, CH3), (M-5443, F, CH3, H, Ph, H), (M-5444, F, CH3, H, Ph, Cl), (M-5445, F, CH3, H, Ph, F), (M-5446, F, CH3, H, Ph, CF3), (M-5447, F, CH3, H, Ph, Br), (M-5448, F, CH3, H, Ph, CH3), (M-5449, F, CH3, H, 4-F-Ph, H), (M-5450, F, CH3, H, 4-F-Ph, Cl), (M-5451, F, CH3, H, 4-F-Ph, F), (M-5452, F, CH3, H, 4-F-Ph, CF3), (M-5453, F, CH3, H, 4-F-Ph, Br), (M-5454, F, CH3, H, 4-F-Ph, CH3), (M-5455, F, CH3, H, 4-CF3-Ph, H), (M-5456, F, CH3, H, 4-CF3-Ph, Cl), (M-5457, F, CH3, H, 4-CF3-Ph, F), (M-5458, F, CH3, H, 4-CF3-Ph, CF3), (M-5459, F, CH3, H, 4-CF3-Ph, Br), (M-5460, F, CH3, H, 4-CF3-Ph, CH3), (M-5461, F, CH3, H, 4-(Me)2N-Ph, H), (M-5462, F, CH3, H, 4-(Me)2N-Ph, Cl), (M-5463, F, CH3, H, 4-(Me)2N-Ph, F), (M-5464, F, CH3, H, 4-(Me)2N-Ph, CF3), (M-5465, F, CH3, H, 4-(Me)2N-Ph, Br), (M-5466, F, CH3, H, 4-(Me)2N-Ph, CH3), (M-5467, F, CH3, H, 4-OH-Ph, H), (M-5468, F, CH3, H, 4-OH-Ph, Cl), (M-5469, F, CH3, H, 4-OH-Ph, F), (M-5470, F, CH3, H, 4-OH-Ph, CF3), (M-5471, F, CH3, H, 4-OH-Ph, Br), (M-5472, F, CH3, H, 4-OH-Ph, CH3), (M-5473, F, CH3, H, 3,4-di-F-Ph, H), (M-5474, F, CH3, H, 3,4-di-F-Ph, Cl), (M-5475, F, CH3, H, 3,4-di-F-Ph, F), (M-5476, F, CH3, H, 3,4-di-F-Ph, CF3), (M-5477, F, CH3, H, 3,4-di-F-Ph, Br), (M-5478, F, CH3, H, 3,4-di-F-Ph, CH3), (M-5479, F, CH3, H, 4-COOH-Ph, H), (M-5480, F, CH3, H, 4-COOH-Ph, Cl), (M-5481, F, CH3, H, 4-COOH-Ph, F), (M-5482, F, CH3, H, 4-COOH-Ph, CF3), (M-5483, F, CH3, H, 4-COOH-Ph, Br), (M-5484, F, CH3, H, 4-COOH-Ph, CH3), (M-5485, F, CH3, H, Bn, H), (M-5486, F, CH3, H, Bn, Cl), (M-5487, F, CH3, H, Bn, F), (M-5488, F, CH3, H, Bn, CF3), (M-5489, F, CH3, H, Bn, Br), (M-5490, F, CH3, H, Bn, CH3), (M-5491, F, CH3, H, 4-F-Bn, H), (M-5492, F, CH3, H, 4-F-Bn, Cl), (M-5493, F, CH3, H, 4-F-Bn, F), (M-5494, F, CH3, H, 4-F-Bn, CF3), (M-5495, F, CH3, H, 4-F-Bu, Br), (M-5496, F, CH3, H, 4-F-Bn, CH3), (M-5497, F, CH3, H, 2-Py, H), (M-5498, F, CH3, H, 2-Py, Cl), (M-5499, F, CH3, H, 2-Py, F), (M-5500, F, CH3, H, 2-Py, CF3), (M-5501, F, CH3, H, 2-Py, Br), (M-5502, F, CH3, H, 2-Py, CH3), (M-5503, F, CH3, H, 3-Py, H), (M-5504, F, CH3, H, 3-Py, Cl), (M-5505, F, CH3, H, 3-Py, F), (M-5506, F, CH3, H, 3-Py, CF3), (M-5507, F, CH3, H, 3-Py, Br), (M-5508, F, CH3, H, 3-Py, CH3), (M-5509, F, CH3, H, 4-Py, H), (M-5510, F, CH3, H, 4-Py, Cl), (M-5511, F, CH3, H, 4-Py, F), (M-5512, F, CH3, H, 4-Py, CF3), (M-5513, F, CH3, H, 4-Py, Br), (M-5514, F, CH3, H, 4-Py, CH3), (M-5515, F, CH3, H, 2-Th, H), (M-5516, F, CH3, H, 2-Th, Cl), (M-5517, F, CH3, H, 2-Th, F), (M-5518, F, CH3, H, 2-Th, CF3), (M-5519, F, CH3, H, 2-Th, Br), (M-5520, F, CH3, H, 2-Th, CH3), (M-5521, F, CH3, H, 3-Th, H), (M-5522, F, CH3, H, 3-Th, Cl), (M-5523, F, CH3, H, 3-Th, F), (M-5524, F, CH3, H, 3-Th, CF3), (M-5525, F, CH3, H, 3-Th, Br), (M-5526, F, CH3, H, 3-Th, CH3), (M-5527, F, CH3, H, pyrrazol-2-yl, H), (M- 5528, F, CH3, H, pyrrazol-2-yl, Cl), (M-5529, F, CH3, H, pyrrazol-2-yl, F), (M-5530, F, CH3, H, pyrrazol-2-yl, CF3), (M-5531, F, CH3, H, pyrrazol-2-yl, Br), (M-5532, F, CH3, H, pyrrazol-2-yl, CH3), (M-5533, F, CH3, H, pyrrazol-3-yl, H), (M-5534, F, CH3, H, pyrrazol-3-yl, Cl), (M-5535, F, CH3, H, pyrrazol-3-yl, F), (M-5536, F, CH3, H, pyrrazol-3-yl, CF3), (M-5537, F, CH3, H, pyrrazol-3-yl, Br), (M-5538, F, CH3, H, pyrrazol-3-yl, CH3), (M-5539, F, CH3, H, pyrimidin-2-yl, H), (M-5540, F, CH3, H, pyrimidin-2-yl, Cl), (M-5541, F, CH3, H, pyrimidin-2-yl, F), (M-5542, F, CH3, H, pyrimidin-2-yl, CF3), (M-5543, F, CH3, H, pyrimidin-2-yl, Br), (M-5544, F, CH3, H, pyrimidin-2-yl, CH3), (M-5545, F, CH3, H, pyrimidin-4-yl, H), (M-5546, F, CH3, H, pyrimidin-4-yl, Cl), (M-5547, F, CH3, H, pyrimidin-4-yl, F), (M-5548, F, CH3, H, pyrimidin-4-yl, CF3), (M-5549, F, CH3, H, pyrimidin-4-yl, Br), (M-5550, F, CH3, H, pyrimidin-4-yl, CH3), (M-5551, F, CH3, H, pyrimidin-5-yl, H), (M-5552, F, CH3, H, pyrimidin-5-yl, Cl), (M-5553, F, CH3, H, pyrimidin-5-yl, F), (M-5554, F, CH3, H, pyrimidin-5-yl, CF3), (M-5555, F, CH3, H, pyrimidin-5-yl, Br), (M-5556, F, CH3, H, pyrimidin-5-yl, CH3), (M-5557, F, CH3, H, HOOCCH2CH2CH2, H), (M-5558, F, CH3, H, HOOCCH2CH2CH2Cl), (M-5559, F, CH3, H, HOOCCH2CH2CH2, F), (M-5560, F, CH3, H, HOOCCH2CH2CH2, CF3), (M-5561, F, CH3, H, HOOCCH2CH2CH2, Br), (M-5562, F, CH3, H, HOOCCH2CH2CH2, CH3), (M-5563, F, CH3, H, HOOCCH2CH2CH2CH2, H), (M-5564, F, CH3, H, HOOCCH2CH2CH2CH2, Cl), (M-5565, F, CH3, H, HOOCCH2CH2CH2CH2, F), (M-5566, F, CH3, H, HOOCCH2CH2CH2CH2, CF3), (M-5567, F, CH3, H, HOOCCH2CH2CH2CH2, Br), (M-5568, F, CH3, H, HOOCCH2CH2CH2CH2, CH3), (M-5569, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, H), (M-5570, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-5571, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, F), (M-5572, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CF3), (M-5573, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-5574, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-6575, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-5676, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-5577, F, CH3, H, (Me)2NCOCH2CH2CH2CH2, CH3, F), (M-5578, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2CF3), (M-5579, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-5580, F, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2CH3), (M-5581, F, CH3, H, MeOCH2, H), (M-5582, F, CH3, H, MeOCH2, Cl), (M-5583, F, CH3, H, MeOCH2, F), (M-5584, F, CH3, H, MeOCH2, CH3), (M-5585, F, CH3, H, MeOCH2, Br), (M-5586, F, CH3, H, MeOCH2, CH3), (M-5587, F, CH3, H, EtOCH2, H), (M-5588, F, CH3, H, EtOCH2, Cl), (M-5589, F, CH3, H, EtOCH2, F), (M-5590, F, CH3, H, EtOCH2, CF3), (M-5591, F, CH3, H, EtOCH2, Br), (M-5592, F, CH3, H, EtOCH2, CH3), (M-5593, F, CH3, H, EtOCH2CH2, H), (M-5594, F, CH3, H, EtOCH2CH2, Cl), (M-5595, F, CH3, H, EtOCH2CH2, F), (M-5596, F, CH3, H, EtOCH2CH2, CF3), (M-5597, F, CH3, H, EtOCH2CH2, Br), (M-5598, F, CH3, H, EtOCH2CH2, CH3), (M-5599, F, CH3, H, MeOCH2CH2OCH2CH2, H), (M-5600, F, CH3, H, MeOCH2CH2OCH2CH2, Cl), (M-5601, F, CH3, H, MeOCH2CH2OCH2CH2, F), (M-5602, F, CH3, H, MeOCH2CH2OCH2CH2, CF3), (M-5603, F, CH3, H, MeOCH2CH2OCH2CH2, Br), (M-5604, F, CH3, H, MeOCH2CH2OCH2CH2, CH3), (M-5605, F, CH3, H, MeOCH2CH2, H), (M-5606, F, CH3, H, MeOCH2CH2, Cl), (M-5607, F, CH3, H, MeOCH2CH2, F), (M-5608, F, CH3, H, MeOCH2CH2, CF3), (M-5609, F, CH3, H, MeOCH2CH2, Br), (M-5610, F, CH3, H, MeOCH2CH2, CH3), (M-5611, F, CH3, H, HOCH2, H), (M-5612, F, CH3, H, HOCH2, Cl), (M-5613, F, CH3, H, HOCH2, F), (M-5614, F, CH3, H, HOCH2, CF3), (M-5615, F, CH3, H, HOCH2, Br), (M-5616, F, CH3, H, HOCH2, CH3), (M-5617, F, CH3, H, HOCH2CH2, H), (M-5618, F, CH3, H, HOCH2CH2, Cl), (M-5619, F, CH3, H, HOCH2CH2, F), (M-5620, F, CH3, H, HOCH2CH2, CF3), (M-5621, F, CH3, H, HOCH2CH2, Br), (M-5622, F, CH3, H, HOCH2CH2, CH3), (M-5623, F, CH3, H, HOCH2CH2CH2, H), (M-5624, F, CH3, H, HOCH2CH2CH2, Cl), (M-5625, F, CH3, H, HOCH2CH2CH2, F), (M-6626, F, CH3, H, HOCH2CH2CH2, CF3), (M-5627, F, CH3, H, HOCH2CH2CH2, Br), (M-5628, F, CH3, H, HOCH2CH2CH2, CH3), (M-5629, F, CH3, H, HOCH2CH2CH2CH2, H), (M-5630, F, CH3, H, HOCH2CH2CH2CH2, Cl), (M-5631, F, CH3, H, HOCH2CH2CH2CH2, F), (M-5632, F, CH3, H, HOCH2CH2CH2CH2, CF3), (M-5633, F, CH3, H, HOCH2CH2CH2CH2, Br), (M-5634, F, CH3, H, HOCH2CH2CH2CH2, CH3), (M-5635, F, CH3, H, HOCH2CH2CH2CH2CH2, H), (M-5636, F, CH3, H, HOCH2CH2CH2CH2CH2Cl), (M-5637, F, CH3, H, HOCH2CH2CH2CH2CH2, F), (M-5638, F, CH3, H, HOCH2CH2CH2CH2CH2CF3), (M-5639, F, CH3, H, HOCH2CH2CH2CH2CH2Br), (M-5640, F, CH3, H, HOCH2CH2CH2CH2CH2CH3), (M-5641, F, CH3, H, HOCH2CH2OCH2CH2, H), (M-6642, F, CH3, H, HOCH2CH2OCH2CH2, Cl), (M-5643, F, CH3, H, HOCH2CH2OCH2CH2, F), (M-5644, F, CH3, H, HOCH2CH2OCH2CH2, CF3), (M-5645, F, CH3, H, HOCH2CH2OCH2CH2, Br), (M-5646, F, CH3, H, HOCH2CH2OCH2CH2, CH3), (M-5647, F, CH3, H, (Me)2N, H), (M-5648, F, CH3, H, (Me)2N, Cl), (M-5649, F, CH3, H, (Me)2N, F), (M-5650, F, CH3, H, (Me)2N, CF3), (M-5651, F, CH3, H, (Me)2N, Br), (M-5652, F, CH3, H, (Me)2N, CH3), (M-5653, F, CH3, H, piperidin-4-yl-methyl, H), (M-5654, F, CH3, H, piperidin-4-yl-methyl, Cl), (M-5655, F, CH3, H, piperidin-4-yl-methyl, F), (M-5656, F, CH3, H, piperidin-4-yl-methyl, CF3), (M-5657, F, CH3, H, piperidin-4-yl-methyl, Br), (M-5658, F, CH3, H, piperidin-4-yl-methyl, CH3), (M-5659, F, CH3, H, cyclohexylmethyl, H), (M-5660, F, CH3, H, cyclohexylmethyl, Cl), (M-5661, F, CH3, H, cyclohexylmethyl, F), (M-5662, F, CH3, H, cyclohexylmethyl, CF3), (M-5663, F, CH3, H, cyclohexylmethyl, Br), (M-5664, F, CH3, H, cyclohexylmethyl, CH3), (M-5665, F, CH3, F, H, H), (M-5666, F, CH3, F, H, Cl), (M-5667, F, CH3, F, H, F), (M-5668, F, CH3, F, H, CF3), (M-5669, F, CH3, F, H, Br), (M-5670, F, CH3, F, H, CH3), (M-5671, F, CH3, F, F, H), (M-5672, F, CH3, F, F, Cl), (M-5673, F, CH3, F, F, F), (M-5674, F, CH3, F, F, CF3), (M-5675, F, CH3, F, F, Br), (M-5676, F, CH3, F, F, CH3), (M-5677, F, CH3, F, Cl, H), (M-5678, F, CH3, F, Cl, Cl), (M-5679, F, CH3, F, Cl, F), (M-5680, F, CH3, F, Cl, CF3), (M-6681, F, CH3, F, Cl, Br), (M-5682, F, CH3, F, Cl, CH3), (M-5683, F, CH3, F, CH3, H), (M-5684, F, CH3, F, CH3, Cl), (M-5685, F, CH3, F, CH3, F), (M-5686, F, CH3, F, CH3, CF3), (M-5687, F, CH3, F, CH3, Br), (M-5688, F, CH3, F, CH3, CH3), (M-5689, F, CH3, F, Et, H), (M-5690, F, CH3, F, Et, Cl), (M-5691, F, CH3, F, Et, F), (M-5692, F, CH3, F, Et, CF3), (M-5693, F, CH3, F, Et, Br), (M-5694, F, CH3, F, Et, CH3), (M-5695, F, CH3, F, n-Pr, H), (M-5696, F, CH3, F, n-Pr, Cl), (M-5697, F, CH3, F, n-Pr, F), (M-5698, F, CH3, F, n-Pr, CF3), (M-5699, F, CH3, F, n-Pr, Br), (M-5700, F, CH3, F, n-Pr, CH3), (M-5701, F, CH3, F, c-Pr, H), (M-5702, F, CH3, F, c-Pr, Cl), (M-5703, F, CH3, F, c-Pr, F), (M-5704, F, CH3, F, c-Pr, CF3), (M-5705, F, CH3, F, c-Pr, Br), (M-5706, F, CH3, F, c-Pr, CH3), (M-5707, F, CH3, F, i-Pr, H), (M-5708, F, CH3, F, i-Pr, Cl), (M-5709, F, CH3, F, i-Pr, F), (M-5710, F, CH3, F, i-Pr, CF3), (M-5711, F, CH3, F, i-Pr, Br), (M-5712, F, CH3, F, i-Pr, CH3), (M-5713, F, CH3, F, n-Bu, H), (M-5714, F, CH3, F, n-Bu, Cl), (M-5715, F, CH3, F, n-Bu, F), (M-5716, F, CH3, F, n-Bu, CF3), (M-5717, F, CH3, F, n-Bu, Br), (M-5718, F, CH3, F, n-Bu, CH3), (M-5719, F, CH3, F, i-Bu, H), (M-5720, F, CH3, F, i-Bu, Cl), (M-5721, F, CH3, F, i-Bu, F), (M-5722, F, CH3, F, i-Bu, CF3), (M-5723, F, CH3, F, i-Bu, Br), (M-5724, F, CH3, F, i-Bu, CH3), (M-5725, F, CH3, F, sec-Bu, H), (M-5726, F, CH3, F, sec-Bu, Cl), (M-5727, F, CH3, F, sec-Bu, F), (M-5728, F, CH3, F, sec-Bu, CF3), (M-5729, F, CH3, F, sec-Bu, Br), (M-5730, F, CH3, F, sec-Bu, CH3), (M-5731, F, CH3, F, n-Pea, H), (M-5732, F, CH3, F, n-Pen, Cl), (M-5733, F, CH3, F, n-Pen, F), (M-5734, F, CH3, F, n-Pen, CF3), (M-5735, F, CH3, F, n-Pen, Br), (M-5736, F, CH3, F, n-Pen, CH3), (M-5737, F, CH3, F, c-Pen, H), (M-5738, F, CH3, F, c-Pen, Cl), (M-5739, F, CH3, F, c-Pen, F), (M-5740, F, CH3, F, c-Pen, CF3), (M-5741, F, CH3, F, c-Pen, Br), (M-5742, F, CH3, F, c-Pen, CH3), (M-5743, F, CH3, F, n-Hex, H), (M-5744, F, CH3, F, n-Hex, Cl), (M-5745, F, CH3, F, n-Hex, F), (M-5746, F, CH3, F, n-Hex, CF3), (M-5747, F, CH3, F, n-Hex, Br), (M-5748, F, CH3, F, n-Hex, CH3), (M-5749, F, CH3, F, c-Hex, H), (M-5750, F, CH3, F, c-Hex, Cl), (M-5751, F, CH3, F, c-Hex, F), (M-5752, F, CH3, F, c-Hex, CF3), (M-5753, F, CH3, F, c-Hex, Br), (M-5754, F, CH3, F, c-Hex, CH3), (M-5755, F, CH3, F, OH, H), (M-5756, F, CH3, F, OH, Cl, (M-5757, F, CH3, F, OH, F), (M-5758, F, CH3, F, OH, CF3), (M-5759, F, CH3, F, OH, Br), (M-5760, F, CH3, F, OH, CH3), (M-5761, F, CH3, F, EtO, H), (M-5762, F, CH3, F, EtO, Cl), (M-5763, F, CH3, F, EtO, F), (M-5764, F, CH3, F, EtO, CF3), (M-5765, F, CH3, F, EtO, Br), (M-5766, F, CH3, F, EtO, CH3), (M-5767, F, CH3, F, n-PrO, H), (M-5768, F, CH3, F, n-PrO, Cl), (M-5769, F, CH3, F, n-PrO, F), (M-5770, F, CH3, F, n-PrO, CF3), (M-5771, F, CH3, F, n-PrO, Br), (M-5772, F, CH3, F, n-PrO, CH3), (M-5773, F, CH3, F, PhO, H), (M-5774, F, CH3, F, PhO, Cl), (M-5775, F, CH3, F, PhO, F), (M-5776, F, CH3, F, PhO, CF3), (M-5777, F, CH3, F, PhO, Br), (M-5778, F, CH3, F, PhO, CH3), (M-5779, F, CH3, F, BnO, H), (M-5780, F, CH3, F, BnO, Cl), (M-5781, F, CH3, F, BnO, F), (M-5782, F, CH3, F, BnO, CF3), (M-5783, F, CH3, F, BnO, Br), (M-5784, F, CH3, F, BnO, CH3), (M-5785, F, CH3, F, PhCH2CH2O, H), (M-5786, F, CH3, F, PhCH2CH2O, Cl), (M-5787, F, CH3, F, PhCH2CH2O, F), (M-5788, F, CH3, F, PhCH2CH2O, CF3), (M-5789, F, CH3, F, PhCH2CH2O, Br), (M-5790, F, CH3, F, PhCH2CH2O, CH3), (M-5791, F, CH3, F, CF3O, H), (M-5792, F, CH3, F, CF3O, Cl), (M-5793, F, CH3, F, CF3O, F), (M-5794, F, CH3, F, CF3O, CF3), (M-5795, F, CH3, F, CF3O, Br), (M-5796, F, CH3, F, CF3O, CH3), (M-5797, F, CH3, F, Ph, H), (M-5798, F, CH3, F, Ph, Cl), (M-5799, F, CH3, F, Ph, F), (M-5800, F, CH3, F, Ph, CF3), (M-5801, F, CH3, F, Ph, Br), (M-5802, F, CH3, F, Ph, CH3), (M-5803, F, CH3, F, 4-F-Ph, H), (M-5804, F, CH3, F, 4-F-Ph, Cl), (M-5805, F, CH3, F, 4-F-Ph, F), (M-5806, F, CH3, F, 4-F-Ph, CH3), (M-5807, F, CH3, F, 4-F-Ph, Br), (M-5808, F, CH3, F, 4-F-Ph, CH3), (M-5809, F, CH3, F, 4-CF3-Ph, H), (M-5810, F, CH3, F, 4-CF3-Ph, Cl), (M-5811, F, CH3, F, 4-CF3-Ph, F), (M-5812, F, CH3, F, 4-CF3-Ph, CF3), (M-5813, F, CH3, F, 4-CF3-Ph, Br), (M-5814, F, CH3, F, 4-CF3-Ph, CH3), (M-5815, F, CH3, F, 4-(Me)2N-Ph, H), (M-5816, F, CH3, F, 4-(Me)3N-Ph, Cl), (M-5817, F, CH3, F, 4-(Me)2N-Ph, F), (M-5818, F, CH3, F, 4-(Me)2N-Ph, CF3), (M-5819, F, CH3, F, 4-(Me)3N-Ph, Br), (M-5820, F, CH3, F, 4-(Me)2N-Ph, CH3), (M-5821, F, CH3, F, 4-OH-Ph, H), (M-5822, F, CH3, F, 4-OH-Ph, Cl), (M-5823, F, CH3, F, 4-OH-Ph, F), (M-5824, F, CH3, F, 4-OH-Ph, CH3), (M-5825, F, CH3, F, 4-OH-Ph, Br), (M-5826, F, CH3, F, 4-OH-Ph, CH3), (M-5827, F, CH3, F, 3,4-di-F-Ph, H), (M-5828, F, CH3, F, 3,4-di-F-Ph, Cl), (M-5829, F, CH3, F, 3,4-di-F-Ph, F), (M-5830, F, CH3, F, 3,4-di-F-Ph, CF3), (M-5831, F, CH3, F, 3,4-di-F-Ph, Br), (M-5832, F, CH3, F, 3,4-di-F-Ph, CH3), (M-5833, F, CH3, F, 4-COOH-Ph, H), (M-5834, F, CH3, F, 4-COOH-Ph, Cl), (M-5835, F, CH3, F, 4-COOH-Ph, F), (M-5836, F, CH3, F, 4-COOH-Ph, CF3), (M-5837, F, CH3, F, 4-COOH-Ph, Br), (M-5838, F, CH3, F, 4-COOH-Ph, CH3), (M-5839, F, CH3, F, Bu, H), (M-5840, F, CH3, F, Bn, Cl), (M-5841, F, CH3, F, Bn, F), (M-5842, F, CH3, F, Bn, CF3), (M-5843, F, CH3, F, Bn, Br), (M-5844, F, CH3, F, Bn, CH3), (M-5845, F, CH3, F, 4-F-Bn, H), (M-5846, F, CH3, F, 4-F-Bn, Cl), (M-5847, F, CH3, F, 4-F-Bn, F), (M-5848, F, CH3, F, 4-F-Bn, CF3), (M-5849, F, CH3, F, 4-F-Bn, Br), (M-5850, F, CH3, F, 4-F-Bn, CH3), (M-5851, F, CH3, F, 2-Py, H), (M-5852, F, CH3, F, 2-Py, Cl), (M-5853, F, CH3, F, 2-Py, F), (M-5854, F, CH3, F, 2-Py, CF3), (M-5855, F, CH3, F, 2-Py, Br), (M-5856, F, CH3, F, 2-Py, CH3), (M-5857, F, CH3, F, 3-Py, H), (M-5858, F, CH3, F, 3-Py, Cl), (M-5859, F, CH3, F, 3-Py, F), (M-5860, F, CH3, F, 3-Py, CF3), (M-5861, F, CH3, F, 3-Py, Br), (M-5862, F, CH3, F, 3-Py, CH3), (M-5863, F, CH3, F, 4-Py, H), (M-5864, F, CH3, F, 4-Py, Cl), (M-5865, F, CH3, F, 4-Py, F), (M-5866, F, CH3, F, 4-Py, CF3), (M-5867, F, CH3, F, 4-Py, Br), (M-5868, F, CH3, F, 4-Py, CH3), (M-5869, F, CH3, F, 2-Th, H), (M-5870, F, CH3, F, 2-Th, Cl), (M-5871, F, CH3, F, 2-Th, F), (M-5872, F, CH3, F, 2-Th, CF3), (M-5873, F, CH3, F, 2-Th, Br), (M-5874, F, CH3, F, 2-Th, CH3), (M-5875, F, CH3, F, 3-Th, H), (M-5876, F, CH3, F, 3-Th, Cl), (M-5877, F, CH3, F, 3-Th, F), (M-5878, F, CH3, F, 3-Th, CF3), (M-5879, F, CH3, F, 3-Th, Br), (M-5880, F, CH3, F, 3-Th, CH3), (M-5881, F, CH3, F, pyrrazol-2-yl, H), (M-5882, F, CH3, F, pyrrazol-2-yl, Cl), (M-5883, F, CH3, F, pyrrazol-2-yl, F), (M-5884, F, CH3, F, pyrrazol-2-yl, CF3), (M-5885, F, CH3, F, pyrrazol-2-yl, Br), (M-5886, F, CH3, F, pyrrazol-2-yl, CH3), (M-5887, F, CH3, F, pyrrazol-3-yl, H), (M-5888, F, CH3, F, pyrrazol-3-yl, Cl), (M-5889, F, CH3, F, pyrrazol-3-yl, F), (M-5890, F, CH3, F, pyrrazol-3-yl, CF3), (M-5891, F, CH3, F, pyrrazol-3-yl, Br), (M-5892, F, CH3, F, pyrrazol-3-yl, CH3), (M-5893, F, CH3, F, pyrimidin-2-yl, H), (M-5894, F, CH3, F, pyrimidin-2-yl, Cl), (M-5895, F, CH3, F, pyrimidin-2-yl, F), (M-5896, F, CH3, F, pyrimidin-2-yl, CF3), (M-5897, F, CH3, F, pyrimidin-2-yl, Br), (M-5898, F, CH3, F, pyrimidin-2-yl, CH3), (M-5899, F, CH3, F, pyrimidin-4-yl, H), (M-5900, F, CH3, F, pyrimidin-4-yl, Cl), (M-5901, F, CH3, F, pyrimidin-4-yl, F), (M-5902, F, CH3, F, pyrimidin-4-yl, CF3), (M-5903, F, CH3, F, pyrimidin-4-yl, Br), (M-5904, F, CH3, F, pyrimidin-4-yl, CH3), (M-5905, F, CH3, F, pyrimidin-5-yl, H), (M-5906, F, CH3, F, pyrimidin-5-yl, Cl), (M-5907, F, CH3, F, pyrimidin-5-yl, F), (M-5908, F, CH3, F, pyrimidin-5-yl, CF3), (M-5909, F, CH3, F, pyrimidin-5-yl, Br), (M-5910, F, CH3, F, pyrimidin-5-yl, CH3), (M-5911, F, CH3, F, HOOCCH2CH2CH2, H), (M-5912, F, CH3, F, HOOCCH2CH2CH2, Cl), (M-5913, F, CH3, F, HOOCCH2CH2CH2, F), (M-5914, F, CH3, F, HOOCCH2CH2CH2, CF3), (M-5915, F, CH3, F, HOOCCH2CH2CH2Br), (M-5916, F, CH3, F, HOOCCH2CH2CH2, CH3), (M-5917, F, CH3, F, HOOCCH2CH2CH2CH2, H), (M-5918, F, CH3, F, HOOCCH2CH2CH2CH2, Cl), (M-5919, F, CH3, F, HOOCCH2CH2CH2CH2, F), (M-5920, F, CH3, F, HOOCCH2CH2CH2CH2, CF3), (M-5921, F, CH3, F, HOOCCH2CH2CH2CH2, Br), (M-5922, F, CH3, F, HOOCCH2CH2CH2CH2, CH3), (M-5923, F, CH3, F, (Me)2NCOCH2CH2CH2CH2, H), (M-5924, F, CH3, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-5925, F, CH3, F, (Me)2NCOCH2CH2CH2CH2, F), (M-5926, F, CH3, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-5927, F, CH3, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-5928, F, CH3, F, (Me)2NCOCH2CH2CH2CH3, CH3), (M-5929, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2H), (M-5930, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-5931, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-5932, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-5933, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2Br), (M-5934, F, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-5935, F, CH3, F, MeOCH2, H), (M-5936, F, CH3, F, MeOCH2, Cl), (M-5937, F, CH3, F, MeOCH2, F), (M-5938, F, CH3, F, MeOCH2, CF3), (M-5939, F, CH3, F, MeOCH2, Br), (M-5940, F, CH3, F, MeOCH2, CH3), (M-5941, F, CH3, F, EtOCH2, H), (M-5942, F, CH3, F, EtOCH2, Cl), (M-5943, F, CH3, F, EtOCH2, F), (M-5944, F, CH3, F, EtOCH2, CF3), (M-5945, F, CH3, F, EtOCH2, Br), (M-5946, F, CH3, F, EtOCH2, CH3), (M-5947, F, CH3, F, EtOCH2CH2, H), (M-5948, F, CH3, F, EtOCH2CH2, Cl), (M-5949, F, CH3, F, EtOCH2CH2, F), (M-5950, F, CH3, F, EtOCH2CH2, CF3), (M-5951, F, CH3, F, EtOCH2CH2, Br), (M-5952, F, CH3, F, EtOCH2CH2, CH3), (M-5953, F, CH3, F, MeOCH2CH2OCH2CH2, H), (M-5954, F, CH3, F, MeOCH2CH2OCH2CH2, Cl), (M-5955, F, CH3, F, MeOCH2CH2OCH2CH2, F), (M-5956, F, CH3, F, MeOCH2CH2OCH2CH2, CF3), (M-5957, F, CH3, F, MeOCH2CH2CH2CH3, Br), (M-5958, F, CH3, F, MeOCH2CH2OCH2CH2, CH3), (M-5959, F, CH3, F, MeOCH2CH2, H), (M-5960, F, CH3, F, MeOCH2CH2, Cl), (M-5961, F, CH3, F, MeOCH2CH2, F), (M-5962, F, CH3, F, MeOCH2CH2, CF3), (M-5963, F, CH3, F, MeOCH2CH2, Br), (M-5964, F, CH3, F, MeOCH2CH2, CH3), (M-5965, F, CH3, F, HOCH2, H), (M-5966, F, CH3, F, HOCH2, Cl), (M-5967, F, CH3, F, HOCH2, F), (M-5968, F, CH3, F, HOCH2, CF3), (M-5969, F, CH3, F, HOCH2, Br), (M-5970, F, CH3, F, HOCH2, CH3), (M-5971, F, CH3, F, HOCH2CH2, H), (M-5972, F, CH3, F, HOCH2CH2, Cl), (M-5973, F, CH3, F, HOCH2CH2, F), (M-5974, F, CH3, F, HOCH2CH2, CF3), (M-5975, F, CH3, F, HOCH2CH2, Br), (M-5976, F, CH3, F, HOCH2CH2, CH3), (M-5977, F, CH3, F, HOCH2CH2CH2, H), (M-5978, F, CH3, F, HOCH2CH2CH2, Cl), (M-5979, F, CH3, F, HOCH2CH2CH2, F), (M-5980, F, CH3, F, HOCH2CH2CH2, CF3), (M-5981, F, CH3, F, HOCH2CH2CH2, Br), (M-5982, F, CH3, F, HOCH2CH2CH2, CH3), (M-5983, F, CH3, F, HOCH2CH2CH2CH2, H), (M-5984, F, CH3, F, HOCH2CH2CH2CH2, Cl), (M-5985, F, CH3, F, HOCH2CH2CH2CH2, F), (M-5986, F, CH3, F, HOCH2CH2CH2CH2, CF3), (M-5987, F, CH3, F, HOCH2CH2CH2CH2, Br), (M-5988, F, CH3, F, HOCH2CH2CH2CH2, CH3), (M-5989, F, CH3, F, HOCH2CH2CH2CH2CH2, H), (M-5990, F, CH3, F, HOCH2CH2CH2CH2CH2Cl), (M-5991, F, CH3, F, HOCH2CH2CH2CH2CH2, F), (M-5992, F, CH3, F, HOCH2CH2CH2CH2CH2CF3), (M-5993, F, CH3, F, HOCH2CH2CH2CH2CH2Br), (M-5994, F, CH3, F, HOCH2CH2CH2CH2CH2CH3), (M-5995, F, CH3, F, HOCH2CH2OCH2CH2, H), (M-5996, F, CH3, F, HOCH2CH2OCH2CH2, Cl), (M-5997, F, CH3, F, HOCH2CH2OCH2CH2, F), (M-5998, F, CH3, F, HOCH2CH2OCH2CH2, CF3), (M-5999, F, CH3, F, HOCH2CH2OCH2CH2, Br), (M-6000, F, CH3, F, HOCH2CH2OCH2CH2, CH3), (M-6001, F, CH3, F, (Me)2N, H), (M-6002, F, CH3, F, (Me)2N, Cl), (M-6003, F, CH3, F, (Me)2N, F), (M-6004, F, CH3, F, (Me)2N, CF3), (M-6005, F, CH3, F, (Me)2N, Br), (M-6006, F, CH3, F, (Me)2N, CH3), (M-6007, F, CH3, F, piperidin-4-yl-methyl, H), (M-6008, F, CH3, F, piperidin-4-yl-methyl, Cl), (M-6009, F, CH3, F, piperidin-4-yl-methyl, F), (M-6010, F, CH3, F, piperidin-4-yl-methyl, CF3), (M-6011, F, CH3, F, piperidin-4-yl-methyl, Br), (M-6012, F, CH3, F, piperidin-4-yl-methyl, CH3), (M-6013, F, CH3, F, cyclohexylmethyl, H), (M-6014, F, CH3, F, cyclohexylmethyl, Cl), (M-6015, F, CH3, F, cyclohexylmethyl, F), (M-6016, F, CH3, F, cyclohexylmethyl, CF3), (M-6017, F, CH3, F, cyclohexylmethyl, Br), (M-6018, F, CH3, F, cyclohexylmethyl, CH3), (M-6019, F, CH3, Cl, H, H), (M-6020, F, CH3, Cl, H, Cl), (M-6021, F, CH3, Cl, H, F), (M-6022, F, CH3, Cl, H, CF3), (M-6023, F, CH3, Cl, H, Br), (M-6024, F, CH3, Cl, H, CH3), (M-6025, F, CH3, Cl, F, H), (M-6026, F, CH3, Cl, F, Cl), (M-6027, F, CH3, Cl, F, F), (M-6028, F, CH3, Cl, F, CF3), (M-6029, F, CH3, Cl, F, Br), (M-6030, F, CH3, Cl, F, CH3), (M-6031, F, CH3, Cl, Cl, H), (M-6032, F, CH3, Cl, Cl, Cl), (M-6033, F, CH3, Cl, Cl, F), (M-6034, F, CH3, Cl, Cl, CF3), (M-6035, F, CH3, Cl, Cl, Br), (M-6036, F, CH3, Cl, Cl, CH3), (M-6037, F, CH3, Cl, CH3, H), (M-6038, F, CH31 Cl, CH3, Cl), (M-6039, F, CH3, Cl, CH3, F), (M-6040, F, CH3, Cl, CH3, CF3), (M-6041, F, CH3, Cl, CH3, Br), (M-6042, F, CH3, Cl, CH3, CH3), (M-6043, F, CH3, Cl, Et, H), (M-6044, F, CH3, Cl, Et, Cl), (M-6045, F, CH3, Cl, Et, F), (M-6046, F, CH3, Cl, Et, CF3), (M-6047, F, CH3, Cl, Et, Br), (M-6048, F, CH3, Cl, Et, CH3), (M-6049, F, CH3, Cl, n-Pr, H), (M-6050, F, CH3, Cl, n-Pr, Cl), (M-6051, F, CH3, Cl, n-Pr, F), (M-6052, F, CH3, Cl, n-Pr, CF3), (M-6053, F, CH3, Cl, n-Pr, Br), (M-6054, F, CH3, Cl, n-Pr, CH3), (M-6055, F, CH3, Cl, c-Pr, H), (M-6056, F, CH3, Cl, c-Pr, Cl), (M-6057, F, CH3, Cl, c-Pr, F), (M-6058, F, CH3, Cl, c-Pr, CF3), (M-6059, F, CH3, Cl, c-Pr, Br), (M-6060, F, CH3, Cl, c-Pr, CH3), (M-6061, F, CH3, Cl, i-Pr, H), (M-6062, F, CH3, Cl, i-Pr, Cl), (M-6063, F, CH3, Cl, i-Pr, F), (M-6064, F, CH3, Cl, i-Pr, CF3), (M-6065, F, CH3, Cl, i-Pr, Br), (M-6066, F, CH3, Cl, i-Pr, CH3), (M-6067, F, CH3, Cl, n-Bu, H), (M-6068, F, CH3, Cl, n-Bu, Cl), (M-6069, F, CH3, Cl, n-Bu, F), (M-6070, F, CH3, Cl, n-Bu, CF3), (M-6071, F, CH3, Cl, n-Bu, Br), (M-6072, F, CH3, Cl, n-Bu, CH3), (M-6073, F, CH3, Cl, i-Bu, H), (M-6074, F, CH3, Cl, i-Bu, Cl), (M-6075, F, CH3, Cl, i-Bu, F), (M-6076, F, CH3, Cl, i-Bu, CF3), (M-6077, F, CH3, Cl, i-Bu, Br), (M-6078, F, CH3, Cl, i-Bu, CH3), (M-6079, F, CH3, Cl, sec-Bu, H), (M-6080, F, CH3, Cl, sec-Bu, Cl), (M-6081, F, CH3, Cl, sec-Bu, F), (M-6082, F, CH3, Cl, sec-Bu, CF3), (M-6083, F, CH3, Cl, sec-Bu, Br), (M-6084, F, CH3, Cl, sec-Bu, CH3), (M-6085, F, CH3, Cl, n-Pen, H), (M-6086, F, CH3, Cl, n-Pen, Cl), (M-6087, F, CH3, Cl, n-Pen, F), (M-6088, F, CH3, Cl, n-Pen, CF3), (M-6089, F, CH3, Cl, n-Pen, Br), (M-6090, F, CH3, Cl, n-Pen, CH3), (M-6091, F, CH3, Cl, c-Pen, H), (M-6092, F, CH3, Cl, c-Pen, Cl), (M-6093, F, CH3, Cl, c-Pen, F), (M-6094, F, CH3, Cl, c-Pen, CF3), (M-6095, F, CH3, Cl, c-Pen, Br), (M-6096, F, CH3, Cl, c-Pen, CH3), (M-6097, F, CH3, Cl, n-Hex, H), (M-6098, F, CH3, Cl, n-Hex, Cl), (M-6099, F, CH3, Cl, n-Hex, F), (M-6100, F, CH3, Cl, n-Hex, CF3), (M-6101, F, CH3, CL n-Hex, Br), (M-6102, F, CH3, Cl, n-Hex, CH3), (M-6103, F, CH3, Cl, c-Hex, H), (M-6104, F, CH3, Cl, c-Hex, Cl), (M-6105, F, CH3, Cl, c-Hex, F), (M-6106, F, CH3, Cl, c-Hex, CF3), (M-6107, F, CH3, Cl, c-Hex, Br), (M-6108, F, CH3, Cl, c-Hex, CH3), (M-6109, F, CH3, Cl, Oil, H), (M-6110, F, CH3, Cl, OH, Cl), (M-6111, F, CH3, Cl, OH, F), (M-6112, F, CH3, Cl, OH, CF3), (M-6113, F, CH3, Cl, OH, Br), (M-6114, F, CH3, Cl, OH, CH3), (M-6115, F, CH3, Cl, EtO, H), (M-6116, F, CH3, Cl, EtO, Cl), (M-6117, F, CH3, Cl, EtO, F), (M-6118, F, CH3, Cl, EtO, CF3), (M-6119, F, CH3, Cl, EtO, Br), (M-6120, F, CH3, Cl, EtO, CH3), (M-6121, F, CH3, Cl, n-PrO, H), (M-6122, F, CH3, Cl, n-PrO, Cl), (M-6123, F, CH3, Cl, n-PrO, F), (M-6124, F, CH3, Cl, n-PrO, CF3), (M-6125, F, CH3, Cl, n-PrO, Br), (M-6126, F, CH3, Cl, n-PrO, CH3), (M-6127, F, CH3, Cl, PhO, H), (M-6128, F, CH3, Cl, PhO, Cl), (M-6129, F, CH3, Cl, PhO, F), (M-6130, F, CH3, Cl, PhO, CF3), (M-6131, F, CH3, Cl, PhO, Br), (M-6132, F, CH3, Cl, PhO, CH3), (M-6133, F, CH3, Cl, BnO, H), (M-6134, F, CH3, Cl, BnO, Cl), (M-6135, F, CH3, Cl, BnO, F), (M-6136, F, CH3, Cl, BnO, CF3), (M-6137, F, CH3, Cl, BnO, Br), (M-6138, F, CH3, Cl, BnO, CH3), (M-6139, F, CH3, Cl, PhCH2CH2O, H), (M-6140, F, CH3, Cl, PhCH2CH2O, Cl), (M-6141, F, CH3, Cl, PhCH2CH2O, F), (M-6142, F, CH3, Cl, PhCH2CH2O, CF3), (M-6143, F, CH3, Cl, PhCH2CH2O, Br), (M-6144, F, CH3, Cl, PhCH2CH2O, CH3), (M-6145, F, CH3, Cl, CF3O, H), (M-6146, F, CH3, Cl, CF3O, Cl), (M-6147, F, CH3, Cl, CF3O, F), (M-6148, F, CH3, Cl, CF3O, CF3), (M-6149, F, CH3, Cl, CF3O, Br), (M-6150, F, CH3, Cl, CF3O, CH3), (M-6151, F, CH3, Cl, Ph, H), (M-6152, F, CH3, Cl, Ph, Cl), (M-6153, F, CH3, Cl, Ph, F), (M-6154, F, CH3, Cl, Ph, CF3), (M-6155, F, CH3, Cl, Ph, Br), (M-6156, F, CH3, Cl, Ph, CH3), (M-6157, F, CH3, Cl, 4-F-Ph, H), (M-6158, F, CH3, Cl, 4-F-Ph, Cl), (M-6159, F, CH3, Cl, 4-F-Ph, F), (M-6160, F, CH3, Cl, 4-F-Ph, CF3), (M-6161, F, CH3, Cl, 4-F-Ph, Br), (M-6162, F, CH3, Cl, 4-F-Ph, CH3), (M-6163, F, CH3, Cl, 4-CF3-Ph, H), (M-6164, F, CH3, Cl, 4-CF3-Ph, Cl), (M-6165, F, CH3, Cl, 4-CF3-Ph, F), (M-6166, F, CH3, Cl, 4-CF3-Ph, CF3), (M-6167, F, CH3, Cl, 4-CF3-Ph, Br), (M-6168, F, CH3, Cl, 4-CF3-Ph, CH3), (M-6169, F, CH3, Cl, 4-(Me)2N-Ph, H), (M-6170, F, CH3, Cl, 4-(Me)2N-Ph, Cl), (M-6171, F, CH3, Cl, 4-(Me)2N-Ph, F), (M-6172, F, CH3, Cl, 4-(Me)2N-Ph, CF3), (M-6173, F, CH3, Cl, 4-(Me)2N-Ph, Br), (M-6174, F, CH3, Cl, 4-(Me)2N-Ph, CH3), (M-6175, F, CH3, Cl, 4-OH-Ph, H), (M-6176, F, CH3, Cl, 4-OH-Ph, Cl), (M-6177, F, CH3, Cl, 4-OH-Ph, F), (M-6178, F, CH3, Cl, 4-OH-Ph, CF3), (M-6179, F, CH3, Cl, 4-OH-Ph, Br), (M-6180, F, CH3, Cl, 4-OH-Ph, CH3), (M-6181, F, CH3, Cl, 3,4-di-F-Ph, H), (M-6182, F, CH3, Cl, 3,4-di-F-Ph, Cl), (M-6183, F, CH3, Cl, 3,4-di-F-Ph, F), (M-6184, F, CH3, Cl, 3,4-di-F-Ph, CF3), (M-6185, F, CH3, Cl, 3,4-di-F-Ph, Br), (M-6186, F, CH3, Cl, 3,4-di-F-Ph, CH3), (M-6187, F, CH3, Cl, 4-COOH-Ph, H), (M-6188, F, CH3, Cl, 4-COOH-Ph, Cl), (M-6189, F, CH3, Cl, 4-COOH-Ph, F), (M-6190, F, CH3, Cl, 4-COOH-Ph, CF3), (M-6191, F, CH3, Cl, 4-COOH-Ph, Br), (M-6192, F, CH3, Cl, 4-COOH-Ph, CH3), (M-6193, F, CH3, Cl, Bn, H), (M-6194, F, CH3, Cl, Bn, Cl), (M-6195, F, CH3, Cl, Bn, F), (M-6196, F, CH3, Cl, Bn, CF3), (M-6197, F, CH3, Cl, Bn, Br), (M-6198, F, CH3, Cl, Bn, CH3), (M-6199, F, CH3, Cl, 4-F-Bn, H), (M-6200, F, CH3, Cl, 4-F-Bn, Cl), (M-6201, F, CH3, Cl, 4-F-Bn, F), (M-6202, F, CH3, Cl, 4-F-Bn, CH3), (M-6203, F, CH3, Cl, 4-F-Bn, Br), (M-6204, F, CH3, Cl, 4-F-Bn, CH3), (M-6205, F, CH3, Cl, 2-Py, H), (M-6206, F, CH3, Cl, 2-Py, Cl), (M-6207, F, CH3, Cl, 2-Py, F), (M-6208, F, CH3, Cl, 2-Py, CF3), (M-6209, F, CH3, Cl, 2-Py, Br), (M-6210, F, CH3, Cl, 2-Py, CH3), (M-6211, F, CH3, Cl, 3-Py, H), (M-6212, F, CH3, Cl, 3-Py, Cl), (M-6213, F, CH3, Cl, 3-Py, F), (M-6214, F, CH3, Cl, 3-Py, CF3), (M-6215, F, CH3, Cl, 3-Py, Br), (M-6216, F, CH3, Cl, 3-Py, CH3), (M-6217, F, CH3, Cl, 4-Py, H), (M-6218, F, CH3, Cl, 4-Py, Cl), (M-6219, F, CH3, Cl, 4-Py, F), (M-6220, F, CH3, Cl, 4-Py, CF3), (M-6221, F, CH3, Cl, 4-Py, Br), (M-6222, F, CH3, Cl, 4-Py, CH3), (M-6223, F, CH3, Cl, 2-Th, H), (M-6224, F, CH3, Cl, 2-Th, Cl), (M-6225, F, CH3, Cl, 2-Th, F), (M-6226, F, CH3, Cl, 2-Th, CF3), (M-6227, F, CH3, Cl, 2-Th, Br), (M-6228, F, CH3, Cl, 2-Th, CH3), (M-6229, F, CH3, Cl, 3-Th, H), (M-6230, F, CH3, Cl, 3-Th, Cl), (M-6231, F, CH3, Cl, 3-Th, F), (M-6232, F, CH3, Cl, 3-Th, CF3), (M-6233, F, CH3, Cl, 3-Th, Br), (M-6234, F, CH3, Cl, 3-Th, CH3), (M-6235, F, CH3, Cl, pyrrazol-2-yl, H), (M-6236, F, CH3, Cl, pyrrazol-2-yl, Cl), (M-6237, F, CH3, Cl, pyrrazol-2-yl, F), (M-6238, F, CH3, Cl, pyrrazol-2-yl, CF3), (M-6239, F, CH3, Cl, pyrrazol-2-yl, Br), (M-6240, F, CH3, Cl, pyrrazol-2-yl, CH3), (M-6241, F, CH3, Cl, pyrrazol-3-yl, H), (M-6242, F, CH3, Cl, pyrrazol-3-yl, Cl), (M-6243, F, CH3, Cl, pyrrazol-3-yl, F), (M-6244, F, CH3, Cl, pyrrazol-3-yl, CF3), (M-6245, F, CH3, Cl, pyrrazol-3-yl, Br), (M-6246, F, CH3, Cl, pyrrazol-3-yl, CH3), (M-6247, F, CH3, Cl, pyrimidin-2-yl, H), (M-6248, F, CH3, Cl, pyrimidin-2-yl, Cl), (M-6249, F, CH3, Cl, pyrimidin-2-yl, F), (M-6250, F, CH3, Cl, pyrimidin-2-yl, CF3), (M-6251, F, CH3, Cl, pyrimidin-2-yl, Br), (M-6252, F, CH3, Cl, pyrimidin-2-yl, CH3), (M-6253, F, CH3, Cl, pyrimidin-4-yl, H), (M-6254, F, CH3, Cl, pyrimidin-4-yl, Cl), (M-6255, F, CH3, Cl, pyrimidin-4-yl, F), (M-6256, F, CH3, Cl, pyrimidin-4-yl, CF3), (M-6257, F, CH3, Cl, pyrimidin-4-yl, Br), (M-6258, F, CH3, Cl, pyrimidin-4-yl, CH3), (M-6259, F, CH3, Cl, pyrimidin-5-yl, H), (M-6260, F, CH3, Cl, pyrimidin-5-yl, Cl), (M-6261, F, CH3, Cl, pyrimidin-5-yl, F), (M-6262, F, CH3, Cl, pyrimidin-5-yl, CF3), (M-6263, F, CH3, Cl, pyrimidin-5-yl, Br), (M-6264, F, CH3, Cl, pyrimidin-5-yl, CH3), (M-6265, F, CH3, Cl, HOOCCH2CH2CH2, H), (M-6266, F, CH3, Cl, HOOCCH2CH2CH2, Cl), (M-6267, F, CH3, Cl, HOOCCH2CH2CH2, F), (M-6268, F, CH3, Cl, HOOCCH2CH2CH2, CF3), (M-6269, F, CH3, Cl, HOOCCH2CH2CH2Br), (M-6270, F, CH3, Cl, HOOCCH2CH2CH2, CH3), (M-6271, F, CH3, Cl, HOOCCH2CH2CH2CH2, H), (M-6272, F, CH3, Cl, HOOCCH2CH2CH2CH2, Cl), (M-6273, F, CH3, Cl, HOOCCH2CH2CH2CH2, F), (M-6274, F, CH3, Cl, HOOCCH2CH2CH2CH2, CF3), (M-6275, F, CH3, Cl, HOOCCH2CH2CH2CH2, Br), (M-6276, F, CH3, Cl, HOOCCH2CH2CH2CH2, CH3), (M-6277, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-6278, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-6279, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-6280, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-6281, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-6282, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-6283, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-6284, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-6285, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-6286, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-6287, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-6288, F, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-6289, F, CH3, Cl, MeOCH2, H), (M-6290, F, CH3, Cl, MeOCH2, Cl), (M-6291, F, CH3, Cl, MeOCH2, F), (M-6292, F, CH3, Cl, MeOCH2, CF3), (M-6293, F, CH3, Cl, MeOCH2, Br), (M-6294, F, CH3, Cl, MeOCH2, CH3), (M-6295, F, CH3, Cl, EtOCH2, H), (M-6296, F, CH3, Cl, EtOCH2, Cl), (M-6297, F, CH3, Cl, EtOCH2, F), (M-6298, F, CH3, Cl, EtOCH2, CF3), (M-6299, F, CH3, Cl, EtOCH2, Br), (M-6300, F, CH3, Cl, EtOCH2, CH3), (M-6301, F, CH3, Cl, EtOCH2CH2, H), (M-6302, F, CH3, Cl, EtOCH2CH2, Cl), (M-6303, F, CH3, Cl, EtOCH2CH2, F), (M-6304, F, CH3, Cl, EtOCH2CH2, CF3), (M-6305, F, CH3, Cl, EtOCH2CH2, Br), (M-6306, F, CH3, Cl, EtOCH2CH2, CH3), (M-6307, F, CH3, Cl, MeOCH2CH2OCH2CH2, H), (M-6308, F, CH3, Cl, MeOCH2CH2OCH2CH2, Cl), (M-6309, F, CH3, Cl, MeOCH2CH2OCH2CH2, F), (M-6310, F, CH3, Cl, MeOCH2CH2OCH2CH2, CF3), (M-6311, F, CH3, Cl, MeOCH2CH2OCH2CH2, Br), (M-6312, F, CH3, Cl, MeOCH2CH2OCH2CH2, CH3), (M-6313, F, CH3, Cl, MeOCH2CH2, H), (M-6314, F, CH3, Cl, MeOCH2CH2, Cl), (M-6315, F, CH3, Cl, MeOCH2CH2, F), (M-6316, F, CH3, Cl, MeOCH2CH2, CF3), (M-6317, F, CH3, Cl, MeOCH2CH2, Br), (M-6318, F, CH3, Cl, MeOCH2CH2, CH3), (M-6319, F, CH3, Cl, HOCH2, H), (M-6320, F, CH3, Cl, HOCH2, Cl), (M-6321, F, CH3, Cl, HOCH2, F), (M-6322, F, CH3, Cl, HOCH2, CF3), (M-6323, F, CH3, Cl, HOCH2, Br), (M-6324, F, CH3, Cl, HOCH2, CH3), (M-6325, F, CH3, Cl, HOCH2CH2, H), (M-6326, F, CH3, Cl, HOCH2CH2, Cl), (M-6327, F, CH3, Cl, HOCH2CH2, F), (M-6328, F, CH3, Cl, HOCH2CH2, CF3), (M-6329, F, CH3, Cl, HOCH2CH2, Br), (M-6330, F, CH3, Cl, HOCH2CH2, CH3), (M-6331, F, CH3, Cl, HOCH2CH2CH2, H), (M-6332, F, CH3, Cl, HOCH2CH2CH2, Cl), (M-6333, F, CH3, Cl, HOCH2CH2CH2, F), (M-6334, F, CH3, Cl, HOCH2CH2CH2, CF3), (M-6335, F, CH3, Cl, HOCH2CH2CH2, Br), (M-6336, F, CH3, Cl, HOCH2CH2CH2, CH3), (M-6337, F, CH3, Cl, HOCH2CH2CH2CH2, H), (M-6338, F, CH3, Cl, HOCH2CH2CH2CH2, Cl), (M-6339, F, CH3, Cl, HOCH2CH2CH2CH2, F), (M-6340, F, CH3, Cl, HOCH2CH2CH2CH2, CF3), (M-6341, F, CH3, Cl, HOCH2CH2CH2CH2, Br), (M-6342, F, CH3, Cl, HOCH2CH2CH2CH2, CH3), (M-6343, F, CH3, Cl, HOCH2CH2CH2CH2CH2, H), (M-6344, F, CH3, Cl, HOCH2CH2CH2CH2CH2Cl), (M-6345, F, CH3, Cl, HOCH2CH2CH2CH2CH3, F), (M-6346, F, CH3, Cl, HOCH2CH2CH2CH2CH2, CF3), (M-6347, F, CH3, Cl, HOCH2CH2CH2CH2CH2, Br), (M-6348, F, CH3, Cl, HOCH2CH2CH2CH2 CH2, CH3), (M-6349, F, CH3, Cl, HOCH2CH2OCH2CH2, H), (M-6350, F, CH3, Cl, HOCH2CH2OCH2CH2, Cl), (M-6351, F, CH3, Cl, HOCH2CH2OCH2CH2, F), (M-6352, F, CH3, Cl, HOCH2CH2OCH2CH2, CF3), (M-6353, F, CH3, Cl, HOCH2CH2OCH2CH2, Br), (M-6354, F, CH3, Cl, HOCH2CH2OCH2CH2, CH3), (M-6355, F, CH3, Cl, (Me)2N, H), (M-6356, F, CH3, Cl, (Me)2N, Cl), (M-6357, F, CH3, Cl, (Me)2N, F), (M-6358, F, CH3, Cl, (Me)2N, CF3), (M-6359, F, CH3, Cl, (Me)2N, Br), (M-6360, F, CH3, Cl, (Me)2H, CH3), (M-6361, F, CH3, Cl, piperidin-4-yl-methyl, H), (M-6362, F, CH3, Cl, piperidin-4-yl-methyl, Cl), (M-6363, F, CH3, Cl, piperidin-4-yl-methyl, F), (M-6364, F, CH3, Cl, piperidin-4-yl-methyl, CF3), (M-6365, F, CH3, Cl, piperidin-4-yl-methyl, Br), (M-6366, F, CH3, Cl, piperidin-4-yl-methyl, CH3), (M-6367, F, CH3, Cl, cyclohexylmethyl, H), (M-6368, F, CH3, Cl, cyclohexylmethyl, Cl), (M-6369, F, CH3, Cl, cyclohexylmethyl, F), (M-6370, F, CH3, Cl, cyclohexylmethyl, CF3), (M-6371, F, CH3, Cl, cyclohexylmethyl, Br), (M-6372, F, CH3, Cl, cyclohexylmethyl, CH3), (M-6373, Cl, H, H, H, H), (M-6374, Cl, H, H, H, Cl), (M-6375, MeO, F, H, H, F), (M-6376, MeO, F, H, H, c-Pr), (M-6377, Cl, H, H, H, Br), (M-6378, Cl, H, H, H, CH3), (M-6379, MeO, H, H, F, c-Pr), (M-6380, Cl, H, H, F, Cl), (M-6381, MeO, H, H, F, F), (M-6382, Cl, H, H, F, CF3), (M-6383, Cl, H, H, F, Br), (M-6384, Cl, H, H, F, CH3), (M-6385, Cl, H, H, Cl, H), (M-6386, MeO, F, H, H, Et), (M-6387, MeO, H, H, Cl, F), (M-6388, Cl, H, H, Cl, CF3), (M-6389, Cl, H, H, Cl, Br), (M-6390, Cl, H, H, Cl, CH3), (M-6391, Cl, H, H, CH3, H), (M-6392, Cl, H, H, CH3, Cl), (M-6393, Cl, H, H, CH3, F), (M-6394, Cl, H, H, CH3, CF3), (M-6395, Cl, H, H, CH3, Br), (M-6396, Cl, H, H, CH3, CH3), (M-6397, Cl, H, H, Et, H), (M-6398, Cl, H, H, Et, Cl), (M-6399, Cl, H, H, Et, F), (M-6400, Cl, H, H, Et, CF3), (M-6401, Cl, H, H, Et, Br), (M-6402, Cl, H, H, Et, CH3), (M-6403, Cl, H, H, n-Pr, H), (M-6404, Cl, H, H, n-Pr, Cl), (M-6405, Cl, H, H, n-Pr, F), (M-6406, Cl, H, H, n-Pr, CF3), (M-6407, Cl, H, H, n-Pr, Br), (M-6408, Cl, H, H, n-Pr, CH3), (M-6409, Cl, H, H, c-Pr, H), (M-6410, Cl, H, H, c-Pr, Cl), (M-6411, Cl, H, H, c-Pr, F), (M-6412, Cl, H, H, c-Pr, CF3), (M-6413, Cl, H, H, c-Pr, Br), (M-6414, Cl, H, H, c-Pr, CH3), (M-6415, Cl, H, H, i-Pr, H), (M-6416, Cl, H, H, i-Pr, Cl), (M-6417, Cl, H, H, i-Pr, F), (M-6418, Cl, H, H, i-Pr, CF3), (M-6419, Cl, H, H, i-Pr, Br), (M-6420, Cl, H, H, i-Pr, CH3), (M-6421, MeO, H, H, n-Bu, H), (M-6422, Cl, H, H, n-Bu, Cl), (M-6423, Cl, H, H, n-Bu, F), (M-6424, Cl, H, H, n-Bu, CF3), (M-6425, Cl, H, H, n-Bu, Br), (M-6426, Cl, H, H, n-Bu, CH3), (M-6427, Cl, H, H, i-Bu, H), (M-6428, Cl, H, H, i-Bu, Cl), (M-6429, CL, H, H, i-Bu, F), (M-6430, Cl, H, H, i-Bu, CF3), (M-6431, Cl, H, H, i-Bu, Br), (M-6432, Cl, H, H, i-Bu, CH3), (M-6433, Cl, H, H, sec-Bu, H), (M-6434, Cl, H, H, sec-Bu, Cl), (M-6435, Cl, H, H, sec-Bu, F), (M-6436, Cl, H, H, sec-Bu, CF3), (M-6437, Cl, H, H, sec-Bu, Br), (M-6438, Cl, H, H, sec-Bu, CH3), (M-6439, Cl, H, H, n-Pen, H), (M-6440, Cl, H, H, n-Pen, Cl), (M-6441, MeO, H, H, n-Pen, F), (M-6442, Cl, H, H, n-Pen, CF3), (M-6443, Cl, H, H, n-Pen, Br), (M-6444, Cl, H, H, n-Pen, CH3), (M-6445, Cl, H, H, c-Pen, H), (M-6446, Cl, H, H, c-Pen, Cl), (M-6447, Cl, H, H, c-Pen, F), (M-6448, Cl, H, H, c-Pen, CF3), (M-6449, Cl, H, H, c-Pen, Br), (M-6450, Cl, H, H, c-Pen, CH3), (M-6451, Cl, H, H, n-Hex, H), (M-6452, Cl, H, H, n-Hex, Cl), (M-6453, Cl, H, H, n-Hex, F), (M-6454, Cl, H, H, n-Hex, CF3), (M-6455, Cl, H, H, n-Hex, Br), (M-6456, Cl, H, H, n-Hex, CH3), (M-6457, Cl, H, H, c-Hex, H), (M-6458, Cl, H, H, c-Hex, Cl), (M-6459, Cl, H, H, c-Hex, F), (M-6460, Cl, H, H, c-Hex, CF3), (M-6461, Cl, H, H, c-Hex, Br), (M-6462, Cl, H, H, c-Hex, CH3), (M-6463, Cl, H, H, OH, H), (M-6464, Cl, H, H, OH, Cl), (M-6465, Cl, H, H, OH, F), (M-6460, Cl, H, H, OH, CF3), (M-6467, Cl, H, H, OH, Br), (M-6468, Cl, H, H, OH, CH3), (M-6469, Cl, H, H, EtO, H), (M-6470, Cl, H, H, EtO, Cl), (M-6471, Cl, H, H, EtO, F), (M-6472, Cl, H, H, EtO, CF3), (M-6473, Cl, H, H, EtO, Br), (M-6474, Cl, H, H, EtO, CH3), (M-6475, Cl, H, H, n-PrO, H), (M-6476, Cl, H, H, n-PrO, Cl), (M-6477, Cl, H, H, n-PrO, F), (M-6478, Cl, H, H, n-PrO, CF3), (M-6479, Cl, H, H, n-PrO, Br), (M-6480, Cl, H, H, n-PrO, CH3), (M-6481, Cl, H, H, PhO, H), (M-6482, Cl, H, H, PhO, Cl), (M-6483, Cl, H, H, PhO, F), (M-6484, Cl, H, H, PhO, CF3), (M-6485, Cl, H, H, PhO, Br), (M-6486, Cl, H, H, PhO, CH3), (M-6487, Cl, H, H, BnO, H), (M-6488, Cl, H, H, BnO, Cl), (M-6489, Cl, H, H, BnO, F), (M-6490, Cl, H, H, BnO, CF3), (M-6491, Cl, H, H, BnO, Br), (M-6492, Cl, H, H, BnO, CH3), (M-6493, Cl, H, H, PhCH2CH2O, H), (M-6494, Cl, H, H, PhCH2CH2O, Cl), (M-6495, Cl, H, H, PhCH2CH2O, F), (M-6496, Cl, H, H, PhCH2CH2O, CF3), (M-6497, Cl, H, H, PhCH2CH2O, Br), (M-6498, Cl, H, H, PhCH2CH2O, CH3), (M-6499, MeO, H, H, CF3O, CF3), (M-6500, Cl, H, H, CF3O, Cl), (M-6501, Cl, H, H, CF3O, F), (M-6502, Cl, H, H, CF3O, CF3), (M-6503, Cl, H, H, CF3O, Br), (M-6504, Cl, H, H, CF3O, CH3), (M-6505, MeO, H, H, Ph, H), (M-6506, Cl, H, H, Ph, Cl), (M-6507, Cl, H, H, Ph, F), (M-6508, Cl, H, H, Ph, CF3), (M-6509, Cl, H, H, Ph, Br), (M-6510, Cl, H, H, Ph, CH3), (M-6511, Cl, H, H, 4-F-Ph, H), (M-6512, Cl, H, H, 4-F-Ph, Cl), (M-6513, Cl, H, H, 4-F-Ph, F), (M-6514, Cl, H, H, 4-F-Ph, CF3), (M-6515, Cl, H, H, 4-F-Ph, Br), (M-6516, Cl, H, H, 4-F-Ph, CH3), (M-6517, Cl, H, H, 4-CF3-Ph, H), (M-6518, Cl, H, H, 4-CF3-Ph, Cl), (M-6519, Cl, H, H, 4-CF3-Ph, F), (M-6520, Cl, H, H, 4-CF3-Ph, CF3), (M-6521, Cl, H, H, 4-CF3-Ph, Br), (M-6522, Cl, H, H, 4-CF3-Ph, CH3), (M-6523, Cl, H, H, 4-(Me)2N-Ph, H), (M-6524, Cl, H, H, 4-(Me)2N-Ph, Cl), (M-6525, Cl, H, H, 4-(Me)2N-Ph, F), (M-6526, Cl, H, H, 4-(Me)2N-Ph, CF3), (M-6527, Cl, H, H, 4-(Me)2N-Ph, Br), (M-6528, Cl, H, H, 4-(Me)2N-Ph, CH3), (M-6529, Cl, H, H, 4-OH-Ph, H), (M-6530, Cl, H, H, 4-OH-Ph, Cl), (M-6531, Cl, H, H, 4-OH-Ph, F), (M-6532, Cl, H, H, 4-OH-Ph, CF3), (M-6533, Cl, H, H, 4-OH-Ph, Br), (M-6534, Cl, H, H, 4-OH-Ph, CH3), (M-6535, Cl, H, H, 3,4-di-F-Ph, H), (M-6536, Cl, H, H, 3,4-di-F-Ph, Cl), (M-6537, Cl, H, H, 3,4-di-F-Ph, F), (M-6538, Cl, H, H, 3,4-di-F-Ph, CF3), (M-6539, Cl, H, H, 3,4-di-F-Ph, Br), (M-6540, Cl, H, H, 3,4-di-F-Ph, CH3), (M-6541, Cl, H, H, 4-COOH-Ph, H), (M-6542, Cl, H, H, 4-COOH-Ph, Cl), (M-6543, Cl, H, H, 4-COOH-Ph, F), (M-6544, Cl, H, H, 4-COOH-Ph, CF3), (M-6545, Cl, H, H, 4-COOH-Ph, Br), (M-6546, Cl, H, H, 4-COOH-Ph, CH3), (M-6547, Cl, H, H, Bn, H), (M-6548, Cl, H, H, Bn, Cl), (M-6049, Cl, H, H, Bn, F), (M-6550, Cl, H, H, Bn, CF3), (M-6551, Cl, H, H, Bn, Br), (M-6552, Cl, H, H, Bn, CH3), (M-6553, Cl, H, H, 4-F-Bn, H), (M-6554, Cl, H, H, 4-F-Bn, Cl), (M-6555, Cl, H, H, 4-F-Bn, F), (M-6556, Cl, H, H, 4-F-Bn, CF3), (M-6557, Cl, H, H, 4-F-Bn, Br), (M-6558, Cl, H, H, 4-F-Bn, CH3), (M-6559, Cl, H, H, 2-Py, H), (M-6560, Cl, H, H, 2-Py, Cl), (M-6561, Cl, H, H, 2-Py, F), (M-6562, Cl, H, H, 2-Py, CF3), (M-6563, Cl, H, H, 2-Py, Br), (M-6564, Cl, H, H, 2-Py, CH3), (M-6565, Cl, H, H, 3-Py, H), (M-6566, Cl, H, H, 3-Py, Cl), (M-6667, Cl, H, H, 3-Py, F), (M-6568, Cl, H, H, 3-Py, CF3), (M-6569, Cl, H, H, 3-Py, Br), (M-6570, Cl, H, H, 3-Py, CH3), (M-6571, Cl, H, H, 4-Py, H), (M-6572, Cl, H, H, 4-Py, Cl), (M-6573, Cl, H, H, 4-Py, F), (M-6574, Cl, H, H, 4-Py, CF3), (M-6575, Cl, H, H, 4-Py, Br), (M-6576, Cl, H, H, 4-Py, CH3), (M-6577, Cl, H, H, 2-Th, H), (M-6578, Cl, H, H, 2-Th, Cl), (M-6579, Cl, H, H, 2-Th, F), (M-6680, Cl, H, H, 2-Th, CF3), (M-6581, Cl, H, H, 2-Th, Br), (M-6582, Cl, H, H, 2-Th, CH3), (M-6583, Cl, H, H, 3-Th, H), (M-6584, Cl, H, H, 3-Th, Cl), (M-6585, Cl, H, H, 3-Th, F), (M-6586, Cl, H, H, 3-Th, CF3), (M-6587, Cl, H, H, 3-Th, Br), (M-6588, Cl, H, H, 3-Th, CH3), (M-6589, Cl, H, H, pyrrazol-2-yl, H), (M-6590, Cl, H, H, pyrrazol-2-yl, Cl), (M-6591, Cl, H, H, pyrrazol-2-yl, F), (M-6592, Cl, H, H, pyrrazol-2-yl, CF3), (M-6593, Cl, H, H, pyrrazol-2-yl, Br), (M-6594, Cl, H, H, pyrrazol-2-yl, CH3), (M-6595, Cl, H, H, pyrrazol-3-yl, H), (M-6596, Cl, H, H, pyrrazol-3-yl, Cl), (M-6597, Cl, H, H, pyrrazol-3-yl, F), (M-6598, Cl, H, H, pyrrazol-3-yl, CF3), (M-6599, Cl, H, H, pyrrazol-3-yl, Br), (M-6600, Cl, H, H, pyrrazol-3-yl, CH3), (M-6601, Cl, H, H, pyrimidin-2-yl, H), (M-6602, Cl, H, H, pyrimidin-2-yl, Cl), (M-6603, Cl, H, H, pyrimidin-2-yl, F), (M-6604, Cl, H, H, pyrimidin-2-yl, CF3), (M-6605, Cl, H, H, pyrimidin-2-yl, Br), (M-6606, Cl, H, H, pyrimidin-2-yl, CH3), (M-6607, Cl, H, H, pyrimidin-4-yl, H), (M-6608, Cl, H, H, pyrimidin-4-yl, Cl), (M-6609, Cl, H, H, pyrimidin-4-yl, F), (M-6610, Cl, H, H, pyrimidin-4-yl, CF3), (M-6611, Cl, H, H, pyrimidin-4-yl, Br), (M-6612, Cl, H, H, pyrimidin-4-yl, CH3), (M-6613, Cl, H, H, pyrimidin-5-yl, H), (M-6614, Cl, H, H, pyrimidin-5-yl, Cl), (M-6615, Cl, H, H, pyrimidin-5-yl, F), (M-6616, Cl, H, H, pyrimidin-5-yl, CF3), (M-6617, Cl, H, H, pyrimidin-5-yl, Br), (M-6618, Cl, H, H, pyrimidin-5-yl, CH3), (M-6619, Cl, H, H, HOOCCH2CH2CH2, H), (M-6620, Cl, H, H, HOOCCH2CH2CH2, Cl), (M-6621, Cl, H, H, HOOCCH2CH2CH2, F), (M-6622, Cl, H, H, HOOCCH2CH2CH2, CF3), (M-6623, Cl, H, H, HOOCCH2CH2CH2, Br), (M-6624, Cl, H, H, HOOCCH2CH2CH2, CH3), (M-6625, Cl, H, H, HOOCCH2CH2CH2CH2, H), (M-6626, Cl, H, H, HOOCCH2CH2CH2CH2, Cl), (M-6627, Cl, H, H, HOOCCH2CH2CH2CH2, F), (M-6628, Cl, H, H, HOOCCH2CH2CH2CH2, CF3), (M-6629, Cl, H, H, HOOCCH2CH2CH2CH2, Br), (M-6630, Cl, H, H, HOOCCH2CH2CH2CH2, CH3), (M-6631, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, H), (M-6632, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-6633, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, F), (M-6634, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-6635, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-6636, Cl, H, H, (Me)2NCOCH2CH2CH2CH2, CH2), (M-6637, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-6638, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-6639, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-6640, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-6641, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-6642, Cl, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-6643, Cl, H, H, MeOCH2, H), (M-6644, Cl, H, H, MeOCH2, Cl), (M-6645, Cl, H, H, MeOCH2, F), (M-6646, Cl, H, H, MeOCH2, CF3), (M-6647, Cl, H, H, MeOCH2, Br), (M-6648, Cl, H, H, MeOCH2, CH3), (M-6649, Cl, H, H, EtOCH2, H), (M-6650, Cl, H, H, EtOCH2, Cl), (M-6651, Cl, H, H, EtOCH2, F), (M-6652, Cl, H, H, EtOCH2, CF3), (M-6653, Cl, H, H, EtOCH2, Br), (M-6654, Cl, H, H, EtOCH2, CH3), (M-6655, Cl, H, H, EtOCH2CH2, H), (M-6656, Cl, H, H, EtOCH2CH2, Cl), (M-6657, Cl, H, H, EtOCH2CH2, F), (M-6658, Cl, H, H, EtOCH2CH2, CF3), (M-6659, Cl, H, H, EtOCH2CH2, Br), (M-6660, Cl, H, H, EtOCH2CH2, CH3), (M-6661, Cl, H, H, MeOCH2CH2OCH2CH2, H), (M-6662, Cl, H, H, MeOCH2CH2OCH2CH2, Cl), (M-6663, Cl, H, H, MeOCH2CH2OCH2CH2, F), (M-6664, Cl, H, H, MeOCH2CH2OCH2CH2, CF3), (M-6665, Cl, H, H, MeOCH2CH2OCH2CH2, Br), (M-6666, Cl, H, H, MeOCH2CH2OCH2CH2, CH3), (M-6667, Cl, H, H, MeOCH2CH2, H), (M-6668, Cl, H, H, MeOCH2CH2, Cl), (M-6669, Cl, H, H, MeOCH2CH2, F), (M-6670, Cl, H, H, MeOCH2CH2, CF3), (M-6671, Cl, H, H, MeOCH2CH2, Br), (M-6672, Cl, H, H, MeOCH2CH2, CH3), (M-6673, Cl, H, H, HOCH2, H), (M-6674, Cl, H, H, HOCH2, Cl), (M-6675, Cl, H, H, HOCH2, F), (M-6676, Cl, H, H, HOCH2, CF3), (M-6677, Cl, H, H, HOCH2, Br), (M-6678, Cl, H, H, HOCH2, CH3), (M-6679, Cl, H, H, HOCH2CH2, H), (M-6680, Cl, H, H, HOCH2CH2, Cl), (M-6681, Cl, H, H, HOCH2CH2, F), (M-6682, Cl, H, H, HOCH2CH2, CF3), (M-6683, Cl, H, H, HOCH2CH2, Br), (M-6684, Cl, H, H, HOCH2CH2, CH3), (M-6685, Cl, H, H, HOCH2CH2CH2, H), (M-6686, Cl, H, H, HOCH2CH2CH2, Cl), (M-6687, Cl, H, H, HOCH2CH2CH2, F), (M-6688, Cl, H, H, HOCH2CH2CH2, CF3), (M-6689, Cl, H, H, HOCH2CH2CH2, Br), (M-6690, Cl, H, H, HOCH2CH2CH2, CH3), (M-6691, Cl, H, H, HOCH2CH2CH2CH2, H), (M-6692, Cl, H, H, HOCH2CH2CH2CH2, Cl), (M-6693, Cl, H, H, HOCH2CH2CH2CH2, F), (M-6694, Cl, H, H, HOCH2CH2CH2CH2, CF3), <M-6695, Cl, H, H, HOCH2CH2CH2CH2, Br), (M-6696, Cl, H, H, HOCH2CH2CH2CH2, CH3), (M-6697, Cl, H, H, HOCH2CH2CH2CH2CH2H), (M-6698, Cl, H, H, HOCH2CH2CH2CH2CH2, Cl), (M-6699, Cl, H, H, HOCH2CH2CH2CH2CH2, F), (M-6700, Cl, H, H, HOCH2CH2CH2CH2CH2, CF3), (M-6701, Cl, H, H, HOCH2CH2CH2CH2CH2, Br), (M-6702, Cl, H, H, HOCH2CH2CH2CH2CH2, CH3), (M-6703, Cl, H, H, HOCH2CH2OCH2CH2, H), (M-6704, Cl, H, H, HOCH2CH2OCH2CH2, Cl), (M-6705, Cl, H, H, HOCH2CH2OCH2CH3, F), (M-6706, Cl, H, H, HOCH2CH2OCH2CH2, CF3), (M-6707, Cl, H, H, HOCH2CH2OCH2CH2, Br), (M-6708, Cl, H, H, HOCH2CH2OCH2CH2, CH3), (M-6709, Cl, H, H, (Me)2N, H), (M-6710, Cl, H, H, (Me)2N, Cl), (M-6711, Cl, H, H, (Me)2N, F), (M-6712, Cl, H, H, (Me)2N, CF3), (M-6713, Cl, H, H, (Me)2N, Br), (M-6714, Cl, H, H, (Me)2N, CH3), (M-6715, Cl, H, H, piperidin-4-yl-methyl, H), (M-6716, Cl, H, H, piperidin-4-yl-methyl, Cl), (M-6717, Cl, H, H, piperidin-4-yl-methyl, F), (M-6718, Cl, H, H, piperidin-4-yl-methyl, CF3), (M-6719, Cl, H, H, piperidin-4-yl-methyl, Br), (M-6720, Cl, H, H, piperidin-4-yl-methyl, CH3), (M-6721, Cl, H, H, cyclohexylmethyl, H), (M-6722, Cl, H, H, cyclohexylmethyl, Cl), (M-6723, Cl, H, H, cyclohexylmethyl, F), (M-6724, Cl, H, H, cyclohexylmethyl, CF3), (M-6725, Cl, H, H, cyclohexylmethyl, Br), (M-6726, Cl, H, H, cyclohexylmethyl, CH3), (M-6727, MeO, H, F, H, H), (M-6728, Cl, H, F, H, Cl), (M-6729, MeO, H, F, H, F), (M-6730, MeO, H, F, H, CF3), (M-6731, MeO, H, F, H, Br), (M-6732, MeO, H, F, H, CH3), (M-6733, MeO, H, F, F, H), (M-6734, Cl, H, F, F, Cl), (M-6735, Cl, H, F, F, F), (M-6736, Cl, H, F, F, CF3), (M-6737, Cl, H, F, F, Br), (M-6738, Cl, H, F, F, CH3), (M-6739, Cl, H, F, Cl, H), (M-6740, Cl, H, F, Cl, Cl), (M-6741, Cl, H, F, Cl, F), (M-6742, Cl, H, F, Cl, CF3), (M-6743, Cl, H, F, Cl, Br), (M-6744, Cl, H, F, Cl, CH3), (M-6745, MeO, H, F, CH3, H), (M-6746, Cl, H, F, CH3, Cl), (M-6747, Cl, H, F, CH3, F), (M-6748, Cl, H, F, CH3, CF3), (M-6749, Cl, H, F, CH3, Br), (M-6750, Cl, H, F, CH3, CH3), (M-6751, MeO, H, F, Et, H), (M-6752, Cl, H, F, Et, Cl), (M-6753, Cl, H, F, Et, F), (M-6754, Cl, H, F, Et, CF3), (M-6755, Cl, H, F, Et, Br), (M-6756, Cl, H, F, Et, CH3), (M-6757, MeO, H, F, n-Pr, H), (M-6758, Cl, H, F, n-Pr, Cl), (M-6759, Cl, H, F, n-Pr, F), (M-6760, Cl, H, F, n-Pr, CF3), (M-6761, MeO, H, F, n-Pr, Br), (M-6762, Cl, H, F, n-Pr, CH3), (M-6763, Cl, H, F, c-Pr, H), (M-6764, Cl, H, F, c-Pr, Cl), (M-6765, Cl, H, F, c-Pr, F), (M-6766, Cl, H, F, c-Pr, CF3), (M-6767, Cl, H, F, c-Pr, Br), (M-6768, Cl, H, F, c-Pr, CH3), (M-6769, Cl, H, F, i-Pr, H), (M-6770, Cl, H, F, i-Pr, Cl), (M-6771, Cl, H, F, i-Pr, F), (M-6772, Cl, H, F, i-Pr, CF3), (M-6773, Cl, H, F, i-Pr, Br), (M-6774, Cl, H, F, i-Pr, CH3), (M-6775, MeO, H, F, n-Bu, H), (M-6776, Cl, H, F, n-Bu, Cl), (M-6777, Cl, H, F, n-Bu, F), (M-6778, Cl, H, F, n-Bu, CF3), (M-6779, Cl, H, F, n-Bu, Br), (M-6780, Cl, H, F, n-Bu, CH3), (M-6781, Cl, H, F, i-Bu, H), (M-6782, Cl, H, F, i-Bu, Cl), (M-6783, Cl, H, F, i-Bu, F), (M-6784, Cl, H, F, i-Bu, CF3), (M-6785, Cl, H, F, i-Bu, Br), (M-6786, Cl, H, F, i-Bu, CH3), (M-6787, Cl, H, F, sec-Bu, H), (M-6788, Cl, H, F, sec-Bu, Cl), (M-6789, Cl, H, F, sec-Bu, F), (M-6790, Cl, H, F, sec-Bu, CF3), (M-6791, Cl, H, F, sec-Bu, Br), (M-6792, Cl, H, F, sec-Bu, CH3), (M-6793, MeO, H, F, n-Pen, H), (M-6794, Cl, H, F, n-Pen, Cl), (M-6795, MeO, H, F, n-Pen, F), (M-6796, Cl, H, F, n-Pen, CF3), (M-6797, Cl, H, F, n-Pen, Br), (M-6798, Cl, H, F, n-Pen, CH3), (M-6799, Cl, H, F, c-Pen, H), (M-6800, Cl, H, F, c-Pen, Cl), (M-6801, Cl, H, F, c-Pen, F), (M-6802, Cl, H, F, c-Pen, CF3), (M-6803, Cl, H, F, c-Pen, Br), (M-6804, Cl, H, F, c-Pen, CH3), (M-6805, MeO, H, F, n-Hex, H), (M-6806, Cl, H, F, n-Hex, Cl), (M-6807, Cl, H, F, n-Hex, F), (M-6808, Cl, H, F, n-Hex, CF3), (M-6809, Cl, H, F, n-Hex, Br), (M-6810, Cl, H, F, n-Hex, CH3), (M-6811, MeO, H, F, c-Hex, H), (M-6812, Cl, H, F, c-Hex, Cl), (M-6813, Cl, H, F, c-Hex, F), (M-6814, Cl, H, F, c-Hex, CF3), (M-6815, Cl, H, F, c-Hex, Br), (M-6816, Cl, H, F, c-Hex, CH3), (M-6817, Cl, H, F, OH, H), (M-6818, Cl, H, F, OH, Cl), (M-6819, Cl, H, F, OH, F), (M-6820, Cl, H, F, OH, CF3), (M-6821, Cl, H, F, OH, Br), (M-6822, Cl, H, F, OH, CH3), (M-6823, MeO, H, F, EtO, H), (M-6824, Cl, H, F, EtO, Cl), (M-6825, Cl, H, F, EtO, F), (M-6826, Cl, H, F, EtO, CF3), (M-6827, Cl, H, F, EtO, Br), (M-6828, Cl, H, F, EtO, CH3), (M-6829, Cl, H, F, n-PrO, H), (M-6830, Cl, H, F, n-PrO, Cl), (M-6831, Cl, H, F, n-PrO, F), (M-6832, Cl, H, F, n-PrO, CF3), (M-6833, Cl, H, F, n-PrO, Br), (M-6834, Cl, H, F, n-PrO, CH3), (M-6835, Cl, H, F, PhO, H), (M-6836, Cl, H, F, PhO, Cl), (M-6837, Cl, H, F, PhO, F), (M-6838, Cl, H, F, PhO, CF3), (M-6839, Cl, H, F, PhO, Br), (M-6840, Cl, H, F, PhO, CH3), (M-6841, Cl, H, F, BnO, H), (M-6842, Cl, H, F, BnO, Cl), (M-6843, Cl, H, F, BnO, F), (M-6844, Cl, H, F, BnO, CF3), (M-6845, Cl, H, F, BnO, Br), (M-6846, Cl, H, F, BnO, CH3), (M-6847, Cl, H, F, PhCH2CH2O, H), (M-6848, Cl, H, F, PhCH2CH2O, Cl), (M-6849, Cl, H, F, PhCH2CH2O, F), (M-6850, Cl, H, F, PhCH2CH2O, CF3), (M-6851, Cl, H, F, PhCH2CH2O, Br), (M-6852, Cl, H, F, PhCH2CH2O, CH3), (M-6853, Cl, H, F, CF3O, H), (M-6854, Cl, H, F, CF3O, Cl), (M-6855, Cl, H, F, CF3O, F), (M-6856, Cl, H, F, CF3O, CF3), (M-6857, Cl, H, F, CF3O, Br), (M-6558, Cl, H, F, CF3O, CH3), (M-6859, MeO, H, F, Ph, H), (M-6860, Cl, H, F, Ph, Cl), (M-6861, MeO, H, F, Ph, F), (M-6862, Cl, H, F, Ph, CF3), (M-6863, Cl, H, F, Ph, Br), (M-6864, Cl, H, F, Ph, CH3), (M-6865, MeO, H, F, 4-F-Ph, H), (M-6866, Cl, H, F, 4-F-Ph, Cl), (M-6867, Cl, H, F, 4-F-Ph, F), (M-6868, Cl, H, F, 4-F-Ph, CF3), (M-6869, Cl, H, F, 4-F-Ph, Br), (M-6870, Cl, H, F, 4-F-Ph, CH3), (M-6871, Cl, H, F, 4-CF3-Ph, H), (M-6872, Cl, H, F, 4-CF3-Ph, Cl), (M-6873, Cl, H, F, 4-CF3-Ph, F), (M-6874, Cl, H, F, 4-CF3-Ph, CF3), (M-6875, Cl, H, F, 4-CF3-Ph, Br), (M-6876, Cl, H, F, 4-CF3-Ph, CH3), (M-6877, Cl, H, F, 4-(Me)2N-Ph, H), (M-6878, Cl, H, F, 4-(Me)2N-Ph, Cl), (M-6879, Cl, H, F, 4-(Me)2N-Ph, F), (M-6880, Cl, H, F, 4-(Me)2N-Ph, CF3), (M-6881, Cl, H, F, 4-(Me)2N-Ph, Br), (M-6882, Cl, H, F, 4-(Me)2N-Ph, CH3), (M-6883, Cl, H, F, 4-OH-Ph, H), (M-6884, Cl, H, F, 4-OH-Ph, Cl), (M-6885, Cl, H, F, 4-OH-Ph, F), (M-6886, Cl, H, F, 4-OH-Ph, CF3), (M-6887, Cl, H, F, 4-OH-Ph, Br), (M-6888, Cl, H, F, 4-OH-Ph, CH3), (M-6889, Cl, H, F, 3,4-di-F-Ph, H), (M-6890, Cl, H, F, 3,4-di-F-Ph, Cl), (M-6891, Cl, H, F, 3,4-di-F-Ph, F), (M-6892, Cl, H, F, 3,4-di-F-Ph, CF3), (M-6893, Cl, H, F, 3,4-di-F-Ph, Br), (M-6894, Cl, H, F, 3,4-di-F-Ph, CH3), (M-6895, Cl, H, F, 4-COOH-Ph, H), (M-6896, Cl, H, F, 4-COOH-Ph, Cl), (M-6897, Cl, H, F, 4-COOH-Ph, F), (M-6898, Cl, H, F, 4-COOH-Ph, CF3), (M-6899, Cl, H, F, 4-COOH-Ph, Br), (M-6900, Cl, H, F, 4-COOH-Ph, CH3), (M-6901, MeO, H, F, Bn, H), (M-6902, Cl, H, F, Bn, Cl), (M-6903, Cl, H, F, Bn, F), (M-6904, Cl, H, F, Bn, CF3), (M-6905, Cl, H, F, Bn, Br), (M-6906, Cl, H, F, Bn, CH3), (M-6907, Cl, H, F, 4-F-Bn, H), (M-6908, Cl, H, F, 4-F-Bn, Cl), (M-6909, Cl, H, F, 4-F-Bn, F), (M-6910, Cl, H, F, 4-F-Bn, CF3), (M-6911, Cl, H, F, 4-F-Bn, Br), (M-6912, Cl, H, F, 4-F-Bn, CH3), (M-6913, Cl, H, F, 2-Py, H), (M-6914, Cl, H, F, 2-Py, Cl), (M-6916, Cl, H, F, 2-Py, F), (M-6916, Cl, H, F, 2-Py, CF3), (M-6917, Cl, H, F, 2-Py, Br), (M-6918, Cl, H, F, 2-Py, CH3), (M-6919, MeO, H, F, 3-Py, H), (M-6920, Cl, H, F, 3-Py, Cl), (M-6921, Cl, H, F, 3-Py, F), (M-6922, Cl, H, F, 3-Py, CF3), (M-6923, Cl, H, F, 3-Py, Br), (M-6924, Cl, H, F, 3-Py, CH3), (M-6925, Cl, H, F, 4-Py, H), (M-6926, Cl, H, F, 4-Py, Cl), (M-6927, Cl, H, F, 4-Py, F), (M-6928, Cl, H, F, 4-Py, CF3), (M-6929, Cl, H, F, 4-Py, Br), (M-6930, Cl, H, F, 4-Py, CH3), (M-6931, Cl, H, F, 2-Th, H), (M-6932, Cl, H, F, 2-Th, Cl), (M-6933, Cl, H, F, 2-Th, F), (M-6934, Cl, H, F, 2-Th, CF3), (M-6935, Cl, H, F, 2-Th, Br), (M-6936, Cl, H, F, 2-Th, CH3), (M-6937, Cl, H, F, 3-Th, H), (M-6938, Cl, H, F, 3-Th, Cl), (M-6939, Cl, H, F, 3-Th, F), (M-6940, Cl, H, F, 3-Th, CF3), (M-6941, Cl, H, F, 3-Th, Br), (M-6942, Cl, H, F, 3-Th, CH3), (M-6943, Cl, H, F, pyrrazol-2-yl, H), (M-6944, Cl, H, F, pyrrazol-2-yl, Cl), (M-6945, Cl, H, F, pyrrazol-2-yl, F), (M-6946, Cl, H, F, pyrrazol-2-yl, CF3), (M-6947, Cl, H, F, pyrrazol-2-yl, Br), (M-6948, Cl, H, F, pyrrazol-2-yl, CH3), (M-6949, Cl, H, F, pyrrazol-3-yl, H), (M-6950, Cl, H, F, pyrrazol-3-yl, Cl), (M-6951, Cl, H, F, pyrrazol-3-yl, F), (M-6952, Cl, H, F, pyrrazol-3-yl, CF3), (M-6953, Cl, H, F, pyrrazol-3-yl, Br), (M-6954, Cl, H, F, pyrrazol-3-yl, CH3), (M-6955, Cl, H, F, pyrimidin-2-yl, H), (M-6956, Cl, H, F, pyrimidin-2-yl, Cl), (M-6957, Cl, H, F, pyrimidin-2-yl, F), (M-6958, Cl, H, F, pyrimidin-2-yl, CF3), (M-6959, Cl, H, F, pyrimidin-2-yl, Br), (M-6960, Cl, H, F, pyrimidin-2-yl, CH3), (M-6961, Cl, H, F, pyrimidin-4-yl, H), (M-6962, Cl, H, F, pyrimidin-4-yl, Cl), (M-6963, Cl, H, F, pyrimidin-4-yl, F), (M-6964, Cl, H, F, pyrimidin-4-yl, CF3), (M-6965, Cl, H, F, pyrimidin-4-yl, Br), (M-6966, Cl, H, F, pyrimidin-4-yl, CH3), (M-6967, Cl, H, F, pyrimidin-5-yl, H), (M-6968, Cl, H, F, pyrimidin-5-yl, Cl), (M-6969, Cl, H, F, pyrimidin-5-yl, F), (M-6970, Cl, H, F, pyrimidin-5-yl, CF3), (M-6971, Cl, H, F, pyrimidin-5-yl, Br), (M-6972, Cl, H, F, pyrimidin-5-yl, CH3), (M-6973, Cl, H, F, HOOCCH2CH2CH2, H), (M-6974, Cl, H, F, HOOCCH2CH2CH2, Cl), (M-6975, Cl, H, F, HOOCCH2CH2CH2, F), (M-6976, Cl, H, F, HOOCCH2CH2CH2, CF3), (M-6977, Cl, H, F, HOOCCH2CH2CH2, Br), (M-6978, Cl, H, F, HOOCCH2CH2CH2, CH3), (M-6979, Cl, H, F, HOOCCH2CH2CH2CH2, H), (M-6980, Cl, H, F, HOOCCH2CH2CH2CH2, Cl), (M-6981, Cl, H, F, HOOCCH2CH2CH2CH2, F), (M-6982, Cl, H, F, HOOCCH2CH2CH2CH2, CF3), (M-6983, Cl, H, F, HOOCCH2CH2CH2CH2, Br), (M-6984, Cl, H, F, HOOCCH2CH2CH2CH2, CH3), (M-6985, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, H), (M-6986, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-6987, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, F), (M-6988, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-6989, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-6990, Cl, H, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-6991, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-6992, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-6993, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-6994, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-6995, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-6996, Cl, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-6997, Cl, H, F, MeOCH2, H), (M-6998, Cl, H, F, MeOCH2, Cl), (M-6999, Cl, H, F, MeOCH2, F), (M-7000, Cl, H, F, MeOCH2, CF3), (M-7001, Cl, H, F, MeOCH2, Br), (M-7002, Cl, H, F, MeOCH2, CH3), (M-7003, Cl, H, F, EtOCH2, H), (M-7004, Cl, H, F, EtOCH2, Cl), (M-7005, Cl, H, F, EtOCH2, F), (M-7006, Cl, H, F, EtOCH2, CF3), (M-7007, Cl, H, F, EtOCH2, Br), (M-7008, Cl, H, F, EtOCH2, CH3), (M-7009, MeO, H, F, EtOCH2CH2, H), (M-7010, Cl, H, F, EtOCH2CH2, Cl), (M-7011, Cl, H, F, EtOCH2CH2, F), (M-7012, Cl, H, F, EtOCH2CH2, CF3), (M-7013, Cl, H, F, EtOCH2CH2, Br), (M-7014, Cl, H, F, EtOCH2CH2, CH3), (M-7015, Cl, H, F, MeOCH2CH2OCH2CH2, H), (M-7016, Cl, H, F, MeOCH2CH2OCH2CH2, Cl), (M-7017, Cl, H, F, MeOCH2CH2OCH2CH2, F), (M-7018, Cl, H, F, MeOCH2CH2OCH2CH2, CF3), (M-7019, Cl, H, F, MeOCH2CH2OCH2CH2, Br), (M-7020, Cl, H, F, MeOCH2CH2OCH2CH2, CH3), (M-7021, Cl, H, F, MeOCH2CH2, H), (M-7022, Cl, H, F, MeOCH2CH2, Cl), (M-7023, Cl, H, F, MeOCH2CH2, F), (M-7024, Cl, H, F, MeOCH2CH2, CF3), (M-7025, Cl, H, F, MeOCH2CH2, Br), (M-7026, Cl, H, F, MeOCH2CH2, CH3), (M-7027, Cl, H, F, HOCH2, H), (M-7028, Cl, H, F, HOCH2, Cl), (M-7029, Cl, H, F, HOCH2, F), (M-7030, Cl, H, F, HOCH2, CF3), (M-7031, Cl, H, F, HOCH2, Br), (M-7032, Cl, H, F, HOCH2, CH3), (M-7033, Cl, H, F, HOCH2CH2, H), (M-7034, Cl, H, F, HOCH2CH2, Cl), (M-7035, Cl, H, F, HOCH2CH2, F), (M-7036, Cl, H, F, HOCH2CH2, CF3), (M-7037, Cl, H, F, HOCH2CH2, Br), (M-7038, Cl, H, F, HOCH2CH2, CH3), (M-7039, Cl, H, F, HOCH2CH2CH2, H), (M-7040, Cl, H, F, HOCH2CH2CH2, Cl), (M-7041, Cl, H, F, HOCH2CH2CH2, F), (M-7042, Cl, H, F, HOCH2CH2CH2, CF3), (M-7043, Cl, H, F, HOCH2CH2CH2, Br), (M-7044, Cl, H, F, HOCH2CH2CH2, CH3), (M-7045, Cl, H, F, HOCH2CH2CH2CH2, H), (M-7046, Cl, H, F, HOCH2CH2CH2CH2, Cl), (M-7047, Cl, H, F, HOCH2CH2CH2CH2, F), (M-7048, Cl, H, F, HOCH2CH2CH2CH2, CF3), (M-7049, Cl, H, F, HOCH2CH2CH2CH2, Br), (M-7050, Cl, H, F, HOCH2CH2CH2CH2, CH3), (M-7051, Cl, H, F, HOCH2CH2CH2CH2CH2, H), (M-7052, Cl, H, F, HOCH2CH2CH2CH2CH2, Cl), (M-7053, Cl, H, F, HOCH2CH2CH2CH2CH2, F), (M-7054, Cl, H, F, HOCH2CH2CH2CH2CH2, CF3), (M-7055, Cl, H, F, HOCH2CH2CH2CH2CH2, Br), (M-7056, Cl, H, F, HOCH2CH2CH2CH2CH2CH3), (M-7057, Cl, H, F, HOCH2CH2OCH2CH2, H), (M-7058, Cl, H, F, HOCH2CH2OCH2CH2, Cl), (M-7059, Cl, H, F, HOCH2CH2OCH2CH2, F), (M-7060, Cl, H, F, HOCH2CH2OCH2CH2, CF3), (M-07061, Cl, H, F, HOCH2CH2OCH2CH2, Br), (M-7062, Cl, H, F, HOCH2CH2OCH2CH2, CH3), (M-7063, Cl, H, F, (Me)2N, H), (M-7064, Cl, H, F, (Me)2N, Cl), (M-7065, Cl, H, F, (Me)2N, F), (M-7066, Cl, H, F, (Me)2N, CF3), (M-7067, Cl, H, F, (Me)2N, Br), (M-7068, Cl, H, F, (Me)2N, CH3), (M-7069, Cl, H, F, piperidin-4-yl-methyl, H), (M-7070, Cl, H, F, piperidin-4-yl-methyl, Cl), (M-7071, Cl, H, F, piperidin-4-yl-methyl, F), (M-7072, Cl, H, F, piperidin-4-yl-methyl, CF3), (M-7073, Cl, H, F, piperidin-4-yl-methyl, Br), (M-7074, Cl, H, F, piperidin-4-yl-methyl, CH3), (M-7075, Cl, H, F, cyclohexylmethyl, H), (M-7076, Cl, H, F, cyclohexylmethyl, Cl), (M-7077, Cl, H, F, cyclohexylmethyl, F), (M-7078, Cl, H, F, cyclohexylmethyl, CF3), (M-7079, Cl, H, F, cyclohexylmethyl, Br), (M-7080, Cl, H, F, cyclohexylmethyl, CH3), (M-7081, Cl, H, Cl, H, H), (M-7082, Cl, H, Cl, H, Cl), (M-7083, Cl, H, Cl, H, F), (M-7084, Cl, H, Cl, H, CF3), (M-7085, Cl, H, Cl, H, Br), (M-7086, Cl, H, Cl, H, CH3), (M-7087, Cl, H, Cl, F, H), (M-7088, Cl, H, Cl, F, Cl), (M-7089, Cl, H, Cl, F, F), (M-7090, Cl, H, Cl, F, CF3), (M-7091, Cl, H, Cl, F, Br), (M-7092, Cl, H, Cl, F, CH3), (M-7093, MeO, H, Cl, Cl, H), (M-7094, Cl, H, Cl, Cl, Cl), (M-7095, Cl, H, Cl, Cl, F), (M-7096, Cl, H, Cl, Cl, CF3), (M-7097, Cl, H, Cl, Cl, Br), (M-7098, Cl, H, Cl, Cl, CH3), (M-7099, Cl, H, Cl, CH3, H), (M-7100, Cl, H, Cl, CH3, Cl), (M-7101, Cl, H, Cl, CH3, F), (M-7102, Cl, H, Cl, CH2, CF3), (M-7103, Cl, H, Cl, CH2, Br), (M-7104, Cl, H, Cl, CH3, CH3), (M-7105, Cl, H, Cl, Et, H), (M-7106, Cl, H, Cl, Et, Cl), (M-7107, Cl, H, Cl, Et, F), (M-7108, Cl, H, Cl, Et, CF3), (M-7109, Cl, H, Cl, Et, Br), (M-7110, Cl, H, Cl, Et, CH3), (M-7111, Cl, H, Cl, n-Pr, H), (M-7112, Cl, H, Cl, n-Pr, Cl), (M-7113, Cl, H, Cl, n-Pr, F), (M-7114, Cl, H, Cl, n-Pr, CF3), (M-7115, Cl, H, Cl, n-Pr, Br), (M-7116, Cl, H, Cl, n-Pr, CH3), (M-7117, Cl, H, Cl, c-Pr, H), (M-7118, Cl, H, Cl, c-Pr, Cl), (M-7119, Cl, H, Cl, c-Pr, F), (M-7120, Cl, H, Cl, c-Pr, CF3), (M-7121, Cl, H, Cl, c-Pr, Br), (M-7122, Cl, H, Cl, c-Pr, CH3), (M-7123, Cl, H, Cl, i-Pr, H), (M-7124, Cl, H, Cl, i-Pr, Cl), (M-7125, Cl, H, Cl, i-Pr, F), (M-7126, Cl, H, Cl, i-Pr, CF3), (M-7127, Cl, H, Cl, i-Pr, Br), (M-7128, Cl, H, Cl, i-Pr, CH3), (M-7129, Cl, H, Cl, n-Bu, H), (M-7130, Cl, H, Cl, n-Bu, Cl), (M-7131, Cl, H, Cl, n-Bu, F), (M-7132, Cl, H, Cl, n-Bu, CF3), (M-7133, Cl, H, Cl, n-Bu, Br), (M-7134, Cl, H, Cl, n-Bu, CH3), (M-7135, Cl, H, Cl, i-Bu, H), (M-7136, Cl, H, Cl, i-Bu, Cl), (M-7137, Cl, H, Cl, i-Bu, F), (M-7138, Cl, H, Cl, i-Bu, CF3), (M-7139, Cl, H, Cl, i-Bu, Br), (M-7140, Cl, H, Cl, i-Bu, CH3), (M-7141, Cl, H, Cl, sec-Bu, H), (M-7142, Cl, H, Cl, sec-Bu, Cl), (M-7143, Cl, H, Cl, sec-Bu, F), (M-7144, Cl, H, Cl, sec-Bu, CF3), (M-7145, Cl, H, Cl, sec-Bu, Br), (M-7146, Cl, H, Cl, sec-Bu, CH3), (M-7147, Cl, H, Cl, n-Pen, H), (M-7148, Cl, H, Cl, n-Pen, Cl), (M-7149, Cl, H, Cl, n-Pen, F), (M-7150, Cl, H, Cl, n-Pen, CF3), (M-7151, Cl, H, Cl, n-Pen, Br), (M-7152, Cl, H, Cl, n-Pen, CH3), (M-7153, Cl, H, Cl, c-Pen, H), (M-7154, Cl, H, Cl, c-Pen, Cl), (M-7155, Cl, H, Cl, c-Pen, F), (M-7156, Cl, H, Cl, c-Pen, CF3), (M-7157, Cl, H, Cl, c-Pen, Br), (M-7158, Cl, H, Cl, c-Pen, CH3), (M-7159, Cl, H, Cl, n-Hex, H), (M-7160, Cl, H, Cl, n-Hex, Cl), (M-7161, Cl, H, Cl, n-Hex, F), (M-7162, Cl, H, Cl, n-Hex, CF3), (M-7163, Cl, H, Cl, n-Hex, Br), (M-7164, Cl, H, Cl, n-Hex, CH3), (M-7165, Cl, H, Cl, c-Hex, H), (M-7166, Cl, H, Cl, c-Hex, Cl), (M-7167, Cl, H, Cl, c-Hex, F), (M-7168, Cl, H, Cl, c-Hex, CF3), (M-7169, Cl, H, Cl, c-Hex, Br), (M-7170, Cl, H, Cl, c-Hex, CH3), (M-7171, Cl, H, Cl, OH, H), (M-7172, Cl, H, Cl, OH, Cl), (M-7173, Cl, H, Cl, OH, F), (M-7174, Cl, H, Cl, OH, CF3), (M-7175, Cl, H, Cl, OH, Br), (M-7176, Cl, H, Cl, OH, CH3), (M-7177, Cl, H, Cl, EtO, H), (M-7178, Cl, H, Cl, EtO, Cl), (M-7179, Cl, H, Cl, EtO, F), (M-7180, Cl, H, Cl, EtO, CF3), (M-7181, Cl, H, Cl, EtO, Br), (M-7182, Cl, H, Cl, EtO, CH3), (M-7183, Cl, H, Cl, n-PrO, H), (M-7184, Cl, H, Cl, n-PrO, Cl), (M-7185, Cl, H, Cl, n-PrO, F), (M-7186, Cl, H, Cl, n-PrO, CF3), (M-7187, Cl, H, Cl, n-PrO, Br), (M-7188, Cl, H, Cl, n-PrO, CH3), (M-7189, Cl, H, Cl, PhO, H), (M-7190, Cl, H, Cl, PhO, Cl), (M-7191, Cl, H, Cl, PhO, F), (M-7192, Cl, H, Cl, PhO, CF3), (M-7193, Cl, H, Cl, PhO, Br), (M-7194, Cl, H, Cl, PhO, CH3), (M-7195, Cl, H, Cl, BnO, H), (M-7196, Cl, H, Cl, BnO, Cl), (M-7197, Cl, H, Cl, BnO, P), (M-7198, Cl, H, Cl, BnO, CF3), (M-7199, Cl, H, Cl, BnO, Br), (M-7200, Cl, H, Cl, BnO, CH3), (M-7201, Cl, H, Cl, PhCH2CH2O, H), (M-7202, Cl, H, Cl, PhCH2CH2O, Cl), (M-7203, Cl, H, Cl, PhCH2CH2O, F), (M-7204, Cl, H, Cl, PhCH2CH2O, CF3), (M-7205, Cl, H, Cl, PhCH2CH2O, Br), (M-7206, Cl, H, Cl, PhCH2CH2O, CH3), (M-7207, Cl, H, Cl, CF3O, H), (M-7208, Cl, H, Cl, CF30, Cl), (M-7209, Cl, H, Cl, CF3O, F), (M-7210, Cl, H, Cl, CF3O, CF3), (M-7211, Cl, H, Cl, CF3O, Br), (M-7212, Cl, H, Cl, CF3O, CH3), (M-7213, Cl, H, Cl, Ph, H), (M-7214, Cl, H, Cl, Ph, Cl), (M-7215, Cl, H, Cl, Ph, F), (M-7216, Cl, H, Cl, Ph, CF3), (M-7217, Cl, H, Cl, Ph, Br), (M-7218, Cl, H, Cl, Ph, CH3), (M-7219, Cl, H, Cl, 4-F-Ph, H), (M-7220, Cl, H, Cl, 4-F-Ph, Cl), (M-7221, Cl, H, Cl, 4-F-Ph, F), (M-7222, Cl, H, Cl, 4-F-Ph, CF3), (M-7223, Cl, H, Cl, 4-F-Ph, Br), (M-7224, Cl, H, Cl, 4-F-Ph, CH3), (M-7225, Cl, H, Cl, 4-CF3-Ph, H), (M-7226, Cl, H, Cl, 4-CF3-Ph, Cl), (M-7227, Cl, H, Cl, 4-CF3-Ph, F), (M-7228, Cl, H, Cl, 4-CF3-Ph, CF3), (M-7229, Cl, H, Cl, 4-CF3-Ph, Br), (M-7230, Cl, H, Cl, 4-CF3-Ph, CH3), (M-7231, Cl, H, Cl, 4-(Me)2N-Ph, H), (M-7232, Cl, H, Cl, 4-(Me)2N-Ph, Cl), (M-7233, Cl, H, Cl, 4-(Me)2N-Ph, F), (M-7234, Cl, H, Cl, 4-(Me)2N-Ph, CF3), (M-7235, Cl, H, Cl, 4-(Me)2N-Ph, Br), (M-7236, Cl, H, Cl, 4-(Me)2N-Ph, CH3), (M-7237, Cl, H, Cl, 4-OH-Ph, H), (M-7238, Cl, H, Cl, 4-OH-Ph, Cl), (M-7239, Cl, H, Cl, 4-OH-Ph, F), (M-7240, Cl, H, Cl, 4-OH-Ph, CF3), (M-7241, Cl, H, Cl, 4-OH-Ph, Br), (M-7242, Cl, H, Cl, 4-OH-Ph, CH3), (M-7243, Cl, H, Cl, 3,4-di-F-Ph, H), (M-7244, Cl, H, Cl, 3,4-di-F-Ph, Cl), (M-7245, Cl, H, Cl, 3,4-di-F-Ph, F), (M-7246, Cl, H, Cl, 3,4-di-F-Ph, CF3), (M-7247, Cl, H, Cl, 3,4-di-F-Ph, Br), (M-7248, Cl, Ft, Cl, 3,4-di-F-Ph, CH3), (M-7249, Cl, H, Cl, 4-COOH-Ph, H), (M-7250, Cl, H, Cl, 4-COOH-Ph, Cl), (M-7251, Cl, H, Cl, 4-COOH-Ph, F), (M-7252, Cl, H, Cl, 4-COOH-Ph, CF3), (M-7253, Cl, H, Cl, 4-COOH-Ph, Br), (M-7254, Cl, H, Cl, 4-COOH-Ph, CH3), (M-7255, Cl, H, Cl, Bn, H), (M-7256, Cl, H, Cl, Bn, Cl), (M-7257, Cl, H, Cl, Bn, F), (M-7258, Cl, H, Cl, Bn, CF3), (M-7259, Cl, H, Cl, Bn, Br), (M-7260, Cl, H, Cl, Bn, CH3), (M-7261, Cl, H, Cl, 4-F-Bn, H), (M-7262, Cl, H, Cl, 4-F-Bn, Cl), (M-7263, Cl, H, Cl, 4-F-Bn, F), (M-7264, Cl, H, Cl, 4-F-Bn, CF3), (M-7265, Cl, H, Cl, 4-F-Bn, Br), (M-7266, Cl, H, Cl, 4-F-Bn, CH3), (M-7267, Cl, H, Cl, 2-Py, H), (M-7268, Cl, H, Cl, 2-Py, Cl), (M-7269, Cl, H, Cl, 2-Py, F), (M-7270, Cl, H, Cl, 2-Py, CF3), (M-7271, Cl, H, Cl, 2-Py, Br), (M-7272, Cl, H, Cl, 2-Py, CH3), (M-7273, Cl, H, Cl, 3-Py, H), (M-7274, Cl, H, Cl, 3-Py, Cl), (M-7275, Cl, H, Cl, 3-Py, F), (M-7276, Cl, H, Cl, 3-Py, CF3), (M-7277, Cl, H, Cl, 3-Py, Br), (M-7278, Cl, H, Cl, 3-Py, CH3), (M-7279, Cl, H, Cl, 4-Py, H), (M-7280, Cl, H, Cl, 4-Py, Cl), (M-7281, Cl, H, Cl, 4-Py, F), (M-7282, Cl, H, Cl, 4-Py, CF3), (M-7283, Cl, H, Cl, 4-Py, Br), (M-7284, Cl, H, Cl, 4-Py, CH3), (M-7285, Cl, H, Cl, 2-Th, H), (M-7286, Cl, H, Cl, 2-Th, Cl), (M-7287, Cl, H, Cl, 2-Th, F), (M-7288, Cl, H, Cl, 2-Th, CF3), (M-7289, Cl, H, Cl, 2-Th, Br), (M-7290, Cl, H, Cl, 2-Th, CH3), (M-7291, Cl, H, Cl, 3-Th, H), (M-7292, Cl, H, Cl, 3-Th, Cl), (M-7293, Cl, H, Cl, 3-Th, F), (M-7294, Cl, H, Cl, 3-Th, CF3), (M-7295, Cl, H, Cl, 3-Th, Br), (M-7296, Cl, H, Cl, 3-Th, CH3), (M-7297, Cl, H, Cl, pyrrazol-2-yl, H), (M-7298, Cl, H, Cl, pyrrazol-2-yl, Cl), (M-7299, Cl, H, Cl, pyrrazol-2-yl, F), (M-7300, Cl, H, Cl, pyrrazol-2-yl, CF3), (M-7301, Cl, H, Cl, pyrrazol-2-yl, Br), (M-7302, Cl, H, Cl, pyrrazol-2-yl, CH3), (M-7303, Cl, H, Cl, pyrrazol-3-yl, H), (M-7304, Cl, H, Cl, pyrrazol-3-yl, Cl), (M-7305, Cl, H, Cl, pyrrazol-3-yl, F), (M-7306, Cl, H, Cl, pyrrazol-3-yl, CF3), (M-7307, Cl, H, Cl, pyrrazol-3-yl, Br), (M-7308, Cl, H, Cl, pyrrazol-3-yl, CH3), (M-7309, Cl, H, Cl, pyrimidin-2-yl, H), (M-7310, Cl, H, Cl, pyrimidin-2-yl, Cl), (M-7311, Cl, H, Cl, pyrimidin-2-yl, F), (M-7312, Cl, H, Cl, pyrimidin-2-yl, CF3), (M-7313, Cl, H, Cl, pyrimidin-2-yl, Br), (M-7314, Cl, H, Cl, pyrimidin-2-yl, CH3), (M-7315, Cl, H, Cl, pyrimidin-4-yl, H), (M-7316, Cl, H, Cl, pyrimidin, 4-yl, Cl), (M-7317, Cl, H, Cl, pyrimidin-4-yl, F), (M-7318, Cl, H, Cl, pyrimidin-4-yl, CF3), (M-7319, Cl, H, Cl, pyrimidin-4-yl, Br), (M-7320, Cl, H, Cl, pyrimidin-4-yl, CH3), (M-7321, Cl, H, Cl, pyrimidin-5-yl, H), (M-7322, Cl, H, Cl, pyrimidin-5-yl, Cl), (M-7323, Cl, H, Cl, pyrimidin-5-yl, F), (M-7324, Cl, H, Cl, pyrimidin-5-yl, CF3), (M-7325, Cl, H, Cl, pyrimidin-5-yl, Br), (M-7326, Cl, H, Cl, pyrimidin-5-yl, CH3), (M-7327, Cl, H, Cl, HOOCCH2CH2CH2, H), (M-7328, Cl, H, Cl, HOOCCH2CH2CH2, Cl), (M-7329, Cl, H, Cl, HOOCCH2CH2CH2, F), (M-7330, Cl, H, Cl, HOOCCH2CH2CH2, CF3), (M-7331, Cl, H, Cl, HOOCCH2CH2CH2, Br), (M-7332, Cl, H, Cl, HOOCCH2CH2CH2, CH3), (M-7333, Cl, H, Cl, HOOCCH2CH2CH2CH2, H), (M-7334, Cl, H, Cl, HOOCCH2CH2CH2CH2, Cl), (M-7335, Cl, H, Cl, HOOCCH2CH2CH2CH2, F), (M-7336, Cl, H, Cl, HOOCCH2CH2CH2CH2, CF3), (M-7337, Cl, H, Cl, HOOCCH2CH2CH2CH2, Br), (M-7338, Cl, H, Cl, HOOCCH2CH2CH2CH2, CH3), (M-7339, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-7340, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-7341, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-7342, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-7343, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-7344, Cl, B, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-7345, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-7346, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-7347, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-7348, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-7349, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-7350, Cl, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-7351, Cl, H, Cl, MeOCH2, H), (M-7352, Cl, H, Cl, MeOCH2, Cl), (M-7353, Cl, H, Cl, MeOCH2, F), (M-7354, Cl, H, Cl, MeOCH2, CF3), (M-7355, Cl, H, Cl, MeOCH2, Br), (M-7356, Cl, H, Cl, MeOCH2, CH3), (M-7357, Cl, H, Cl, EtOCH2, H), (M-7358, Cl, H, Cl, EtOCH2, Cl), (M-7359, Cl, H, Cl, EtOCH2, F), (M-7360, Cl, H, Cl, EtOCH2, CF3), (M-7361, Cl, H, Cl, EtOCH2, Br), (M-7362, Cl, H, Cl, EtOCH2, CH3), (M-7363, Cl, H, Cl, EtOCH2CH2, H), (M-7364, Cl, H, Cl, EtOCH2CH2, Cl), (M-7365, Cl, H, Cl, EtOCH2CH2, F), (M-7366, Cl, H, Cl, EtOCH2CH2, CF3), (M-7367, Cl, H, Cl, EtOCH2CH2, Br), (M-7368, Cl, H, Cl, EtOCH2CH2, CH3), (M-7369, Cl, H, Cl, MeOCH2CH2OCH2CH2, H), (M-7370, Cl, H, Cl, MeOCH2CH2OCH2CH2, Cl), (M-7371, Cl, H, Cl, MeOCH2CH2OCH2CH2, F), (M-7372, Cl, H, Cl, MeOCH2CH2OCH2CH2, CF3), (M-7373, Cl, H, Cl, MeOCH2CH2OCH2CH2, Br), (M-7374, Cl, H, Cl, MeOCH2CH2OCH2CH2, CH3), (M-7375, Cl, H, Cl, MeOCH2CH2, H), (M-7376, Cl, H, Cl, MeOCH2CH2, Cl), (M-7377, Cl, H, Cl, MeOCH2CH2, F), (M-7378, Cl, H, Cl, MeOCH2CH2, CF3), (M-7379, Cl, H, Cl, MeOCH2CH2, Br), (M-7380, Cl, H, Cl, MeOCH2CH2, CH3), (M-7381, Cl, H, Cl, HOCH2, H), (M-7382, Cl, H, Cl, HOCH2, Cl), (M-7383, Cl, H, Cl, HOCH2, F), (M-7384, Cl, H, Cl, HOCH2, CF3), (M-7385, Cl, H, Cl, HOCH2, Br), (M-7386, Cl, H, Cl, HOCH2, CH3), (M-7387, Cl, H, Cl, HOCH2CH2, H), (M-7388, Cl, H, Cl, HOCH2CH2, Cl), (M-7389, Cl, H, Cl, HOCH2CH2, F), (M-7390, Cl, H, Cl, HOCH2CH2, CF3), (M-7391, Cl, H, Cl, HOCH2CH2, Br), (M-7392, Cl, H, Cl, HOCH2CH2, CH3), (M-7393, Cl, H, Cl, HOCH2CH2CH2, H), (M-7394, Cl, H, Cl, HOCH2CH2CH2, Cl), (M-7396, Cl, H, Cl, HOCH2CH2CH2, F), (M-7396, Cl, H, Cl, HOCH2CH2CH2, CF3), (M-7397, Cl, H, Cl, HOCH2CH2CH2, Br), (M-7398, Cl, H, Cl, HOCH2CH2CH2, CH3), (M-7399, Cl, H, Cl, HOCH2CH2CH2CH2, H), (M-7400, Cl, H, Cl, HOCH2CH2CH2CH2, Cl), (M-7401, Cl, H, Cl, HOCH2CH2CH2CH2, F), (M-7402, Cl, H, Cl, HOCH2CH2CH2CH2, CF3), (M-7403, Cl, H, Cl, HOCH2CH2CH2CH2, Br), (M-7404, Cl, H, Cl, HOCH2CH2CH2CH2, CH3), (M-7405, Cl, H, Cl, HOCH2CH2CH2CH2CH2, H), (M-7406, Cl, H, Cl, HOCH2CH2CH2CH2CH2, Cl), (M-7407, Cl, H, Cl, HOCH2CH2CH2CH2CH2, F), (M-7408, Cl, H, Cl, HOCH2CH2CH2CH2CH2, CF3), (M-7409, Cl, H, Cl, HOCH2CH2CH2CH2CH2, Br), (M-7410, Cl, H, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-7411, Cl, H, Cl, HOCH2CH2OCH2CH2, H), (M-7412, Cl, H, Cl, HOCH2CH2OCH2CH2, Cl), (M-7413, Cl, H, Cl, HOCH2CH2OCH2CH2, F), (M-7414, Cl, H, Cl, HOCH2CH2OCH2CH2, CF3), (M-7415, Cl, H, Cl, HOCH2CH2OCH2CH2, Br), (M-7416, Cl, H, Cl, HOCH2CH2OCH2CH2, CH3), (M-7417, Cl, H, Cl, (Me)2N, H), (M-7418, Cl, H, Cl, (Me)2N, Cl), (M-7419, Cl, H, Cl, (Me)2N, F), (M-7420, Cl, H, Cl, (Me)2N, CF3), (M-7421, Cl, H, Cl, (Me)2N, Br), (M-7422, Cl, H, Cl, (Me)2N, CH3), (M-7423, Cl, H, Cl, piperidin-4-yl-methyl, H), (M-7424, Cl, H, Cl, piperidin-4-yl-methyl, Cl), (M-7425, Cl, H, Cl, piperidin-4-yl-methyl, F), (M-7426, Cl, H, Cl, piperidin-4-yl-methyl, CF3), (M-7427, Cl, H, Cl, piperidin-4-yl-methyl, Br), (M-7428, Cl, H, Cl, piperidin-4-yl-methyl, CH3), (M-7429, Cl, H, Cl, cyclohexylmethyl, H), (M-7430, Cl, H, Cl, cyclohexylmethyl, Cl), (M-7431, Cl, H, Cl, cyclohexylmethyl, F), (M-7432, Cl, H, Cl, cyclohexylmethyl, CF3), (M-7433, Cl, H, Cl, cyclohexylmethyl, Br), (M-7434, Cl, H, Cl, cyclohexylmethyl, CH3), (M-7435, Cl, F, H, H, H), (M-7436, Cl, F, H, H, Cl), (M-7437, Cl, F, H, H, F), (M-7438, Cl, F, H, H, CF3), (M-7439, Cl, F, H, H, Br), (M-7440, Cl, F, H, H, CH3), (M-7441, Cl, F, H, F, H), (M-7442, Cl, F, H, F, Cl), (M-7443, Cl, F, H, F, F), (M-7444, Cl, F, H, F, CF3), (M-7445, Cl, F, H, F, Br), (M-7446, Cl, F, H, F, CH3), (M-7447, Cl, F, H, Cl, H), (M-7448, Cl, F, H, Cl, Cl), (M-7449, Cl, F, H, Cl, F), (M-7450, Cl, F, H, Cl, CF3), (M-7451, Cl, F, H, Cl, Br), (M-7452, Cl, F, H, Cl, CH3), (M-7453, Cl, F, H, CH3, H), (M-7454, Cl, F, H, CH3, Cl), (M-7455, Cl, F, H, CH3, F), (M-7456, Cl, F, H, CH3, CF3), (M-7457, Cl, F, H, CH3, Br), (M-7458, Cl, F, H, CH3, CH3), (M-7459, Cl, F, H, Et, H), (M-7460, Cl, F, H, Et, Cl), (M-7461, Cl, F, H, Et, F), (M-7462, Cl, F, H, Et, CF2), (M-7463, Cl, F, H, Et, Br), (M-7464, Cl, F, H, Et, CH3), (M-7465, Cl, F, H, n-Pr, H), (M-7466, Cl, F, H, n-Pr, Cl), (M-7467, Cl, F, H, n-Pr, F), (M-7468, Cl, F, H, n-Pr, CF3), (M-7469, Cl, F, H, n-Pr, Br), (M-7470, Cl, F, H, n-Pr, CH3), (M-7471, Cl, F, H, c-Pr, H), (M-7472, Cl, F, H, c-Pr, Cl), (M-7473, Cl, F, H, c-Pr, F), (M-7474, Cl, F, H, c-Pr, CF3), (M-7475, Cl, F, H, c-Pr, Br), (M-7476, Cl, F, H, c-Pr, CH3), (M-7477, Cl, F, H, i-Pr, H), (M-7478, Cl, F, H, i-Pr, Cl), (M-7479, Cl, F, H, i-Pr, F), (M-7480, Cl, F, H, i-Pr, CF3), (M-7481, Cl, F, ft, i-Pr, Br), (M-7482, Cl, F, H, i-Pr, CH3), (M-7483, MeO, F, H, n-Bu, H), (M-7484, Cl, F, H, n-Bu, Cl), (M-7480, Cl, F, H, n-Bu, F), (M-7486, Cl, F, H, n-Bu, CF3), (M-7487, Cl, F, H, n-Bu, Br), (M-7488, Cl, F, H, n-Bu, CH3), (M-7489, Cl, F, H, i-Bu, H), (M-7490, Cl, F, H, i-Bu, Cl), (M-7491, Cl, F, H, i-Bu, F), (M-7492, Cl, F, H, i-Bu, CF3), (M-7493, Cl, F, H, i-Bu, Br), (M-7494, Cl, F, H, i-Bu, CH3), (M-7495, Cl, F, H, sec-Bu, H), (M-7496, Cl, F, H, sec-Bu, Cl), (M-7497, Cl, F, H, sec-Bu, F), (M-7498, Cl, F, H, sec-Bu, CF3), (M-7499, Cl, F, H, sec-Bu, Br), (M-7500, Cl, F, H, sec-Bu, CH3), (M-7501, Cl, F, H, n-Pen, H), (M-7502, Cl, F, H, n-Pen, Cl), (M-7503, Cl, F, H, n-Pen, F), (M-7504, Cl, F, H, n-Pen, CF3), (M-7505, Cl, F, H, n-Pen, Br), (M-7506, CL F, H, n-Pen, CH3), (M-7507, Cl, F, H, c-Pen, H), (M-7508, Cl, F, H, c-Pen, Cl), (M-7509, Cl, F, H, c-Pen, F), (M-7510, Cl, F, H, c-Pen, CF3), (M-7511, Cl, F, H, c-Pen, Br), (M-7512, Cl, F, H, c-Pen, CH3), (M-7513, Cl, F, H, n-Hex, H), (M-7514, Cl, F, H, n-Hex, Cl), (M-7515, Cl, F, H, n-Hex, F), (M-7516, Cl, F, H, n-Hex, CF3), (M-7517, Cl, F, H, n-Hex, Br), (M-7518, Cl, F, H, n-Hex, CH3), (M-7519, Cl, F, H, c-Hex, H), (M-7520, Cl, F, H, c-Hex, Cl), (M-7521, Cl, F, H, c-Hex, F), (M-7522, Cl, F, H, c-Hex, CF3), (M-7523, Cl, F, H, c-Hex, Br), (M-7524, Cl, F, H, c-Hex, CH3), (M-7525, Cl, F, H, OH, H), (M-7526, Cl, F, H, OH, Cl), (M-7527, Cl, F, H, OH, F), (M-7528, Cl, F, H, OH, CF3), (M-7529, Cl, F, H, OH, Br), (M-7530, Cl, F, H, OH, CH3), (M-7531, Cl, F, H, EtO, H), (M-7532, Cl, F, H, EtO, Cl), (M-7533, Cl, F, H, EtO, F), (M-7534, C), F, H, EtO, CF3), (M-7535, Cl, F, H, EtO, Br), (M-7536, Cl, F, H, EtO, CH3), (M-7537, Cl, F, H, n-PrO, H), (M-7538, Cl, F, H, n-PrO, Cl), (M-7539, Cl, F, H, n-PrO, F), (M-7540, Cl, F, H, n-PrO, CF3), (M-7541, Cl, F, H, n-PrO, Br), (M-7542, Cl, F, H, n-PrO, CH3), (M-7543, Cl, F, H, PhO, H), (M-7544, Cl, F, H, PhO, Cl), (M-7545, Cl, F, H, PhO, F), (M-7546, Cl, F, H, PhO, CF3), (M-7547, Cl, F, H, PhO, Br), (M-7548, Cl, F, H, PhO, CH3), (M-7549, Cl, F, H, BnO, H), (M-7550, Cl, F, H, BnO, Cl), (M-7551, Cl, F, H, BnO, F), (M-7552, Cl, F, H, BnO, CF3), (M-7553, Cl, F, H, BnO, Br), (M-7554, Cl, F, H, BnO, CH3), (M-7555, Cl, F, H, PhCH2CH2O, H), (M-7556, Cl, F, H, PhCH2CH2O, Cl), (M-7557, Cl, F, H, PhCH2CH2O, F), (M-7558, Cl, F, H, PhCH2CH2O, CF3), (M-7559, Cl, F, H, PhCH2CH2O, Br), (M-7560, Cl, F, H, PhCH2CH2O, CH3), (M-7561, Cl, F, H, CF3O, H), (M-7562, Cl, F, H, CF3O, Cl), (M-7563, Cl, F, H, CF3O, F), (M-7564, Cl, F, H, CF3O, CF3), (M-7565, Cl, F, H, CF3O, Br), (M-7566, Cl, F, H, CF3O, CH3), (M-7567, Cl, F, H, Ph, H), (M-7568, Cl, F, H, Ph, Cl), (M-7569, Cl, F, H, Ph, F), (M-7570, Cl, F, H, Ph, CF3), (M-7571, Cl, F, H, Ph, Br), (M-7572, Cl, F, H, Ph, CH3), (M-7573, Cl, F, H, 4-F-Ph, H), (M-7574, Cl, F, H, 4-F-Ph, Cl), (M-7575, Cl, F, H, 4-F-Ph, F), (M-7576, Cl, F, H, 4-F-Ph, CF3), (M-7577, Cl, F, H, 4-F-Ph, Br), (M-7578, Cl, F, H, 4-F-Ph, CH3), (M-7579, Cl, F, H, 4-CF3-Ph, H), (M-7580, Cl, F, H, 4-CF3-Ph, Cl), (M-7581, Cl, F, H, 4-CF3-Ph, F), (M-7582, Cl, F, H, 4-CF3-Ph, CF3), (M-7583, Cl, F, H, 4-CF3-Ph, Br), (M-7584, Cl, F, H, 4-CF3-Ph, CH3), (M-7585, Cl, F, H, 4-(Me)2N-Ph, H), (M-7586, Cl, F, H, 4-(Me)2N-Ph, Cl), (M-7587, Cl, F, H, 4-(Me)2N-Ph, F), (M-7588, Cl, F, H, 4-(Me)2N-Ph, CF3), (M-7589, Cl, F, H, 4-(Me)2N-Ph, Br), (M-7590, Cl, F, H, 4-(Me)2N-Ph, CH3), (M-7591, Cl, F, H, 4-OH-Ph, H), (M-7592, Cl, F, H, 4-OH-Ph, Cl), (M-7593, Cl, F, H, 4-OH-Ph, F), (M-7594, Cl, F, H, 4-OH-Ph, CF3), (M-7595, Cl, F, H, 4-OH-Ph, Br), (M-7596, Cl, F, H, 4-OH-Ph, CH3), (M-7597, Cl, F, H, 3,4-di-F-Ph, H), (M-7598, Cl, F, H, 3,4-di-F-Ph, Cl), (M-7599, Cl, F, H, 3,4-di-F-Ph, F), (M-7600, Cl, F, H, 3,4-di-F-Ph, CF3), (M-7601, Cl, F, H, 3,4-di-F-Ph, Br), (M-7602, Cl, F, H, 3,4-di-F-Ph, CH3), (M-7603, Cl, F, H, 4-COOH-Ph, H), (M-7604, Cl, F, H, 4-COOH-Ph, Cl), (M-7605, Cl, F, H, 4-COOH-Ph, F), (M-7606, Cl, F, H, 4-COOH-Ph, CF3), (M-7607, Cl, F, H, 4-COOH-Ph, Br), (M-7608, Cl, F, H, 4-COOH-Ph, CH3), (M-7609, Cl, F, H, Bn, H), (M-7610, Cl, F, H, Bn, Cl), (M-7611, Cl, F, H, Bn, F), (M-7612, Cl, F, H, Bn, CF3), (M-7613, Cl, F, H, Bn, Br), (M-7614, Cl, F, H, Bn, CH3), (M-7615, Cl, F, H, 4-F-Bn, H), (M-7616, Cl, F, H, 4-F-Bn, Cl), (M-7617, Cl, F, H, 4-F-Bn, F), (M-7618, Cl, F, H, 4-F-Bn, CF3), (M-7619, Cl, F, H, 4-F-Bn, Br), (M-7620, Cl, F, H, 4-F-Bn, CH3), (M-7621, Cl, F, H, 2-Py, H), (M-7622, Cl, F, H, 2-Py, Cl), (M-7623, Cl, F, H, 2-Py, F), (M-7624, Cl, F, H, 2-Py, CF3), (M-7625, Cl, F, H, 2-Py, Br), (M-7626, Cl, F, H, 2-Py, CH3), (M-7627, Cl, F, H, 3-Py, H), (M-7628, Cl, F, H, 3-Py, Cl), (M-7629, Cl, F, H, 3-Py, F), (M-7630, Cl, F, H, 3-Py, CF3), (M-7631, Cl, F, H, 3-Py, Br), (M-7632, Cl, F, H, 3-Py, CH3), (M-7633, Cl, F, H, 4-Py, H), (M-7634, Cl, F, H, 4-Py, Cl), (M-7635, Cl, F, H, 4-Py, F), (M-7636, Cl, F, H, 4-Py, CF3), (M-7637, Cl, F, H, 4-Py, Br), (M-7638, Cl, F, H, 4-Py, CH3), (M-7639, Cl, F, H, 2-Th, H), (M-7640, Cl, F, H, 2-Th, Cl), (M-7641, Cl, F, H, 2-Th, F), (M-7642, Cl, F, H, 2-Th, CF3), (M-7643, Cl, F, H, 2-Th, Br), (M-7644, Cl, F, H, 2-Th, CH3), (M-7645, Cl, F, H, 3-Th, H), (M-7646, Cl, F, H, 3-Th, Cl), (M-7647, Cl, F, H, 3-Th, F), (M-7648, Cl, F, H, 3-Th, CF3), (M-7649, Cl, F, H, 3-Th, Br), (M-7650, Cl, F, H, 3-Th, CH3), (M-7651, Cl, F, H, pyrrazol-2-yl, H), (M-7652, Cl, F, H, pyrrazol-2-yl, Cl), (M-7653, Cl, F, H, pyrrazol-2-yl, F), (M-7654, Cl, F, H, pyrrazol-2-yl, CF3), (M-7655, Cl, F, H, pyrrazol-2-yl, Br), (M-7656, Cl, F, H, pyrrazol-2-yl, CH3), (M-7657, Cl, F, H, pyrrazol-3-yl, H), (M-7658, Cl, F, H, pyrrazol-3-yl, Cl), (M-7659, Cl, F, H, pyrrazol-3-yl, F), (M-7660, Cl, F, H, pyrrazol-3-yl, CF3), (M-7661, Cl, F, H, pyrrazol-3-yl, Br), (M-7662, Cl, F, H, pyrrazol-3-yl, CH3), (M-7663, Cl, F, H, pyrimidin-2-yl, H), (M-7664, Cl, F, H, pyrimidin-2-yl, Cl), (M-7665, Cl, F, H, pyrimidin-2-yl, F), (M-7666, Cl, F, H, pyrimidin-2-yl, CF3), (M-7667, Cl, F, H, pyrimidin-2-yl, Br), (M-7668, Cl, F, H, pyrimidin-2-yl, CH3), (M-7669, Cl, F, H, pyrimidin-4-yl, H), (M-7670, Cl, F, H, pyrimidin-4-yl, Cl), (M-7671, Cl, F, H, pyrimidin-4-yl, F), (M-7672, Cl, F, H, pyrimidin-4-yl, CF3), (M-7673, Cl, F, H, pyrimidin-4-yl, Br), (M-7674, Cl, F, H, pyrimidin-4-yl, CH3), (M-7675, Cl, F, H, pyrimidin-5-yl, H), (M-7676, Cl, F, H, pyrimidin-5-yl, Cl), (M-7677, Cl, F, H, pyrimidin-5-yl, F), (M-7678, Cl, F, H, pyrimidin-5-yl, CF3), (M-7679, Cl, F, H, pyrimidin-5-yl, Br), (M-7680, Cl, F, H, pyrimidin-5-yl, CH3), (M-7681, Cl, F, H, HOOCCH2CH2CH2, H), (M-7682, Cl, F, H, HOOCCH2CH2CH2, Cl), (M-7683, Cl, F, H, HOOCCH2CH2CH2, F), (M-7684, Cl, F, H, HOOCCH2CH2CH2, CF3), (M-7685, Cl, F, H, HOOCCH2CH2CH2, Br), (M-7686, Cl, F, H, HOOCCH2CH2CH2, CH3), (M-7687, Cl, F, H, HOOCCH2CH2CH2CH2, H), (M-7688, Cl, F, H, HOOCCH2CH2CH2CH2, Cl), (M-7689, Cl, F, H, HOOCCH2CH2CH2CH2, F), (M-7690, Cl, F, H, HOOCCH2CH2CH2CH2, CF3), (M-7691, Cl, F, H, HOOCCH2CH2CH2CH2, Br), (M-7692, Cl, F, H, HOOCCH2CH2CH2CH2, CH3), (M-7693, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, H), (M-7694, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-7695, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, F), (M-7696, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-7697, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-7698, Cl, F, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-7699, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-7700, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-7701, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-7702, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-7703, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-7704, Cl, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-7705, Cl, F, H, MeOCH2, H), (M-7706, Cl, F, H, MeOCH2, Cl), (M-7707, Cl, F, H, MeOCH2, F), (M-7708, Cl, F, H, MeOCH2, CF3), (M-7709, Cl, F, H, MeOCH2, Br), (M-7710, Cl, F, H, MeOCH2, CH3), (M-7711, Cl, F, H, EtOCH2, H), (M-7712, Cl, F, H, EtOCH2, Cl), (M-7713, Cl, F, H, EtOCH2, F), (M-7714, Cl, F, H, EtOCH2, CF3), (M-7715, Cl, F, H, EtOCH2, Br), (M-7716, Cl, F, H, EtOCH2, CH3), (M-7717, Cl, F, H, EtOCH2CH2, H), (M-7718, Cl, F, H, EtOCH2CH2, Cl), (M-7719, Cl, F, H, EtOCH2CH2, F), (M-7720, Cl, F, H, EtOCH2CH2, CF3), (M-7721, Cl, F, H, EtOCH2CH2, Br), (M-7722, Cl, F, H, EtOCH2CH2, CH3), (M-7723, Cl, F, H, MeOCH2CH2OCH2CH2, H), (M-7724, Cl, F, H, MeOCH2CH2OCH2CH2, Cl), (M-7725, Cl, F, H, MeOCH2CH2OCH2CH2, F), (M-7726, Cl, F, H, MeOCH2CH2OCH2CH2, CF3), (M-7727, Cl, F, H, MeOCH2CH2OCH2CH2, Br), (M-7728, Cl, F, H, MeOCH2CH2OCH2CH2, CH3), (M-7729, Cl, F, H, MeOCH2CH2, H), (M-7730, Cl, F, H, MeOCH2CH2, Cl), (M-7731, Cl, F, H, MeOCH2CH2, F), (M-7732, Cl, F, H, MeOCH2CH2, CF3), (M-7733, Cl, F, H, MeOCH2CH2, Br), (M-7734, Cl, F, H, MeOCH2CH2, CH3), (M-7735, Cl, F, H, HOCH2, H), (M-7736, Cl, F, H, HOCH2, Cl), (M-7737, Cl, F, H, HOCH2, F), (M-7738, Cl, F, H, HOCH2, CF3), (M-7739, Cl, F, H, HOCH2, Br), (M-7740, Cl, F, H, HOCH2, CH3), (M-7741, Cl, F, H, HOCH2CH2, H), (M-7742, Cl, F, H, HOCH2CH2, Cl), (M-7743, Cl, F, H, HOCH2CH2, F), (M-7744, Cl, F, H, HOCH2CH2, CF3), (M-7745, Cl, F, H, HOCH2CH2, Br), (M-7746, Cl, F, H, HOCH2CH2, CH3), (M-7747, Cl, F, H, HOCH2CH2CH2, H), (M-7748, Cl, F, H, HOCH2CH2CH2, Cl), (M-7749, Cl, F, H, HOCH2CH2CH2, F), (M-7750, Cl, F, H, HOCH2CH2CH2, CF3), (M-7751, Cl, F, H, HOCH2CH2CH2, Br), (M-7752, Cl, F, H, HOCH2CH2CH2, CH3), (M-7753, Cl, F, H, HOCH2CH2CH2CH2, H), (M-7754, Cl, F, H, HOCH2CH2CH2CH2, Cl), (M-7755, Cl, F, H, HOCH2CH2CH2CH2, F), (M-7756, Cl, F, H, HOCH2CH2CH2CH2, CF3), (M-7757, Cl, F, H, HOCH2CH2CH2CH2, Br), (M-7758, Cl, F, H, HOCH2CH2CH2CH2, CH3), (M-7759, Cl, F, H, HOCH2CH2CH2CH2CH2H), (M-7760, Cl, F, H, HOCH2CH2CH2CH2CH2, Cl), (M-7761, Cl, F, H, HOCH2CH2CH2CH2CH2, F), (M-7762, Cl, F, H, HOCH2CH2CH2CH2CH2CF3), (M-7763, Cl, F, H, HOCH2CH2CH2CH2CH2Br), (M-7764, Cl, F, H, HOCH2CH2CH2CH2CH2CH3), (M-7765, Cl, F, H, HOCH2CH2OCH2CH2, H), (M-7766, Cl, F, H, HOCH2CH2OCH2CH2, Cl), (M-7767, Cl, F, H, HOCH2CH2OCH2CH2, F), (M-7768, Cl, F, H, HOCH2CH2OCH2CH2, CF3), (M-7769, Cl, F, H, HOCH2CH2OCH2CH2, Br), (M-7770, Cl, F, H, HOCH2CH2OCH2CH2, CH3), (M-7771, Cl, F, H, (Me)2N, H), (M-7772, Cl, F, H, (Me)2N, Cl), (M-7773, Cl, F, H, (Me)2N, F), (M-7774, Cl, F, H, (Me)2N, CF3), (M-7775, Cl, F, H, (Me)2N, Br), (M-7776, Cl, F, H, (Me)2N, CH3), (M-7777, Cl, F, H, piperidin-4-yl-methyl, H), (M-7778, Cl, F, H, piperidin-4-yl-methyl, Cl), (M-7779, Cl, F, H, piperidin-4-yl-methyl, F), (M-7780, Cl, F, H, piperidin-4-yl-methyl, CF3), (M-7781, Cl, F, H, piperidin-4-yl-methyl, Br), (M-7782, Cl, F, H, piperidin-4-yl-methyl, CH3), (M-7783, Cl, F, H, cyclohexylmethyl, H), (M-7784, Cl, F, H, cyclohexylmethyl, Cl), (M-7785, Cl F, H, cyclohexylmethyl, F), (M-7786, Cl, F, H, cyclohexylmethyl, CF3), (M-7787, Cl, F, H, cyclohexylmethyl, Br), (M-7788, Cl, F, H, cyclohexylmethyl, CH3), (M-7789, Cl, F, F, H, H), (M-7790, Cl, F, F, H, Cl), (M-7791, Cl, F, F, H, F), (M-7792, Cl, F, F, H, CF3), (M-7793, Cl, F, F, H, Br), (M-7794, Cl, F, F, H, CH3), (M-7795, Cl, F, F, F, H), (M-7796, Cl, F, F, F, Cl), (M-7797, Cl, F, F, F, F), (M-7798, Cl, F, F, F, CF3), (M-7799, Cl, F, F, F, Br), (M-7800, Cl, F, F, F, CH3), (M-7801, Cl, F, F, Cl, H), (M-7802, Cl, F, F, Cl, Cl), (M-7803, Cl, F, F, Cl, F), (M-7804, Cl, F, F, Cl, CF3), (M-7805, Cl, F, F, Cl, Br), (M-7806, Cl, F, F, Cl, CH3), (M-7807, Cl, F, F, CH3, H), (M-7808, Cl, F, F, CH3, Cl), (M-7809, Cl, F, F, CH3, F), (M-7810, Cl, F, F, CH3, CF3), (M-7811, Cl, F, F, CH3, Br), (M-7812, Cl, F, F, CH3, CH3), (M-7813, Cl, F, F, Et, H), (M-7814, Cl, F, F, Et, Cl), (M-7815, Cl, F, F, Et, F), (M-7816, Cl, F, F, Et, CF3), (M-7817, Cl, F, F, Et, Br), (M-7818, Cl, F, F, Et, CH3), (M-7819, Cl, F, F, n-Pr, H), (M-7820, Cl, F, F, n-Pr, Cl), (M-7821, Cl, F, F, n-Pr, F), (M-7822, Cl, F, F, n-Pr, CF3), (M-7823, Cl, F, F, n-Pr, Br), (M-7824, Cl, F, F, n-Pr, CH3), (M-7825, Cl, F, F, c-Pr, H), (M-7826, Cl, F, F, c-Pr, Cl), (M-7827, Cl, F, F, c-Pr, F), (M-7828, Cl, F, F, c-Pr, CF3), (M-7829, Cl, F, F, c-Pr, Br), (M-7830, Cl, F, F, c-Pr, CH3), (M-7831, Cl, F, F, i-Pr, H), (M-7832, Cl, F, F, i-Pr, Cl), (M-7833, Cl, F, F, i-Pr, F), (M-7834, Cl, F, F, i-Pr, CF3), (M-7835, Cl, F, F, i-Pr, Br), (M-7836, Cl, F, F, i-Pr, CH3), (M-7837, Cl, F, F, n-Bu, H), (M-7838, Cl, F, F, n-Bu, Cl), (M-7839, Cl, F, F, n-Bu, F), (M-7840, Cl, F, F, n-Bu, CF3), (M-7841, Cl, F, F, n-Bu, Br), (M-7842, Cl, F, F, n-Bu, CH3), (M-7843, Cl, F, F, i-Bu, H), (M-7844, Cl, F, F, i-Bu, Cl), (M-7845, Cl, F, F, i-Bu, F), (M-7846, Cl, F, F, i-Bu, CF3), (M-7847, Cl, F, F, i-Bu, Br), (M-7848, Cl, F, F, i-Bu, CH3), (M-7849, Cl, F, F, sec-Bu, H), (M-7850, Cl, F, F, sec-Bu, Cl), (M-7851, Cl, F, F, sec-Bu, F), (M-7852, Cl, F, F, sec-Bu, CF3), (M-7853, Cl, F, F, sec-Bu, Br), (M-7854, Cl, F, F, sec-Bu, CH3), (M-7855, Cl, F, F, n-Pen, H), (M-7856, Cl, F, F, n-Pen, Cl), (M-7857, Cl, F, F, Q-Pen, F), (M-7858, Cl, F, F, n-Pen, CF3), (M-7859, Cl, F, F, n-Pen, Br), (M-7860, Cl, F, F, n-Pen, CH3), (M-7861, Cl, F, F, c-Pen, H), (M-7862, Cl, F, F, c-Pen, Cl), (M-7863, Cl, F, F, c-Pen, F), (M-7864, Cl, F, F, c-Pen, CF3), (M-7865, Cl, F, F, c-Pen, Br), (M-7866, Cl, F, F, c-Pen, CH3), (M-7867, Cl, F, F, n-Hex, H), (M-7868, Cl, F, F, n-Hex, Cl), (M-7869, Cl, F, F, n-Hex, F), (M-7870, Cl, F, F, n-Hex, CF3), (M-7871, Cl, F, F, n-Hex, Br), (M-7872, Cl, F, F, n-Hex, CH3), (M-7873, Cl, F, F, c-Hex, H), (M-7874, Cl, F, F, c-Hex, Cl), (M-7875, Cl, F, F, c-Hex, F), (M-7876, Cl, F, F, c-Hex, CF3), (M-7877, Cl, F, F, c-Hex, Br), (M-7878, Cl, F, F, c-Hex, CH3), (M-7879, Cl, F, F, OH, H), (M-7880, Cl, F, F, OH, Cl), (M-7881, Cl, F, F, OH, F), (M-7882, Cl, F, F, OH, CF3), (M-7883, Cl, F, F, OH, Br), (M-7884, Cl, F, F, OH, CH3), (M-7885, Cl, F, F, EtO, H), (M-7886, Cl, F, F, EtO, Cl), (M-7887, Cl, F, F, EtO, F), (M-7888, Cl, F, F, EtO, CF3), (M-7889, Cl, F, F, EtO, Br), (M-7890, Cl, F, F, EtO, CH3), (M-7891, Cl, F, F, n-PrO, H), (M-7892, Cl, F, F, n-PrO, Cl), (M-7893, Cl, F, F, n-PrO, F), (M-7894, Cl, F, F, n-PrO, CF3), (M-7895, Cl, F, F, n-PrO, Br), (M-7896, Cl, F, F, n-PrO, CH3), (M-7897, Cl, F, F, PhO, H), (M-7898, Cl, F, F, PhO, Cl), (M-7899, Cl, F, F, PhO, F), (M-7900, Cl, F, F, PhO, CF3), (M-7901, Cl, F, F, PhO, Br), (M-7902, Cl, F, F, PhO, CH3), (M-7903, Cl, P, F, BnO, H), (M-7904, Cl, F, F, BnO, Cl), (M-7905, Cl, F, F, BnO, F), (M-7906, Cl, F, F, BnO, CF3), (M-7907, Cl, F, F, BnO, Br), (M-7908, Cl, F, F, BnO, CH3), (M-7909, Cl, F, F, PhCH2CH2O, H), (M-7910, Cl, F, F, PhCH2CH2O, Cl), (M-7911, Cl, F, F, PhCH2CH2O, F), (M-7912, Cl, F, F, PhCH2CH2O, CF3), (M-7913, Cl, F, F, PhCH2CH2O, Br), (M-7914, Cl, F, F, PhCH2CH2O, CH3), (M-7915, Cl, F, F, CF3O, H), (M-7916, Cl, F, F, CF3O, Cl), (M-7917, Cl, F, F, CF3O, F), (M-7918, Cl, F, F, CF3O, CF3), (M-7919, Cl, F, F, CF3O, Br), (M-7920, Cl, F, F, CF3O, CH3), (M-7921, Cl, F, F, Ph, H), (M-7922, Cl, F, F, Ph, Cl), (M-7923, Cl, F, F, Ph, F), (M-7924, Cl, F, F, Ph, CF3), (M-7925, Cl, F, F, Ph, Br), (M-7926, Cl, F, F, Ph, CH3), (M-7927, Cl, F, F, 4-F-Ph, H), (M-7928, Cl, F, F, 4-F-Ph, Cl), (M-7929, Cl, F, F, 4-F-Ph, F), (M-7930, Cl, F, F, 4-F-Ph, CF3), (M-7931, Cl, F, F, 4-F-Ph, Br), (M-7932, Cl, F, F, 4-F-Ph, CH3), (M-7933, Cl, F, F, 4-CF3-Ph, H), (M-7934, Cl, F, F, 4-CF3-Ph, Cl), (M-7935, Cl, F, F, 4-CF3-Ph, F), (M-7936, Cl, F, F, 4-CF3-Ph, CF3), (M-7937, Cl, F, F, 4-CF3-Ph, Br), (M-7938, Cl, F, F, 4-CF3-Ph, CH3), (M-7939, Cl, F, F, 4-(Me)2N-Ph, H), (M-7940, Cl, F, F, 4-(Me)3N-Ph, Cl), (M-7941, Cl, F, F, 4-(Me)2N-Ph, F), (M-7942, Cl, F, F, 4-(Me)2M-Ph, CF3), (M-7943, Cl, F, F, 4-(Me)2N-Ph, Br), (M-7944, Cl, F, F, 4-(Me)2N-Ph, CH3), (M-7945, Cl, F, F, 4-OH-Ph, H), (M-7946, Cl, F, F, 4-OH-Ph, Cl), (M-7947, Cl, F, F, 4-OH-Ph, F), (M-7948, Cl, F, F, 4-OH-Ph, CF3), (M-7949, Cl, F, F, 4-OH-Ph, Br), (M-7950, Cl, F, F, 4-OH-Ph, CH3), (M-7951, Cl, F, F, 3,4-di-F-Ph, H), (M-7952, Cl, F, F, 3,4-di-F-Ph, Cl), (M-7953, Cl, F, F, 3,4-di-F-Ph, F), (M-7954, Cl, F, F, 3,4-di-F-Ph, CF3), (M-7955, Cl, F, F, 3,4-di-F-Ph, Br), (M-7956, Cl, F, F, 3,4-di-F-Ph, CH3), (M-7957, Cl, F, F, 4-COOH-Ph, H), (M-7958, Cl, F, F, 4-COOH-Ph, Cl), (M-7959, Cl, F, F, 4-COOH-Ph, F), (M-7960, Cl, F, F, 4-COOH-Ph, CF3), (M-7961, Cl, F, F, 4-COOH-Ph, Br), (M-7962, Cl, F, F, 4-COOH-Ph, CH3), (M-7963, Cl, F, F, Bn, H), (M-7964, Cl, F, F, Bn, Cl), (M-7965, Cl, F, F, Bn, F), (M-7966, Cl, F, F, Bn, CF3), (M-7967, Cl, F, F, Bn, Br), (M-7968, Cl, F, F, Bn, CH3), (M-7969, Cl, F, F, 4-F-Bn, H), (M-7970, Cl, F, F, 4-F-Bn, Cl), (M-7971, Cl, F, F, 4-F-Bn, F), (M-7972, Cl, F, F, 4-F-Bn, CF3), (M-7973, Cl, F, F, 4-F-Bn, Br), (M-7974, Cl, F, F, 4-F-Bn, CH3), (M-7975, Cl, F, F, 2-Py, H), (M-7976, Cl, F, F, 2-Py, Cl), (M-7977, Cl, F, F, 2-Py, F), (M-7978, Cl, F, F, 2-Py, CF3), (M-7979, Cl, F, F, 2-Py, Br), (M-7980, Cl, F, F, 2-Py, CH3), (M-7981, Cl, F, F, 3-Py, H), (M-7982, Cl, F, F, 3-Py, Cl), (M-7983, Cl, F, F, 3-Py, F), (M-7984, Cl, F, F, 3-Py, CF3), (M-7985, Cl, F, F, 3-Py, Br), (M-7986, Cl, F, F, 3-Py, CH3), (M-7987, Cl, F, F, 4-Py, H), (M-7988, Cl, F, F, 4-Py, Cl), (M-7989, Cl, F, F, 4-Py, F), (M-7990, Cl, F, F, 4-Py, CF3), (M-7991, Cl, F, F, 4-Py, Br), (M-7992, Cl, F, F, 4-Py, CH3), (M-7993, Cl, F, F, 2-th, H), (M-7994, Cl, F, F, 2-Th, Cl), (M-7995, Cl, F, F, 2-Th, F), (M-7996, Cl, F, F, 2-Th, CF3), (M-7997, Cl, F, F, 2-Th, Br), (M-7998, Cl, F, F, 2-Th, CH3), (M-7999, Cl, F, F, 3-Th, H), (M-8000, Cl, F, F, 3-Th, Cl), (M-8001, Cl, F, F, 3-Th, F), (M-8002, Cl, F, F, 3-Th, CF3), (M-8003, Cl, F, F, 3-Th, Br), (M-8004, Cl, F, F, 3-Th, CH3), (M-8005, Cl, F, F, pyrrazol-2-yl, H), (M-8006, Cl, F, F, pyrrazol-2-yl, Cl), (M-8007, Cl, F, F, pyrrazol-2-yl, F), (M-8008, Cl, F, F, pyrrazol-2-yl, CF3), (M-8009, Cl, F, F, pyrrazol-2-yl, Br), (M-8010, Cl, F, E, pyrrazol-2-yl, CH3), (M-8011, Cl, F, F, pyrrazol-3-yl, H), (M-8012, Cl, F, F, pyrrazol-3-yl, Cl), (M-8013, Cl, F, F, pyrrazol-3-yl, F), (M-8014, Cl, F, F, pyrrazol-3-yl, CF3), (M-8015, Cl, F, F, pyrrazol-3-yl, Br), (M-8016, Cl, F, F, pyrrazol-3-yl, CH3), (M-8017, Cl, F, F, pyrimidin-2-yl, H), (M-8018, Cl, F, F, pyrimidin-2-yl, Cl), (M-8019, Cl, F, F, pyrimidin-2-yl, F), (M-8020, Cl, F, F, pyrimidin-2-yl, CF3), (M-8021, Cl, F, F, pyrimidin-2-yl, Br), (M-8022, Cl, F, F, pyrimidin-2-yl, CH3), (M-8023, Cl, F, F, pyrimidin-4-yl, H), (M-8024, Cl, F, F, pyrimidin-4-yl, Cl), (M-8025, Cl, F, F, pyrimidin-4-yl, F), (M-8026, Cl, F, F, pyrimidin-4-yl, CF3), (M-8027, Cl, F, F, pyrimidin-4-yl, Br), (M-8028, Cl, F, F, pyrimidin-4-yl, CH3), (M-8029, Cl, F, F, pyrimidin-5-yl, H), (M-8030, Cl, F, F, pyrimidin-5-yl, Cl), (M-8031, Cl, F, F, pyrimidin-5-yl, F), (M-8032, Cl, F, F, pyrimidin-5-yl, CF3), (M-8033, Cl, F, F, pyrimidin-5-yl, Br), (M-8034, Cl, F, F, pyrimidin-5-yl, CH3), (M-8035, Cl, F, F, HOOCCH2CH2CH2, H), (M-8036, Cl, F, F, HOOCCH2CH2CH2, Cl), (M-8037, Cl, F, F, HOOCCH2CH2CH2, F), (M-8038, Cl, F, F, HOOCCH2CH2CH2, CF3), (M-8039, Cl, F, F, HOOCCH2CH2CH2, Br), (M-8040, Cl, F, F, HOOCCH2CH2CH2, CH3), (M-8041, Cl, F, F, HOOCCH2CH2CH2CH2, H), (M-8042, Cl, F, F, HOOCCH2CH2CH2CH2, Cl), (M-8043, Cl, F, F, HOOCCH2CH2CH2CH2, F), (M-8044, Cl, F, F, HOOCCH2CH2CH2CH2, CF3), (M-8045, Cl, F, F, HOOCCH2CH2CH2CH2, Br), (M-8046, Cl, F, F, HOOCCH2CH2CH2CH2, CH3), (M-8047, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, H), (M-8048, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-8049, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, F), (M-8050, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-8051, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-8052, Cl, F, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-8053, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-8054, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-8055, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-8056, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-8057, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-8058, Cl, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-8059, Cl, F, F, MeOCH2, H), (M-8060, Cl, F, F, MeOCH2, Cl), (M-8061, Cl, F, F, MeOCH2, F), (M-8062, Cl, F, F, MeOCH2, CF3), (M-8063, Cl, F, F, MeOCH2, Br), (M-8064, Cl, F, F, MeOCH2, CH3), (M-8065, Cl, F, F, EtOCH2, H), (M-8066, Cl, F, F, EtOCH2, Cl), (M-8067, Cl, F, F, EtOCH2, F), (M-8068, Cl, F, F, EtOCH2, CF3), (M-8069, Cl, F, F, EtOCH2, Br), (M-8070, Cl, F, F, EtOCH2, CH3), (M-8071, Cl, F, F, EtOCH2CH2, H), (M-8072, Cl, F, F, EtOCH2CH2, Cl), (M-8073, Cl, F, F, EtOCH2CH2, F), (M-8074, Cl, F, F, EtOCH2CH2, CF3), (M-8075, Cl, F, F, EtOCH2CH2, Br), (M-8076, Cl, F, F, EtOCH2CH2, CH3), (M-8077, Cl, F, F, MeOCH2CH2OCH2CH2, H), (M-8078, Cl, F, F, MeOCH2CH2OCH2CH2, Cl), (M-8079, Cl, F, F, MeOCH2CH2OCH2CH2, F), (M-8080, Cl, F, F, MeOCH2CH2OCH2CH2, CF3), (M-8081, Cl, F, F, MeOCH2CH2OCH2CH2, Br), (M-8082, Cl, F, F, MeOCH2CH2OCH2CH2, CH3), (M-8083, Cl, F, F, MeOCH2CH2, H), (M-8084, Cl, F, F, MeOCH2CH2, Cl), (M-8085, Cl, F, F, MeOCH2CH2, F), (M-8086, Cl, F, F, MeOCH2CH2, CF3), (M-8087, Cl, F, F, MeOCH2CH2, Br), (M-8088, Cl, F, F, MeOCH2CH2, CH3), (M-8089, Cl, F, F, HOCH2, H), (M-8090, Cl, F, F, HOCH2, Cl), (M-8091, Cl, F, F, HOCH2, F), (M-8092, Cl, F, F, HOCH2, CF3), (M-8093, Cl, F, F, HOCH2, Br), (M-8094, Cl, F, F, HOCH2, CH3), (M-8095, Cl, F, F, HOCH2CH2, H), (M-8096, Cl, F, F, HOCH2CH2, Cl), (M-8097, Cl, F, F, HOCH2CH2, F), (M-8098, Cl, F, F, HOCH2CH2, CF3), (M-8099, Cl, F, F, HOCH2CH2, Br), (M-8100, Cl, F, F, HOCH2CH2, CH3), (M-8101, Cl, F, F, HOCH2CH2CH2, H), (M-8102, Cl, F, F, HOCH2CH2CH2, Cl), (M-8103, Cl, F, F, HOCH2CH2CH2, F), (M-8104, Cl, F, F, HOCH2CH2CH2, CF3), (M-8105, Cl, F, F, HOCH2CH2CH2, Br), (M-8106, Cl, F, F, HOCH2CH2CH2, CH3), (M-8107, Cl, F, F, HOCH2CH2CH2CH2, H), (M-8108, Cl, F, F, HOCH2CH2CH2CH2, Cl), (M-8109, Cl, F, F, HOCH2CH2CH2CH2, F), (M-8110, Cl, F, F, HOCH2CH2CH2CH2, CF3), (M-8111, Cl, F, F, HOCH2CH2CH2CH2, Br), (M-8112, Cl, F, F, HOCH2CH2CH2CH2, CH3), (M-8113, Cl, F, F, HOCH2CH2CH2CH2CH2H), (M-8114, Cl, F, F, HOCH2CH2CH2CH2CH2, Cl), (M-8115, Cl, F, F, HOCH2CH2CH2CH2CH2, F), (M-8116, Cl, F, F, HOCH2CH2CH2CH2CH2, CF3), (M-8117, Cl, F, F, HOCH2CH2CH2CH2CH2Br), (M-8118, Cl, F, F, HOCH2CH2CH2CH2CH2, CH3), (M-8119, Cl, F, F, HOCH2CH2OCH2CH2, H), (M-8120, Cl, F, F, HOCH2CH2OCH2CH2, Cl), (M-8121, Cl, F, F, HOCH2CH2OCH2CH2, F), (M-8122, Cl, F, F, HOCH2CH2OCH2CH2, CF3), (M-8123, Cl, F, F, HOCH2CH2OCH2CH2, Br), (M-8124, Cl, F, F, HOCH2CH2OCH2CH2, CH3), (M-8125, Cl, F, F, (Me)2N, H), (M-8126, Cl, F, F, (Me)2N, Cl), (M-8127, Cl, F, F, (Me)2N, F), (M-8128, Cl, F, F, (Me)2N, CF3), (M-8129, Cl, F, F, (Me)2N, Br), (M-8130, Cl, F, F, (Me)2N, CH3), (M-8131, Cl, F, F, piperidin-4-yl-methyl, H), (M-8132, Cl, F, F, piperidin-4-yl-methyl, Cl), (M-8133, Cl, F, F, piperidin-4-yl-methyl, F), (M-8134, Cl, F, F, piperidin-4-yl-methyl, CF3), (M-8185, Cl, F, F, piperidin-4-yl-methyl, Br), (M-8136, Cl, F, F, piperidin-4-yl-methyl, CH3), (M-8137, Cl, F, F, cyclohexylmethyl, H), (M-8138, Cl, F, F, cyclohexylmethyl, Cl), (M-8139, Cl, F, F, cyclohexylmethyl, F), (M-8140, Cl, F, F, cyclohexylmethyl, CF3), (M-8141, Cl, F, F, cyclohexylmethyl, Br), (M-8142, Cl, F, F, cyclohexylmethyl, CH3), (M-8143, Cl, F, Cl, H, H), (M-8144, Cl, F, Cl, H, Cl), (M-8145, Cl, F, Cl, H, F), (M-8146, Cl, F, Cl, H, CF3), (M-8147, Cl, F, Cl, H, Br), (M-8148, Cl, F, Cl, H, CH3), (M-8149, Cl, F, Cl, F, H), (M-8150, Cl, F, Cl, F, Cl), (M-8151, Cl, F, Cl, F, F), (M-8152, Cl, F, Cl, F, CF3), (M-8153, Cl, F, Cl, F, Br), (M-8154, Cl, F, Cl, F, CH3), (M-8155, Cl, F, Cl, Cl, H), (M-8156, Cl, F, Cl, Cl, Cl), (M-8157, Cl, F, Cl, Cl, F), (M-8158, Cl, F, CU Cl, CF3), (M-8159, Cl, F, Cl, Cl, Br), (M-8160, Cl, F, Cl, Cl, CH3), (M-8161, Cl, F, Cl, CH3, H), (M-8162, Cl, F, Cl, CH3, Cl), (M-8163, Cl, F, Cl, CH3, F), (M-8164, Cl, F, Cl, CH3, CF3), (M-8165, Cl, F, Cl, CH3, Br), (M-8166, Cl, F, Cl, CH3, CH3), (M-8167, Cl, F, Cl, Et, H), (M-8168, Cl, F, Cl, Et, Cl), (M-8169, Cl, F, Cl, Et, F), (M-8170, Cl, F, Cl, Et, CF3), (M-8171, Cl, F, Cl, Et, Br), (M-8172, Cl, F, Cl, Et, CH3), (M-8173, Cl, F, Cl, n-Pr, H), (M-8174, Cl, F, Cl, n-Pr, Cl), (M-8175, Cl, F, Cl, n-Pr, F), (M-8176, Cl, F, Cl, n-Pr, CF3), (M-8177, Cl, F, Cl, n-Pr, Br), (M-8178, Cl, F, Cl, n-Pr, CH3), (M-8179, Cl, F, Cl, c-Pr, H), (M-8180, Cl, F, Cl, c-Pr, Pr, Cl), (M-8181, Cl, F, Cl, c-Pr, F), (M-8182, Cl, F, Cl, c-Pr, CF3), (M-8183, Cl, F, Cl, c-Pr, Br), (M-8184, Cl, F, Cl, c-Pr, CH3), (M-8185, Cl, F, Cl, i-Pr, H), (M-8186, Cl, F, Cl, i-Pr, Cl), (M-8187, Cl, F, Cl, i-Pr, F), (M-8188, Cl, F, Cl, i-Pr, CF3), (M-8189, Cl, F, Cl, i-Pr, Br), (M-8190, Cl, F, Cl, i-Pr, CH3), (M-8191, Cl, F, Cl, n-Bu, H), (M-8192, Cl, F, Cl, n-Bu, Cl), (M-8193, Cl, F, Cl, n-Bu, F), (M-8194, Cl, F, Cl, n-Bu, CF3), (M-8195, Cl, F, Cl, n-Bu, Br), (M-8196, Cl, F, Cl, n-Bu, CH3), (M-8197, Cl, F, Cl, i-Bu, H), (M-8198, Cl, F, Cl, i-Bu, Cl), (M-8199, Cl, F, Cl, i-Bu, F), (M-8200, Cl, F, Cl, i-Bu, CF3), (M-8201, Cl, F, Cl, i-Bu, Br), (M-8202, Cl, F, Cl, i-Bu, CH3), (M-8203, Cl, F, Cl, sec-Bu, H), (M-8204, Cl, F, Cl, sec-Bu, Cl), (M-8205, Cl, F, Cl, sec-Bu, F), (M-8206, Cl, F, Cl, sec-Bu, CF3), (M-8207, Cl, F, Cl, sec-Bu, Br), (M-8208, Cl, F, Cl, sec-Bu, CH3), (M-8209, Cl, F, Cl, n-Pen, H), (M-8210, Cl, F, Cl, n-Pen, Cl), (M-8211, Cl, F, Cl, n-Pen, F), (M-8212, Cl, F, Cl, n-Pen, CF3), (M-8213, Cl, F, Cl, n-Pen, Br), (M-8214, Cl, F, Cl, n-Pen, CH3), (M-8215, Cl, F, Cl, c-Pen, H), (M-8216, Cl, F, Cl, c-Pen, Cl), (M-8217, Cl, F, Cl, c-Pen, F), (M-8218, Cl, F, Cl, c-Pen, CF3), (M-8219, Cl, F, Cl, c-Pen, Br), (M-8220, Cl, F, Cl, c-Pen, CH3), (M-8221, Cl, F, Cl, n-Hex, H), (M-8222, Cl, F, Cl, n-Hex, Cl), (M-8223, Cl, F, Cl, n-Hex, F), (M-8224, Cl, F, Cl, n-Hex, CF3), (M-8225, Cl, F, Cl, n-Hex, Br), (M-8226, Cl, F, Cl, n-Hex, CH3), (M-8227, Cl, F, Cl, c-Hex, H), (M-8228, Cl, F, Cl, c-Hex, Cl), (M-8229, Cl, F, Cl, c-Hex, F), (M-8230, Cl, F, Cl, c-Hex, CF3), (M-8231, Cl, F, Cl, c-Hex, Br), (M-8232, Cl, F, Cl, c-Hex, CH3), (M-8233, Cl, F, Cl, OH, H), (M-8234, Cl, F, Cl, OH, Cl), (M-8235, Cl, F, Cl, OH, F), (M-8236, Cl, F, Cl, OH, CF3), (M-8237, Cl, F, Cl, OH, Br), (M-8238, Cl, F, Cl, OH, CH3), (M-8239, Cl, F, Cl, EtO, H), (M-8240, Cl, F, Cl, EtO, Cl), (M-8241, Cl, F, Cl, EtO, F), (M-8242, Cl, F, Cl, EtO, CF3), (M-8243, Cl, F, Cl, EtO, Br), (M-8244, Cl, F, Cl, EtO, CH3), (M-8245, Cl, F, Cl, n-PrO, H), (M-8246, Cl, F, Cl, n-PrO, Cl), (M-8247, Cl, F, Cl, n-PrO, F), (M-8248, Cl, F, Cl, n-PrO, CF3), (M-8249, Cl, F, Cl, n-PrO, Br), (M-8250, Cl, F, Cl, n-PrO, CH3), (M-8251, Cl, F, Cl, PhO, H), (M-8252, Cl, F, Cl, PhO, Cl), (M-8253, Cl, F, Cl, PhO, F), (M-8254, Cl, F, Cl, PhO, CF3), (M-8255, Cl, F, Cl, PhO, Br), (M-8256, Cl, F, Cl, PhO, CH3), (M-8257, Cl, F, Cl, BuO, H), (M-8258, Cl, F, Cl, BnO, Cl), (M-8259, Cl, F, Cl, BnO, F), (M-8260, Cl, F, Cl, BnO, CF3), (M-8261, Cl, F, Cl, BnO, Br), (M-8262, Cl, F, Cl, BnO, CH3), (M-8263, Cl, F, Cl, PhCH2CH2O, H), (M-8264, Cl, F, Cl, PhCH2CH2O, Cl), (M-8265, Cl, F, Cl, PhCH2CH2O, F), (M-8266, Cl, F, Cl, PhCH2CH2O, CF3), (M-8267, Cl, F, Cl, PhCH2CH2O, Br), (M-8268, Cl, F, Cl, PhCH2CH2O, CH3), (M-8269, Cl, F, Cl, CF3O, H), (M-8270, Cl, F, Cl, CF3O, Cl), (M-8271, Cl, F, Cl, CF3O, F), (M-8272, Cl, F, Cl, CF3O, CF3), (M-8273, Cl, F, Cl, CF3O, Br), (M-8274, Cl, F, Cl, CF3O, CH3), (M-8275, Cl, F, Cl, Ph, H), (M-8276, Cl, F, Cl, Ph, Cl), (M-8277, Cl, F, Cl, Ph, F), (M-8278, Cl, F, Cl, Ph, CF3), (M-8279, Cl, F, Cl, Ph, Br), (M-8280, Cl, F, Cl, Ph, CH3), (M-8281, Cl, F, Cl, 4-F-Ph, H), (M-8282, Cl, F, Cl, 4-F-Ph, Cl), (M-8283, Cl, F, Cl, 4-F-Ph, F), (M-8284, Cl, F, Cl, 4-F-Ph, CH3), (M-8285, Cl, F, Cl, 4-F-Ph, Br), (M-8286, Cl, F, Cl, 4-F-Ph, CH3), (M-8287, Cl, F, Cl, 4-CF3-Ph, H), (M-8288, Cl, F, Cl, 4-CF3-Ph, Cl), (M-8289, Cl, F, Cl, 4-CF3-Ph, F), (M-8290, Cl, F, Cl, 4-CF3-Ph, CF3), (M-8291, Cl, F, Cl, 4-CF3-Ph, Br), (M-8292, Cl, F, Cl, 4-CF3-Ph, CH3), (M-8293, Cl, F, Cl, 4-(Me)2N-Ph, H), (M-8294, Cl, F, Cl, 4-(Me)2N-Ph, Cl), (M-8295, Cl, F, Cl, 4-(Me)2N-Ph, F), (M-8296, Cl, F, Cl, 4-(Me)2N-Ph, CF3), (M-8297, Cl, F, Cl, 4-(Me)2N-Ph, Br), (M-8298, Cl, F, Cl, 4-(Me)2N-Ph, CH3), (M-8299, Cl, F, Cl, 4-OH-Ph, H), (M-8300, Cl, F, Cl, 4-OH-Ph, Cl), (M-8301, Cl, F, Cl, 4-OH-Ph, F), (M-8302, Cl, F, Cl, 4-OH-Ph, CF3), (M-8303, Cl, F, Cl, 4-OH-Ph, Br), (M-8304, Cl, F, Cl, 4-OH-Ph, CH3), (M-8305, Cl, F, Cl, 3,4-di-F-Ph, H), (M-8306, Cl, F, Cl, 3,4-di-F-Ph, Cl), (M-8307, Cl, F, Cl, 3,4-di-F-Ph, F), (M-8308, Cl, F, Cl, 3,4-di-F-Ph, CF3), (M-8309, Cl, F, Cl, 3,4-di-F-Ph, Br), (M-8310, Cl, F, Cl, 3,4-di-F-Ph, CH3), (M-8311, Cl, F, Cl, 4-COOH-Ph, H), (M-8312, Cl, F, Cl, 4-COOH-Ph, Cl), (M-8313, Cl, F, Cl, 4-COOH-Ph, F), (M-8314, Cl, F, Cl, 4-COOH-Ph, CF3), (M-8315, Cl, F, Cl, 4-COOH-Ph, Br), (M-8316, Cl, F, Cl, 4-COOH-Ph, CH3), (M-8317, C), F, Cl, Bn, H), (M-8318, Cl, F, Cl, Bn, Cl), (M-8319, Cl, F, Cl, Bn, F), (M-8320, Cl, F, Cl, Bn, CF3), (M-8321, Cl, F, Cl, Bn, Br), (M-8322, Cl, F, Cl, Bn, CH3), (M-8323, Cl, F, Cl, 4-F-Bu, H), (M-8324, Cl, F, Cl, 4-F-Bn, Cl), (M-8325, Cl, F, Cl, 4-F-Bn, F), (M-8326, Cl, F, Cl, 4-F-Bn, CF3), (M-8327, Cl, F, Cl, 4-F-Bn, Br), (M-8328, Cl, F, Cl, 4-F-Bn, CH3), (M-8329, Cl, F, Cl, 2-Py, H), (M-8330, Cl, F, Cl, 2-Py, Cl), (M-8331, Cl, F, Cl, 2-Py, F), (M-8332, Cl, F, Cl, 2-Py, CF3), (M-8333, Cl, F, Cl, 2-Py, Br), (M-8334, Cl, F, Cl, 2-Py, CH3), (M-8335, Cl, F, Cl, 3-Py, H), (M-8336, Cl, F, Cl, 3-Py, Cl), (M-8337, Cl, F, Cl, 3-Py, F), (M-8338, Cl, F, Cl, 3-Py, CF3), (M-8339, Cl, F, Cl, 3-Py, Br), (M-8340, Cl, F, Cl, 3-Py, CH3), (M-8341, Cl, F, Cl, 4-Py, H), (M-8342, Cl, F, Cl, 4-Py, Cl), (M-8343, Cl, F, Cl, 4-Py, F), (M-8344, Cl, F, Cl, 4-Py, CF3), (M-8345, Cl, F, Cl, 4-Py, Br), (M-8346, Cl, F, Cl, 4-Py, CH3), (M-8347, Cl, F, Cl, 2-Th, H), (M-8348, Cl, F, Cl, 2-Th, Cl), (M-8349, Cl, F, Cl, 2-Th, F), (M-8350, Cl, F, Cl, 2-th, CF3), (M-8351, Cl, F, Cl, 2-Th, Br), (M-8352, Cl, F, Cl, 2-Th, CH3), (M-8353, Cl, F, Cl, 3-Th, H), (M-8354, Cl, F, Cl, 3-Th, Cl), (M-8355, Cl, F, Cl, 3-Th, F), (M-8356, Cl, F, Cl, 3-Th, CF3), (M-8357, Cl, F, Cl, 3-Th, Br), (M-8358, Cl, F, Cl, 3-Th, CH3), (M-8359, Cl, F, Cl, pyrrazol-2-yl, H), (M-8360, Cl, F, Cl, pyrrazol-2-yl, Cl), (M-8361, Cl, F, Cl, pyrrazol-2-yl, F), (M-8362, Cl, F, Cl, pyrrazol-2-yl, CF3), (M-8363, Cl, F, Cl, pyrrazol-2-yl, Br), (M-8364, Cl, F, Cl, pyrrazol-2-yl, CH3), (M-8365, Cl, F, Cl, pyrrazol-3-yl, H), (M-8366, Cl, F, Cl, pyrrazol-3-yl, Cl), (M-8367, Cl, F, Cl, pyrrazol-3-yl, F), (M-8368, Cl, F, Cl, pyrrazol-3-yl, CF3), (M-8369, Cl, F, Cl, pyrrazol-3-yl, Br), (M-8370, Cl, F, Cl, pyrrazol-3-yl, CH3), (M-8371, Cl, F, Cl, pyrimidin-2-yl, H), (M-8372, Cl, F, Cl, pyrimidin-2-yl, Cl), (M-8373, Cl, F, Cl, pyrimidin-2-yl, F), (M-8374, Cl, F, Cl, pyrimidin-2-yl, CF3), (M-8375, Cl, F, Cl, pyrimidin-2-yl, Br), (M-8376, Cl, F, Cl, pyrimidin-2-yl, CH3), (M-8377, Cl, F, Cl, pyrimidin-4-yl, H), (M-8378, Cl, F, Cl, pyrimidin-4-yl, Cl), (M-8379, Cl, F, Cl, pyrimidin-4-yl, F), (M-8380, Cl, F, Cl, pyrimidin-4-yl, CF3), (M-8381, Cl, F, Cl, pyrimidin-4-yl, Br), (M-8382, Cl, F, Cl, pyrimidin-4-yl, CH3), (M-8383, Cl, F, Cl, pyrimidin-5-yl, H), (M-8384, Cl, F, Cl, pyrimidin-5-yl, Cl), (M-8385, Cl, F, Cl, pyrimidin-5-yl, F), (M-8386, Cl, F, Cl, pyrimidin-5-yl, CF3), (M-8387, Cl, F, Cl, pyrimidin-5-yl, Br), (M-8388, Cl, F, Cl, pyrimidin-5-yl, CH3), (M-8389, Cl, F, Cl, HOOCCH2CH2CH2, H), (M-8390, Cl, F, Cl, HOOCCH2CH2CH2, Cl), (M-8391, Cl, F, Cl, HOOCCH2CH2CH2, F), (M-8392, Cl, F, Cl, HOOCCH2CH2CH2, CF3), (M-8393, Cl, F, Cl, HOOCCH2CH2CH2Br), (M-8394, Cl, F, Cl, HOOCCH2CH2CH2, CH3), (M-8395, Cl, F, Cl, HOOCCH2CH2CH2CH2, H), (M-8396, Cl, F, Cl, HOOCCH2CH2CH2CH2, Cl), (M-8397, Cl, F, Cl, HOOCCH2CH2CH2CH2, F), (M-8398, Cl, F, Cl, HOOCCH2CH2CH2CH2, CF3), (M-8399, Cl, F, Cl, HOOCCH2CH2CH2CH2, Br), (M-8400, Cl, F, Cl, HOOCCH2CH2CH2CH2, CH3), (M-8401, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-8402, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-8403, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-8404, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-8405, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-8406, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-8407, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2H), (M-8408, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-8409, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-8410, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-8411, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-8412, Cl, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-8413, Cl, F, Cl, MeOCH2, H), (M-8414, Cl, F, Cl, MeOCH2, Cl), (M-8415, Cl, F, Cl, MeOCH2, F), (M-8416, Cl, F, Cl, MeOCH2, CF3), (M-8417, Cl, F, Cl, MeOCH2, Br), (M-8418, Cl, F, Cl, MeOCH2, CH3), (M-8419, Cl, F, Cl, EtOCH2, H), (M-8420, Cl, F, Cl, EtOCH2, Cl), (M-8421, Cl, F, Cl, EtOCH2, F), (M-8422, Cl, F, Cl, EtOCH2, CF3), (M-8423, Cl, F, Cl, EtOCH2, Br), (M-8424, Cl, F, Cl, EtOCH2, CH3), (M-8425, Cl, F, Cl, EtOCH2CH2, H), (M-8426, Cl, F, Cl, EtOCH2CH2, Cl), (M-8427, Cl, F, Cl, EtOCH2CH2, F), (M-8428, Cl, F, Cl, EtOCH2CH2, CF3), (M-8429, Cl, F, Cl, EtOCH2CH2, Br), (M-8430, Cl, F, Cl, EtOCH2CH2, CH3), (M-8431, Cl, F, Cl, MeOCH2CH2OCH2CH2, H), (M-8432, Cl, F, Cl, MeOCH2CH2OCH2CH2, Cl), (M-8433, Cl, F, Cl, MeOCH2CH2OCH2CH2, F), (M-8434, Cl, F, Cl, MeOCH2CH2OCH2CH2, CF3), (M-8435, Cl, F, Cl, MeOCH2CH2OCH2CH2, Br), (M-8436, Cl, F, Cl, MeOCH2CH2OCH2CH2, CH3), (M-8437, Cl, F, Cl, MeOCH2CH2, H), (M-8438, Cl, F, Cl, MeOCH2CH2, Cl), (M-8439, Cl, F, Cl, MeOCH2CH2, F), (M-8440, Cl, F, Cl, MeOCH2CH2, CF3), (M-8441, Cl, F, Cl, MeOCH2CH2, Br), (M-8442, Cl, F, Cl, MeOCH2CH2, CH3), (M-8443, Cl, F, Cl, HOCH2, H), (M-8444, Cl, F, Cl, HOCH2, Cl), (M-8445, Cl, F, Cl, HOCH2, F), (M-8446, Cl, F, Cl, HOCH2, CF3), (M-8447, Cl, F, Cl, HOCH2, Br), (M-8448, Cl, F, Cl, HOCH2, CH3), (M-8449, Cl, F, Cl, HOCH2CH2H), (M-8450, Cl, F, Cl, HOCH2CH2, Cl), (M-8451, Cl, F, Cl, HOCH2CH2, F), (M-8452, Cl, F, Cl, HOCH2CH2, CF3), (M-8453, Cl, F, Cl, HOCH2CH2, Br), (M-8454, Cl, F, Cl, HOCH2CH2, CH3), (M-8455, Cl, F, Cl, HOCH2CH2CH2, H), (M-8456, Cl, F, Cl, HOCH2CH2CH2, Cl), (M-8457, Cl, F, Cl, HOCH2CH2CH2, F), (M-8458, Cl, F, Cl, HOCH2CH2CH2, CF3), (M-8459, Cl, F, Cl, HOCH2CH2CH2, Br), (M-8460, Cl, F, Cl, HOCH2CH2CH2, CH3), (M-8461, Cl, F, Cl, HOCH2CH2CH2CH2, H), (M-8462, Cl, F, Cl, HOCH2CH2CH2CH2, Cl), (M-8463, Cl, F, Cl, HOCH2CH2CH2CH2, F), (M-8464, Cl, F, Cl, HOCH2CH2CH2CH2, CF3), (M-8465, Cl, F, Cl, HOCH2CH2CH2CH2, Br), (M-8466, Cl, F, Cl, HOCH2CH2CH2CH2, CH3), (M-8467, Cl, F, Cl, HOCH2CH2CH2CH2CH2H), (M-8468, Cl, F, Cl, HOCH2CH2CH2CH2CH2Cl), (M-8469, Cl, F, Cl, HOCH2CH2CH2CH2CH2, F), (M-8470, Cl, F, Cl, HOCH2CH2CH2CH2CH2CF3), (M-8471, Cl, F, Cl, HOCH2CH2CH2CH2CH2Br), (M-8472, Cl, F, Cl, HOCH2CH2CH2CH2CH2CH3), (M-8473, Cl, F, Cl, HOCH2CH2OCH2CH2, H), (M-8474, Cl, F, Cl, HOCH2CH2OCH2CH2, Cl), (M-8475, Cl, F, Cl, HOCH2CH2OCH2CH2, F), (M-8476, Cl, F, Cl, HOCH2CH2OCH2CH2, CF3), (M-8477, Cl, F, Cl, HOCH2CH2OCH2CH2, Br), (M-8478, Cl, F, Cl, HOCH2CH2OCH1CH2, CH3), (M-8479, Cl, F, Cl, (Me)2N, H), (M-8480, Cl, F, Cl, (Me)2N, Cl), (M-8481, Cl, F, Cl, (Me)2N, F), (M-8482, Cl, F, Cl, (Me)2N, CF3), (M-8483, Cl, F, Cl, (Me)2N, Br), (M-8484, Cl, F, Cl, (Me)2N, CH3), (M-8485, Cl, F, Cl, piperidin-4-yl-methyl, H), (M-8486, Cl, F, Cl, piperidin-4-yl-methyl, Cl), (M-8487, Cl, F, Cl, piperidin-4-yl-methyl, F), (M-8488, Cl, F, Cl, piperidin-4-yl-methyl, CF3), (M-8489, Cl, F, Cl, piperidin-4-yl-methyl, Br), (M-8490, Cl, F, Cl, piperidin-4-yl-methyl, CH3), (M-8491, Cl, F, Cl, cyclohexylmethyl, H), (M-8492, Cl, F, Cl, cyclohexylmethyl, Cl), (M-8493, Cl, F, Cl, cyclohexylmethyl, F), (M-8494, Cl, F, Cl, cyclohexylmethyl, CF3), (M-8495, Cl, F, Cl, cyclohexylmethyl, Br), (M-8496, Cl, F, Cl, cyclohexylmethyl, CH3), (M-8497, Cl, CH3, H, H, H), (M-8498, Cl, CH3, H, H, Cl), (M-8499, Cl, CH3, H, H, F), (M-8500, Cl, CH3, H, H, CF3), (M-8501, Cl, CH3, H, H, Br), (M-8502, Cl, CH3, H, H, CH3), (M-8503, Cl, CH3, H, F, H), (M-8504, Cl, CH3, H, F, Cl), (M-8505, Cl, CH3, H, F, F), (M-8506, Cl, CH3, H, F, CF3), (M-8507, Cl, CH3, H, F, Br), (M-8508, Cl, CH3, H, F, CH3), (M-8509, Cl, CH3, H, Cl, H), (M-8510, Cl, CH3, H, Cl, Cl), (M-8511, Cl, CH3, H, Cl, F), (M-8512, Cl, CH3, H, Cl, CF3), (M-8513, Cl, CH3, H, Cl, Br), (M-8514, Cl, CH3, H, Cl, CH3), (M-8515, Cl, CH3, H, CH3, H), (M-8516, Cl, CH3, H, CH3, Cl), (M-8517, Cl, CH3, H, CH3, F), (M-8518, Cl, CH3, H, CH3, CF3), (M-8519, Cl, CH3, H, CH3, Br), (M-8520, Cl, CH3, H, CH3, CH3), (M-8521, Cl, CH3, H, Et, H), (M-8522, Cl, CH3, H, Et, Cl), (M-8523, Cl, CH3, H, Et, F), (M-8524, Cl, CH3, H, Et, CF3), (M-8525, Cl, CH3, H, Et, Br), (M-8526, Cl, CH3, H, Et, CH3), (M-8527, Cl, CH3, H, n-Pr, H), (M-8528, Cl, CH3, H, n-Pr, Cl), (M-8529, Cl, CH3, H, n-Pr, F), (M-8530, Cl, CH3, H, n-Pr, CF3), (M-8531, Cl, CH3, H, n-Pr, Br), (M-8532, Cl, CH3, H, n-Pr, CH3), (M-8533, Cl, CH3, H, c-Pr, H), (M-8534, Cl, CH3, H, c-Pr, Cl), (M-8535, Cl, CH3, H, c-Pr, F), (M-8536, Cl, CH3, H, c-Pr, CF3), (M-8537, Cl, CH3, H, c-Pr, Br), (M-8538, Cl, CH3, H, c-Pr, CH3), (M-8539, Cl, CH3, H, i-Pr, H), (M-8540, Cl, CH3, H, i-Pr, Cl), (M-8541, Cl, CH3, H, i-Pr, F), (M-8542, Cl, CH3, H, i-Pr, CF3), (M-8543, Cl, CH3, H, i-Pr, Br), (M-8544, Cl, CH3, H, i-Pr, CH3), (M-8545, Cl, CH3, H, n-Bu, H), (M-8546, Cl, CH3, H, n-Bu, Cl), (M-8547, Cl, CH3, H, n-Bu, F), (M-8548, Cl, CH3, H, n-Bu, CF3), (M-8549, Cl, CH3, H, n-Bu, Br), (M-8550, Cl, CH3, H, n-Bu, CH3), (M-8551, Cl, CH3, H, i-Bu, H), (M-8552, Cl, CH3, H, i-Bu, Cl), (M-8553, Cl, CH3, H, i-Bu, F), (M-8554, Cl, CH3, H, i-Bu, CF3), (M-8555, Cl, CH3, H, i-Bu, Br), (M-8556, Cl, CH3, H, i-Bu, CH3), (M-8557, Cl, CH3, H, sec-Bu, H), (M-8558, Cl, CH3, H, sec-Bu, Cl), (M-8559, Cl, CH3, H, sec-Bu, F), (M-8560, Cl, CH3, H, sec-Bu, CF3), (M-8561, Cl, CH3, H, sec-Bu, Br), (M-8562, Cl, CH3, H, sec-Bu, CH3), (M-8563, Cl, CH3, H, n-Pen, H), (M-8564, Cl, CH3, H, n-Pen, Cl), (M-8565, Cl, CH3, H, n-Pen, F), (M-8566, Cl, CH3, H, n-Pen, CF3), (M-8567, Cl, CH3, H, n-Pen, Br), (M-8568, Cl, CH3, H, n-Pen, CH3), (M-8569, Cl, CH3, H, c-Pen, H), (M-8570, Cl, CH3, H, c-Pen, Cl), (M-8571, Cl, CH3, H, c-Pen, F), (M-8572, Cl, CH3, H, c-Pen, CF3), (M-8573, Cl, CH3, H, c-Pen, Br), (M-8574, Cl, CH3, H, c-Pen, CH3), (M-8575, Cl, CH3, H, n-Hex, H), (M-8576, Cl, CH3, H, n-Hex, Cl), (M-8577, Cl, CH3, H, n-Hex, F), (M-8578, Cl, CH3, H, n-Hex, CF3), (M-8579, Cl, CH3, H, n-Hex, Br), (M-8580, Cl, CH3, H, n-Hex, CH3), (M-8581, Cl, CH3, H, c-Hex, H), (M-8582, Cl, CH3, H, c-Hex, Cl), (M-8583, Cl, CH3, H, c-Hex, F), (M-8584, Cl, CH3, H, c-Hex, CF3), (M-8585, Cl, CH3, H, c-Hex, Br), (M-8586, Cl, CH3, H, c-Hex, CH3), (M-8587, Cl, CH3, H, OH, H), (M-8588, Cl, CH3, H, OH, Cl), (M-8589, Cl, CH3, H, OH, F), (M-8590, Cl, CH3, H, OH, CF3), (M-8591, Cl, CH3, H, OH, Br), (M-8592, Cl, CH3, H, OH, CH3), (M-8593, Cl, CH3, H, EtO, H), (M-8594, Cl, CH3, H, EtO, Cl), (M-8595, Cl, CH3, H, EtO, F), (M-8596, Cl, CH3, H, EtO, CF3), (M-8597, Cl, CH3, H, EtO, Br), (M-8598, Cl, CH3, H, EtO, CH3), (M-8599, Cl, CH3, H, n-PrO, H), (M-8600, Cl, CH3, H, n-PrO, Cl), (M-8601, Cl, CH3, H, n-PrO, P), (M-8602, Cl, CH3, H, n-PrO, CF3), (M-8603, Cl, CH3, H, n-PrO, Br), (M-8604, CL, CH3, H, n-PrO, CH3), (M-8605, Cl, CH3, H, PhO, H), (M-8606, Cl, CH3, H, PhO, Cl), (M-8607, Cl, CH3, H, PhO, F), (M-8608, Cl, CH3, H, PhO, CF3), (M-8609, Cl, CH3, H, PhO, Br), (M-8610, Cl, CH3, H, PhO, CH3), (M-8611, Cl, CH3, H, BnO, H), (M-8612, Cl, CH3, H, BnO, Cl), (M-8613, Cl, CH3, H, BnO, F), (M-8614, Cl, CH3, H, BnO, CF3), (M-8615, Cl, CH3, H, BnO, Br), (M-8616, Cl, CH3, H, BnO, CH3), (M-8617, Cl, CH3, H, PhCH2CH2O, H), (M-8618, Cl, CH3, H, PhCH2CH2O, Cl), (M-8619, Cl, CH3, H, PhCH2CH2O, P), (M-8620, Cl, CH3, H, PhCH2CH2O, CF3), (M-8621, Cl, CH3, H, PhCH2CH2O, Br), (M-8622, Cl, CH3, H, PhCH2CH2O, CH3), (M-8623, Cl, CH3, H, CF3O, H), (M-8624, Cl, CH3, H, CF3O, Cl), (M-8625, Cl, CH3, H, CF3O, F), (M-8626, Cl, CH3, H, CF3O, CF3), (M-8627, Cl, CH3, H, CF3O, Br), (M-8628, Cl, CH3, H, CF3O, CH3), (M-8629, Cl, CH3, H, Ph, H), (M-8630, Cl, CH3, H, Ph, Cl), (M-8631, Cl, CH3, H, Ph, F), (M-8632, Cl, CH3, H, Ph, CF3), (M-8633, Cl, CH3, H, Ph, Br), (M-8634, Cl, CH3, H, Ph, CH3), (M-8635, Cl, CH3, H, 4-F-Ph, H), (M-8636, Cl, CH3, H, 4-F-Ph, Cl), (M-8637, Cl, CH3, H, 4-F-Ph, F), (M-8638, Cl, CH3, H, 4-F-Ph, CF3), (M-8639, Cl, CH3, H, 4-F-Ph, Br), (M-8640, Cl, CH3, H, 4-F-Ph, CH3), (M-8641, Cl, CH3, H, 4-CF3-Ph, H), (M-8642, Cl, CH3, H, 4-CF3-Ph, Cl), (M-8643, Cl, CH3, H, 4-CF3-Ph, F), (M-8644, Cl, CH3, H, 4-CF3-Ph, CF3), (M-8645, Cl, CH3, H, 4-CF3-Ph, Br), (M-8646, Cl, CH3, H, 4-CF3-Ph, CH3), (M-8647, Cl, CH3, H, 4-(Me)2N-Ph, H), (M-8648, Cl, CH3, H, 4-(Me)2N-Ph, Cl), (M-8649, CL, CH3, H, 4-(Me)2N-Ph, F), (M-8650, Cl, CH3, H, 4-(Me)2N-Ph, CF3), (M-8651, Cl, CH3, H, 4-(Me)2N-Ph, Br), (M-8652, Cl, CH3, H, 4-(Me)2N-Ph, CH3), (M-8653, Cl, CH3, H, 4-OH-Ph, H), (M-8654, Cl, CH3, H, 4-OH-Ph, Cl), (M-8655, Cl, CH3, H, 4-OH-Ph, F), (M-8656, Cl, CH3, H, 4-OH-Ph, CF3), (M-8657, Cl, CH3, H, 4-OH-Ph, Br), (M-8658, Cl, CH3, H, 4-OH-Ph, CH3), (M-8659, Cl, CH3, H, 3,4-di-F-Ph, H), (M-8660, Cl, CH3, H, 3,4-di-F-Ph, Cl), (M-8661, Cl, CH3, H, 3,4-di-F-Ph, F), (M-8662, Cl, CH3, H, 3,4-di-F-Ph, CF3), (M-8663, Cl, CH3, H, 3,4-di-F-Ph, Br), (M-8664, Cl, CH3, H, 3,4-di-F-Ph, CH3), (M-8665, Cl, CH3, H, 4-COOH-Ph, H), (M-8666, Cl, CH3, H, 4-COOH-Ph, Cl), (M-8667, Cl, CH3, H, 4-COOH-Ph, F), (M-8668, Cl, CH3, H, 4-COOH-Ph, CF3), (M-8669, Cl, CH3, H, 4-COOH-Ph, Br), (M-8670, Cl, CH3, H, 4-COOH-Ph, CH3), (M-8671, Cl, CH3, H, Bn, H), (M-8672, Cl, CH3, H, Bn, Cl), (M-8673, Cl, CH3, H, Bn, F), (M-8674, Cl, CH3, H, Bn, CF3), (M-8675, Cl, CH3, H, Bn, Br), (M-8676, Cl, CH3, H, Bn, CH3), (M-8677, Cl, CH3, H, 4-F-Bu, H), (M-8678, Cl, CH3, H, 4-F-Bu, Cl), (M-8679, Cl, CH3, H, 4-F-Bn, F), (M-8680, Cl, CH3, H, 4-F-Bn, CF3), (M-8681, Cl, CH3, Ft, 4-F-Bn, Br), (M-8682, Cl, CH3, H, 4-F-Bn, CH3), (M-8683, Cl, CH3, H, 2-Py, H), (M-8684, Cl, CH3, H, 2-Py, Cl), (M-8685, Cl, CH3, H, 2-Py, F), (M-8686, Cl, CH3, H, 2-Py, CF3), (M-8687, Cl, CH3, H, 2-Py, Br), (M-8688, Cl, CH3, H, 2-Py, CH3), (M-8689, Cl, CH3, H, 3-Py, H), (M-8690, Cl, CH3, H, 3-Py, Cl), (M-8691, Cl, CH3, H, 3-Py, F), (M-8692, Cl, CH3, H, 3-Py, CF3), (M-8693, Cl, CH3, H, 3-Py, Br), (M-8694, Cl, CH3, H, 3-Py, CH3), (M-8695, Cl, CH3, H, 4-Py, H), (M-8696, Cl, CH3, H, 4-Py, Cl), (M-8697, Cl, CH3, H, 4-Py, F), (M-8698, Cl, CH3, H, 4-Py, CF3), (M-8699, Cl, CH3, H, 4-Py, Br), (M-8700, Cl, CH3, H, 4-Py, CH3), (M-8701, Cl, CH3, H, 2-Th, H), (M-8702, Cl, CH3, H, 2-Th, Cl), (M-8703, Cl, CH3, H, 2-Th, F), (M-8704, Cl, CH3, H, 2-Th, CF3), (M-8705, Cl, CH3, H, 2-Th, Br), (M-8706, Cl, CH3, H, 2-Th, CH3), (M-8707, Cl, CH3, H, 3-Th, H), (M-8708, Cl, CH3, H, 3-Th, Cl), (M-8709, Cl, CH3, H, 3-Th, F), (M-8710, Cl, CH3, H, 3-Th, CF3), (M-8711, Cl, CH3, H, 3-Th, Br), (M-8712, Cl, CH3, H, 3-Th, CH3), (M-8713, Cl, CH3, H, pyrrazol-2-yl, H), (M-8714, Cl, CH3, H, pyrrazol-2-yl, Cl), (M-8715, Cl, CH3, H, pyrrazol-2-yl, F), (M-8716, Cl, CH3, H, pyrrazol-2-yl, CF3), (M-8717, Cl, CH3, H, pyrrazol-2-yl, Br), (M-8718, Cl, CH3, H, pyrrazol-2-yl, CH3), (M-8719, Cl, CH3, H, pyrrazol-3-yl, H), (M-8720, Cl, CH3, H, pyrrazol-3-yl, Cl), (M-8721, Cl, CH3< H, pyrrazol-3-yl, F), (M-8722, Cl, CH3, H, pyrrazol-3-yl, CF3), (M-8723, Cl, CH3, H, pyrrazol-3-yl, Br), (M-8724, Cl, CH3, H, pyrrazol-3-yl, CH3), (M-8725, Cl, CH3, H, pyrimidin-2-yl, H), (M-8726, Cl, CH3, H, pyrimidin-2-yl, Cl), (M-8727, Cl, CH3, H, pyrimidin-2-yl, F), (M-8728, Cl, CH3, H, pyrimidin-2-yl, CF3), (M-8729, Cl, CH3, H, pyrimidin-2-yl, Br), (M-8730, Cl, CH3, H, pyrimidin-2-yl, CH3), (M-8731, Cl, CH3, H, pyrimidin-4-yl, H), (M-8732, Cl, CH3, H, pyrimidin-4-yl, Cl), (M-8733, Cl, CH3, H, pyrimidin-4-yl, F), (M-8734, Cl, CH3, H, pyrimidin-4-yl, CF3), (M-8735, Cl, CH3, H, pyrimidin-4-yl, Br), (M-8736, Cl, CH3, H, pyrimidin-4-yl, CH3), (M-8737, Cl, CH3, H, pyrimidin-5-yl, H), (M-8738, Cl, CH3, H, pyrimidin-5-yl, Cl), (M-8739, Cl, CH3, H, pyrimidin-5-yl, F), (M-8740, Cl, CH3, H, pyrimidin-5-yl, CF3), (M-8741, Cl, CH3, H, pyrimidin-6-yl, Br), (M-8742, Cl, CH3, H, pyrimidin-5-yl, CH3), (M-8743, Cl, CH3, H, HOOCCH2CH2CH2, H), (M-8744, Cl, CH3, H, HOOCCH2CH2CH2, Cl), (M-8745, Cl, CH3, H, HOOCCH2CH2CH2, F), (M-8746, Cl, CH3, H, HOOCCH2CH2CH2, CF3), (M-8747, Cl, CH3, H, HOOCCH2CH2CH2, Br), (M-8748, Cl, CH3, H, HOOCCH2CH2CH2, CH3), (M-8749, Cl, CH3, H, HOOCCH2CH2CH2CH2, H), (M-8750, Cl, CH3, H, HOOCCH2CH2CH2CH2, Cl), (M-8751, Cl, CH3, H, HOOCCH2CH2CH2CH2, F), (M-8752, Cl, CH3, H, HOOCCH2CH2CH2CH2, CF3), (M-8753, Cl, CH3, H, HOOCCH2CH2CH2CH3, Br), (M-8754, Cl, CH3, H, HOOCCH2CH2CH2CH2, CH3), (M-8755, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, H), (M-8756, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-8757, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, F), (M-8758, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-8759, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-8760, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-8761, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2H), (M-8762, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-8763, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-8764, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-8765, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-8766, Cl, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-8767, Cl, CH3, H, MeOCH2, H), (M-8768, Cl, CH3, H, MeOCH2, Cl), (M-8769, Cl, CH3, H, MeOCH2, F), (M-8770, Cl, CH3, H, MeOCH2, CF3), (M-8771, Cl, CH3, H, MeOCH2, Br), (M-8772, Cl, CH3, H, MeOCH2, CH3), (M-8773, Cl, CH3, H, EtOCH2, H), (M-8774, Cl, CH3, H, EtOCH2, Cl), (M-8775, Cl, CH3, H, EtOCH2, F), (M-8776, Cl, CH3, H, EtOCH2, CF3), (M-8777, Cl, CH3, H, EtOCH2, Br), (M-8778, Cl, CH3, H, EtOCH2, CH3), (M-8779, Cl, CH3, H, EtOCH2CH2, H), (M-8780, Cl, CH3, H, EtOCH2CH2, Cl), (M-8781, Cl, CH3, H, EtOCH2CH2, F), (M-8782, Cl, CH3, H, EtOCH2CH2, CF3), (M-8783, Cl, CH3, H, EtOCH2CH2, Br), (M-8784, Cl, CH3, H, EtOCH2CH2, CH3), (M-8785, Cl, CH3, H, MeOCH2CH2OCH2CH2, H), (M-8786, Cl, CH3, H, MeOCH2CH2OCH2CH2, Cl), (M-8787, Cl, CH3, H, MeOCH2CH2OCH2CH2, F), (M-8788, Cl, CH3, H, MeOCH2CH2OCH2CH2, CF3), (M-8789, Cl, CH3, H, MeOCH2CH2OCH2CH2, Br), (M-8790, Cl, CH3, H, MeOCH2CH2OCH2CH2, CH3), (M-8791, Cl, CH3, H, MeOCH2CH2, H), (M-8792, Cl, CH3, H, MeOCH2CH2, Cl), (M-8793, Cl, CH3, H, MeOCH2CH2, F), (M-8794, Cl, CH3, H, MeOCH2CH2, CF3), (M-8795, Cl, CH3, H, MeOCH2CH2, Br), (M-8796, Cl, CH3, H, MeOCH2CH2, CH3), (M-8797, Cl, CH3, H, HOCH2, H), (M-8798, Cl, CH3, H, HOCH2, Cl), (M-8799, Cl, CH3, H, HOCH2, F), (M-8800, Cl, CH3, H, HOCH2, CF3), (M-8801, Cl, CH3, H, HOCH2, Br), (M-8802, Cl, CH3, H, HOCH2, CH3), (M-8803, Cl, CH3, H, HOCH2CH2, H), (M-8804, Cl, CH3, H, HOCH2CH2, Cl), (M-8805, Cl, CH3, H, HOCH2CH2, F), (M-8806, Cl, CH3, H, HOCH2CH2, CF3), (M-8807, Cl, CH3, H, HOCH2CH2, Br), (M-8808, Cl, CH3, H, HOCH2CH2, CH3), (M-8809, Cl, CH3, H, HOCH2CH2CH2, H), (M-8810, Cl, CH3, H, HOCH2CH2CH2, Cl), (M-8811, Cl, CH3, H, HOCH2CH2CH2, F), (M-8812, Cl, CH3, H, HOCH2CH2CH2, CF3), (M-8813, Cl, CH3, H, HOCH2CH2CH2, Br), (M-8814, Cl, CH3, H, HOCH2CH2CH2, CH3), (M-8815, Cl, CH3, H, HOCH2CH2CH2CH2, H), (M-8816, Cl, CH3, H, HOCH2CH2CH2CH2, Cl), (M-8817, Cl, CH3, H, HOCH2CH2CH2CH2, F), (M-8818, Cl, CH3, H, HOCH2CH2CH2CH2, CF3), (M-8819, Cl, CH3, H, HOCH2CH2CH2CH2, Br), (M-8820, Cl, CH3, H, HOCH2CH2CH2CH2, CH3), (M-8821, Cl, CH3, H, HOCH2CH2CH2CH2CH2H), (M-8822, Cl, CH3, H, HOCH2CH2CH2CH2CH2Cl), (M-8823, Cl, CH3, H, HOCH2CH2CH2CH2CH2, F), (M-8824, Cl, CH3, H, HOCH2CH2CH2CH2CH2CF3), (M-8825, Cl, CH3, H, HOCH2CH2CH2CH2CH2Br), (M-8826, Cl, CH3, H, HOCH2CH2CH2CH2CH2CH3), (M-8827, Cl, CH3, H, HOCH2CH2OCH2CH2, H), (M-8828, Cl, CH3, H, HOCH2CH2OCH2CH2, Cl), (M-8829, Cl, CH3, H, HOCH2CH2OCH2CH2, F), (M-8830, Cl, CH3, H, HOCH2CH2OCH2 CH2, CF3), (M-8831, Cl, CH3, H, HOCH2CH2OCH2CH2, Br), (M-8832, Cl, CH3, H, HOCH2CH2OCH2CH2, CH3), (M-8833, Cl, CH3, H, (Me)2N, H), (M-8834, Cl, CH3, H, (Me)2N, Cl), (M-8835, Cl, CH3, H, (Me)2N, F), (M-8836, Cl, CH3, H, (Me)2N, CF3), (M-8837, Cl, CH3, H, (Me)2N, Br), (M-8838, Cl, CH3, H, (Me)2N, CH3), (M-8839, Cl, CH3, H, piperidin-4-yl-methyl, H), (M-8840, Cl, CH3, H, piperidin-4-yl-methyl, Cl), (M-8841, Cl, CH3, H, piperidin-4-yl-methyl, F), (M-8842, Cl, CH3, H, piperidin-4-yl-methyl, CF3), (M-8843, Cl, CH3, H, piperidin-4-yl-methyl, Br), (M-8844, Cl, CH3, H, piperidin-4-yl-methyl, CH3), (M-8845, Cl, CH3, H, cyclohexylmethyl, H), (M-8846, Cl, CH3, H, cyclohexylmethyl, Cl), (M-8847, Cl, CH3, H, cyclohexylmethyl, F), (M-8848, Cl, CH3, H, cyclohexylmethyl, CF3), (M-8849, Cl, CH3, H, cyclohexylmethyl, Br), (M-8850, Cl, CH3, H, cyclohexylmethyl, CH3), (M-8851, Cl, CH3, F, H, H), (M-8852, Cl, CH3, F, H, Cl), (M-8853, MeO, CH3, F, H, F), (M-8854, Cl, CH3, F, H, CF3), (M-8855, Cl, CH3, F, H, Br), (M-8856, Cl, CH3, F, H, CH3), (M-8857, Cl, CH3, F, F, H), (M-8858, Cl, CH3, F, F, Cl), (M-8859, Cl, CH3, F, F, F), (M-8860, Cl, CH3, F, F, CF3), (M-8861, Cl, CH3, F, F, Br), (M-8862, Cl, CH3, F, F, CH3), (M-8863, Cl, CH3, F, Cl, H), (M-8864, Cl, CH3, F, Cl, Cl), (M-8865, Cl, CH3, F, Cl, F), (M-8866, Cl, CH3, F, Cl, CF3), (M-8867, Cl, CH3, F, Cl, Br), (M-8868, Cl, CH3, F, Cl, CH3), (M-8869, Cl, CH3, F, CH3, H), (M-8870, Cl, CH3, F, CH3, Cl), (M-8871, Cl, CH3, F, CH3, F), (M-8872, Cl, CH3, F, CH3, CF3), (M-8873, Cl, CH3, F, CH3, Br), (M-8874, Cl, CH3, F, CH3, CH3), (M-8875, Cl, CH3, F, Et, H), (M-8876, Cl, CH3, F, Et, Cl), (M-8877, Cl, CH3, F, Et, F), (M-8878, Cl, CH3, F, Et, CF3), (M-8879, Cl, CH3, F, Et, Br), (M-8880, Cl, CH3, F, Et, CH3), (M-8881, Cl, CH3, F, n-Pr, H), (M-8882, Cl, CH3, F, n-Pr, Cl), (M-8883, Cl, CH3, F, n-Pr, F), (M-8884, Cl, CH3, F, n-Pr, CF3), (M-8885, Cl, CH3, F, n-Pr, Br), (M-8886, Cl, CH3, F, n-Pr, CH3), (M-8887, Cl, CH3, F, c-Pr, H), (M-8888, Cl, CH3, F, c-Pr, Cl), (M-8889, Cl, CH3, F, c-Pr, F), (M-8890, Cl, CH3, F, c-Pr, CF3), (M-8891, Cl, CH3, F, c-Pr, Br), (M-8892, Cl, CH3, F, c-Pr, CH3), (M-8893, Cl, CH3, F, i-Pr, H), (M-8894, Cl, CH3, F, i-Pr, Cl), (M-8895, Cl, CH3, F, i-Pr, F), (M-8896, Cl, CH3, F, i-Pr, CF3), (M-8897, Cl, CH3, F, i-Pr, Br), (M-8898, Cl, CH3, F, i-Pr, CH3), (M-8899, Cl, CH3, F, n-Bu, H), (M-8900, Cl, CH3, F, n-Bu, Cl), (M-8901, Cl, CH3, F, n-Bu, F), (M-8902, Cl, CH3, F, n-Bu, CF3), (M-8903, Cl, CH3, F, n-Bu, Br), (M-8904, Cl, CH3, F, n-Bu, CH3), (M-8905, Cl, CH3, F, i-Bu, H), (M-8906, Cl, CH3, F, i-Bu, Cl), (M-8907, Cl, CH3, F, i-Bu, F), (M-8908, Cl, CH3, F, i-Bu, CF3), (M-8909, Cl, CH3, F, i-Bu, Br), (M-8910, Cl, CH3, F, i-Bu, CH3), (M-8911, Cl, CH3, F, sec-Bu, H), (M-8912, Cl, CH3, F, sec-Bu, Cl), (M-8913, Cl, CH3, F, sec-Bu, F), (M-8914, Cl, CH3, F, sec-Bu, CF3), (M-8915, Cl, CH3, F, sec-Bu, Br), (M-8916, Cl, CH3, F, sec-Bu, CH3), (M-8917, Cl, CH3, F, n-Pen, H), (M-8918, Cl, CH3, F, n-Pen, Cl), (M-8919, Cl, CH3, F, n-Pen, F), (M-8920, Cl, CH3, F, n-Pen, CF3), (M-8921, Cl, CH3, F, n-Pen, Br), (M-8922, Cl, CH3, F, n-Pen, CH3), (M-8923, Cl, CH3, F, c-Pen, H), (M-8924, Cl, CH31 F, c-Pen, Cl), (M-8925, Cl, CH3, F, c-Pen, F), (M-8926, Cl, CH3, F, c-Pen, CF3), (M-8927, Cl, CH3, F, c-Pen, Br), (M-8928, Cl, CH3, F, c-Pen, CH3), (M-8929, Cl, CH3, F, n-Hex, H), (M-8930, Cl, CH3, F, n-Hex, Cl), (M-8931, Cl, CH3, F, n-Hex, F), (M-8932, Cl, CH3, F, n-Hex, CF3), (M-8933, Cl, CH3, F, n-Hex, Br), (M-8934, Cl, CH3, F, n-Hex, CH3), (M-8935, Cl, CH3, F, c-Hex, H), (M-8936, Cl, CH3, F, c-Hex, Cl), (M-8937, Cl, CH3, F, c-Hex, F), (M-8938, Cl, CH3, F, c-Hex, CF3), (M-8939, Cl, CH3, F, c-Hex, Br), (M-8940, Cl, CH3, F, c-Hex, CH3), (M-8941, Cl, CH3, F, OH, H), (M-8942, Cl, CH3, F, OH, Cl), (M-8943, Cl, CH3, F, OH, F), (M-8944, Cl, CH3, F, OH, CF3), (M-8945, Cl, CH3, F, OH, Br), (M-8946, Cl, CH3, F, OH, CH3), (M-8947, Cl, CH3, F, EtO, H), (M-8948, Cl, CH3, F, EtO, Cl), (M-8949, Cl, CH3, F, EtO, F), (M-8950, Cl, CH3, F, EtO, CF3), (M-8951, Cl, CH3, F, EtO, Br), (M-8952, Cl, CH3, F, EtO, CH3), (M-8953, Cl, CH3, F, n-PrO, H), (M-8954, Cl, CH3, F, n-PrO, Cl), (M-8955, Cl, CH3, F, n-PrO, F), (M-8956, Cl, CH3, F, n-PrO, CF3), (M-8957, Cl, CH3, F, n-PrO, Br), (M-8958, Cl, CH3, F, n-PrO, CH3), <M-8959, Cl, CH3, F, PhO, H), (M-8960, Cl, CH3, F, PhO, Cl), (M-8961, Cl, CH3, F, PhO, F), (M-8962, Cl, CH3, F, PhO, CF3), (M-8963, Cl, CH3, F, PhO, Br), (M-8964, Cl, CH3, F, PhO, CH3), (M-8965, Cl, CH3, F, BnO, H), (M-8966, Cl, CH3, F, BnO, Cl), (M-8967, Cl, CH3, F, BnO, F), (M-8968, Cl, CH3, F, BnO, CF3), (M-8969, Cl, CH3, F, BnO, Br), (M-8970, Cl, CH3, F, BnO, CH3), (M-8971, Cl, CH3, F, PhCH2CH2O, H), (M-8972, Cl, CH3, F, PhCH2CH2O, Cl), (M-8973, Cl, CH3, F, PhCH2CH2O, F), (M-8974, Cl, CH3, F, PhCH2CH2O, CF3), (M-8975, Cl, CH3, F, PhCH2CH2O, Br), (M-8976, Cl, CH3, F, PhCH2CH2O, CH3), (M-8977, Cl, CH3, F, CF3O, H), (M-8978, Cl, CH3, F, CF3O, Cl), (M-8979, Cl, CH3, F, CF3O, F), (M-8980, Cl, CH3, F, CF3O, CF3), (M-8981, Cl, CH3, F, CF3O, Br), (M-8982, Cl, CH3, F, CF3O, CH3), (M-8983, Cl, CH3, F, Ph, H), (M-8984, Cl, CH3, F, Ph, Cl), (M-8985, Cl, CH3, F, Ph, F), (M-8986, Cl, CH3, F, Ph, CF3), (M-8987, Cl, CH3, F, Ph, Br), (M-8988, Cl, CH3, F, Ph, CH3), (M-8989, Cl, CH3, F, 4-F-Ph, H), (M-8990, Cl, CH3, F, 4-F-Ph, Cl), (M-8991, Cl, CH3, F, 4-F-Ph, F), (M-8992, Cl, CH3, F, 4-F-Ph, CF3), (M-8993, Cl, CH3, F, 4-F-Ph, Br), (M-8994, Cl, CH3, F, 4-F-Ph, CH3), (M-8995, Cl, CH3, F, 4-CF3-Ph, H), (M-8996, Cl, CH3, F, 4-CF3-Ph, Cl), (M-8997, Cl, CH3, F, 4-CF3-Ph, F), (M-8998, Cl, CH3, F, 4-CF3-Ph, CF3), (M-8999, Cl, CH3, F, 4-CF3-Ph, Br), (M-9000, Cl, CH3, F, 4-CF3-Ph, CH3), (M-9001, Cl, CH3, F, 4-(Me)2N-Ph, H), (M-9002, Cl, CH3, F, 4-(Me)2N-Ph, Cl), (M-9003, Cl, CH3, F, 4-(Me)2N-Ph, F), (M-9004, Cl, CH3, F, 4-(Me)2N-Ph, CF3), (M-9005, Cl, CH3, F, 4-(Me)2N-Ph, Br), (M-9006, Cl, CH3, F, 4-(Me)2N-Ph, CH3), (M-9007, Cl, CH3, F, 4-OH-Ph, H), (M-9008, Cl, CH3, F, 4-OH-Ph, Cl), (M-9009, Cl, CH3, F, 4-OH-Ph, F), (M-9010, Cl, CH3, F, 4-OH-Ph, CF3), (M-9011, Cl, CH3, F, 4-OH-Ph, Br), (M-9012, Cl, CH3, F, 4-OH-Ph, CH3), (M-9013, Cl, CH3, F, 3,4-di-F-Ph, H), (M-9014, Cl, CH3, F, 3,4-di-F-Ph, Cl), (M-9015, Cl, CH3, F, 3,4-di-F-Ph, F), (M-9016, Cl, CH3, F, 3,4-di-F-Ph, CF3), (M-9017, Cl, CH3, F, 3,4-di-F-Ph, Br), (M-9018, Cl, CH3, F, 3,4-di-F-Ph, CH3), (M-9019, Cl, CH3, F, 4-COOH-Ph, H), (M-9020, Cl, CH3, F, 4-COOH-Ph, Cl), (M-9021, Cl, CH3, F, 4-COOH-Ph, F), (M-9022, Cl, CH3, F, 4-COOH-Ph, CF3), (M-9023, Cl, CH3, F, 4-COOH-Ph, Br), (M-9024, Cl, CH3, F, 4-COOH-Ph, CH3), (M-9025, Cl, CH3, F, Bn, H), (M-9026, Cl, CH3, F, Bn, Cl), (M-9027, Cl, CH3, F, Bn, F), (M-9028, Cl, CH3, F, Bn, CF3), (M-9029, Cl, CH3, F, Bn, Br), (M-9030, Cl, CH3, F, Bn, CH3), (M-9031, Cl, CH3, F, 4-F-Bn, H), (M-9032, Cl, CH3, F, 4-F-Bn, Cl), (M-9033, Cl, CH3, F, 4-F-Bn, F), (M-9034, Cl, CH3, F, 4-F-Bn, CF3), (M-9035, Cl, CH3, F, 4-F-Bn, Br), (M-9036, Cl, CH3, F, 4-F-Bn, CH3), (M-9037, Cl, CH3, F, 2-Py, H), (M-9038, Cl, CH3, F, 2-Py, Cl), (M-9039, Cl, CH3, F, 2-Py, F), (M-9040, Cl, CH3, F, 2-Py, CF3), (M-9041, Cl, CH3, F, 2-Py, Br), (M-9042, Cl, CH3, F, 2-Py, CH3), (M-9043, Cl, CH3, F, 3-Py, H), (M-9044, Cl, CH3, F, 3-Py, Cl), (M-9045, Cl, CH3, F, 3-Py, F), (M-9046, Cl, CH3, F, 3-Py, CF3), (M-9047, Cl, CH3, F, 3-Py, Br), (M-9048, Cl, CH3, F, 3-Py, CH3), (M-9049, Cl, CH3, F, 4-Py, H), (M-9050, Cl, CH3, F, 4-Py, Cl), (M-9051, Cl, CH3, F, 4-Py, F), (M-9052, Cl, CH3, F, 4-Py, CF3), (M-9053, Cl, CH3, F, 4-Py, Br), (M-9054, Cl, CH3, F, 4-Py, CH3), (M-9055, Cl, CH3, F, 2-Th, H), (M-9056, Cl, CH3, F, 2-Th, Cl), (M-9057, Cl, CH3, F, 2-Th, F), (M-9058, Cl, CH3, F, 2-Th, CF3), (M-9059, Cl, CH3, F, 2-Th, Br), (M-9060, Cl, CH3, F, 2-Th, CH3), (M-9061, Cl, CH3, F, 3-Th, H), (M-9062, Cl, CH3, F, 3-Th, Cl), (M-9063, Cl, CH3, F, 3-Th, F), (M-9064, Cl, CH3, F, 3-Th, CF3), (M-9065, Cl, CH3, F, 3-Th, Br), (M-9066, Cl, CH3, F, 3-Th, CH3), (M-9067, Cl, CH3, F, pyrrazol-2-yl, H), (M-9068, Cl, CH3, F, pyrrazol-2-yl, Cl), (M-9069, Cl, CH3, F, pyrrazol-2-yl, F), (M-9070, Cl, CH3, F, pyrrazol-2-yl, CF3), (M-9071, Cl, CH3, F, pyrrazol-2-yl, Br), (M-9072, Cl, CH3, F, pyrrazol-2-yl, CH3), (M-9073, Cl, CH3, F, pyrrazol-3-yl, H), (M-9074, Cl, CH3, F, pyrrazol-3-yl, Cl), (M-9075, Cl, CH3, F, pyrrazol-3-yl, F), (M-9076, Cl, CH3, F, pyrrazol-3-yl, CF3), (M-9077, Cl, CH3, F, pyrrazol-5-yl, Br), (M-9078, Cl, CH3, F, pyrrazol-3-yl, CH3), (M-9079, Cl, CH3, F, pyrimidin-2-yl, H), (M-9080, Cl, CH3, F, pyrimidin-2-yl, Cl), (M-9081, Cl, CH3, F, pyrimidin-2-yl, F), (M-9082, Cl, CH3, F, pyrimidin-2-yl, CF3), (M-9083, Cl, CH3, F, pyrimidin-2-yl, Br), (M-9084, Cl, CH3, F, pyrimidin-2-yl, CH3), (M-9085, Cl, CH3, F, pyrimidin-4-yl, H), (M-9086, Cl, CH3, F, pyrimidin-4-yl, Cl), (M-9087, Cl, CH3, F, pyrimidin-4-yl, F), (M-9088, Cl, CH3, F, pyrimidin-4-yl, CF3), (M-9089, Cl, CH3, F, pyrimidin-4-yl, Br), (M-9090, Cl, CH3, F, pyrimidin-4-yl, CH3), (M-9091, Cl, CH3, F, pyrimidin-5-yl, H), (M-9092, Cl, CH3, F, pyrimidin-5-yl, Cl), (M-9093, Cl, CH3, F, pyrimidin-5-yl, F), (M-9094, Cl, CH3, F, pyrimidin-5-yl, CF3), (M-9095, Cl, CH3, F, pyrimidin-5-yl, Br), (M-9096, Cl, CH3, F, pyrimidin-5-yl, CF3), (M-9097, Cl, CH3, F, HOOCCH2CH2CH2, H), (M-9098, Cl, CH3, F, HOOCCH2CH2CH2, Cl), (M-9099, Cl, CH3, F, HOOCCH2CH2CH2, F), (M-9100, Cl, CH3, F, HOOCCH2CH2CH2, CF3), (M-9101, Cl, CH3, F, HOOCCH2CH2CH2, Br), (M-9102, Cl, CH3, F, HOOCCH2CH2CH2, CH3), (M-9103, Cl, CH3, F, HOOCCH2CH2CH2CH2, H), (M-9104, Cl, CH3, F, HOOCCH2CH2CH2CH2, Cl), (M-9105, Cl, CH3, F, HOOCCH2CH2CH2CH2, F), (M-9106, Cl, CH3, F, HOOCCH2CH2CH2CH2, CF3), (M-9107, Cl, CH3, F, HOOCCH2CH2CH2CH2, Br), (M-9108, Cl, CH3, F, HOOCCH2CH2CH2CH2, CH3), (M-9109, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2, H), (M-9110, Cl, CH3, P, (Me)2NCOCH2CH2CH2CH2, Cl), (M-9111, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2, F), (M-9112, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-9113, Cl, CH3, F, (Me)3NCOCH2CH2CH2CH2Br), (M-9114, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-9115, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-9116, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-9117, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-9118, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-9119, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-9120, Cl, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-9121, Cl, CH3, F, MeOCH2, H), (M-9122, Cl, CH3, F, MeOCH2, Cl), (M-9123, Cl, CH3, F, MeOCH2, F), (M-9124, Cl, CH3, F, MeOCH2, CH3), (M-9125, Cl, CH3, F, MeOCH2, Br), (M-9126, Cl, CH3, F, MeOCH2, CH3), (M-9127, Cl, CH3, F, EtOCH2, H), (M-9128, Cl, CH3, F, EtOCH2, Cl), (M-9129, Cl, CH3, F, EtOCH2, F), (M-9130, Cl, CH3, F, EtOCH2, CF3), (M-9131, Cl, CH3, F, EtOCH2, Br), (M-9132, Cl, CH3, F, EtOCH2, CH3), (M-9133, Cl, CH3, F, EtOCH2CH2, H), (M-9134, Cl, CH3, F, EtOCH2CH2, Cl), (M-9135, Cl, CH3, F, EtOCH2CH2, F), (M-9136, Cl, CH3, F, EtOCH2CH2, CF3), (M-9137, Cl, CH3, F, EtOCH2CH2, Br), (M-9138, Cl, CH3, F, EtOCH2CH2, CH3), (M-9139, Cl, CH3, F, MeOCH2CH2OCH2CH2, H), (M-9140, Cl, CH3, F, MeOCH2CH2OCH2CH3, Cl), (M-9141, Cl, CH3, F, MeOCH2CH2OCH2CH2, F), (M-9142, Cl, CH3, F, MeOCH2CH2OCH2CH2, CF3), (M-9143, Cl, CH3, F, MeOCH2CH2OCH2CH2, Be), (M-9144, Cl, CH3, F, MeOCH2CH2OCH2CH2, CH3), (M-9145, Cl, CH3, F, MeOCH2CH2, H), (M-9146, Cl, CH3, F, MeOCH2CH2, Cl), (M-9147, Cl, CH3, F, MeOCH2CH2, F), (M-9148, Cl, CH3, F, MeOCH2CH2, CF3), (M-9149, Cl, CH3, F, MeOCH2CH2, Br), (M-9150, Cl, CH3, F, MeOCH2CH2, CH3), (M-9151, Cl, CH3, F, HOCH2, H), (M-9152, Cl, CH3, F, HOCH2, Cl), (M-9153, Cl, CH3, F, HOCH2, F), (M-9154, Cl, CH3, F, HOCH2, CF3), (M-9155, Cl, CH3, F, HOCH2, Br), (M-9156, Cl, CH3, F, HOCH2, CH3), (M-9157, Cl, CH3, F, HOCH2CH2, H), (M-9158, Cl, CH3, F, HOCH2CH2, Cl), (M-9159, Cl, CH3, F, HOCH2CH2, F), (M-9160, Cl, CH3, F, HOCH2CH2, CF3), (M-9161, Cl, CH3, F, HOCH2CH2, Br), (M-9162, Cl, CH3, F, HOCH2CH2, CH3), (M-9163, Cl, CH3, F, HOCH2CH2CH2, H), (M-9164, Cl, CH3, F, HOCH2CH2CH3, Cl), (M-9165, Cl, CH3, F, HOCH2CH2CH2, F), (M-9166, Cl, CH3, F, HOCH2CH2CH2, CF3), (M-9167, Cl, CH3, F, HOCH2CH2CH2, Br), (M-9168, Cl, CH3, F, HOCH2CH2CH2, CH3), (M-9169, Cl, CH3, F, HOCH2CH2CH2CH2, H), (M-9170, Cl, CH3, F, HOCH2CH2CH2CH2, Cl), (M-9171, Cl, CH3, F, HOCH2CH2CH2CH2, F), (M-9172, Cl, CH3, F, HOCH2CH2CH2CH2, CF3), (M-9173, Cl, CH3, F, HOCH2CH2CH2CH2, Br), (M-9174, Cl, CH3, F, HOCH2CH2CH2CH2, CH3), (M-9175, Cl, CH3, F, HOCH2CH2CH2CH2CH2, H), (M-9176, Cl, CH3, F, HOCH2CH2CH2CH2CH2Cl), (M-9177, Cl, CH3, F, HOCH2CH2CH2CH2CH2, F), (M-9178, Cl, CH3, F, HOCH2CH2CH2CH2CH2, CF3), (M-9179, Cl, CH3, F, HOCH2CH2CH2CH2CH2Br), (M-9180, Cl, CH3, F, HOCH2CH2CH2CH2CH3, CH3), (M-9181, Cl, CH3, F, HOCH2CH2OCH2CH2, H), (M-9182, Cl, CH3, F, HOCH2CH2OCH2CH2, Cl), (M-9183, Cl, CH3, F, HOCH2CH2OCH2CH2, F), (M-9184, Cl, CH3, F, HOCH2CH2OCH2CH2, CF3), (M-9185, Cl, CH3, F, HOCH2CH2OCH2CH2, Br), (M-9186, Cl, CH3, F, HOCH2CH2OCH3CH3, CH3), (M-9187, Cl, CH3, F, (Me)2N, H), (M-9188, Cl, CH3, F, (Me)2N, Cl), (M-9189, Cl, CH3, F, (Me)2N, F), (M-9190, Cl, CH3, F, (Me)2N, CF3), (M-9191, Cl, CH3, F, (Me)2N, Br), (M-9192, Cl, CH3, F, (Me)2N, CH3), (M-9193, Cl, CH3, F, piperidin-4-yl-methyl, H), (M-9194, Cl, CH3, F, piperidin-4-yl-methyl, Cl), (M-9195, Cl, CH3, F, piperidin-4-yl-methyl, F), (M-9196, Cl, CH3, F, piperidin-4-yl-methyl, CF3), (M-9197, Cl, CH3, F, piperidin-4-yl-methyl, Br), (M-9198, Cl, CH3, F, piperidin-4-yl-methyl, CH3), (M-9199, Cl, CH3, F, cyclohexylmethyl, H), (M-9200, Cl, CH3, F, cyclohexylmethyl, Cl), (M-9201, Cl, CH3, F, cyclohexylmethyl, F), (M-9202, Cl, CH3, F, cyclohexylmethyl, CF3), (M-9203, Cl, CH3, F, cyclohexylmethyl, Br), (M-9204, Cl, CH3, F, cyclohexylmethyl, CH3), (M-9205, Cl, CH3, Cl, H, H), (M-9206, Cl, CH3, Cl, H, Cl), (M-9207, Cl, CH3, Cl, H, F), (M-9208, Cl, CH3, CL H, CF3), (M-9209, Cl, CH3, Cl, H, Br), (M-9210, Cl, CH3, Cl, H, CH3), (M-9211, Cl, CH3, Cl, F, H), (M-9212, CL, CH3, Cl, F, Cl), (M-9213, Cl, CH3, Cl, F, F), (M-9214, Cl, CH3, Cl, F, CF3), (M-9215, Cl, CH3, Cl, F, Br), (M-9216, Cl, CH3, Cl, F, CH3), (M-9217, Cl, CH3, Cl, Cl, H), (M-9218, Cl, CH3, Cl, Cl, Cl), (M-9219, Cl, CH3, Cl, Cl, F), (M-9220, Cl, CH3, Cl, Cl, CF3), (M-9221, Cl, CH3, Cl, Cl, Br), (M-9222, Cl, CH3, Cl, Cl, CH3), (M-9223, Cl, CH3, Cl, CH3, H), (M-9224, Cl, CH3, Cl, CH3, Cl), (M-9225, Cl, CH3, Cl, CH3, F), (M-9226, Cl, CH3, Cl, CH3, CF3), (M-9227, Cl, CH3, Cl, CH3, Br), (M-9228, Cl, CH3, Cl, CH3, CH3), (M-9229, Cl, CH3, Cl, Et, H), (M-9230, Cl, CH3, Cl, Et, Cl), (M-9231, Cl, CH3, Cl, Et, F), (M-9232, Cl, CH3, Cl, Et, CF3), (M-9233, Cl, CH3, Cl, Et, Br), (M-9234, Cl, CH3, Cl, Et, CH3), (M-9235, Cl, CH3, Cl, N-Pr, H), (M-9236, Cl, CH3, Cl, n-Pr, Cl), (M-9237, Cl, CH3, Cl, n-Pr, F), (M-9238, Cl, CH3, Cl, n-Pr, CF3), (M-9239, Cl. CH3, Cl, n-Pr, Br), (M-9240, Cl, CH3, Cl, n-Pr, CH3), (M-9241, Cl, CH3, Cl, c-Pr, H), (M-9242, Cl, CH3, Cl, c-Pr, Cl), (M-9243, Cl, CH3, Cl, c-Pr, F), (M-9244, Cl, CH3, Cl, c-Pr, CF3), (M-9245, Cl, CH3, Cl, c-Pr, Br), (M-9246, Cl, CH3, Cl, c-Pr, CH3), (M-9247, Cl, CH3, Cl, i-Pr, H), (M-9248, Cl, CH3, Cl, i-Pr, Cl), (M-9249, Cl, CH3, Cl, i-Pr, F), (M-9250, Cl, CH3, Cl, i-Pr, CF3), (M-9251, Cl, CH3, Cl, i-Pr, Br), (M-9252, Cl, CH3, Cl, i-Pr, CH3), (M-9253, Cl, CH3, Cl, n-Bu, H), (M-9254, Cl, CH3, Cl, n-Bu, Cl), (M-9255, Cl, CH3, Cl, n-Bu, F), (M-9256, Cl, CH3, Cl, n-Bu, CF3), (M-9257, Cl, CH3, Cl, n-Bu, Br), (M-9258, Cl, CH3, Cl, n-Bu, CH3), (M-9259, Cl, CH3, Cl, i-Bu, H), (M-9260, Cl, CH3, Cl, i-Bu, Cl), (M-9261, Cl, CH3, Cl, i-Bu, F), (M-9262, Cl, CH3, Cl, i-Bu, CF3), (M-9263, Cl, CH3, Cl, i-Bu, Br), (M-9264, Cl, CH3, Cl, i-Bu, CH3), (M-9265, Cl, CH3, Cl, sec-Bu, H), (M-9266, Cl, CH3, Cl, sec-Bu, Cl), (M-9267, Cl, CH3, Cl, sec-Bu, F), (M-9268, Cl, CH3, Cl, sec-Bu, CF3), (M-9269, Cl, CH3, Cl, sec-Bu, Br), (M-9270, Cl, CH3, Cl, sec-Bu, CH3), (M-9271, Cl, CH3, Cl, n-Pen, H), (M-9272, Cl, CH3, Cl, n-Pen, Cl), (M-9273, Cl, CH3, Cl, n-Pen, F), (M-9274, Cl, CH3, Cl, n-Pen, CF3), (M-9275, Cl, CH3, Cl, n-Pen, Br), (M-9276, Cl, CH3, Cl, n-Pen, CH3), (M-9277, Cl, CH3, Cl, c-Pen, H), (M-9278, Cl, CH3, Cl, c-Pen, Cl), (M-9279, Cl, CH3, Cl, c-Pen, F), (M-9280, Cl, CH3, Cl, c-Pen, CF3), (M-9281, Cl, CH3, Cl, c-Pen, Br), (M-9282, Cl, CH3, Cl, c-Pen, CH3), (M-9283, Cl, CH3, Cl, n-Hex, H), (M-9284, Cl, CH3, Cl, n-Hex, Cl), (M-9285, Cl, CH3, Cl, n-Hex, F), (M-9286, Cl, CH3, Cl, n-Hex, CF3), (M-9287, Cl, CH3, Cl, n-Hex, Br), (M-9288, Cl, CH3, Cl, n-Hex, CH3), (M-9289, Cl, CH3, CJ, c-Hex, H), (M-9290, Cl, CH3, Cl, c-Hex, Cl), (M-9291, Cl, CH3, Cl, c-Hex, F), (M-9292, Cl, CH3, Cl, c-Hex, CF3), (M-9293, Cl, CH3, Cl, c-Hex, Br), (M-9294, Cl, CH3, Cl, c-Hex, CH3), (M-9295, Cl, CH3, Cl, OH, H), (M-9296, Cl, CH3, Cl, OH, Cl), (M-9297, Cl, CH3, Cl, OH, F), (M-9298, Cl, CH3, Cl, OH, CF3), (M-9299, Cl, CH3, Cl, OH, Br), (M-9300, Cl, CH3, Cl, OH, CH3), (M-9301, Cl, CH3, Cl, EtO, H), (M-9302, Cl, CH3, Cl, EtO, Cl), (M-9303, Cl, CH3, Cl, EtO, F), (M-9304, Cl, CH3, Cl, EtO, CF3), (M-9305, Cl, CH3, Cl, EtO, Br), (M-9306, Cl, CH3, Cl, EtO, CH3), (M-9307, Cl, CH3, Cl, n-PrO, H), (M-9308, Cl, CH3, Cl, n-PrO, Cl), (M-9309, Cl, CH3, Cl, n-PrO, F), (M-9310, Cl, CH3, Cl, n-PrO, CF3), (M-9311, Cl, CH3, Cl, n-PrO, Br), (M-9312, Cl, CH3, Cl, n-PrO, CH3), (M-9313, Cl, CH3, Cl, PhO, H), (M-9314, Cl, CH3, Cl, PhO, Cl), (M-9315, Cl, CH3, Cl, PhO, F), (M-9316, Cl, CH3, Cl, PhO, CF3), (M-9317, Cl, CH3, Cl, PhO, Br), (M-9318, Cl, CH3, Cl, PhO, CH3), (M-9319, Cl, CH3, Cl, BnO, H), (M-9320, Cl, CH3, Cl, BnO, Cl), (M-9321, Cl, CH3, Cl, BnO, P), (M-9322, Cl, CH3, Cl, BnO, CF3), (M-9323, Cl, CH3, Cl, BnO, Br), (M-9324, Cl, CH3, Cl, BnO, CH3), (M-9325, Cl, CH3, Cl, PhCH2CH2O, H), (M-9321, Cl, CH3, Cl, PhCH2CH2O, Cl), (M-9327, Cl, CH3, Cl, PhCH2CH2O, F), (M-9328, Cl, CH3, Cl, PhCH2CH2O, CF3), (M-9329, Cl, CH3, Cl, PhCH2CH2O, Br), (M-9330, Cl, CH3, Cl, PhCH2CH2O, CH3), (M-9331, Cl, CH3, Cl, CF3O, H), (M-9332, Cl, CH3, Cl, CF3O, Cl), (M-9333, Cl, CH3, Cl, CF3O, F), (M-9334, Cl, CH3, Cl, CF3O, CF3), (M-9335, Cl, CH3, Cl, CF3O, Br), (M-9336, Cl, CH3, Cl, CF3O, CH3), (M-9337, Cl, CH3, Cl, Ph, H), (M-9338, Cl, CH3, Cl, Ph, Cl), (M-9339, Cl, CH3, Cl, Ph, F), (M-9340, Cl, CH3, Cl, Ph, CF3), (M-9341, Cl, CH3, Cl, Ph, Br), (M-9342, Cl, CH3, Cl, Ph, CH3), (M-9343, Cl, CH3, Cl, 4-F-Ph, H), (M-9344, Cl, CH3, Cl, 4-F-Ph, Cl), (M-9345, Cl, CH3, Cl, 4-F-Ph, F), (M-9346, Cl, CH3, Cl, 4-F-Ph, CF3), (M-9347, Cl, CH3, Cl, 4-F-Ph, Br), (M-9348, Cl, CH3, Cl, 4-F-Ph, CH3), (M-9349, Cl, CH3, Cl, 4-CF3-Ph, H), (M-9350, Cl, CH3, Cl, 4-CF3-Ph, Cl), (M-9351, Cl, CH3, Cl, 4-CF3-Ph, F), (M-9352, Cl, CH3, Cl, 4-CF3-Ph, CF3), (M-9353, Cl, CH3, Cl, 4-CF3-Ph, Br), (M-9354, Cl, CH3, Cl, 4-CF3-Ph, CH3), (M-9355, Cl, CH3, Cl, 4-(Me)2N-Ph, H), (M-9356, Cl, CH3, Cl, 4-(Me)2N-Ph, Cl), (M-9357, Cl, CH3, Cl, 4-(Me)2N-Ph, F), (M-9358, Cl, CH3, Cl, 4-(Me)2N-Ph, CF3), (M-9359, Cl, CH3, Cl, 4-(Me)2N-Ph, Br), (M-9360, Cl, CH3, Cl, 4-(Me)2N-Ph, CH3), (M-9361, Cl, CH3, Cl, 4-OH-Ph, H), (M-9362, Cl, CH3, Cl, 4-OH-Ph, Cl), (M-9363, Cl, CH3, Cl, 4-OH-Ph, F), (M-9364, Cl, CH3, Cl, 4-OH-Ph, CF3), (M-9365, Cl, CH3, Cl, 4-OH-Ph, Br), (M-9366, Cl, CH3, Cl, 4-OH-Ph, CH3), (M-9367, Cl, CH3, Cl, 3,4-di-F-Ph, H), (M-9368, Cl, CH3, Cl, 3,4-di-F-Ph, Cl), (M-9369, Cl, CH3, Cl, 3,4-di-F-Ph, F), (M-9370, Cl, CH3, Cl, 3,4-di-F-Ph, CF3), (M-9371, Cl, CH3, Cl, 3,4-di-F-Ph, Br), (M-9372, Cl, CH3, Cl, 3,4-di-F-Ph, CH3), (M-9373, Cl, CH3, Cl, 4-COOH-Ph, H), (M-9374, Cl, CH3, Cl, 4-COOH-Ph, Cl), (M-9375, Cl, CH3, Cl, 4-COOH-Ph, F), (M-9376, Cl, CH3, Cl, 4-COOH-Ph, CF3), (M-9377, Cl, CH3, Cl, 4-COOH-Ph, Br), (M-9378, Cl, CH3, Cl, 4-COOH-Ph, CH3), (M-9379, Cl, CH3, Cl, Bn, H), (M-9380, Cl, CH3, Cl, Bn, Cl), (M-9381, Cl, CH3, Cl, Bn, F), (M-9382, Cl, CH3, Cl, Bn, CF3), (M-9383, Cl, CH3, Cl, Bn, Br), (M-9384, Cl, CH3, Cl, Bn, CH3), (M-9385, Cl, CH3, Cl, 4-F-Bn, H), (M-9386, Cl, CH3, Cl, 4-F-Bn, Cl), (M-9387, Cl, CH3, Cl, 4-F-Bn, F), (M-9388, Cl, CH3, Cl, 4-F-Bn, CF3), (M-9389, Cl, CH3, Cl, 4-F-Bn, Br), (M-9390, Cl, CH3, Cl, 4-F-Bn, CH3), (M-9391, Cl, CH3, Cl, 2-Py, H), (M-9392, Cl, CH3, Cl, 2-Py, Cl), (M-9393, Cl, CH3, Cl, 2-Py, F), (M-9394, Cl, CH3, Cl, 2-Py, CF3), (M-9395, Cl, CH3, Cl, 2-Py, Br), (M-9396, Cl, CH3, Cl, 2-Py, CH3), (M-9397, Cl, CH3, Cl, 3-Py, H), (M-9398, Cl, CH3, Cl, 3-Py, Cl), (M-9399, Cl, CH3, Cl, 3-Py, F), (M-9400, Cl, CH3, Cl, 3-Py, CF3), (M-9401, Cl, CH3, Cl, 3-Py, Br), (M-9402, Cl, CH3, Cl, 3-Py, CH3), (M-9403, Cl, CH3, Cl, 4-Py, H), (M-9404, Cl, CH3, Cl, 4-Py, Cl), (M-9405, Cl, CH3, Cl, 4-Py, F), (M-9406, Cl, CH3, Cl, 4-Py, CF3), (M-9407, Cl, CH3, Cl, 4-Py, Br), (M-9408, Cl, CH3, Cl, 4-Py, CH3), (M-9409, Cl, CH3, Cl, 2-Th, H), (M-9410, Cl, CH3, Cl, 2-Th, Cl), (M-9411, Cl, CH3, Cl, 2-Th, F), (M-9412, Cl, CH3, Cl, 2-Th, CF3), (M-9413, Cl, CH3, Cl, 2-Th, Br), (M-9414, Cl, CH3, Cl, 2-Th, CH3), (M-9415, Cl, CH3, Cl, 3-Th, H), (M-9416, Cl, CH3, Cl, 3-Th, Cl), (M-9417, Cl, CH3, Cl, 3-Th, F), (M-9418, Cl, CH3, Cl, 3-Th, CF3), (M-9419, Cl, CH3, Cl, 3-Th, Br), (M-9420, Cl, CH3, Cl, 3-Th, CH3), (M-9421, Cl, CH3, Cl, pyrrazol-2-yl, H), (M-9422, Cl, CH3, Cl, pyrrazol-2-yl, Cl), (M-9423, Cl, CH3, Cl, pyrrazol-2-yl, F), (M-9424, Cl, CH3, Cl, pyrrazol-2-yl, CF3), (M-9425, Cl, CH3, Cl, pyrrazol-2-yl, Br), (M-9426, Cl, CH3, Cl, pyrrazol-2-yl, CH3), (M-9427, Cl, CH3, Cl, pyrrazol-3-yl, H), (M-9428, Cl, CH3, Cl, pyrrazol-3-yl, Cl), (M-9429, Cl, CH3, Cl, pyrrazol-3-yl, F), (M-9430, Cl, CH3, Cl, pyrrazol-3-yl, CF3), (M-9431, Cl, CH3, Cl, pyrrazol-3-yl, Br), (M-9432, Cl, CH3, Cl, pyrrazol-3-yl, CH3), (M-9433, Cl, CH3, Cl, pyrimidin-2-yl, H), (M-9434, Cl, CH3, Cl, pyrimidin-2-yl, Cl), (M-9435, Cl, CH3, Cl, pyrimidin-2-yl, F), (M-9436, Cl, CH3, Cl, pyrimidin-2-yl, CF3), (M-9437, Cl, CH3, Cl, pyrimidin-2-yl, Br), (M-9438, Cl, CH3, Cl, pyrimidin-2-yl, CH3), (M-9439, Cl, CH3, Cl, pyrimidin-4-yl, H), (M-9440, Cl, CH3, Cl, pyrimidin-4-yl, Cl), (M-9441, Cl, CH3, Cl, pyrimidin-4-yl, F), (M-9442, Cl, CH3, Cl, pyrimidin-4-yl, CF3), (M-9443, Cl, CH3, Cl, pyrimidin-4-yl, Br), (M-9444, Cl, CH3, Cl, pyrimidin-4-yl, CH3), (M-9445, Cl, CH3, Cl, pyrimidin-5-yl, H), (M-9446, Cl, CH3, Cl, pyrimidin-5-yl, Cl), (M-9447, Cl, CH3, Cl, pyrimidin-5-yl, F), (M-9448, Cl, CH3, Cl, pyrimidin-5-yl, CF3), (M-9449, Cl, CH3, Cl, pyrimidin-5-yl, Br), (M-9450, Cl, CH3, Cl, pyrimidin-5-yl, CH3), (M-9451, Cl, CH3, Cl, HOOCCH2CH2CH2, H), (M-9452, Cl, CH3, Cl, HOOCCH2CH2CH2, Cl), (M-9453, Cl, CH3, Cl, HOOCCH2CH2CH2, F), (M-9454, Cl, CH3, Cl, HOOCCH2CH2CH2, CF3), (M-9455, Cl, CH3, Cl, HOOCCH2CH2CH2, Br), (M-9456, Cl, CH3, Cl, HOOCCH2CH2CH2, CH3), (M-9457, Cl, CH3, Cl, HOOCCH2CH2CH2CH2, H), (M-9458, Cl, CH3, Cl, HOOCCH2CH2CH2CH2, Cl), (M-9459, Cl, CH3, Cl, HOOCCH1CH2CH2CH2, F), (M-9460, Cl, CH3, Cl, HOOCCH2CH2CH2CH2, CF3), (M-9461, Cl, CH3, Cl, HOOCCH2CH2CH2CH2, Br), (M-9462, Cl, CH3, Cl, HOOCCH2CH2CH2CH2, CH3), (M-9463, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-9464, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-9465, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-9466, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-9467, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-9468, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-9469, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-9470, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-9471, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-9472, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-9473, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-9474, Cl, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-9475, Cl, CH3, Cl, MeOCH2, H), (M-9476, Cl, CH3, Cl, MeOCH2, Cl), (M-9477, Cl, CH3, Cl, MeOCH2, F), (M-9478, Cl, CH3, Cl, MeOCH2, CF3), (M-9479, Cl, CH3, Cl, MeOCH2, Br), (M-9480, Cl, CH3, Cl, MeOCH2, CH3), (M-9481, Cl, CH3, Cl, EtOCH2, H), (M-9482, Cl, CH3, Cl, EtOCH2, Cl), (M-9483, Cl, CH3, Cl, EtOCH2, F), (M-9484, Cl, CH3, Cl, EtOCH2, CF3), (M-9485, Cl, CH3, Cl, EtOCH2, Br), (M-9486, Cl, CH3, Cl, EtOCH2, CH3), (M-9487, Cl, CH3, Cl, EtOCH2CH2, H), (M-9488, Cl, CH3, Cl, EtOCH2CH2, Cl), (M-9489, Cl, CH3, Cl, EtOCH2CH2, F), (M-9490, Cl, CH3, Cl, EtOCH2CH2, CF3), (M-9491, Cl, CH3, Cl, EtOCH2CH2, Br), (M-9492, Cl, CH3, Cl, EtOCH2CH2, CH3), (M-9493, Cl, CH3, Cl, MeOCH2CH2OCH2CH2, H), (M-9494, Cl, CH3, Cl, MeOCH2CH2OCH2CH2, Cl), (M-9495, Cl, CH3, Cl, (MeOCH2CH2OCH2CH2, F), (M-9496, Cl, CH3, Cl, MeOCH2CH2OCH2CH2, CF3), (M-9497, Cl, CH3, Cl, MeOCH2CH2OCH2CH2, Br), (M-9498, Cl, CH3, Cl, MeOCH2CH2OCH2CH2, CH3), (M-9499, Cl, CH3, Cl, MeOCH2CH2, H), (M-9500, Cl, CH3, Cl, MeOCH2CH2, Cl), (M-9501, Cl, CH3, Cl, MeOCH2CH2, F), (M-9502, Cl, CH3, Cl, MeOCH2CH2, CF3), (M-9503, Cl, CH3, Cl, MeOCH2CH2, Br), (M-9504, Cl, CH3, Cl, MeOCH2CH2, CH3), (M-9505, Cl, CH3, Cl, HOCH2, H), (M-9506, Cl, CH3, Cl, HOCH2, Cl), (M-9507, Cl, CH3, Cl, HOCH2, F), (M-9508, Cl, CH3, Cl, HOCH2, CF3), (M-9509, Cl, CH3, Cl, HOCH2, Br), (M-9510, Cl, CH3, Cl, HOCH2, CH3), (M-9511, Cl, CH3, Cl, HOCH2CH2, H), (M-9512, Cl, CH3, Cl, HOCH2CH2, Cl), (M-9513, Cl, CH3, Cl, HOCH2CH2, F), (M-9514, Cl, CH3, Cl, HOCH2CH2, CF3), (M-9515, Cl, CH3, Cl, HOCH2CH2, Br), (M-9516, Cl, CH3, Cl, HOCH2CH2, CH3), (M-9517, Cl, CH3, Cl, HOCH2CH2CH2, H), (M-9518, Cl, CH3, Cl, HOCH2CH2CH2, Cl), (M-9519, Cl, CH3, Cl, HOCH2CH2CH2, F), (M-9520, Cl, CH3, Cl, HOCH2CH2CH2, CF3), (M-9521, Cl, CH3, Cl, HOCH2CH2CH2, Br), (M-9522, Cl, CH3, Cl, HOCH2CH2CH2, CH3), (M-9523, Cl, CH3, Cl, HOCH2CH2CH2CH2, H), (M-9524, Cl, CH3, Cl, HOCH2CH2CH2CH2, Cl), (M-9525, Cl, CH3, Cl, HOCH2CH2CH2CH2, F), (M-9526, Cl, CH3, Cl, HOCH2CH2CH2CH2, CF3), (M-9527, Cl, CH3, Cl, HOCH2CH2CH2CH2, Br), (M-9528, Cl, CH3, Cl, HOCH2CH2CH2CH2, CH3), (M-9529, CL, CH3, Cl, HOCH2CH2CH2CH2CH2, H), (M-9530, Cl, CH3, Cl, HOCH2CH2CH2CH2CH2, Cl), (M-9531, Cl, CH3, Cl, HOCH2CH2CH2CH2CH2, F), (M-9532, Cl, CH3, Cl, HOCH2CH2CH2CH2CH2, CF3), (M-9533, Cl, CH3, Cl, HOCH2CH2CH2 CH2CH2, Br), (M-9534, Cl, CH3, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-9535, Cl, CH3, Cl, HOCH2CH2OCH2CH2, H), (M-9536, Cl, CH3, Cl, HOCH2CH2OCH3CH3, Cl), (M-9537, Cl, CH3, Cl, HOCH2CH2OCH2CH2, F), (M-9538, Cl, CH3, Cl, HOCH2CH2OCH2CH2, CF3), (M-9539, Cl, CH3, Cl, HOCH2CH2OCH2CH2, Br), (M-9540, Cl, CH3, Cl, HOCH2CH2OCH2CH2, CH3), (M-9541, Cl, CH3, Cl, (Me)2N, H), (M-9542, Cl, CH3, Cl, (Me)2N, Cl), (M-9543, Cl, CH3, Cl, (Me)2N, F), (M-9544, Cl, CH3, Cl, (Me)2N, CF3), (M-9545, Cl, CH3, Cl, (Me)2N, Br), (M-9546, Cl, CH3, Cl, (Me)2N, CH3), (M-9547, Cl, CH3, Cl, piperidin-4-yl-methyl, H), (M-9548, Cl, CH3, Cl, piperidin-4-yl-methyl, Cl), (M-9549, Cl, CH3, Cl, piperidin-4-yl-methyl, F), (M-9550, Cl, CH3, Cl, piperidin-4-yl-methyl, CF3), (M-9551, Cl, CH3, Cl, piperidin-4-yl-methyl, Br), (M-9552, Cl, CH3, Cl, piperidin-4-yl-methyl, CH3), (M-9553, Cl, CH3, Cl, cyclohexylmethyl, H), (M-9554, Cl, CH3, Cl, cyclohexylmethyl, Cl), (M-9555, Cl, CH3, Cl, cyclohexylmethyl, F), (M-9556, Cl, CH3, Cl, cyclohexylmethyl, CF3), (M-9557, Cl, CH3, Cl, cyclohexylmethyl, Br), (M-9558, Cl, CH3, Cl, cyclohexylmethyl, CH3), (M-9559, CH3, H, H, H, H), (M-9560, CH3, H, H, H, Cl), (M-9561, MeO, H, H, H, F), (M-9562, MeO, H, H, H, CF3), (M-9563, CH3, H, H, H, Br), (M-9564, CH3, H, H, H, CH3), (M-9565, MeO, H, H, F, H), (M-9566, CH3, H, H, F, Cl), (M-9567, MeO, F, H, F, F), (M-9568, CH3, H, H, F, CF3), (M-9569, CH3, H, H, F, Br), (M-9570, CH3, H, H, F, CH3), (M-9571, CH3, H, H, Cl, H), (M-9572, MeO, F, H, H, i-Pr), (M-9573, CH3, H, H, Cl, F), (M-9574, CH3, H, H, Cl, CF3), (M-9575, CH3, H, H, Cl, Br), (M-9576, CH3, H, H, Cl, CH3), (M-9577, CH3, H, H, CH3, H), (M-9578, CH3, H, H, CH3, Cl), (M-9579, CH3, H, H, CH3, F), (M-9580, CH3, H, H, CH3, CF3), (M-9581, CH3, H, H, CH3, Br), (M-9582, CH3, H, H, CH3, CH3), (M-9583, CH3, H, H, Et, H), (M-9584, CH3, H, H, Et, Cl), (M-9585, CH3, H, H, Et, F), (M-9586, CH3, H, H, Et, CF3), (M-9587, CH3, H, H, Et, Br), (M-9588, CH3, H, H, Et, CH3), (M-9589, CH3, H, H, n-Pr, H), (M-9590, CH3, H, H, n-Pr, Cl), (M-9591, CH3, H, H, n-Pr, F), (M-9592, CH3, H, H, n-Pr, CF3), (M-9593, CH3, H, H, n-Pr, Br), (M-9594, CH3, H, H, n-Pr, CH3), (M-9595, Et, CH3, H, H, c-Pr, H), (M-9596, CH3, H, H, c-Pr, Cl), (M-9597, CH3, H, H, c-Pr, F), (M-9598, CH3, H, H, c-Pr, CF3), (M-9599, CH3, H, H, c-Pr, Br), (M-9600, CH3, H, H, c-Pr, CH3), (M-9601, CH3, H, H, i-Pr, H), (M-9602, CH3, H, H, i-Pr, Cl), (M-9603, CH3, H, H, i-Pr, F), (M-9604, CH3, H, H, i-Pr, CF3), (M-9605, CH3, H, H, i-Pr, Br), (M-9606, CH3, H, H, i-Pr, CH3), (M-9607, CH3, H, H, n-Bu, H), (M-9608, CH3, H, H, n-Bu, Cl), (M-9609, CH3, H, H, n-Bu, F), (M-9610, CH3, H, H, n-Bu, CF3), (M-9611, CH3, H, H, n-Bu, Br), (M-9612, CH3, H, H, n-Bu, CH3), (M-9613, CH3, H, H, i-Bu, H), (M-9614, CH3, H, H, i-Bu, Cl), (M-9615, CH3, H, H, i-Bu, F), (M-9616, CH3, H, H, i-Bu, CF3), (M-9617, CH3, H, H, i-Bu, Br), (M-9618, CH3, H, H, i-Bu, CH3), (M-9619, CH3, H, H, sec-Bu, H), (M-9620, CH3, H, H, sec-Bu, Cl), (M-9621, CH3, H, H, sec-Bu, F), (M-9622, CH3, H, H, sec-Bu, CF3), (M-9623, CH3, H, H, sec-Bu, Br), (M-9624, CH3, H, H, sec-Bu, CH3), (M-9625, CH3, H, H, n-Pen, H), (M-9626, CH3, H, H, n-Pen, Cl), (M-9627, CH3, H, H, n-Pen, F), (M-9628, CH3, H, H, n-Pen, CF3), (M-9629, CH3, H, H, n-Pen, Br), (M-9630, CH3, H, H, n-Pen, CH3), (M-9631, CH3, H, H, c-Pen, H), (M-9632, CH3, H, H, c-Pen, Cl), (M-9633, CH3, H, H, c-Pen, F), (M-9634, CH3, H, H, c-Pen, CF3), (M-9635, CH3, H, H, c-Pen, Br), (M-9636, CH3, H, H, c-Pen, CH3), (M-9637, CH3, H, H, n-Hex, H), (M-9638, CH3, H, H, n-Hex, Cl), (M-9639, CH3, H, H, n-Hex, F), (M-9640, CH3, H, H, n-Hex, CF3), (M-9641, CH3, H, H, n-Hex, Br), (M-9642, CH3, H, H, n-Hex, CH3), (M-9643, CH3, H, H, c-Hex, H), (M-9644, CH3, H, H, c-Hex, Cl), (M-9645, CH3, H, H, c-Hex, F), (M-9646, CH3, H, H, c-Hex, CF3), (M-9647, CH3, H, H, c-Hex, Br), (M-9648, CH3, H, H, c-Hex, CH3), (M-9649, CH3, H, H, OH, H), (M-9650, CH3, H, H, OH, Cl), (M-9651, CH3, H, H, OH, F), (M-9652, CH3, H, H, OH, CF3), (M-9653, CH3, H, H, OH, Br), (M-9654, CH3, H, H, OH, CH3), (M-9655, CH3, H, H, EtO, H), (M-9656, CH3, H, H, EtO, Cl), (M-9657, CH3, H, H, EtO, F), (M-9658, CH3, H, H, EtO, CF3), (M-9659, CH3, H, H, EtO, Br), (M-9660, CH3, H, H, EtO, CH3), (M-9661, CH3, H, H, n-PrO, H), (M-9662, CH3, H, H, n-PrO, Cl), (M-9663, CH3, H, H, n-PrO, F), (M-9664, CH3, H, H, n-PrO, CF3), (M-9665, CH3, H, H, n-PrO, Br), (M-9666, CH3, H, H, n-PrO, CH3), (M-9667, CH3, H, H, PhO, H), (M-9668, CH3, H, H, PhO, Cl), (M-9669, CH3, H, H, PhO, F), (M-9670, CH3, H, H, PhO, CF3), (M-9671, CH3, H, H, PhO, Br), (M-9672, CH3, H, H, PhO, CH3), (M-9673, CH3, H, H, BnO, H), (M-9674, CH3, H, H, BnO, Cl), (M-9675, CH3, H, H, BnO, F), (M-9676, CH3, H, H, BnO, CF3), (M-9677, CH3, H, H, BnO, Br), (M-9678, CH3, H, H, BnO, CH3), (M-9679, CH3, H, H, PhCH2CH2O, H), (M-9680, CH3, H, H, PhCH2CH2O, Cl), (M-9681, CH3, H, H, PhCH2CH2O, F), (M-9682, CH3, H, H, PhCH2CH2O, CF3), (M-9683, CH3, H, H, PhCH2CH2O, Br), (M-9684, CH3, H, H, PhCH2CH2O, CH3), (M-9685, MeO, H, H, CF3O, H), (M-9686, CH3, H, H, CF3O, Cl), (M-9687, CH3, H, H, CF3O, F), (M-9688, CH3, H, H, CF3O, CF3), (M-9689, CH3, H, H, CF3O, Br), (M-9690, CH3, H, H, CF30, CH3), (M-9691, CH3, H, H, Ph, H), (M-9692, CH3, H, H, Ph, Cl), (M-9693, CH3, H, H, Ph, F), (M-9694, CH3, H, H, Ph, CF3), (M-9695, CH3, H, H, Ph, Br), (M-9696, CH3, H, H, Ph, CH3), (M-9697, CH3, H, H, 4-F-Ph, H), (M-9698, CH3, H, H, 4-F-Ph, Cl), (M-9699, CH3, H, H, 4-F-Ph, F), (M-9700, CH3, H, H, 4-F-Ph, CF3), (M-9701, CH3, H, H, 4-F-Ph, Br), (M-9702, CH3, H, H, 4-F-Ph, CH3), (M-9703, CH3, H, H, 4-CF3-Ph, H), (M-9704, CH3, H, H, 4-CF3-Ph, Cl), (M-9705, CH3, H, H, 4-CF3-Ph, F), (M-9706, CH3, H, H, 4-CF3-Ph, CF3), (M-9707, CH3, H, H, 4-CF3-Ph, Br), (M-9708, CH3, H, H, 4-CF3-Ph, PhCH3), (M-9709, CH3, H, H, 4-<Me)2N-Ph, H), (M-9710, CH3, H, H, 4-(Me)2N-Ph, Cl), (M-9711, CH3, H, H, 4-(Me)2N-Ph, F), (M-9712, CH3, H, H, 4-(Me)2N-Ph, CF3), (M-9713, CH3, H, H, 4-(Me)2N-Ph, Br), (M-9714, CH3, H, H, 4-(Me)2N-Ph, CH3), (M-9715, CH3, H, H, 4-OH-Ph, H), (M-9716, CH3, H, H, 4-OH-Ph, Cl), (M-9717, CH3, H, H, 4-OH-Ph, F), (M-9718, CH3, H, H, 4-OH-Ph, CF3), (M-9719, CH3, H, H, 4-OH-Ph, Br), (M-9720, CH3, H, H, 4-OH-Ph, CH3), (M-9721, CH3, H, H, 3,4-di-F-Ph, H), (M-9722, CH3, H, H, 3,4-di-F-Ph, Cl), (M-9723, CH3, H, H, 3,4-di-F-Ph, F), (M-9724, CH3, H, H, 3,4-di-F-Ph, CF3), (M-9725, CH3, H, H, 8,4-di-F-Ph, Br), (M-9726, CH3, H, H, 3,4-di-F-Ph, CH3), (M-9727, CH3, H, H, 4-COOH-Ph, H), (M-9728, CH3, H, H, 4-COOH-Ph, Cl), (M-9729, CH3, H, H, 4-COOH-Ph, F), (M-9730, CH3, H, H, 4-COOH-Ph, CF3), (M-9731, CH3, H, H, 4-COOH-Ph, Br), (M-9732, CH3, H, H, 4-COOH-Ph, CH3), (M-9733, CH3, H, H, Bn, H), (M-9734, CH3, H, H, Bn, Cl), (M-9735, CH3, H, H, Bn, F), (M-9736, CH3, H, H, Bn, CF3), (M-9737, CH3, H, H, Bn, Br), (M-9738, CH3, H, H, Bn, CH3), (M-9739, CH3, H, H, 4-F-Bn, H), (M-9740, CH3, H, H, 4-F-Bn, Cl), (M-9741, CH3, H, H, 4-F-Bn, F), (M-9742, CH3, H, H, 4-F-Bn, CF3), (M-9743, CH3, H, H, 4-F-Bn, Br), (M-9744, CH3, H, H, 4-F-Bn, CH3), (M-9745, CH3, H, H, 2-Py, H), (M-9746, CH3, H, H, 2-Py, Cl), (M-9747, CH3, H, H, 2-Py, F), (M-9748, CH3, H, H, 2-Py, CF3), (M-9749, CH3, H, H, 2-Py, Br), (M-9750, CH3, H, H, 2-Py, CH3), (M-9751, CH3, H, H, 3-Py, H), (M-9752, CH3, H, H, 3-Py, Cl), (M-9753, CH3, H, H, 3-Py, F), (M-9754, CH3, H, H, 3-Py, CF3), (M-9755, CH3, H, H, 3-Py, Br), (M-9756, CH3, H, H, 3-Py, CH3), (M-9757, CH3, H, H, 4-Py, H), (M-9758, CH3, H, H, 4-Py, Cl), (M-9759, CH3, H, H, 4-Py, F), (M-9760, CH3, H, H, 4-Py, CF3), (M-9761, CH3, H, H, 4-Py, Br), (M-9762, CH3, H, H, 4-Py, CH3), (M-9763, CH3, H, H, 2-Th, H), (M-9764, CH3, H, H, 2-Th, Cl), (M-9765, CH3, H, H, 2-Th, F), (M-9766, CH3, H, H, 2-Th, CF3), (M-9767, CH3, H, H, 2-Th, Br), (M-9768, CH3, H, H, 2-Th, CH3), (M-9769, CH3, H, H, 3-Th, H), (M-9770, CH3, H, H, 3-Th, Cl), (M-9771, CH3, H, H, 3-Th, F), (M-9772, CH3, H, H, 3-Th, CF3), (M-9773, CH3, H, H, 3-Th, Br), (M-9774, CH3, H, H, 3-Th, CH3), (M-9775, CH3, H, H, pyrrazol-2-yl, H), (M-9776, CH3, H, H, pyrrazol-2-yl, Cl), (M-9777, CH3, H, H, pyrrazol-2-yl, F), (M-9778, CH3, H, H, pyrrazol-2-yl, CF3), (M-9779, CH3, H, H, pyrrazol-2-yl, Br), (M-9780, CH3, H, H, pyrrazol-2-yl, CH3), (M-9781, CH3, H, H, pyrrazol-3-yl, H), (M-9782, CH3, H, H, pyrrazol-3-yl, Cl), (M-9783, CH3, H, H, pyrrazol-3-yl, F), (M-9784, CH3, H, H, pyrrazol-3-yl, CF3), (M-9785, CH3, H, H, pyrrazol-3-yl, Br), (M-9786, CH3, H, H, pyrrazol-3-yl, CH3), (M-9787, CH3, H, H, pyrimidin-2-yl, H), (M-9788, CH3, H, H, pyrimidin-2-yl, Cl), (M-9789, CH3, H, H, pyrimidin-2-yl, F), (M-9790, CH3, H, H, pyrimidin-2-yl, CF3), (M-9791, CH3, H, H, pyrimidin-2-yl, Br), (M-9792, CH3, H, H, pyrimidin-2-yl, CH3), (M-9793, CH3, H, H, pyrimidin-4-yl, H), (M-9794, CH3, H, H, pyrimidin-4-yl, Cl), (M-9795, CH3, H, H, pyrimidin-4-yl, F), (M-9796, CH3, H, H, pyrimidin-4-yl, CF3), (M-9797, CH3, H, H, pyrimidin-4-yl, Br), (M-9798, CH3, H, H, pyrimidin-4-yl, CH3), (M-9799, CH3, H, H, pyrimidin-5-yl, H), (M-9800, CH3, H, H, pyrimidin-5-yl, Cl), (M-9801, CH3, H, H, pyrimidin-5-yl, F), (M-9802, CH3, H, H, pyrimidin-5-yl, CF3), (M-9803, CH3, H, H, pyrimidin-5-yl, Br), (M-9804, CH3, H, H, pyrimidin-5-yl, CH3), (M-9805, CH3, H, H, HOOCCH2CH2CH2H), (M-9806, CH3, H, H, HOOCCH2CH2CH2Cl), (M-9807, CH3, H, H, HOOCCH2CH2CH2, F), (M-9808, CH3, H, H, HOOCCH2CH2CH2, CF3), (M-9809, CH3, H, H, HOOCCH2CH2CH2, Br), (M-9810, CH3, H, H, HOOCCH2CH2CH2CH3), (M-9811, CH3, H, H, HOOCCH2CH2CH2CH2, H), (M-9812, CH3, H, H, HOOCCH2CH2CH2CH2, Cl), (M-9813, CH3, H, H, HOOCCH2CH2CH2CH2, F), (M-9814, CH3, H, H, HOOCCH2CH2CH2CH2, CF3), (M-9815, CH3, H, H, HOOCCH2CH2CH2CH2, Br), (M-9816, CH3, H, H, HOOCCH2CH2CH2CH2, CH3), (M-9817, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, H), (M-9818, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-9819, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, F), (M-9820, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-9821, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-9822, CH3, H, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-9823, CH3, H, H, (Me)2NCOCH2CH2CH2CH2CH3, H), (M-9824, CH3, H, H, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-9825, CH3, H, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-9826, CH3, H H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-9827, CH3, H, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-9828, CH3, H, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-9829, CH3, H, H, MeOCH2, H), (M-9830, CH3, H, H, MeOCH2, Cl), (M-9831, CH3, H, H, MeOCH2, F), (M-9832, CH3, H, H, MeOCH2, CF3), (M-9833, CH3, H, H, MeOCH2, Br), (M-9834, CH3, H, H, MeOCH2, CH3), (M-9835, CH3, H, H, EtOCH2, H), (M-9836, CH3, H, H, EtOCH2, Cl), (M-9837, CH3, H, H, EtOCH2, F), (M-9838, CH3, H, H, EtOCH2, CF3), (M-9839, CH3, H, H, EtOCH2, Br), (M-9840, CH3, H, H, EtOCH2, CH3), (M-9841, CH3, H, H, EtOCH2CH2, H), (M-9842, CH3, H, H, EtOCH2CH2, Cl), (M-9843, CH3, H, H, EtOCH2CH2, F), (M-9844, CH3, H, H, EtOCH2CH2, CF3), (M-9845, CH3, H, H, EtOCH2CH2, Br), (M-9846, CH3, H, H, EtOCH2CH2, CH3), (M-9847, CH3, H, H, MeOCH2CH2OCH2CH2, H), (M-9848, CH3, H, H, MeOCH2CH2OCH2CH2, Cl), (M-9849, CH3, H, H, MeOCH2CH2OCH2CH2, F), (M-9850, CH3, H, H, MeOCH2CH2OCH2CH2, CF3), (M-9851, CH3, H, H, MeOCH2CH2OCH2CH2, Br), (M-9852, CH3, H, H, MeOCH2CH2OCH2CH2, CH3), (M-9853, CH3, H, H, MeOCH2CH2, H), (M-9854, CH3, H, H, MeOCH2CH2, Cl), (M-9855, CH3, H, H, MeOCH2CH2, F), (M-9856, CH3, H, H, MeOCH2CH2, CF3), (M-9857, CH3, H, H, MeOCH2CH2, Br), (M-9858, CH3, H, H, MeOCH2CH2, CH3), (M-9859, CH3, H, H, HOCH2, H), (M-9860, CH3, H, H, HOCH2, Cl), (M-9861, CH3, H, H, HOCH2, F), (M-9862, CH3, H, H, HOCH2, CF3), (M-9863, CH3, H, H, HOCH2, Br), (M-9864, CH3, H, H, HOCH2, CH3), (M-9865, CH3, H, H, HOCH2CH2, H), (M-9866, CH3, H, H, HOCH2CH2, Cl), (M-9867, CH3, H, H, HOCH2CH2, F), (M-9868, CH3, H, H, HOCH2CH2, CF3), (M-9869, CH3, H, H, HOCH2CH2, Br), (M-9870, CH3, H, H, HOCH2CH2, CH3), (M-9871, CH3, H, H, HOCH2CH2CH2, H), (M-9872, CH3, H, H, HOCH2CH2CH2, Cl), (M-9873, CH3, H, H, HOCH2CH2CH2, F), (M-9874, CH3, H, H, HOCH2CH2CH2, CF3), (M-9875, CH3, H, H, HOCH2CH2CH2, Br), (M-9876, CH3, H, H, HOCH2CH2CH2, CH3), (M-9877, CH3, H, H, HOCH2CH2CH2CH2, H), (M-9878, CH3, H, H, HOCH2CH2CH2CH2, Cl), (M-9879, CH3, H, H, HOCH2CH2CH2CH2, F), (M-9880, CH3, H, H, HOCH2CH2CH2CH2, CF3), (M-9881, CH3, H, H, HOCH2CH2CH2CH2, Br), (M-9882, CH3, H, H, HOCH2CH2CH2CH2, CH3), (M-9883, CH3, H, H, HOCH2CH2CH2CH2CH2H), (M-9884, CH3, H, H, HOCH2CH2CH2CH3CH3, Cl), (M-9885, CH3, H, H, HOCH2CH2CH2CH2CH2, F), (M-9886, CH3, H, H, HOCH2CH2CH2CH2CH2, CF3), (M-9887, CH3, H, H, HOCH2CH2CH2CH2CH2Br), (M-9888, CH3, H, H, HOCH2CH2CH2CH2CH2CH3), (M-9889, CH3, H, H, HOCH2CH2OCH2CH2, H), (M-9890, CH3, H, H, HOCH2CH2OCH2CH2, Cl), (M-9891, CH3, H, H, HOCH2CH2OCH2CH2, F), (M-9892, CH3, H, H, HOCH2CH2OCH2CH2, CF3), (M-9893, CH3, H, H, HOCH2CH2OCH2CH2, Br), (M-9894, CH3, H, H, HOCH2CH2OCH2CH2, CH3), (M-9895, CH3, H, H, (Me)3N, H), (M-9896, CH3, H, H, (Me)2N, Cl), (M-9897, CH3, H, H, (Me)2H, F), (M-9898, CH3, H, H, (Me)2N, CF3), (M-9899, CH3, H, H, (Me)2N, Br), (M-9900, CH3, H, H, (Me)2N, CH3), (M-9901, CH3, H, H, piperidin-4-yl-methyl, H), (M-9902, CH3, H, H, piperidin-4-yl-methyl, Cl), (M-9903, CH3, H, H, piperidin-4-yl-methyl, F), (M-9904, CH3, H, H, piperidin-4-yl-methyl, CF3), (M-9905, CH3, H, H, piperidin-4-yl-methyl, Br), (M-9906, CH3, H, H, piperidin-4-yl-methyl, CH3), (M-9907, CH3, H, H, cyclohexylmethyl, H), (M-9908, CH3, H, H, cyclohexylmethyl, Cl), (M-9909, CH3, H, H, cyclohexylmethyl, F), (M-9910, CH3, H, H, cyclohexylmethyl, CF3), (M-9911, CH3, H, H, cyclohexylmethyl, Br), (M-9912, CH3, H, H, cyclohexylmethyl, CH3), (M-9913, CH3, H, F, H, H), (M-9914, CH3, H, F, H, Cl), (M-9915, CH3, H, F, H, F), (M-9916, CH3, H, F, H, CF3), (M-9917, CH3, H, F, H, Br), (M-9918, CH3, H, F, H, CH3), (M-9919, CH3, H, F, F, H), (M-9920, CH3, H, F, F, Cl), (M-9921, CH3, H, F, F, F), (M-9922, CH3, H, F, F, CF3), (M-9923, CH3, H, F, F, Br), (M-9924, CH3, H, F, F, CH3), (M-9925, CH3, H, F, Cl, H), (M-9926, CH3, H, F, Cl, Cl), (M-9927, CH3, H, F, Cl, F), (M-9928, CH3, H, F, Cl, CF3), (M-9929, CH3, H, F, Cl, Br), (M-9930, CH3, H, F, Cl, CH3), (M-9931, CH3, H, F, CH3, H), (M-9932, CH3, H, F, CH3, Cl), (M-9933, CH3, H, F, CH3, F), (M-9934, CH3, H, F, CH3, CF3), (M-9935, CH3, H, F, CH3, Br), (M-9936, CH3, H, F, CH3, CH3), (M-9937, CH3, H, F, Et, H), (M-9938, CH3, H, F, Et, Cl), (M-9939, CH3, H, F, Et, F), (M-9940, CH3, H, F, Et, CF3), (M-9941, CH3, H, F, Et, Br), (M-9942, CH3, H, F, Et, CH3), (M-9943, CH3, H, F, n-Pr, H), (M-9944, CH3, H, F, n-Pr, Cl), (M-9945, CH3, H, F, n-Pr, F), (M-9946, CH3, H, F, n-Pr, CF3), (M-9947, CH3, H, F, n-Pr, Br), (M-9948, CH3, H, F, n-Pr, CH3), (M-9949, CH3, H, F, c-Pr, H), (M-9950, CH3, H, F, c-Pr, Cl), (M-9951, CH3, H, F, c-Pr, F), (M-9952, CH3, H, F, c-Pr, CF3), (M-9953, CH3, H, F, c-Pr, Br), (M-9954, CH3, H, F, c-Pr, CH3), (M-9955, CH3, H, F, i-Pr, H), (M-9956, CH3, H, F, i-Pr, Cl), (M-9957, CH3, H, F, i-Pr, F), (M-9958, CH3, H, F, i-Pr, CF3), (M-9959, CH3, H, F, i-Pr, Br), (M-9960, CH3, H, F, i-Pr, CH3), (M-9961, CH3, H, F, n-Bu, H), (M-9962, CH3, H, F, n-Bu, Cl), (M-9963, CH3, H, F, n-Bu, F), (M-9964, CH3, H, F, n-Bu, CF3), (M-9965, CH3, H, F, n-Bu, Br), (M-9966, CH3, H, F, n-Bu, CH3), (M-9967, CH3, H, F, i-Bu, H), (M-9968, CH3, H, F, i-Bu, Cl), (M-9969, CH3, H, F, i-Bu, F), (M-9970, CH3, H, F, i-Bu, CF3), (M-9971, CH3, H, F, i-Bu, Br), (M-9972, CH3, H, F, i-Bu, CH3), (M-9973, CH3, H, F, sec-Bu, H), (M-9974, CH3, H, F, sec-Bu, Cl), (M-9975, CH3, H, F, sec-Bu, F), (M-9976, CH3, H, F, sec-Bu, CF3), (M-9977, CH3, H, F, sec-Bu, Br), (M-9978, CH3, H, F, sec-Bu, CH3), (M-9979, CH3, H, F, n-Pen, H), (M-9980, CH3, H, F, n-Pea, Cl), (M-9981, CH3, H, F, n-Pen, F), (M-9982, CH3, H, F, n-Pen, CF3), (M-9983, CH3, H, F, n-Pen, Br), (M-9984, CH3, H, F, n-Pen, CH3), (M-9985, CH3, H, F, c-Pen, H), (M-9986, CH3, H, F, c-Pen, Cl), (M-9987, CH3, H, F, c-Pen, F), (M-9988, CH3, H, F, c-Pen, CF3), (M-9989, CH3, H, F, c-Pen, Br), (M-9990, CH3, H, F, c-Pen, CH3), (M-9991, CH3, H, F, n-Hex, H), (M-9992, CH3, H, F, n-Hex, Cl), (M-9993, CH3, H, F, n-Hex, F, (M-9994, CH3, H, F, n-Hex, CF3), (M-9995, CH3, H, F, n-Hex, Br), (M-9996, CH3, H, F, n-Hex, CH3), (M-9997, CH3, H, F, c-Hex, H), (M-9998, CH3, H, F, c-Hex, Cl), (M-9999, CH3, H, F, c-Hex, F), (M-10000, CH3, H, F, c-Hex, CF3), (M-10001, CH3, H, F, c-Hex, Br), (M-10002, CH3, H, F, c-Hex, CH3), (M-10003, CH3, H, F, OH, H), (M-10004, CH3, H, F, OH, Cl), (M-10005, CH3, H, F, OH, F), (M-10006, CH3, H, F, OH, CF3), (M-10007, CH3, H, F, OH, Br), (M-10008, CH3, H, F, OH, CH3), (M-10009, CH3, H, F, EtO, H), (M-10010, CH3, H, F, EtO, Cl), (M-10011, CH3, H, F, EtO, F), (M-10012, CH3, H, F, EtO, CF3), (M-10013, CH3, H, F, EtO, Br), (M-10014, CH3, H, F, EtO, CH3), (M-10015, CH3, H, F, n-PrO, H), (M-10016, CH3, H, F, n-PrO, Cl), (M-10017, CH3, H, F, n-PrO, F), (M-10018, CH3, H, F, n-PrO, CF3), (M-10019, CH3, H, F, n-PrO, Br), (M-10020, CH3, H, F, n-PrO, CH3), (M-10021, CH3, H, F, PhO, H), (M-10022, CH3, H, F, PhO, Cl), (M-10023, CH3, H, F, PhO, F), (M-10024, CH3, H, F, PhO, CF3), (M-10025, CH3, H, F, PhO, Br), (M-10026, CH3, H, F, PhO, CH3), (M-10027, CH3, H, F, BnO, H), (M-10028, CH3, H, F, BnO, Cl), (M-10029, CH3, H, F, BnO, F), (M-10030, CH3, H, F, BnO, CF3), (M-10031, CH3, H, F, BnO, Br), (M-10032, CH3, H, F, BnO, CH3), (M-10033, CH3, H, F, PhCH2CH2O, H), (M-10034, CH3, H, F, PhCH2CH2O, Cl), (M-10035, CH3, H, F, PhCH2CH2O, F), (M-10036, CH3, H, F, PhCH2CH2O, CF3), (M-10037, CH3, H, F, PhCH2CH2O, Br), (M-10038, CH3, H, F, PhCH2CH2O, CH3), (M-10039, CH3, H, F, CF3O, H), (M-10040, CH3, H, F, CF30, Cl), (M-10041, CH3, H, F, CF3O, F), (M-10042, CH3, H, F, CF3O, CF3), (M-10043, CH3, H, F, CF3O, Br), (M-10044, CH3, H, F, CF3O, CH3), (M-10045, CH3, H, F, Ph, H), (M-10046, CH3, H, F, Ph, Cl), (M-10047, CH3, H, F, Ph, F), (M-10048, CH3, H, F, Ph, CF3), (M-10049, CH3, H, F, Ph, Br), (M-10050, CH3, H, P, Ph, CF3), (M-10051, CH3, H, F, 4-F-Ph, H), (M-10052, CH3, H, F, 4-F-Ph, Cl), (M-10053, CH3, H, F, 4-F-Ph, F), (M-10054, CH3, H, F, 4-F-Ph, CF3), (M-10055, CH3, H, F, 4-F-Ph, Br), (M-10056, CH3, H, F, 4-F-Ph, CH3), (M-10057, CH3, H, F, 4-CF3-Ph, H), (M-10058, CH3, H, F, 4-CF3-Ph, Cl), (M-10059, CH3, H, F, 4-CF3-Ph, F), (M-10060, CH3, H, F, 4-CF3-Ph, CF3), (M-10061, CH3, H, F, 4-CF3-Ph, Br), (M-10062, CH3, H, F, 4-CF3-Ph, CH3), (M-10063, CH3, H, F, 4-(Me)2N-Ph, H), (M-10064, CH3, H, F, 4-(Me)2N-Ph, Cl), (M-10065, CH3, H, F, 4-(Me)2N-Ph, F), (M-10066, CH3, H, F, 4-(Me)2N-Ph, CF3), (M-10067, CH3, H, F, 4-(Me)2N-Ph, Br), (M-10068, CH3, H, F, 4-(Me)2N-Ph, CH3), (M-10069, CH3, H, F, 4-OH-Ph, H), (M-10070, CH3, H, F, 4-OH-Ph, Cl), (M-10071, CH3, H, F, 4-OH-Ph, F), (M-10072, CH3, H, E, 4-OH-Ph, CF3), (M-10073, CH3, H, F, 4-OH-Ph, Br), (M-10074, CH3, H, F, 4-OH-Ph, CH3), (M-10075, CH3, H, F, 3,4-di-F-Ph, H), (M-10076, CH3, H, F, 3,4-di-F-Ph, Cl), (M-10077, CH3, H, F, 3,4-di-F-Ph, F), (M-10078, CH3, H, F, 3,4-di-F-Ph, CF3), (M-10079, CH3, H, F, 3,4-di-F-Ph, Br), (M-10080, CH3, H, F, 3,4-di-F-Ph, CH3), (M-10081, CH3, H, F, 4-COOH-Ph, H), (M-10082, CH3, H, F, 4-COOH-Ph, Cl), (M-10083, CH3, H, F, 4-COOH-Ph, F), (M-10084, CH3, H, F, 4-COOH-Ph, CF3), (M-10085, CH3, H, F, 4-COOH-Ph, Br), (M-10086, CH3, H, F, 4-COOH-Ph, CH3), (M-10087, CH3, H, F, Bn, H), (M-10088, CH3, H, F, Bn, Cl), (M-10089, CH3, H, F, Bn, F), (M-10090, CH3, H, F, Bn, CF3), (M-10091, CH3, H, F, Bn, Br), (M-10092, CH3, H, F, Bn, CH3), (M-10093, CH3, H, F, 4-F-Bn, H), (M-10094, CH3, H, F, 4-F-Bn, Cl), (M-10095, CH3, H, F, 4-F-Bn, F), (M-10096, CH3, H, F, 4-F-Bn, CF3), (M-10097, CH3, H, F, 4-F-Bn, Br), (M-10098, CH3, H, F, 4-F-Bn, CH3), (M-10099, CH3, H, F, 2-Py, H), (M-10100, CH3, H, F, 2-Py, Cl), (M-10101, CH3, H, F, 2-Py, F), M-10102, CH3, H, F, 2-Py, CF3), (M-10103, CH3, H, F, 2-Py, Br), (M-10104, CH3, H, F, 2-Py, CH3), (M-10105, CH3, H, F, 3-Py, H), (M-10106, CH3, H, F, 3-Py, Cl), (M-10107, CH3, H, F, 3-Py, F), (M-10108, CH3, H, F, 3-Py, CF3), (M-10109, CH3, H, F, 3-Py, Br), (M-10110, CH3, H, F, 3-Py, CH3), (M-10111, CH3, H, F, 4-Py, H), (M-10112, CH3, H, F, 4-Py, Cl), (M-10113, CH3, H, F, 4-Py, F), (M-10114, CH3, H, F, 4-Py, CF3), (M-10115, CH3, H, F, 4-Py, Br), (M-10116, CH3, H, F, 4-Py, CH3), (M-10117, CH3, H, F, 2-Th, H), (M-10118, CH3, H, F, 2-Th, Cl), (M-10119, CH3, H, F, 2-Th, F), (M-10120, CH3, H, F, 2-Th, CF3), (M-10121, CH3, H, F, 2-Th, Br), (M-10122, CH3, H, F, 2-Th, CH3), (M-10123, CH3, H, F, 3-Th, H), (M-10124, CH3, H, F, 3-Th, Cl), (M-10125, CH3, H, F, 3-Th, F), (M-10126, CH3, H, F, 3-Th, CF3), (M-10127, CH3, H, F, 3-Th, Br), (M-10128, CH3, H, F, 3-Th, CH3), (M-10129, CH3, H, F, pyrrazol-2-yl, H), (M-10130, CH3, H, F, pyrrazol-2-yl, Cl), (M-10131, CH3, H, F, pyrrazol-2-yl, F), (M-10132, CH3, H, F, pyrrazol-2-yl, CF3), (M-10133, CH3, H, F, pyrrazol-2-yl, Br), (M-10134, CH3, H, F, pyrrazol-2-yl, CH3), (M-10135, CH3, H, F, pyrrazol-3-yl, H), (M-10136, CH3, H, F, pyrrazol-3-yl, Cl), (M-10137, CH3, H, F, pyrrazol-3-yl, F), (M-10138, CH3, H, F, pyrrazol-3-yl, CF3), (M-10139, CH3, H, F, pyrrazol-3-yl, Br), (M-10140, CH3, H, F, pyrrazol-3-yl, CH3), (M-10141, CH3, H, F, pyrimidin-2-yl, H), (M-10142, CH3, H, F, pyrimidin-2-yl, Cl), (M-10143, CH3, H, F, pyrimidin-2-yl, F), (M-10144, CH3, H, F, pyrimidin-2-yl, CF3), (M-10145, CH3, H, F, pyrimidin-2-yl, Br), (M-10146, CH3, H, F, pyrimidin-2-yl, CH3), (M-10147, CH3, H, F, pyrimidin-4-yl, H), (M-10148, CH3, H, F, pyrimidin-4-yl, Cl), (M-10149, CH3, H, F, pyrimidin-4-yl, F), (M-10150, CH3, H, F, pyrimidin-4-yl, CF3), (M-10151, CH3, H, F, pyrimidin-4-yl, Br), (M-10152, CH3, H, F, pyrimidin-4-yl, CH3), (M-10153, CH3, H, F, pyrimidin-5-yl, H), (M-10154, CH3, H, F, pyrimidin-5-yl, Cl), (M-10155, CH3, H, F, pyrimidin-5-yl, F), (M-10156, CH3, H, F, pyrimidin-5-yl, CF3), (M-10157, CH3, H, F, pyrimidin-5-yl, Br), (M-10158, CH3, H, F, pyrimidin-5-yl, CH3), (M-10159, CH3, H, F, HOOCCH2CH2CH2, H), (M-10160, CH3, H, F, HOOCCH2CH2CH2Cl), (M-10161, CH3, H, F, HOOCCH2CH2CH2, F), (M-10162, CH3, H, F, HOOCCH2CH2CH2CF3), (M-10163, CH3, H, F, HOOCCH2CH2CH2Br), (M-10164, CH3, H, F, HOOCCH2CH2CH2CH3), (M-10165, CH3, H, F, HOOCCH2CH2CH2CH2, H), (M-10166, CH3, H, F, HOOCCH2CH2CH2CH2, Cl), (M-10167, CH3, H, F, HOOCCH2CH2CH2CH2, F), (M-10168, CH3, H, F, HOOCCH2CH2CH2CH2, CF3), (M-10169, CH3, H, F, HOOCCH2CH2CH2CH2, Br), (M-10170, CH3, H, F, HOOCCH2CH2CH2CH2, CH3), (M-10171, CH3, H, F, (Me)2NCOCH2CH2CH2CH2, H), (M-10172, CH3, H, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-10173, CH3, H, F, (Me)2NCOCH2CH2CH2CH2, F), (M-10174, CH3, H, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-10175, CH3, H, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-10176, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH3), (M-10177, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-10178, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-10179, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-10180, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-10181, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-10182, CH3, H, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-10183, CH3, H, F, MeOCH2, H), (M-10184, CH3, H, F, MeOCH2, Cl), (M-10185, CH3, H, F, MeOCH2, F), (M-10186, CH3, H, F, MeOCH2, CF3), (M-10187, CH3, H, F, MeOCH2, Br), (M-10188, CH3, H, F, MeOCH2, CH3), (M-10189, CH3, H, F, EtOCH2, H), (M-10190, CH3, H, F, EtOCH2, Cl), (M-10191, CH3, H, F, EtOCH2, F), (M-10192, CH3, H, F, EtOCH2, CF3), (M-10193, CH3, H, F, EtOCH2, Br), (M-10194, CH3, H, F, EtOCH2, CH3), (M-10195, CH3, H, F, EtOCH2CH2, H), (M-10196, CH3, H, F, EtOCH2CH2, Cl), (M-10197, CH3, H, F, EtOCH2CH2, F), (M-10198, CH3, H, F, EtOCH2CH2, CF3), (M-10199, CH3, H, F, EtOCH2CH2, Br), (M-10200, CH3, H, F, EtOCH2CH2, CH3), (M-10201, CH3, H, F, MeOCH2CH2OCH2CH2, H), (M-10202, CH3, H, F, MeOCH2CH2OCH2CH2, Cl), (M-10203, CH3, H, F, MeOCH2CH2OCH2CH2, F), (M-10204, CH3, H, F, MeOCH2CH2OCH2CH2, CF3), (M-10205, CH3, H, F, MeOCH2CH2OCH2CH2, Br), (M-10206, CH3, H, F, MeOCH2CH2OCH2CH2, CH3), (M-10207, CH3, H, F, MeOCH2CH2, H), (M-10208, CH3, H, F, MeOCH2CH2, Cl), (M-10209, CH3, H, F, MeOCH2CH2, F), (M-10210, CH3, H, F, MeOCH2CH2, CF3), (M-10211, CH3, H, F, MeOCH2CH2, Br), (M-10212, CH3, H, F, MeOCH2CH2, CH3), (M-10213, CH3, H, F, HOCH2, H), (M-10214, CH3, H, F, HOCH2, Cl), (M-10215, CH3, H, F, HOCH2, F), (M-10216, CH3, H, F, HOCH2, CF3), (M-10217, CH3, H, F, HOCH2, Br), (M-10218, CH3, H, F, HOCH2, CH3), (M-10219, CH3, H, F, HOCH2CH2, H), (M-10220, CH3, H, F, HOCH2CH2, Cl), (M-10221, CH3, H, F, HOCH2CH2, F), (M-10222, CH3, H, F, HOCH2CH2, CF3), (M-10223, CH3, H, F, HOCH2CH2, Br), (M-10224, CH3, H, F, HOCH2CH2, CH3), (M-10225, CH3, H, F, HOCH2CH2CH2, H), (M-10226, CH3, H, F, HOCH2CH2CH2, Cl), (M-10227, CH3, H, F, HOCH2CH2CH2, F), (M-10228, CH3, H, F, HOCH2CH2CH2, CF3), (M-10229, CH3, H, F, HOCH2CH2CH2, Br), (M-10230, CH3, H, F, HOCH2CH2CH2, CH3), (M-10231, CH3, H, F, HOCH2CH2CH2CH3, H), (M-10232, CH3, H, F, HOCH2CH2CH2CH2, Cl), (M-10233, CH3, H, F, HOCH2CH2CH2CH2, F), (M-10234, CH3, H, F, HOCH2CH2CH2CH2, CF3), (M-10235, CH3, H, F, HOCH2CH2CH2CH2, Br), (M-10236, CH3, H, F, HOCH2CH2CH2CH2, CH3), (M-10237, CH3, H, F, HOCH2CH2CH2CH2CH2H), (M-10238, CH3, H, F, HOCH2CH2CH2CH2CH2, Cl), (M-10239, CH3, H, F, HOCH2CH2CH2CH2CH2, F), (M-10240, CH3, H, F, HOCH2CH2CH2CH2CH2CF3), (M-10241, CH3, H, F, HOCH2CH2CH2CH2CH2, Br), (M-10242, CH3, H, F, HOCH2CH2CH2CH2CH2CH3), (M-10243, CH3, H, F, HOCH2CH2OCH2CH2, H), (M-10244, CH3, H, F, HOCH2CH2OCH2CH2, Cl), (M-10245, CH3, H, F, HOCH2CH2OCH2CH2, F), (M-10246, CH3, H, F, HOCH2CH2OCH2CH2, CF3), (M-10247, CH3, H, F, HOCH2CH2OCH2CH2, Br), (M-10248, CH3, H, F, HOCH2CH2OCH2CH2, CH3), (M-10249, CH3, H, F, (Me)2N, H), (M-10250, CH3, H, F, (Me)2N, Cl), (M-10251, CH3, H, F, (Me)2N, F), (M-10252, CH3, H, F, (Me)2N, CF3), (M-10253, CH3, H, F, (Me)2N, Br), (M-10254, CH3, H, F, (Me)2N, CH3), (M-10255, CH3, H, F, piperidin-4-yl-methyl, H), (M-10256, CH3, H, F, piperidin-4-yl-methyl, Cl), (M-J 0257, CH3, H, F, piperidin-4-yl-methyl, F), (M-10258, CH3, H, F, piperidin-4-yl-methyl, CF3), (M-10259, CH3, H, F, piperidin-4-yl-methyl, Br), (M-10260, CH3, H, F, piperidin-4-yl-methyl, CH3), (M-10261, CH3, H, F, cyclohexylmethyl, H), (M-10262, CH3, H, F, cyclohexylmethyl, Cl), (M-10263, CH3, H, F, cyclohexylmethyl, F), (M-10264, CH3, H, F, cyclohexylmethyl, CF3), (M-10265, CH3, H, F, cyclohexylmethyl, Br), (M-10266, CH3, H, F, cyclohexylmethyl, CH3), (M-102671, CH3, H, Cl, H, H), (M-10268, CH3, H, Cl, H, Cl), (M-10269, CH3, H, Cl, H, F), (M-10270, CH3, H, Cl, H, CF3), (M-10271, CH3, H, Cl, H, Br), (M-10272, CH3, H, Cl, H, CH3), (M-10273, CH3, H, Cl, F, H), (M-10274, CH3, H, Cl, F, Cl), (M-10275, CH3, H, Cl, F, F), (M-10276, CH3, H, Cl, F, CF3), (M-10277, CH3, H, Cl, F, Br), (M-10278, CH3, H, Cl, F, CH3), (M-10279, CH3, H, Cl, Cl, H), (M-10280, CH3, H, Cl, Cl, Cl), (M-10281, CH3, H, Cl, Cl, F), (M-10282, CH3, H, Cl, Cl, CF3), (M-10283, CH3, H, Cl, Cl, Br), (M-10284, CH3, H, Cl, Cl, CH3), (M-10285, CH3, H, Cl, CH3, H), (M-10286, CH3, H, Cl, CH3, Cl), (M-10287, CH3, H, Cl, CH3, F), (M-10288, CH3, H, Cl, CH3, CF3), (M-10289, CH3, H, Cl, CH3, Br), (M-10290, CH3, H, Cl, CH3, CH3), (M-10291, CH3, H, Cl, Et, H), (M-10292, CH3, H, Cl, Et, Cl), (M-10293, CH3, H, Cl, Et, F), (M-10294, CH3, H, Cl, Et, CF3), (M-10295, CH3, H, Cl, Et, Br), (M-10296, CH3, H, Cl, Et, CH3), (M-10297, CH3, H, Cl, n-Pr, H), (M-10298, CH3, H, Cl, n-Pr, Cl), (M-10299, CH3, H, Cl, n-Pr, F), (M-10300, CH3, H, Cl, n-Pr, CF3), (M-10301, CH3, H, Cl, n-Pr, Br), (M-10302, CH3, H, Cl, n-Pr, CH3), (M-10303, CH3, H, Cl, c-Pr, H), (M-10304, CH3, H, Cl, c-Pr, Cl), (M-10305, CH3, H, Cl, c-Pr, F), (M-10306, CH3, H, Cl, c-Pr, CF3), (M-10307, CH3, H, Cl, c-Pr, Br), (M-10308, CH3, H, Cl, c-Pr, CH3), (M-10309, CH3, H, Cl, i-Pr, H), (M-10310, CH3, H, Cl, i-Pr, Cl), (M-10311, CH3, H, Cl, i-Pr, F), (M-10312, CH3, H, Cl, i-Pr, CF3), (M-10313, CH3, H, Cl, i-Pr, Br), (M-10314, CH3, H, Cl, i-Pr, CH3), (M-10315, CH3, H, Cl, n-Bu, H), (M-10316, CH3, H, Cl, n-Bu, Cl), (M-10317, CH3, H, Cl, n-Bu, F), (M-10318, CH3, H, Cl, n-Bu, CF3), (M-10319, CH3, H, Cl, n-Bu, Br), (M-10820, CH3, H, Cl, n-Bu, CH3), (M-10321, CH3, H, Cl, i-Bu, H), (M-10322, CH3, H, Cl, i-Bu, Cl), (M-10323, CH3, H, Cl, i-Bu, F), (M-10324, CH3, H, Cl, i-Bu, CF3), (M-10325, CH3, H, Cl, i-Bu, Br), (M-10326, CH3, H, Cl, i-Bu, CH3), (M-10327, CH3, H, Cl, sec-Bu, H), (M-10328, CH3, H, Cl, sec-Bu, Cl), (M-10329, CH3, H, Cl, sec-Bu, F), (M-10330, CH3, H, Cl, sec-Bu, CF3), (M-10331, CH3, H, Cl, sec-Bu, Br), (M-10332, CH3, H, Cl, sec-Bu, CH3), (M-10333, CH3, H, Cl, n-Pen, H), (M-10334, CH3, H, Cl, n-Pen, Cl), (M-10335, CH3, H, Cl, n-Pen, F), (M-10336, CH3, H, Cl, n-Pen, CF3), (M-10337, CH3, H, Cl, n-Pen, Br), (M-10338, CH3, H, Cl, n-Pen, CH3), (M-10339, CH3, H, Cl, c-Pen, H), (M-10340, CH3, H, Cl, c-Pen, Cl), (M-10341, CH3, H, Cl, c-Pen, F), (M-10342, CH3, H, Cl, c-Pen, CF3), (M-10343, CH3, H, Cl, c-Pen, Br), (M-10344, CH3, H, Cl, c-Pen, CH3), (M-10345, CH3, H, Cl, n-Hex, H), (M-10346, CH3, H, Cl, n-Hex, Cl), (M-10347, CH3, H, Cl, n-Hex, F), (M-10348, CH3, H, Cl, n-Hex, CF3), (M-10349, CH3, H, Cl, n-Hex, Br), (M-10350, CH3, H, Cl, n-Hex, CH3), (M-10351, CH3, H, Cl, c-Hex, H), (M-10352, CH3, H, Cl, c-Hex, Cl), (M-10353, CH3, H, Cl, c-Hex, F), (M-10354, CH3, H, Cl, c-Hex, CF3), (M-10355, CH3, H, Cl, c-Hex, Br), (M-10356, CH3, H, Cl, c-Hex, CH3), (M-10357, CH3, H, Cl, OH, H), (M-10358, CH3, H, Cl, OH, Cl), (M-10359, CH3, H, Cl, OH, F), (M-10360, CH3, H, Cl, OH, CF3), (M-10361, CH3, H, Cl, OH, Br), (M-10362, CH3, H, Cl, OH, CH3), (M-10363, CH3, H, Cl, EtO, H), (M-10364, CH3, H, Cl, EtO, Cl), (M-10365, CH3, H, Cl, EtO, F), (M-10366, CH3, H, Cl, EtO, CF3), (M-10367, CH3, H, Cl, EtO, Br), (M-10368, CH3, H, Cl, EtO, CH3), (M-10369, CH3, H, Cl, n-PrO, H), (M-10370, CH3, H, Cl, n-PrO, Cl), (M-10371, CH3, H, Cl, n-PrO, F), (M-10372, CH3, H, Cl, n-PrO, CF3), (M-10373, CH3, H, Cl, n-PrO, Br), (M-10374, CH3, H, Cl, n-PrO, CH3), (M-10375, CH3, H, Cl, PhO, H), (M-10376, CH3, H, Cl, PhO, Cl), (M-10377, CH3, H, Cl, PhO, F), (M-10378, CH3, H, Cl, PhO, CF3), (M-10379, CH3, H, Cl, PhO, Br), (M-10380, CH3, H, Cl, PhO, CH3), (M-10381, CH3, H, Cl, BnO, H), (M-10382, CH3, H, Cl, BnO, Cl), (M-10383, CH3, H, Cl, BnO, F), (M-10384, CH3, H, Cl, BnO, CF3), (M-10385, CH3, H, Cl, BnO, Br), (M-10386, CH3, H, Cl, BnO, CH3), (M-10387, CH3, H, Cl, PhCH2CH2O, H), (M-10388, CH3, H, Cl, PhCH1CH2O, Cl), (M-10389, CH3, H, Cl, PhCH2CH2O, F), (M-10390, CH3, H, Cl, PhCH2CH2O, CF3), (M-10391, CH3, H, Cl, PhCH2CH2O, Br), (M-10392, CH3, H, Cl, PhCH2CH2O, CH3), (M-10393, CH3, H, Cl, CF3O, H), (M-10394, CH3, H, Cl, CF3O, Cl), (M-10395, CH3, H, Cl, CF3O, F), (M-10396, CH3, H, Cl, CF3O, CF3), (M-10397, CH3, H, Cl, CF3O, Br), (M-10398, CH3, H, Cl, CF3O, CH3), (M-10399, CH3, H, Cl, Ph, H), (M-10400, CH3, H, Cl, Ph, Cl), (M-10401, CH3, H, Cl, Ph, F), (M-10402, CH3, H, Cl, Ph, CF3), (M-10403, CH3, H, Cl, Ph, Br), (M-10404, CH3, H, Cl, Ph, CH3), (M-10405, CH3, H, Cl, 4-F-Ph, H), (M-10406, CH3, H, Cl, 4-F-Ph, Cl), (M-10407, CH3, H, Cl, 4-F-Ph, F), (M-10408, CH3, H, Cl, 4-F-Ph, CF3), (M-10409, CH3, H, Cl, 4-F-Ph, Br), (M-10410, CH3, H, Cl, 4-F-Ph, CH3), (M-10411, CH3, H, Cl, 4-CF3-Ph, H), (M-10412, CH3, H, Cl, 4-CF3-Ph, Cl), (M-10413, CH3, H, Cl, 4-CF3-Ph, F), (M-10414, CH3, H, Cl, 4-CF3-Ph, CF3), (M-10415, CH3, H, Cl, 4-CF3-Ph, Br), (M-10416, CH3, H, Cl, 4-CF3-Ph, CF3), (M-10417, CH3, H, Cl, 4-(Me)2N-Ph, H), (M-10418, CH3, H, Cl, 4-(Me)2N-Ph, Cl), (M-10419, CH3, H, Cl, 4-(Me)2N-Ph, F), (M-10420, CH3, H, Cl, 4-(Me)2N-Ph, CF3), (M-10421, CH3, H, Cl, 4-(Me)2N-Ph, Br), (M-10422, CH3, H, Cl, 4-(Me)2N-Ph, CH3), (M-10423, CH3, H, Cl, 4-OH-Ph, H), (M-10424, CH3, H, Cl, 4-OH-Ph, Cl), (M-10425, CH3, H, Cl, 4-OH-Ph, F), (M-10426, CH3, H, Cl, 4-OH-Ph, CF3), (M-10427, CH3, H, Cl, 4-OH-Ph, Br), (M-10428, CH3, H, Cl, 4-OH-Ph, CH3), (M-10429, CH3, H, Cl, 3,4-di-F-Ph, H), (M-10430, CH3, H, Cl, 3,4-di-F-Ph, Cl), (M-10431, CH3, H, Cl, 3,4-di-F-Ph, F), (M-10432, CH3, H, Cl, 3,4-di-F-Ph, CF3), (M-10433, CH3, H, Cl, 3,4-di-F-Ph, Br), (M-10434, CH3, H, Cl, 3,4-di-F-Ph, CH3), (M-10435, CH3, H, Cl, 4-COOH-Ph, H), (M-10436, CH3, H, Cl, 4-COOH-Ph, Cl), (M-10437, CH3, H, Cl, 4-COOH-Ph, F), (M-10438, CH3, H, Cl, 4-COOH-Ph, CF3), (M-10439, CH3, H, Cl, 4-COOH-Ph, Br), (M-10440, CH3, H, Cl, 4-COOH-Ph, CH3), (M-10441, CH3, H, Cl, Bn, H), (M-10442, CH3, H, Cl, Bn, Cl), (M-10443, CH3, H, Cl, Bn, F), (M-10444, CH3, H, Cl, Bn, CF3), (M-10445, CH3, H, Cl, Bn, Br), (M-10446, CH3, H, Cl, Bn, CH3), (M-10447, CH3, H, Cl, 4-F-Bn, H), (M-10448, CH3, H, Cl, 4-F-Bn, Cl), (M-10449, CH3, H, Cl, 4-F-Bn, F), (M-10450, CH3, H, Cl, 4-F-Bn, CF3), (M-10451, CH3, H, Cl, 4-F-Bn, Br), (M-10452, CH3, H, Cl, 4-F-Bn, CH3), (M-10453, CH3, H, Cl, 2-Py, H), (M-10454, CH3, H, Cl, 2-Py, Cl), (M-10455, CH3, H, Cl, 2-Py, F), (M-10456, CH3, H, Cl, 2-Py, CF3), (M-10457, CH3, H, Cl, 2-Py, Br), (M-10458, CH3, H, Cl, 2-Py, CH3), (M-10459, CH3, H, Cl, 3-Py, H), (M-10460, CH3, H, Cl, 3-Py, Cl), (M-10461, CH3, H, Cl, 3-Py, F), (M-10462, CH3, H, Cl, 3-Py, CF3), (M-10463, CH3, H, Cl, 3-Py, Br), (M-10464, CH3, H, Cl, 3-Py, CH3), (M-10465, CH3, H, Cl, 4-Py, H), (M-10466, CH3, H, Cl, 4-Py, Cl), (M-10467, CH3, H, Cl, 4-Py, F), (M-10468, CH3, H, Cl, 4-Py, CF3), (M-10469, CH3, H, Cl, 4-Py, Br), (M-10470, CH3, H, Cl, 4-Py, CH3), (M-10471, CH3, H, Cl, 2-Th, H), (M-10472, CH3, H, Cl, 2-Th, Cl), (M-10473, CH3, H, Cl, 2-Th, F), (M-10474, CH3, H, Cl, 2-Th, CF3), (M-10475, CH3, H, Cl, 2-Th, Br), (M-10476, CH3, H, Cl, 2-Th, CH3), (M-10477, CH3, H, Cl, 3-Th, H), (M-10478, CH3, H, Cl, 3-Th, Cl), (M-10479, CH3, H, Cl, 3-Th, F), (M-10480, CH3, H, Cl, 3-Th, CF3), (M-10481, CH3, H, Cl, 3-Th, Br), (M-10482, CH3, H, Cl, 3-Th, CH3), (M-10483, CH3, H, Cl, pyrrazol-2-yl, H), (M-10484, CH3, H, Cl, pyrrazol-2-yl, Cl), (M-10485, CH3, H, Cl, pyrrazol-2-yl, F), (M-10486, CH3, H, Cl, pyrrazol-2-yl, CF3), (M-10487, CH3, H, Cl, pyrrazol-2-yl, Br), (M-10488, CH3, H, Cl, pyrrazol-2-yl, CH3), (M-10489, CH3, H, Cl, pyrrazol-3-yl, H), (M-10490, CH3, H, Cl, pyrrazol-3-yl, Cl), (M-10491, CH3, H, Cl, pyrrazol-3-yl, F), (M-10492, CH3, H, Cl, pyrrazol-3-yl, CF3), (M-10493, CH3, H, Cl, pyrrazol-3-yl, Br), (M-10494, CH3, H, Cl, pyrrazol-3-yl, CH3), (M-10495, CH3, H, Cl, pyrimidin-2-yl, H), (M-10496, CH3, H, Cl, pyrimidin-2-yl, Cl), (M-10497, CH3, H, Cl, pyrimidin-2-yl, F), (M-10498, CH3, H, Cl, pyrimidin-2-yl, CF3), (M-10499, CH3, H, Cl, pyrimidin-2-yl, Br), (M-10500, CH3, H, Cl, pyrimidin-2-yl, CH3), (M-10501, CH3, H, Cl, pyrimidin-4-yl, H), (M-10502, CH3, H, Cl, pyrimidin-4-yl, Cl), (M-10503, CH3, H, Cl, pyrimidin-4-yl, F), (M-10504, CH3, H, Cl, pyrimidin-4-yl, CF3), (M-10505, CH3, H, Cl, pyrimidin-4-yl, Br), (M-10506, CH3, H, Cl, pyrimidin-4-yl, CH3), (M-10507, CH3, H, Cl, pyrimidin-5-yl, H), (M-10508, CH3, H, Cl, pyrimidin-5-yl, Cl), (M-10509, CH3, H, Cl, pyrimidin-5-yl, F), (M-10510, CH3, H, Cl, pyrimidin-5-yl, CF3), (M-10511, CH3, H, Cl, pyrimidin-5-yl, Br), (M-10512, CH3, H, Cl, pyrimidin-5-yl, CH3), (M-10513, CH3, H, Cl, HOOCCH2CH2CH2, H), (M-10514, CH3, H, Cl, HOOCCH2CH2CH2, Cl), (M-10616, CH3, H, Cl, HOOCCH2CH2CH2, F), (M-10516, CH3, H, Cl, HOOCCH2CH2CH2, CF3), (M-10517, CH3, H, Cl, HOOCCH2CH2CH2, Br), (M-10518, CH3, H, Cl, HOOCCH2CH2CH2, CH3), (M-10519, CH3, H, Cl, HOOCCH2CH2CH2CH2, H), (M-10520, CH3, H, Cl, HOOCCH2CH2CH2CH2, Cl), (M-10521, CH3, H, Cl, HOOCCH2CH2CH2CH2, F), (M-10522, CH3, H, Cl, HOOCCH2CH2CH2CH2, CF3), (M-10523, CH3, H, Cl, HOOCCH2CH2CH2CH21 Br), (M-10524, CH3, H, Cl, HOOCCH2CH2CH2CH2, CH3), (M-10525, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-10526, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-10527, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-10528, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-10529, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-10530, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-10531, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-10532, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-10533, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-10534, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-10535, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-10536, CH3, H, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-10537, CH3, H, Cl, MeOCH2, H), (M-10538, CH3, H, Cl, MeOCH2, Cl), (M-10539, CH3, H, Cl, MeOCH2, F), (M-10540, CH3, H, Cl, MeOCH2, CF3), (M-10541, CH3, H, Cl, MeOCH2, Br), (M-10542, CH3, H, Cl, MeOCH2, CH3), (M-10543, CH3, H, Cl, EtOCH2, H), (M-10544, CH3, H, Cl, EtOCH2, Cl), (M-10545, CH3, H, Cl, EtOCH2, F), (M-10546, CH3, H, Cl, EtOCH2, CF3), (M-10547, CH3, H, Cl, EtOCH2, Br), (M-10548, CH3, H, Cl, EtOCH2, CH3), (M-10549, CH3, H, Cl, EtOCH2CH2, H), (M-10550, CH3, H, Cl, EtOCH2CH2, Cl), (M-10551, CH3, H, Cl, EtOCH2CH2, F), (M-10552, CH3, H, Cl, EtOCH2CH2, CF3), (M-10553, CH3, H, Cl, EtOCH2CH2, Br), (M-10554, CH3, H, Cl, EtOCH2CH2, CH3), (M-10555, CH3, H, Cl, MeOCH2CH2OCH2CH2, H), (M-10556, CH3, H, Cl, MeOCH2CH2OCH2CH2, Cl), (M-10557, CH3, H, Cl, MeOCH2CH2OCH2CH2, F), (M-10558, CH3, H, Cl, MeOCH2CH2OCH2CH3, CF3), (M-10559, CH3, H, Cl, MeOCH2CH2OCH2CH2, Br), (M-10560, CH3, H, Cl, MeOCH2CH2OCH2CH2, CH3), (M-10561, CH3, H, Cl, MeOCH2CH2, H), (M-10562, CH3, H, Cl, MeOCH2CH2, Cl), (M-10563, CH3, H, Cl, MeOCH2CH2, F), (M-10564, CH3, H, Cl, MeOCH2CH2, CF3), (M-10565, CH3, H, Cl, MeOCH2CH2, Br), (M-10566, CH3, H, Cl, MeOCH2CH2, CH3), (M-10567, CH3, H, Cl, HOCH2, H), (M-10568, CH3, H, Cl, HOCH2, Cl), (M-10569, CH3, H, Cl, HOCH2, F), (M-10570, CH3, H, Cl, HOCH2, CF3), (M-10571, CH3, H, Cl, HOCH2, Br), (M-10572, CH3, H, Cl, HOCH2, CH3), (M-10573, CH3, H, Cl, HOCH2CH2, H), (M-10574, CH3, H, Cl, HOCH2CH2, Cl), (M-10575, CH3, H, Cl, HOCH2CH2, F), (M-10576, CH3, H, Cl, HOCH2CH2, CF3), (M-10577, CH3, H, Cl, HOCH2CH2, Br), (M-10578, CH3, H, Cl, HOCH2CH2, CH3), (M-10579, CH3, H, Cl, HOCH2CH2CH2, H), (M-10580, CH3, H, Cl, HOCH2CH2CH2, Cl), (M-10581, CH3, H, Cl, HOCH2CH2CH2, F), (M-10582, CH3, H, Cl, HOCH2CH2CH2, CF3), (M-10583, CH3, H, Cl, HOCH2CH2CH2, Br), (M-10584, CH3, H, Cl, HOCH2CH2CH2, CH3), (M-10585, CH3, H, Cl, HOCH2CH2CH2CH2, H), (M-10586, CH3, H, Cl, HOCH2CH2CH2CH2, Cl), (M-10587, CH3, H, Cl, HOCH2CH2CH2CH2, F), (M-10588, CH3, H, Cl, HOCH2CH2CH2CH2, CF3), (M-10589, CH3, H, Cl, HOCH2CH2CH2CH2, Br), (M-10590, CH3, H, Cl, HOCH2CH2CH2CH2, CH3), (M-10591, CH3, H, Cl, HOCH2CH2CH2CH2CH2, H), (M-10592, CH3, H, Cl, HOCH2CH2CH2CH2CH2Cl), (M-10593, CH3, H, Cl, HOCH2CH2CH2CH2CH2, F), (M-10594, CH3, H, Cl, HOCH2CH2CH2CH2CH2CF3), (M-10595, CH3, H, Cl, HOCH2CH2CH2CH2CH2Br), (M-10596, CH3, H, Cl, HOCH2CH2CH2CH2CH2CH3), (M-10597, CH3, H, Cl, HOCH2CH2OCH2CH2, H), (M-10598, CH3, H, Cl, HOCH2CH2OCH2CH3, Cl), (M-10599, CH3, H, Cl, HOCH2CH2OCH2CH2, F), (M-10600, CH3, H, Cl, HOCH2CH2OCH2CH2, CF3), (M-10601, CH3, H, Cl, HOCH2CH2OCH2CH2, Br), (M-10602, CH3, H, Cl, HOCH2CH2OCH2CH2, CH3), (M-10603, CH3, H, Cl, (Me)2N, H), (M-10604, CH3, H, Cl, (Me)2N, Cl), (M-10605, CH3, H, Cl, (Me)2N, F), (M-10606, CH3, H, Cl, (Me)2N, CF3), (M-10607, CH3, H, Cl, (Me)2N, Br), (M-10608, CH3, H, Cl, (Me)2N, CH3), (M-10609, CH3, H, Cl, piperidin-4-yl-methyl, H), (M-10610, CH3, H, Cl, piperidin-4-yl-methyl, Cl), (M-10611, CH3, H, Cl, piperidin-4-yl-methyl, F), (M-10612, CH3, H, Cl, piperidin-4-yl-methyl, CF3), (M-10613, CH3, H, Cl, piperidin-4-yl-methyl, Br), (M-10614, CH3, H, Cl, piperidin-4-yl-methyl, CH3), (M-10615, CH3, H, Cl, cyclohexylmethyl, H), (M-10616, CH3, H, Cl, cyclohexylmethyl, Cl), (M-10617, CH3, H, Cl, cyclohexylmethyl, F), (M-10618, CH3, H, Cl, cyclohexylmethyl, CF3), (M-10619, CH3, H, Cl, cyclohexylmethyl, Br), (M-10620, CH3, H, Cl, cyclohexylmethyl, CH3), (M-10621, CH3, F, H, H, H), (M-10622, CH3, F, H, H, Cl), (M-10623, CH3, F, H, H, F), (M-10624, CH3, F, H, H, CF3), (M-10625, CH3, F, H, H, Br), (M-10626, CH3, F, H, H, CH3), (M-10627, CH3, F, PI, F, H), (M-10628, CH3, F, H, F, Cl), (M-10629, CH3, F, H, F, F), (M-10630, CH3, F, H, F, CF3), (M-10631, CH3, F, H, F, Br), (M-10632, CH3, F, H, F, CH3), (M-10633, CH3, F, H, Cl, H), (M-10634, CH3, F, H, Cl, Cl), (M-10635, CH3, F, H, Cl, F), (M-10636, CH3, F, H, Cl, CF3), (M-10637, CH3, F, H, Cl, Br), (M-10638, CH3, F, H, Cl, CH3), (M-10639, CH3, F, H, CH3, H), (M-10640, CH3, F, H, CH3, Cl), (M-10641, CH3, F, H, CH3, F), (M-10642, CH3, F, H, CH3, CF3), (M-10643, CH3, F, H, CH3, Br), (M-10644, CH3, F, H, CH3, CH3), (M-10645, CH3, F, H, Et, H), (M-10646, CH3, F, H, Et, Cl), (M-10647, CH3, F, H, Et, F), (M-10648, CH3, F, H, Et, CF3), (M-10649, CH3, F, H, Et, Br), (M-10650, CH3, F, H, Et, CH3), (M-10651, CH3, F, H, n-Pr, H), (M-10652, CH3, F, H, n-Pr, Cl), (M-10653, CH3, F, H, n-Pr, F), (M-10654, CH3, F, H, n-Pr, CF3), (M-10655, CH3, F, H, n-Pr, Br), (M-10656, CH3, F, H, n-Pr, CH3), (M-10657, CH3, F, H, c-Pr, H), (M-10658, CH3, F, H, c-Pr, Cl), (M-10659, CH3, F, H, c-Pr, F), (M-10660, CH3, F, H, c-Pr, CF3), (M-10661, CH3, F, H, c-Pr, Br), (M-10662, CH3, F, H, c-Pr, CH3), (M-10663, CH3, F, H, i-Pr, H), (M-10664, CH3, F, H, i-Pr, Cl), (M-10665, CH3, F, H, i-Pr, F), (M-10666, CH3, F, H, i-Pr, CF3), (M-10667, CH3, F, H, i-Pr, Br), (M-10668, CH3, F, H, i-Pr, CH3), (M-10669, CH3, F, H, n-Bu, H), (M-10670, CH3, F, H, n-Bu, Cl), (M-10671, CH3, F, H, n-Bu, F), (M-10672, CH3, F, H, n-Bu, CF3), (M-10673, CH3, F, H, n-Bu, Br), (M-10674, CH3, F, H, n-Bu, CH3), (M-10675, CH3, F, H, i-Bu, H), (M-10676, CH3, F, H, i-Bu, Cl), (M-10677, CH3, F, H, i-Bu, F), (M-10678, CH3, F, H, i-Bu, CF3), (M-10679, CH3, F, H, i-Bu, Br), (M-10680, CH3, F, H, i-Bu, CH3), (M-10681, CH3, F, H, sec-Bu, H), (M-10682, CH3, F, H, sec-Bu, Cl), (M-10683, CH3, F, H, sec-Bu, F), (M-10684, CH3, F, H, sec-Bu, CF3), (M-10685, CH3, F, H, sec-Bu, Br), (M-10686, CH3, F, H, sec-Bu, CH3), (M-10687, CH3, F, H, n-Pen, H), (M-10688, CH3, F, H, n-Pen, Cl), (M-10689, CH3, F, H, n-Pen, F), (M-10690, CH3, F, H, n-Pen, CF3), (M-10691, CH3, F, H, n-Pen, Br), (M-10692, CH3, F, H, n-Pen, CH3), (M-10693, CH3, F, H, c-Pen, H), (M-10694, CH3, F, H, c-Pen, Cl), (M-10695, CH3, F, H, c-Pen, F), (M-10696, CH3, F, H, c-Pen, CF3), (M-10697, CH3, F, H, c-Pen, Br), (M-10698, CH3, F, H, c-Pen, CH3), (M-10699, CH3, F, H, n-Hex, H), (M-10700, CH3, F, H, n-Hex, Cl), (M-10701, CH3, F, H, n-Hex, F), (M-10702, CH3, F, H, n-Hex, CF3), (M-10703, CH3, F, H, n-Hex, Br), (M-10704, CH3, F, H, n-Hex, CH3), (M-10705, CH3, F, H, c-Hex, H), (M-10706, CH3, F, H, c-Hex, Cl), (M-10707, CH3, F, H, c-Hex, F), (M-10708, CH3, F, H, c-Hex, CF3), (M-10709, CPIs, F, H, c-Hex, Br), (M-10710, CH3, F, H, c-Hex, CH3), (M-10711, CH3, F, H, OH, H), (M-10712, CH3, F, H, OH, Cl), (M-10713, CH3, F, H, OH, F), (M-10714, CH3, F, H, OH, CF3), (M-10715, CH3, F, H, OH, Br), (M-10716, CH3, F, H, OH, CH3), (M-10717, CH3, F, H, EtO, H), (M-10718, CH3, F, H, EtO, Cl), (M-10719, CH3, F, H, EtO, F), (M-10720, CH3, F, H, EtO, CF3), (M-10721, CH3, F, H, EtO, Br), (M-10722, CH3, F, H, EtO, CH3), (M-10723, CH3, F, H, n-PrO, H), (M-10724, CH3, F, H, n-PrO, Cl), (M-10725, CH3, F, H, n-PrO, F), (M-10726, CH3, F, H, n-PrO, CF3), (M-10727, CH3, F, H, n-PrO, Br), (M-10728, CH3, F, H, n-PrO, CH3), (M-10729, CH3, F, H, PhO, H), (M-10730, CH3, F, H, PhO, Cl), (M-10731, CH3, F, H, PhO, F), (M-10732, CH3, F, H, PhO, CF3), (M-10733, CH3, F, H, PhO, Br), (M-10734, CH3, F, H, PhO, CH3), (M-10735, CH3, F, H, BnO, H), (M-10736, CH3, F, H, BnO, Cl), (M-10737, CH3, F, H, BnO, F), (M-10738, CH3, F, H, BnO, CF3), (M-10739, CPIs, F, H, BnO, Br), (M-10740, CH3, F, H, BnO, CH3), (M-10741, CH3, F, H, PhCH2CH2O, H), (M-10742, CH3, F, H, PhCH2CH2O, Cl), (M-10743, CH3, F, H, PhCH2CH2O, F), (M-10744, CH3, F, H, PhCH2CH2O, CF3), (M-10745, CH3, F, H, PhCH2CH2O, Br), (M-10746, CH3, F, H, PhCH2CH2O, CH3), (M-10747, CH3, F, H, CF3O, H), (M-10748, CH3, F, H, CF3O, Cl), (M-10749, CH3, F, H, CF3O, F), (M-10750, CH3, F, H, CF3O, CF3), (M-10751, CH3, F, H, CF3O, Br), (M-10752, CH3, F, H, CF3O, CH3), (M-10753, CH3, F, H, Ph, H), (M-10754, CH3, F, H, Ph, Cl), (M-10755, CH3, F, H, Ph, F), (M-10756, CH3, F, H, Ph, CF3), (M-10757, CH3, F, H, Ph, Br), (M-10758, CH3, F, H, Ph, CH3), (M-10759, CH3, F, H, 4-F-Ph, H), (M-10760, CH3, F, H, 4-F-Ph, Cl), (M-10761, CH3, F, H, 4-F-Ph, F), (M-10762, CH3, F, H, 4-F-Ph, CF3), (M-10763, CH3, F, H, 4-F-Ph, Br), (M-10764, CH3, F, H, 4-F-Ph, CH3), (M-10765, CH3, F, H, 4-CF3-Ph, H), (M-10766, CH3, F, H, 4-CF3-Ph, Cl), (M-10767, CH3, F, H, 4-CF3-Ph, F), (M-10768, CH3, F, H, 4-CF3-Ph, CF3), (M-10769, CH3, F, H, 4-CF3-Ph, Br), (M-10770, CH3, F, H, 4-CF3-Ph, CH3), (M-10771, CH3, F, H, 4-(Me)2N-Ph, H), (M-10772, CH3, F, H, 4-(Me)2N-Ph, Cl), (M-10773, CH3, F, H, 4-(Me)2N-Ph, F), (M-10774, CH3, F, H, 4-(Me)2N-Ph, CF3), (M-10775, CH3, F, H, 4-(Me)2N-Ph, Br), (M-10776, CH3, F, H, 4-(Me)2N-Ph, CH3), (M-10777, CH3, F, H, 4-OH-Ph, H), (M-10778, CH3, F, H, 4-OH-Ph, Cl), (M-10779, CH3, F, H, 4-OH-Ph, F), (M-10780, CH3, F, H, 4-OH-Ph, CF3), (M-10781, CH3, F, H, 4-OH-Ph, Br), (M-10782, CH3, F, H, 4-OH-Ph, CH3), (M-10783, CH3, F, H, 3,4-di-F-Ph, H), (M-10784, CH3, F, H, 3,4-di-F-Ph, Cl), (M-10785, CH3, F, H, 3,4-di-F-Ph, F), (M-10786, CH3, F, H, 3,4-di-F-Ph, CF3), (M-10787, CH3, F, H, 3,4-di-F-Ph, Br), (M-10788, CH3, F, H, 3,4-di-F-Ph, CH3), (M-10789, CH3, F, H, 4-COOH-Ph, H), (M-10790, CH3, F, H, 4-COOH-Ph, Cl), (M-10791, CH3, F, H, 4-COOH-Ph, F), (M-10792, CH3, F, H, 4-COOH-Ph, CF3), (M-10793, CH3, F, H, 4-COOH-Ph, Br), (M-10794, CH3, F, H, 4-COOH-Ph, CH3), (M-10795, CH3, F, H, Bn, H), (M-10796, CH3, F, H, Bn, Cl), (M-10797, CH3, F, H, Bn, F), (M-10798, CH3, F, H, Bn, CF3), (M-10799, CH3, F, H, Bn, Br), (M-10800, CH3, F, H, Bn, CH3), (M-10801, CH3, F, H, 4-F-Bn, H), (M-10802, CH3, F, H, 4-F-Bn, Cl), (M-10803, CH3, F, H, 4-F-Bn, F), (M-10804, CH3, F, H, 4-F-Bn, CF3), (M-10805, CH3, F, H, 4-F-Bn, Br), (M-10806, CH3, F, H, 4-F-Bn, CH3), (M-10807, CH3, F, H, 2-Py, H), (M-10808, CH3, F, H, 2-Py, Cl), (M-10809, CH3, F, H, 2-Py, F), (M-10810, CH3, F, H, 2-Py, CF3), (M-10811, CH3, F, H, 2-Py, Br), (M-10812, CH3, F, H, 2-Py, CH3), (M-10813, CH3, F, H, 3-Py, H), (M-10814, CH3, F, H, 3-Py, Cl), (M-10815, CH3, F, H, 3-Py, F), (M-10816, CH3, F, H, 3-Py, CF3), (M-10817, CH3, F, H, 3-Py, Br), (M-10818, CH3, F, H, 3-Py, CH3), (M-10819, CH3, F, H, 4-Py, H), (M-10820, CH3, F, H, 4-Py, Cl), (M-10821, CH3, F, H, 4-Py, F), (M-10822, CH3, F, H, 4-Py, CF3), (M-10823, CH3, F, H, 4-Py, Br), (M-10824, CH3, F, H, 4-Py, CH3), (M-10825, CH3, F, H, 2-Th, H), (M-10826, CH3, F, H, 2-Th, Cl), (M-10827, CH3, F, H, 2-Th, F), (M-10828, CH3, F, H, 2-Th, CF3), (M-10829, CH3, F, H, 2-Th, Br), (M-10830, CH3, F, H, 2-Th, CH3), (M-10831, CH3, F, H, 3-Th, H), (M-10832, CH3, F, H, 3-Th, Cl), (M-10833, CH3, F, H, 3-Th, F), (M-10834, CH3, F, H, 3-Th, CF3), (M-10835, CH3, F, H, 3-Th, Br), (M-10836, CH3, F, H, 3-Th, CH3), (M-10837, CH3, F, H, pyrrazol-2-yl, H), (M-10838, CH3, F, H, pyrrazol-2-yl, Cl), (M-10839, CH3, F, H, pyrrazol-2-yl, F), (M-10840, CH3, F, H, pyrrazol-2-yl, CF3), (M-10841, CH3, F, H, pyrrazol-2-yl, Br), (M-10842, CH3, F, H, pyrrazol-2-yl, CH3), (M-10843, CH3, F, H, pyrrazol-3-yl, H), (M-10844, CH3, F, H, pyrrazol-3-yl, Cl), (M-10845, CH3, F, H, pyrrazol-3-yl, F), (M-10846, CH3, F, H, pyrrazol-3-yl, CF3), (M-10847, CH3, F, H, pyrrazol-3-yl, Br), (M-10848, CH3, F, H, pyrrazol-3-yl, CH3), (M-10849, CH3, F, H, pyrimidin-2-yl, H), (M-10850, CH3, F, H, pyrimidin-2-yl, Cl), (M-10851, CH3, F, H, pyrimidin-2-yl, F), (M-10852, CH3, F, H, pyrimidin-2-yl, CF3), (M-10853, CH3, F, H, pyrimidin-2-yl, Br), (M-10854, CH3, F, H, pyrimidin-2-yl, CH3), (M-10855, CH3, F, H, pyrimidin-4-yl, H), (M-10856, CH3, F, H, pyrimidin-4-yl, Cl), (M-10857, CH3, F, H, pyrimidin-4-yl, F), (M-10858, CH3, F, H, pyrimidin-4-yl, CF3), (M-10859, CH3, F, H, pyrimidin-4-yl, Br), (M-10860, CH3, F, H, pyrimidin-4-yl, CH3), (M-10861, CH3, F, H, pyrimidin-5-yl, H), (M-10862, CH3, F, H, pyrimidin-5-yl, Cl), (M-10863, CH3, F, H, pyrimidin-5-yl, F), (M-10864, CH3, F, H, pyrimidin-5-yl, CF3), (M-10865, CH3, F, H, pyrimidin-5-yl, Br), (M-10866, CH3, F, H, pyrimidin-5-yl, CH3), (M-10867, CH3, F, H, HOOCCH2CH2CH2, H), (M-10868, CH3, F, H, HOOCCH2CH2CH2, Cl), (M-10869, CH3, F, H, HOOCCH2CH2CH2, F), (M-10870, CH3, F, H, HOOCCH2CH2CH2, CF3), (M-10871, CH3, F, H, HOOCCH2CH2CH2Br), (M-10872, CH3, F, H, HOOCCH2CH2CH2, CH3), (M-10873, CH3, F, H, HOOCCH2CH2CH2CH2, H), (M-10874, CH3, F, H, HOOCCH2CH2CH2CH2, Cl), (M-10875, CH3, F, H, HOOCCH2CH2CH2CH2, F), (M-10876, CH3, F, H, HOOCCH2CH2CH2CH2, CF3), (M-10877, CH3, F, H, HOOCCH2CH2CH2CH2, Br), (M-10878, CH3, F, H, HOOCCH2CH2CH2CH2, CH3), (M-10879, CH3, F, H, (Me)2NCOCH2CH2CH2CH2, H), (M-10880, CH3, F, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-10881, CH3, F, H, (Me)2NCOCH2CH2CH2CH3, F), (M-10882, CH3, F, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-10883, CH3, F, H, (Me)3NCOCH2CH2CH2CH2Br), (M-10884, CH3, F, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-10885, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-10886, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-10887, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-10888, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-10889, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-10890, CH3, F, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-10891, CH3, F, H, MeOCH2, H), (M-10892, CH3, F, H, MeOCH2, Cl), (M-10893, CH3, F, H, MeOCH2, F), (M-10894, CH3, F, H, MeOCH2, CF3), (M-10895, CH3, F, H, MeOCH2, Br), (M-10896, CH3, F, H, MeOCH2, CH3), (M-10897, CH3, F, H, EtOCH2, H), (M-10898, CH3, F, H, EtOCH2, Cl), (M-10899, CH3, F, H, EtOCH2, F), (M-10900, CH3, F, H, EtOCH2, CF3), (M-10901, CH3, F, H, EtOCH2, Br), (M-10902, CH3, F, H, EtOCH2, CH3), (M-10903, CH3, F, H, EtOCH2CH2, H), (M-10904, CH3, F, H, EtOCH2CH2, Cl), (M-10905, CH3, F, H, EtOCH2CH2, F), (M-10906, CH3, F, H, EtOCH2CH2, CF3), (M-10907, CH3, F, H, EtOCH2CH2, Br), (M-10908, CH3, F, H, EtOCH2CH2, CH3), (M-10909, CH3, F, H, MeOCH2CH2OCH2CH2, H), (M-10910, CH3, F, H, MeOCH2CH2OCH2CH2, Cl), (M-10911, CH3, F, H, MeOCH2CH2OCH2CH2, F), (M-10912, CH3, F, H, MeOCH2CH2OCH2CH2, CF3), (M-10913, CH3, F, H, MeOCH2CH2OCH2CH2, Br), (M-10914, CH3, F, H, MeOCH2CH2OCH2CH2, CH3), (M-10915, CH3, F, H, MeOCH2CH2, H), (M-10916, CH3, F, H, MeOCH2CH2, Cl), (M-10917, CH3, F, H, MeOCH2CH2, F), (M-10918, CH3, F, H, MeOCH2CH2, CF3), (M-10919, CH3, F, H, MeOCH2CH2, Br), (M-10920, CH3, F, H, MeOCH2CH2, CH3), (M-10921, CH3, F, H, HOCH2, H), (M-10922, CH3, F, H, HOCH2, Cl), (M-10923, CH3, F, H, HOCH2, F), (M-10924, CH3, F, H, HOCH2, CF3), (M-10925, CH3, F, H, HOCH2, Br), (M-10926, CH3, F, H, HOCH2, CH3), (M-10927, CH3, F, H, HOCH2CH2, H), (M-10928, CH3, F, H, HOCH2CH2, Cl), (M-10929, CH3, F, H, HOCH2CH2, F), (M-10930, CH3, F, H, HOCH2CH2, CF3), (M-10931, CH3, F, H, HOCH2CH2, Br), (M-10932, CH3, F, H, HOCH2CH2, CH3), (M-10933, CH3, F, H, HOCH2CH2CH2, H), (M-10934, CH3, F, H, HOCH2CH2CH2, Cl), (M-10935, CH3, F, H, HOCH2CH2CH2, F), (M-10936, CH3, F, H, HOCH2CH2CH2, CF3), (M-10937, CH3, F, H, HOCH2CH2CH2, Br), (M-10938, CH3, F, H, HOCH2CH2CH2, CH3), (M-10939, CH3, F, H, HOCH2CH2CH2CH2, H), (M-10940, CH3, F, H, HOCH2CH2CH2CH2, Cl), (M-10941, CH3, F, H, HOCH2CH2CH2CH2, F), (M-10942, CH3, F, H, HOCH2CH2CH2CH2, CF3), (M-10943, CH3, F, H, HOCH2CH2CH2CH2, Br), (M-10944, CH3, F, H, HOCH2CH2CH2CH2, CH3), (M-10945, CH3, F, H, HOCH2CH2CH2CH2CH2H), (M-10946, CH3, F, H, HOCH2CH2CH2CH2CH2Cl), (M-10947, CH3, F, H, HOCH2CH2CH2CH2CH2, F), (M-10948, CH3, F, H, HOCH2CH2CH2CH2CH2, CF3), (M-10949, CH3, F, H, HOCH2CH2CH2CH2CH2, Br), (M-10950, CH3, F, H, HOCH2CH2CH2CH2CH2, CH3), (M-10951, CH3, F, H, HOCH2CH2OCH2CH2, H), (M-10952, CH3, F, H, HOCH2CH2OCH2CH2, Cl), (M-10953, CH3, F, H, HOCH2CH2OCH2CH2, F), (M-10954, CH3, F, H, HOCH2CH2OCH2CH2, CF3), (M-10955, CH3, F, H, HOCH2CH2OCH2CH2, Br), (M-10956, CH3, F, H, HOCH2CH2OCH2CH2, CH3), (M-10957, CH3, F, H, (Me)2N, H), (M-10958, CH3, F, H, (Me)2N, Cl), (M-10959, CH3, F, H, (Me)2N, F), (M-10960, CH3, F, H, (Me)2N, CF3), (M-10961, CH3, F, H, (Me)2N, Br), (M-10962, CH3, F, H, (Me)2N, CH3), (M-10963, CH3, F, H, piperidin-4-yl-methyl, H), (M-10964, CH3, F, H, piperidin-4-yl-methyl, Cl), (M-10965, CH3, F, H, piperidin-4-yl-methyl, F), (M-10966, CH3, F, H, piperidin-4-yl-methyl, CF3), (M-10967, CH3, F, H, piperidin-4-yl-methyl, Br), (M-10968, CH3, F, Ft, piperidin-4-yl-methyl, CH3), (M-10969, CH3, F, H, cyclohexylmethyl, H), (M-10970, CH3, F, H, cyclohexylmethyl, Cl), (M-10971, CH3, F, H, cyclohexylmethyl, F), (M-10972, CH3, F, H, cyclohexylmethyl, CF3), (M-10973, CH3, F, H, cyclohexylmethyl, Br), (M-10974, CH3, F, H, cyclohexylmethyl, CH3), (M-10975, CH3, F, F, H, H), (M-10976, CH3, F, F, H, Cl), (M-10977, CH3, F, F, H, F), (M-10978, CH3, F, F, H, CF3), (M-10979, CH3, F, F, H, Br), (M-10980, CH3, F, F, H, CH3), (M-10981, CH3, F, F, F, H), (M-10982, CH3, F, F, F, Cl), (M-10983, CH3, F, F, F, F), (M-10984, CH3, F, F, F, CF3), (M-10985, CH3, F, F, F, Br), (M-10986, CH3, F, F, F, CH3), (M-10987, CH3, F, F, Cl, H), (M-10988, CH3, F, F, Cl, Cl), (M-10989, CH3, F, F, Cl, F), (M-10990, CH3, F, F, Cl, CF3), (M-10991, CH3, F, F, Cl, Br), (M-10992, CH3, F, F, Cl, CH3), (M-10993, CH3, F, F, CH3, H), (M-10994, CH3, F, F, CH3, Cl), (M-10995, CH3, F, F, CH3, F), (M-10996, CH3, F, F, CH3, CF3), (M-10997, CH3, F, F, CH3, Br), (M-10998, CH3, F, F, CH3, CH3), (M-10999, CH3, F, F, Et, H), (M-11000, CH3, F, F, Et, Cl), (M-11001, CH3, F, F, Et, F), (M-11002, CH3, F, F, Et, CF3), (M-11003, CH3, F, F, Et, Br), (M-11004, CH3, F, F, Et, CH3), (M-11005, CH3, F, F, n-Pr, H), (M-11006, CH3, F, F, n-Pr, Cl), (M-11007, CH3, F, F, n-Pr, F), (M-11008, CH3, F, F, n-Pr, CF3), (M-11009, CH3, F, F, n-Pr, Br), (M-11010, CH3, F, F, n-Pr, CH3), (M-11011, CH3, F, F, c-Pr, H), (M-11012, CH3, F, F, c-Pr, Cl), (M-11013, CH3, F, F, c-Pr, F), (M-11014, CH3, F, F, c-Pr, CF3), (M-11015, CH3, F, F, c-Pr, Br), (M-11016, CH3, F, F, c-Pr, CH3), (M-11017, CH3, F, F, i-Pr, H), (M-11018, CH3, F, F, i-Pr, Cl), (M-11019, CH3, F, F, i-Pr, F), (M-11020, CH3, F, F, i-Pr, CF3), (M-11021, CH3, F, F, i-Pr, Br), (M-11022, CH3, F, F, i-Pr, CH3), (M-11023, CH3, F, F, n-Bu, H), (M-11024, CH3, F, F, n-Bu, Cl), (M-11025, CH3, F, F, n-Bu, F), (M-11026, CH3, F, F, n-Bu, CF3), (M-11027, CH3, F, F, n-Bu, Br), (M-11028, CH3, F, F, n-Bu, CH3), (M-11029, CH3, F, F, i-Bu, H), (M-11030, CH3, F, F, i-Bu, Cl), (M-11031, CH3, F, F, i-Bu, F), (M-11032, CH3, F, F, i-Bu, CF3), (M-11033, CH3, F, F, i-Bu, Br), (M-11034, CH3, F, F, i-Bu, CH3), (M-11035, CH3, F, F, sec-Bu, H), (M-11036, CH3, F, F, sec-Bu, Cl), (M-11037, CH3, F, F, sec-Bu, F), (M-11038, CH3, F, F, sec-Bu, CF3), (M-11039, CH3, F, F, sec-Bu, Br), (M-11040, CH3, F, F, sec-Bu, CH3), (M-11041, CH3, F, F, n-Pen, H), (M-11042, CH3, F, F, n-Pen, Cl), (M-11043, CH3, F, F, n-Pen, F), (M-11044, CH3, F, F, n-Pen, CF3), (M-11045, CH3, F, F, n-Pen, Br), (M-11046, CH3, F, F, n-Pen, CH3), (M-11047, CH3, F, F, c-Pen, H), (M-11048, CH3, F, F, c-Pen, Cl), (M-11049, CH3, F, F, c-Pen, F), (M-11050, CH3, F, F, c-Pen, CF3), (M-11051, CH3, F, F, c-Pen, Br), (M-11052, CH3, F, F, c-Pen, CH3), (M-11053, CH3, F, F, n-Hex, H), (M-11054, CH3, F, F, n-Hex, Cl), (M-11055, CH3, F, F, n-Hex, F), (M-11056, CH3, F, F, n-Hex, CF3), (M-11057, CH3, F, F, n-Hex, Br), (M-11058, CH3, F, F, n-Hex, CH3), (M-11059, CH3, F, F, c-Hex, H), (M-11060, CH3, F, F, c-Hex, Cl), (M-11061, CH3, F, F, c-Hex, F), (M-11062, CH3, F, F, c-Hex, CF3), (M-11063, CH3, F, F, c-Hex, Br), (M-11064, CH3, F, F, c-Hex, CH3), (M-11065, CH3, F, F, OH, H), (M-11066, CH3, F, F, OH, Cl), (M-11067, CH3, F, F, OH, F), (M-11068, CH3, F, F, OH, CF3), (M-11069, CH3, F, F, OH, Br), (M-11070, CH3, F, F, OH, CH3), (M-11071, CH3, F, F, EtO, H), (M-11072, CH3, F, F, EtO, Cl), (M-11073, CH3, F, F, EtO, F), (M-11074, CH3, F, F, EtO, CF3), (M-11075, CH3, F, F, EtO, Br), (M-11076, CH3, F, F, EtO, CH3), (M-11077, CH3, F, F, n-PrO, H), (M-11078, CH3, F, F, n-PrO, Cl), (M-11079, CH3, F, F, n-PrO, F), (M-11080, CH3, F, F, n-PrO, CF3), (M-11081, CH3, F, F, n-PrO, Br), (M-11082, CH3, F, F, n-PrO, CH3), (M-11083, CH3, F, F, PhO, H), (M-11084, CH3, F, F, PhO, Cl), (M-11085, CH3, F, F, PhO, F), (M-11086, CH3, F, F, PhO, CF3), (M-11087, CH3, F, F, PhO, Br), (M-11088, CH3, F, F, PhO, CH3), (M-11089, CH3, F, F, BnO, H), (M-11090, CH3, F, F, BnO, Cl), (M-11091, CH3, F, F, BnO, F), (M-11092, CH3, F, F, BnO, CF3), (M-11093, CH3, F, F, BnO, Br), (M-11094, CH3, F, F, BnO, CH3), (M-11095, CH3, F, F, PhCH2CH2O, H), (M-11096, CH3, F, F, PhCH2CH2O, Cl), (M-11097, CH3, F, F, PhCH2CH2O, F), (M-11098, CH3, F, F, PhCH2CH2O, CF3), (M-11099, CH3, F, F, PhCH2CH2O, Br), (M-11100, CH3, F, F, PhCH2CH2O, CH3), (M-11101, CH3, F, F, CF3O, H), (M-11102, CH3, F, F, CF3O, Cl), (M-11103, CH3, F, F, CF3O, F), (M-11104, CH3, F, F, CF3O, CH3), (M-11105, CH3, F, F, CF3O, Br), (M-11106, CH3, F, F, CF3O, CH3), (M-11107, CH3, F, F, Ph, H), (M-11108, CH3, F, F, Ph, Cl), (M-11109, CH3, F, F, Ph, F), (M-11110, CH3, F, F, Ph, CF3), (M-11111, CH3, F, F, Ph, Br), (M-11112, CH3, F, F, Ph, CH3), (M-11113, CH3, F, F, 4-F-Ph, H), (M-11114, CH3, F, F, 4-F-Ph, Cl), (M-11115, CH3, F, F, 4-F-Ph, F), (M-11116, CPIs, F, F, 4-F-Ph, CF3), (M-11117, CH3, F, F, 4-F-Ph, Br), (M-11118, CH3, F, F, 4-F-Ph, CH3), (M-11119, CH3, F, F, 4-CF3-Ph, H), (M-11120, CH3, F, F, 4-CF3-Ph, Cl), (M-11121, CH3, F, F, 4-CF3-Ph, F), (M-11122, CH3, F, F, 4-CF3-Ph, CF3), (M-11123, CH3, F, F, 4-CF3-Ph, Br), (M-11124, CH3, F, F, 4-CF3-Ph, CH3), (M-11125, CH3, F, F, 4-(Me)2N-Ph, H), (M-11126, CH3, F, F, 4-(Me)2N-Ph, Cl), (M-11127, CH3, F, F, 4-(Me)2N-Ph, F), (M-11128, CH3, F, F, 4-(Me)2N-Ph, CF3), (M-11129, CH3, F, F, 4-(Me)2N-Ph, Br), (M-11130, CH3, F, F, 4-(Me)2N-Ph, CH3), (M-11131, CH3, F, F, 4-OH-Ph, H), (M-11132, CH3, F, F, 4-OH-Ph, Cl), (M-11133, CH3, F, F, 4-OH-Ph, F), (M-11134, CH3, F, F, 4-OH-Ph, CF3), (M-11135, CH3, F, F, 4-OH-Ph, Br), (M-11136, CH3, F, F, 4-OH-Ph, CH3), (M-11137, CH3, F, F, 3,4-di-F-Ph, H), (M-11138, CH3, F, F, 3,4-di-F-Ph, Cl), (M-11139, CH3, F, F, 3,4-di-F-Ph, F), (M-11140, CH3, F, F, 3,4-di-F-Ph, CF3), (M-11141, CH3, F, F, 3,4-di-F-Ph, Br), (M-11142, CH3, F, F, 3,4-di-F-Ph, CH3), (M-11143, CH3, F, F, 4-COOH-Ph, H), (M-11144, CH3, F, F, 4-COOH-Ph, Cl), (M-11145, CH3, F, F, 4-COOH-Ph, F), (M-11146, CH3, F, F, 4-COOH-Ph, CF3), (M-11147, CH3, F, F, 4-COOH-Ph, Br), (M-11148, CH3, F, F, 4-COOH-Ph, CH3), (M-11149, CH3, F, F, Bn, H), (M-11150, CH3, F, F, Bn, Cl), (M-11151, CH3, F, F, Bn, F), (M-11152, CH3, F, F, Bn, CF3), (M-11153, CH3, F, F, Bn, Br), (M-11154, CH3, F, F, Bn, CH3), (M-11155, CH3, F, F, 4-F-Bn, H), (M-11156, CH3, F, F, 4-F-Bn, Cl), (M-11157, CH3, F, F, 4-F-Bn, F), (M-11158, CH3, F, F, 4-F-Bn, CF3), (M-11159, CH3, F, F, 4-F-Bn, Br), (M-11160, CH3, F, F, 4-F-Bn, CH3), (M-11161, CH3, F, F, 2-Py, H), (M-11162, CH3, F, F, 2-Py, Cl), (M-11163, CH3, F, F, 2-Py, F), (M-11164, CH3, F, F, 2-Py, CF3), (M-11165, CH3, F, F, 2-Py, Br), (M-11166, CH3, F, F, 2-Py, CH3), (M-11167, CH3, F, F, 3-Py, H), (M-11168, CH3, F, F, 3-Py, Cl), (M-11169, CH3, F, F, 3-Py, F), (M-11170, CH3, F, F, 3-Py, CF3), (M-11171, CH3, F, F, 3-Py, Br), (M-11172, CH3, F, F, 3-Py, CH3), (M-11173, CH3, F, F, 4-Py, H), (M-11174, CH3, F, F, 4-Py, Cl), (M-11175, CH3, F, F, 4-Py, F), (M-11176, CH3, F, F, 4-Py, CF3), (M-11177, CH3, F, F, 4-Py, Br), (M-11178, CH3, F, F, 4-Py, CH3), (M-11179, CH3, F, F, 2-Th, H), (M-11180, CH3, F, F, 2-Th, Cl), (M-11181, CH3, F, F, 2-Th, F), (M-11182, CH3, F, F, 2-Th, CF3), (M-11183, CH3, F, F, 2-Th, Br), (M-11184, CH3, F, F, 2-Th, CH3), (M-11185, CH3, F, F, 3-Th, H), (M-11186, CH3, F, F, 3-Th, Cl), (M-11187, CH3, F, F, 3-Th, F), (M-11188, CH3, F, F, 3-Th, CF3), (M-11189, CH3, F, F, 3-Th, Br), (M-11190, CH3, F, F, 3-Th, CH3), (M-11191, CH3, F, F, pyrrazol-2-yl, H), (M-11192, CH3, F, F, pyrrazol-2-yl, Cl), (M-11193, CH3, F, F, pyrrazol-2-yl, F), (M-11194, CH3, F, F, pyrrazol-2-yl, CF3), (M-11195, CH3, F, F, pyrrazol-2-yl, Br), (M-11196, CH3, F, F, pyrrazol-2-yl, CH3), (M-11197, CH3, F, F, pyrrazol-3-yl, H), (M-11198, CH3, F, F, pyrrazol-3-yl, Cl), (M-11199, CH3, F, F, pyrrazol-3-yl, F), (M-11200, CH3, F, F, pyrrazol-3-yl, CF3), (M-11201, CH3, F, F, pyrrazol-3-yl, Br), (M-11202, CH3, F, F, pyrrazol-3-yl, CH3), (M-11203, CH3, F, F, pyrimidin-2-yl, H), (M-11204, CH3, F, F, pyrimidin-2-yl, Cl), (M-11205, CH3, F, F, pyrimidin-2-yl, F), (M-11206, CH3, F, F, pyrimidin-2-yl, CF3), (M-11207, CH3, F, F, pyrimidin-2-yl, Br), (M-11208, CH3, F, F, pyrimidin-2-yl, CH3), (M-11209, CH3, F, F, pyrimidin-4-yl, H), (M-11210, CH3, F, F, pyrimidin-4-yl, Cl), (M-11211, CH3, F, F, pyrimidin-4-yl, F), (M-11212, CH3, F, F, pyrimidin-4-yl, CF3), (M-11213, CH3, F, F, pyrimidin-4-yl, Br), (M-11214, CH3, F, F, pyrimidin-4-yl, CH3), (M-11215, CH3, F, F, pyrimidin-5-yl, H), (M-11216, CH3, F, F, pyrimidin-5-yl, Cl), (M-11217, CH3, F, F, pyrimidin-5-yl, F), (M-11218, CH3, F, F, pyrimidin-5-yl, CF3), (M-11219, CH3, F, F, pyrimidin-5-yl, Br), (M-11220, CH3, F, F, pyrimidin-5-yl, CH3), (M-11221, CH3, F, F, HOOCCH2CH2CH2, H), (M-11222, CH3, F, F, HOOCCH26H2CH2, Cl), (M-11223, CH3, F, F, HOOCCH2CH2CH2, F), (M-11224, CH3, F, F, HOOCCH2CH2CH2CF3), (M-11225, CH3, F, F, HOOCCH2CH2CH2, Br), (M-11226, CH3, F, F, HOOCCH2CH2CH2, CH3), (M-11227, CH3, F, F, HOOCCH2CH2CH2CH2, H), (M-11228, CH3, F, F, HOOCCH2CH2CH2CH2, Cl), (M-11229, CH3, F, F, HOOCCH2CH2CH2CH2, F), (M-11230, CH3, F, F, HOOCCH2CH2CH2CH2, CF3), (M-11231, CH3, F, F, HOOCCH2CH2CH2CH2, Br), (M-11232, CH3, F, F, HOOCCH2CH2CH2CH2, CH3), (M-11233, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, H), (M-11234, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-11235, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, F), (M-11236, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, CF3), (M-11237, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-11238, CH3, F, F, (Me)2NCOCH2CH2CH2CH2, CH3), (M-11239, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-11240, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-11241, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-11242, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2CF3), (M-11243, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-11244, CH3, F, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-11245, CH3, F, F, MeOCH2, H), (M-11246, CH3, F, F, MeOCH2, Cl), (M-11247, CH3, F, F, MeOCH2, F), (M-11248, CH3, F, F, MeOCH2, CF3), (M-11249, CH3, F, F, MeOCH2, Br), (M-11250, CH3, F, F, MeOCH2, CH3), (M-11251, CH3, F, F, EtOCH2, H), (M-11252, CH3, F, F, EtOCH2, Cl), (M-11253, CH3, F, F, EtOCH2, F), (M-11254, CH3, F, F, EtOCH2, CF3), (M-11255, CH3, F, F, EtOCH2, Br), (M-11256, CH3, F, F, EtOCH2, CH3), (M-11257, CH3, F, F, EtOCH2CH2, H), (M-11258, CH3, F, F, EtOCH2CH2, Cl), (M-11259, CH3, F, F, EtOCH2CH2, F), (M-11260, CH3, F, F, EtOCH2CH2, CF3), (M-11261, CH3, F, F, EtOCH2CH2, Br), (M-11262, CH3, F, F, EtOCH2CH2, CH3), (M-11263, CH3, F, F, MeOCH2CH2OCH2CH2, H), (M-11264, CH3, F, F, MeOCH2CH2OCH2CH2, Cl), (M-11265, CH3, F, F, MeOCH2CH2OCH2CH2, F), (M-11266, CH3, F, F, MeOCH2CH2OCH2CH2, CF3), (M-11267, CH3, F, F, MeOCH2CH2OCH2CH2, Br), (M-11268, CH3, F, F, MeOCH2CH2OCH2CH2, CH3), (M-11269, CH3, F, F, MeOCH2CH2, H), (M-11270, CH3, F, F, MeOCH2CH2, Cl), (M-11271, CH3, F, F, MeOCH2CH2, F), (M-11272, CH3, F, F, MeOCH2CH2, CF3), (M-11273, CH3, F, F, MeOCH2CH2, Br), (M-11274, CH3, F, F, MeOCH2CH2, CH3), (M-11275, CH3, F, F, HOCH2, H), (M-11276, CH3, F, F, HOCH2, Cl), (M-11277, CH3, F, F, HOCH2, F), (M-11278, CH3, F, F, HOCH2, CF3), (M-11279, CH3, F, F, HOCH2, Br), (M-11280, CH3, F, F, HOCH2, CH3), (M-11281, CH3, F, F, HOCH2CH2, H), (M-11282, CH3, F, F, HOCH2CH2, Cl), (M-11283, CH3, F, F, HOCH2CH2, F), (M-11284, CH3, F, F, HOCH2CH2, CF3), (M-11286, CH3, F, F, HOCH2CH2, Br), (M-11286, CH3, F, F, HOCH2CH2, CH3), (M-11287, CH3, F, F, HOCH2CH2CH2, H), (M-11288, CH3, F, F, HOCH2CH2CH2, Cl), (M-11289, CH3, F, F, HOCH2CH2CH2, F), (M-11290, CH3, F, F, HOCH2CH2CH2, CF3), (M-11291, CH3, F, F, HOCH2CH2CH2, Br), (M-11292, CH3, F, F, HOCH2CH2CH2, CH3), (M-11293, CH3, F, F, HOCH2CH2CH2CH2, H), (M-11294, CH3, F, F, HOCH2CH2CH2CH2, Cl), (M-11295, CH3, F, F, HOCH2CH2CH2CH2, F), (M-11296, CH3, F, F, HOCH2CH2CH2CH2, CF3), (M-11297, CH3, F, F, HOCH2CH2CH2CH2, Br), (M-11298, CH3, F, F, HOCH2CH2CH2CH2, CH3), (M-11299, CH3, F, F, HOCH2CH2CH2CH2CH2H), (M-11300, CH3, F, F, HOCH2CH2CH2CH2CH2, Cl), (M-11301, CH3, F, F, HOCH2CH2CH2CH2CH2, F), (M-11302, CH3, F, F, HOCH2CH2CH2CH2CH2CF3), (M-11303, CH3, F, F, HOCH2CH2CH2CH2CH2Br), (M-11304, CH3, F, F, HOCH2CH2CH2CH2CH2CH3), (M-11306, CH3, F, F, HOCH2CH2OCH2CH2, H), (M-11306, CH3, F, F, HOCH2CH2OCH2CH2, Cl), (M-11307, CH3, F, F, HOCH2CH2OCH2CH2, F), (M-11308, CH3, F, F, HOCH2CH2OCH2CH2, CF3), (M-11309, CH3, F, F, HOCH2CH2OCH2CH2, Br), (M-11310, CH3, F, F, HOCH2CH2OCH2CH2, CH3), (M-11311, CH3, F, F, (Me)2N, H), (M-11312, CH3, F, F, (Me)2N, Cl), (M-11313, CH3, F, F, (Me)2N, F), (M-11314, CH3, F, F, (Me)2N, CF3), (M-11315, CH3, F, F, (Me)2N, Br), (M-11316, CH3, F, F, (Me)2N, CH3), (M-11317, CH3, F, F, piperidin-4-yl-methyl, H), (M-11318, CH3, F, F, piperidin-4-yl-methyl, Cl), (M-11319, CH3, F, F, piperidin-4-yl-methyl, F), (M-11320, CH3, F, F, piperidin-4-yl-methyl, CF3), (M-11321, CH3, F, F, piperidin-4-yl-methyl, Br), (M-11322, CH3, F, F, piperidin-4-yl-methyl, CH3), (M-11323, CH3, F, F, cyclohexylmethyl, H), (M-11324, CH3, F, F, cyclohexylmethyl, Cl), (M-11325, CH3, F, F, cyclohexylmethyl, F), (M-11326, CH3, F, F, cyclohexylmethyl, CF3), (M-11327, CH3, F, F, cyclohexylmethyl, Br), (M-11328, CH3, F, F, cyclohexylmethyl, CH3), (M-11329, CH3, F, Cl, H, H), (M-11330, CH3, F, Cl, H, Cl), (M-11331, CH3, F, Cl, H, F), (M-11332, CH3, F, Cl, H, CF3), (M-11333, CH3, F, Cl, H, Br), (M-11334, CH3, F, Cl, H, CH3), (M-11335, CH3, F, Cl, F, H), (M-11336, CH3, F, Cl, F, Cl), (M-11337, CH3, F, Cl, F, F), (M-11338, CH3, F, Cl, F, CF3), (M-11339, CH3, F, Cl, F, Br), (M-11340, CH3, F, Cl, F, CH3), (M-11341, CH3, F, Cl, Cl, H), (M-11342, CH3, F, Cl, Cl, Cl), (M-11343, CH3, F, Cl, Cl, F), (M-11344, CH3, F, Cl, Cl, CF3), (M-11345, CH3, F, Cl, Cl, Br), (M-11346, CH3, F, Cl, Cl, CH3), (M-11347, CH3, F, Cl, CH3, H), (M-11348, CH3, F, Cl, CH3, Cl), (M-11349, CH3, F, Cl, CH3, F), (M-11350, CH3, F, Cl, CH3, CF3), (M-11351, CH3, F, Cl, CH3, Br), (M-11352, CH3, F, Cl, CH3, CH3), (M-11353, CH3, F, Cl, Et, H), (M-11354, CH3, F, Cl, Et, Cl), (M-11355, CH3, F, Cl, Et, F), (M-11356, CH3, F, Cl, Et, CF3), (M-11357, CH3, F, Cl, Et, Br), (M-11358, CH3, F, Cl, Et, CH3), (M-11359, CH3, F, Cl, n-Pr, H), (M-11360, CH3, F, Cl, n-Pr, Cl), (M-11361, CH3, F, Cl, n-Pr, F), (M-11362, CH3, F, Cl, n-Pr, CF3), (M-11363, CH3, F, Cl, n-Pr, Br), (M-11364, CH3, F, Cl, n-Pr, CH3), (M-11365, CH3, F, Cl, c-Pr, H), (M-11366, CH3, F, Cl, c-Pr, Cl), (M-11367, CH3, F, Cl, c-Pr, F), (M-11368, CH3, F, Cl, c-Pr, CF3), (M-11369, CH3, F, Cl, c-Pr, Br), (M-11370, CH3, F, Cl, c-Pr, CH3), (M-11371, CH3, F, Cl, i-Pr, H), (M-11372, CH3, F, Cl, i-Pr, Cl), (M-11373, CH3, F, Cl, i-Pr, F), (M-11374, CH3, F, Cl, i-Pr, CF3), (M-11375, CH3, F, Cl, i-Pr, Br), (M-11376, CH3, F, Cl, i-Pr, CH3), (M-11377, CH3, F, Cl, n-Bu, H), (M-11378, CH3, F, Cl, n-Bu, Cl), (M-11379, CH3, F, Cl, n-Bu, F), (M-11380, CH3, F, Cl, n-Bu, CF3), (M-11381, CH3, F, Cl, n-Bu, Br), (M-11382, CH3, F, Cl, n-Bu, CH3), (M-11383, CH3, F, Cl, i-Bu, H), (M-11384, CH3, F, Cl, i-Bu, Cl), (M-11385, CH3, F, Cl, i-Bu, F), (M-11386, CH3, F, Cl, i-Bu, CF3), (M-11387, CH3, F, Cl, i-Bu, Br), (M-11388, CH3, F, Cl, i-Bu, CH3), (M-11389, CH3, F, Cl, sec-Bu, H), (M-11390, CH3, F, Cl, sec-Bu, Cl), (M-11391, CH3, F, Cl, sec-Bu, F), (M-11392, CH3, F, Cl, sec-Bu, CF3), (M-11393, CH3, F, Cl, sec-Bu, Br), (M-11394, CH3, F, Cl, sec-Bu, CH3), (M-11395, CH3, F, Cl, n-Pen, H), (M-11396, CH3, F, Cl, n-Pen, Cl), (M-11397, CH3, F, Cl, n-Pen, F), (M-11398, CH3, F, Cl, n-Pen, CF3), (M-11399, CH3, F, Cl, n-Pen, Br), (M-11400, CH3, F, Cl, n-Pen, CH3), (M-11401, CH3, F, Cl, c-Pen, H), (M-11402, CH3, F, Cl, c-Pen, Cl), (M-11403, CH3, F, Cl, c-Pen, F), (M-11404, CH3, F, Cl, c-Pen, CF3), (M-11405, CH3, F, Cl, c-Pen, Br), (M-11406, CH3, F, Cl, c-Pen, CH3), (M-11407, CH3, F, Cl, n-Hex, H), (M-11408, CH3, F, Cl, n-Hex, Cl), (M-11409, CH3, F, Cl, n-Hex, F), (M-11410, CH3, F, Cl, n-Hex, CF3), (M-11411, CH3, F, Cl, n-Hex, Br), (M-11412, CH3, F, Cl, n-Hex, CH3), (M-11413, CH3, F, Cl, c-Hex, H), (M-11414, CH3, F, Cl, c-Hex, Cl), (M-11415, CH3, F, Cl, c-Hex, F), (M-11416, CH3, F, Cl, c-Hex, CF3), (M-11417, CH3, F, Cl, c-Hex, Br), (M-11418, CH3, F, Cl, c-Hex, CH3), (M-11419, CH3, F, Cl, OH, H), (M-11420, CH3, F, Cl, OH, Cl), (M-11421, CH3, F, Cl, OH, F), (M-11422, CH3, F, Cl, OH, CF3), (M-11423, CH3, F, Cl, OH, Br), (M-11424, CH3, F, Cl, OH, CH3), (M-11425, CH3, F, Cl, EtO, H), (M-11426, CH3, F, Cl, EtO, Cl), (M-11427, CH3, F, Cl, EtO, F), (M-11428, CH3, F, Cl, EtO, CF3), (M-11429, CH3, F, Cl, EtO, Br), (M-11430, CH3, F, Cl, EtO, CH3), (M-11431, CH3, F, Cl, n-PrO, H), (M-11432, CH3, F, Cl, n-PrO, Cl), (M-11433, CH3, F, Cl, n-PrO, F), (M-11434, CH3, F, Cl, n-PrO, CF3), (M-11435, CH3, F, Cl, n-PrO, Br), (M-11436, CH3, F, Cl, n-PrO, CH3), (M-11437, CH3, F, Cl, PhO, H), (M-11438, CH3, F, Cl, PhO, Cl), (M-11439, CH3, F, Cl, PhO, F), (M-11440, CH3, F, Cl, PhO, CF3), (M-11441, CH3, F, Cl, PhO, Br), (M-11442, CH3, F, Cl, PhO, CH3), (M-11443, CH3, F, Cl, BnO, H), (M-11444, CH3, F, Cl, BnO, Cl), (M-11445, CH3, F, Cl, BnO, F), (M-11446, CH3, F, Cl, BnO, CF3), (M-11447, CH3, F, Cl, BnO, Br), (M-11448, CH3, F, Cl, BnO, CH3), (M-11449, CH3, F, Cl, PhCH2CH2O, H), (M-11450, CH3, F, Cl, PhCH2CH2O, Cl), (M-11451, CH3, F, Cl, PhCH2CH2O, F), (M-11452, CH3, F, Cl, PhCH2CH2O, CF3), (M-11453, CH3, F, Cl, PhCH2CH2O, Br), (M-11454, CH3, F, Cl, PhCH2CH2O, CH3), (M-11455, CH3, F, Cl, CF3O, H), (M-11456, CH3, F, Cl, CF3O, Cl), (M-11457, CH3, F, Cl, CF3O, F), (M-11458, CH3, F, Cl, CF3O, CF3), (M-11459, CH3, F, Cl, CF3O, Br), (M-11460, CH3, F, Cl, CF3O, CH3), (M-11461, CH3, F, Cl, Ph, H), (M-11462, CH3, F, Cl, Ph, Cl), (M-11463, CH3, F, Cl, Ph, F), (M-11464, CH3, F, Cl, Ph, CF3), (M-11465, CH3, F, Cl, Ph, Br), (M-11466, CH3, F, Cl, Ph, CH3), (M-11467, CH3, F, Cl, 4-F-Ph, H), (M-11468, CH3, F, Cl, 4-F-Ph, Cl), (M-11469, CH3, F, Cl, 4-F-Ph, F), (M-11470, CH3, F, Cl, 4-F-Ph, CF3), (M-11471, CH3, F, Cl, 4-F-Ph, Br), (M-11472, CH3, F, Cl, 4-F-Ph, CH3), (M-11473, CH3, F, Cl, 4-CF3-Ph, H), (M-11474, CH3, F, Cl, 4-CF3-Ph, Cl), (M-11475, CH3, F, Cl, 4-CF3-Ph, F), (M-11476, CH3, F, Cl, 4-CF3-Ph, CF3), (M-11477, CH3, F, Cl, 4-CF3-Ph, Br), (M-11478, CH3, F, Cl, 4-CF3-Ph, CH3), (M-11479, CH3, F, Cl, 4-(Me)2N-Ph, H), (M-11480, CH3, F, Cl, 4-(Me)2N, Ph, Cl), (M-11481, CH3, F, Cl, 4-(Me)2N-Ph, F), (M-11482, CH3, F, Cl, 4-(Me)2N-Ph, CF3), (M-11483, CH3, F, Cl, 4-(Me)2N-Ph, Br), (M-11484, CH3, F, Cl, 4-(Me)2N-Ph, CH3), (M-11485, CH3, F, Cl, 4-OH-Ph, H), (M-11486, CH3, F, Cl, 4-OH-Ph, Cl), (M-11487, CH3, F, Cl, 4-OH-Ph, F), (M-11488, CH3, F, Cl, 4-OH-Ph, CF3), (M-11489, CH3, F, Cl, 4-OH-Ph, Br), (M-11490, CH3, F, Cl, 4-OH-Ph, CH3), (M-11491, CH3, F, Cl, 3,4-di-F-Ph, H), (M-11492, CH3, F, Cl, 3,4-di-F-Ph, Cl), (M-11493, CH3, F, Cl, 3,4-di-F-Ph, F), (M-11494, CH3, F, Cl, 3,4-di-F-Ph, CF3), (M-11495, CH3, F, Cl, 3,4-di-F-Ph, Br), (M-11496, CH3, F, Cl, 3,4-di-F-Ph, CH3), (M-11497, CH3, F, Cl, 4-COOH-Ph, H), (M-11498, CH3, F, Cl, 4-COOH-Ph, Cl), (M-11499, CH3, F, Cl, 4-COOH-Ph, F), (M-11500, CH3, F, Cl, 4-COOH-Ph, CF3), (M-11501, CH3, F, Cl, 4-COOH-Ph, Br), (M-11502, CH3, F, Cl, 4-COOH-Ph, CH3), (M-11503, CH3, F, Cl, Bn, H), (M-11504, CH3, F, Cl, Bn, Cl), (M-11505, CH3, F, Cl, Bn, F), (M-11506, CH3, F, Cl, Bn, CF3), (M-11507, CH3, F, Cl, Bn, Br), (M-11508, CH3, F, Cl, Bn, CH3), (M-11509, CH3, F, Cl, 4-F-Bn, H), (M-11510, CH3, F, Cl, 4-F-Bn, Cl), (M-11511, CH3, F, Cl, 4-F-Bn, F), (M-11512, CH3, F, Cl, 4-F-Bn, CF3), (M-11513, CH3, F, Cl, 4-F-Bo, Br), (M-11514, CH3, F, Cl, 4-F-Bn, CH3), (M-11510, CH3, F, Cl, 2-Py, H), (M-11516, CH3, F, Cl, 2-Py, Cl), (M-11517, CH3, F, Cl, 2-Py, F), (M-11518, CH3, F, Cl, 2-Py, CF3), (M-11519, CH3, F, Cl, 2-Py, Br), (M-11520, CH3, F, Cl, 2-Py, CH3), (M-11521, CH3, F, Cl, 3-Py, H), (M-11522, CH3, F, Cl, 3-Py, Cl), (M-11523, CH3, F, Cl, 3-Py, P), (M-11524, CH3, F, Cl, 3-Py, CF3), (M-11525, CH3, F, Cl, 3-Py, Br), (M-11526, CH3, F, Cl, 3-Py, CH3), (M-11527, CH3, F, Cl, 4-Py, H), (M-11528, CH3, F, Cl, 4-Py, Cl), (M-11529, CH3, F, Cl, 4-Py, F), (M-11530, CH3, F, Cl, 4-Py, CF3), (M-11531, CH3, F, Cl, 4-Py, Br), (M-11532, CH3, F, Cl, 4-Py, CH3), (M-11533, CH3, F, Cl, 2-Th, H), (M-11534, CH3, F, Cl, 2-Th, Cl), (M-11535, CH3, F, Cl, 2-Th, F), (M-11536, CH3, F, Cl, 2-Th, CF3), (M-11537, CH3, F, Cl, 2-Th, Br), (M-11538, CH3, F, Cl, 2-Th, CH3), (M-11539, CH3, F, Cl, 3-Th, H), (M-11540, CH3, F, Cl, 3-Th, Cl), (M-11541, CH3, F, Cl, 3-Th, F), (M-11542, CH3, F, Cl, 3-Th, CF3), (M-11543, CH3, F, Cl, 3-Th, Br), (M-11544, CH3, F, Cl, 3-Th, CH3), (M-11545, CH3, F, Cl, pyrrazol-2-yl, H), (M-11546, CH3, F, Cl, pyrrazol-2-yl, Cl), (M-11547, CH3, F, Cl, pyrrazol-2-yl, F), (M-11548, CH3, F, Cl, pyrrazol-2-yl, CF3), (M-11549, CH3, F, Cl, pyrrazol-2-yl, Br), (M-11550, CH3, F, Cl, pyrrazol-2-yl, CH3), (M-11551, CH3, F, Cl, pyrrazol-3-yl, H), (M-11552, CH3, F, Cl, pyrrazol-3-yl, Cl), (M-11553, CH3, F, Cl, pyrrazol-3-yl, F), (M-11554, CH3, F, Cl, pyrrazol-3-yl, CF3), (M-11555, CH3, F, Cl, pyrrazol-3-yl, Br), (M-11556, CH3, F, Cl, pyrazol-3-yl, CH3), (M-11557, CH3, F, Cl, pyrimidin-2-yl, H), (M-11558, CH3, F, Cl, pyrimidin-2-yl, Cl), (M-11559, CH3, F, Cl, pyrimidin-2-yl, F), (M-11560, CH3, F, Cl, pyrimidin-2-yl, CF3), (M-11561, CH3, F, Cl, pyrimidin-2-yl, Br), (M-11562, CH3, F, Cl, pyrimidin-2-yl, CH3), (M-11563, CH3, F, Cl, pyrimidin-4-yl, H), (M-11564, CH3, F, Cl, pyrimidin-4-yl, Cl), (M-11565, CH3, F, Cl, pyrimidin-4-yl, F), (M-11566, CH3, F, Cl, pyrimidin-4-yl, CF3), (M-11567, CH3, F, Cl, pyrimidin-4-yl, Br), (M-11568, CH3, F, Cl, pyrimidin-4-yl, CH3), (M-11569, CH3, F, Cl, pyrimidin-5-yl, H), (M-11570, CH3, F, Cl, pyrimidin-5-yl, Cl), (M-11571, CH3, F, Cl, pyrimidin-5-yl, F), (M-11572, CH3, F, Cl, pyrimidin-5-yl, CF3), (M-11573, CH3, F, Cl, pyrimidin-5-yl, Br), (M-11574, CH3, F, Cl, pyrimidin-5-yl, CH3), (M-11575, CH3, F, Cl, HOOCCH2CH2CH2, H), (M-11576, CH3, F, Cl, HOOCCH2CH2CH2, Cl), (M-11577, CH3, F, Cl, HOOCCH2CH2CH2, F), (M-11578, CH3, F, Cl, HOOCCH2CH2CH2, CF3), (M-11579, CH3, F, Cl, HOOCCH2CH2CH2, Br), (M-11580, CH3, F, Cl, HOOCCH2CH2CH2, CH3), (M-11581, CH3, F, Cl, HOOCCH2CH2CH2CH2, H), (M-11582, CH3, F, Cl, HOOCCH2CH2CH2CH2, Cl), (M-11583, CH3, F, Cl, HOOCCH2CH2CH2CH2, F), (M-11584, CH3, F, Cl, HOOCCH2CH2CH2CH2, CF3), (M-11585, CH3, F, Cl, HOOCCH2CH2CH2CH2, Br), (M-11586, CH3, F, Cl, HOOCCH2CH2CH2CH2, CH3), (M-11587, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-11588, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-11589, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-11590, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-11591, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-11592, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-11593, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2C2, H), (M-11594, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-11595, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-11596, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-11597, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-11598, CH3, F, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-11599, CH3, F, Cl, MeOCH2, H), (M-11600, CH3, F, Cl, MeOCH2, Cl), (M-11601, CH3, F, Cl, MeOCH2, F), (M-11602, CH3, F, Cl, MeOCH2, CF3), (M-11603, CH3, F, Cl, MeOCH2, Br), (M-11604, CH3, F, Cl, MeOCH2, CH3), (M-11605, CH3, F, Cl, EtOCH2, H), (M-11606, CH3, F, Cl, EtOCH2, Cl), (M-11607, CH3, F, Cl, EtOCH2, F), (M-11608, CH3, F, Cl, EtOCH2, CF3), (M-11609, CH3, F, Cl, EtOCH2, Br), (M-101610, CH3, F, Cl, EtOCH2, CH3), (M-11611, CH3, F, Cl, EtOCH2CH2, H), (M-11612, CH3, F, Cl, EtOCH2CH2, Cl), (M-11613, CH3, F, Cl, EtOCH2CH2, F), (M-11614, CH3, F, Cl, EtOCH2CH2, CF3), (M-11615, CH3, F, Cl, EtOCH2CH2, Br), (M-11616, CH3, F, Cl, EtOCH2CH2, CH3), (M-11617, CH3, F, Cl, MeOCH2CH2OCH2CH2, H), (M-11618, CH3, F, Cl, MeOCH2CH2OCH2CH2, Cl), (M-11619, CH3, F, Cl, MeOCH2CH2OCH2CH2, F), (M-11620, CH3, F, Cl, MeOCH2CH2OCH2CH2, CF3), (M-11621, CH3, F, Cl, MeOCH2CH2OCH2CH2, Br), (M-11622, CH3, F, Cl, MeOCH2CH2OCH2CH2, CH3), (M-11623, CH3, F, Cl, MeOCH2CH2, H), (M-11624, CH3, F, Cl, MeOCH2CH2, Cl), (M-11625, CH3, F, Cl, MeOCH2CH2, F), (M-11626, CH3, F, Cl, MeOCH2CH2, CF3), (M-11627, CH3, F, Cl, MeOCH2CH2, Br), (M-11628, CH3, F, Cl, MeOCH2CH2, CH3), (M-11629, CH3, F, Cl, HOCH2, H), (M-11630, CH3, F, Cl, HOCH2, Cl), (M-11631, CH3, F, Cl, HOCH2, F), (M-11632, CH3, F, Cl, HOCH2, CF3), (M-11633, CH3, F, Cl, HOCH2, Br), (M-11634, CH3, F, Cl, HOCH2, CH3), (M-11635, CH3, F, Cl, HOCH2CH2, H), (M-11636, CH3, F, Cl, HOCH2CH2, Cl), (M-11637, CH3, F, Cl, HOCH2CH2, F), (M-11638, CH3, F, Cl, HOCH2CH2, CF3), (M-11639, CH3, F, Cl, HOCH2CH2, Br), (M-11640, CH3, F, Cl, HOCH2CH2, CH3), (M-11641, CH3, F, Cl, HOCH2CH2CH2, H), (M-11642, CH3, F, Cl, HOCH2CH2CH2, Cl), (M-11643, CH3, F, Cl, HOCH2CH2CH2, F), (M-11644, CH3, F, Cl, HOCH2CH2CH2, CF3), (M-11645, CH3, F, Cl, HOCH2CH2CH2, Br), (M-11646, CH3, F, Cl, HOCH2CH2CH2, CH3), (M-11647, CH3, F, Cl, HOCH2CH2CH2CH2, H), (M-11648, CH3, F, Cl, HOCH2CH2CH2CH2, Cl), (M-11649, CH3, F, Cl, HOCH2CH2CH2CH2, F), (M-11650, CH3, F, Cl, HOCH2CH2CH2CH2, CF3), (M-11651, CH3, F, Cl, HOCH2CH2CH2CH2, Br), (M-11652, CH3, F, Cl, HOCH2CH2CH2CH2, CH3), (M-11653, CH3, F, Cl, HOCH2CH2CH2CH2CH2H), (M-11654, CH3, F, Cl, HOCH2CH2CH2CH2CH2, Cl), (M-11655, CH3, F, Cl, HOCH2CH2CH2CH2CH2, F), (M-11656, CH3, F, Cl, HOCH2CH2CH2CH2CH2CF3), (M-11657, CH3, F, Cl, HOCH2CH2CH2CH2CH2, Br), (M-11658, CH3, F, Cl, HOCH2CH2CH2CH2CH2, CH3), (M-11659, CH3, F, Cl, HOCH2CH2OCH2CH2, H), (M-11860, CH3, F, Cl, HOCH2CH2OCH2CH2, Cl), (M-11661, CH3, F, Cl, HOCH2CH2OCH2CH2, F), (M-11662, CH3, F, Cl, HOCH2CH2OCH2CH2, CF3), (M-11663, CH3, F, Cl, HOCH2CH2OCH2CH2, Br), (M-11664, CH3, F, Cl, HOCH2CH2OCH2CH2, CH3), (M-11665, CH3, F, Cl, (Me)2N, H), (M-11666, CH3, F, Cl, (Me)2N, Cl), (M-11667, CH3, F, Cl, (Me)2N, F), (M-11668, CH3, F, Cl, (Me)2N, CF3), (M-11669, CH3, F, Cl, (Me)2N, Br), (M-11670, CH3, F, Cl, (Me)2N, CH3), (M-11671, CH3, F, Cl, piperidin-4-yl-methyl, H), (M-11672, CH3, F, Cl, piperidin-4-yl-methyl, Cl), (M-11673, CH3, F, Cl, piperidin-4-yl-methyl, F), (M-11674, CH3, F, Cl, piperidin-4-yl-methyl, CF3), (M-11675, CH3, F, Cl, piperidin-4-yl-methyl, Br), (M-11676, CH3, F, Cl, piperidin-4-yl-methyl, CH3), (M-11677, CH3, F, Cl, cyclohexylmethyl, H), (M-11678, CH3, F, Cl, cyclohexylmethyl, Cl), (M-11679, CH3, F, Cl, cyclohexylmethyl, F), (M-11680, CH3, F, Cl, cyclohexylmethyl, CF3), (M-11681, CH3, F, Cl, cyclohexylmethyl, Br), (M-11682, CH3, F, Cl, cyclohexylmethyl, CH3), (M-11683, CH3, CH3, H, H, H), (M-11684, CH3, CH3, H, H, Cl), (M-11685, CH3, CH3, H, H, F), (M-11686, CH3, CH3, H, H, CF3), (M-11687, CH3, CH3, H, H, Br), (M-11688, CH3, CH3, H, H, CH3), (M-11689, CH3, CH3, H, F, H), (M-11690, CH3, CH3, H, F, Cl), (M-11691, CH3, CH3, H, F, F), (M-11692, CH3, CH3, H, F, CF3), (M-11693, CH3, CH3, H, F, Br), (M-11694, CH3, CH3, H, F, CH3), (M-11695, CH3, CH3, H, Cl, H), (M-11696, CH3, CH3, H, Cl, Cl), (M-11697, CH3, CH3, H, Cl, F), (M-11698, CH3, CH3, H, Cl, CF3), (M-11699, CH3, CH3, H, Cl, Br), (M-11700, CH3, CH3, H, Cl, CH3), (M-11701, CH3, CH3, H, CH3, H), (M-11702, CH3, CH3, H, CH3, Cl), (M-11703, CH3, CH3, H, CH3, F), (M-11704, CH3, CH3, H, CH3, CF3), (M-11705, CH3, CH3, H, CH3, Br), (M-11706, CH3, CH3, H, CH3, CH3), (M-11707, CH3, CH3, H, Et, H), (M-11708, CH3, CH3, H, Et, Cl), (M-11709, CH2, CH3, H, Et, F), (M-11710, CH3, CH3, H, Et, CF3), (M-11711, CH3, CH3, H, Et, Br), (M-11712, CH3, CH3, H, Et, CH3), (M-11713, CH3, CH3, H, n-Pr, H), (M-11714, CH3, CH3, H, n-Pr, CL), (M-11715, CH3, CH3, H, n-Pr, F), (M-11716, CH3, CH3, H, n-Pr, CF3), (M-11717, CH3, CH3, H, n-Pr, Br), (M-11718, CH3, CH3, H, n-Pr, CH3), (M-11719, CH3, CH3, H, c-Pr, H), (M-11720, CH3, CH3, H, c-Pr, Cl), (M-11721, CH3, CH3, H, c-Pr, F), (M-11722, CH3, CH3, H, c-Pr, CF3), (M-11723, CH3, CH3, H, c-Pr, Br), (M-11724, CH3, CH3, H, c-Pr, CH3), (M-11725, CH3, CH3, H, i-Pr, H), (M-11726, CH3, CH3, H, i-Pr, Cl), (M-11727, CH3, CH3, H, i-Pr, F), (M-11728, CH3, CH3, H, i-Pr, CF3), (M-11729, CH3, CH3, H, i-Pr, Br), (M-11730, CH3, CH3, H, i-Pr, CH3), (M-11731, CH3, CH3, H, n-Bu, H), (M-11732, CH3, CH3, H, n-Bu, Cl), (M-11733, CH3, CH3, H, n-Bu, F), (M-11734, CH3, CH3, H, n-Bu, CF3), (M-11735, CH3, CH3, H, n-Bu, Br), (M-11736, CH3, CH3, H, n-Bu, CH3), (M-11737, CH3, CH3, H, i-Bu, H), (M-11738, CH3, CH3, H, i-Bu, Cl), (M-11739, CH3, CH3, H, i-Bu, F), (M-11740, CH3, CH3, H, i-Bu, CF3), (M-11741, CH3, CH3, H, i-Bu, Br), (M-11742, CH3, CH3, H, i-Bu, CH3), (M-11743, CH3, CH3, H, sec-Bu, H), (M-11744, CH3, CH3, H, sec-Bu, Cl), (M-11745, CH3, CH3, H, sec-Bu, F), (M-11746, CH3, CH3, H, sec-Bu, CF3), (M-11747, CH3, CH3, H, sec-Bu, Br), (M-11748, CH3, CH3, H, sec-Bu, CH3), (M-11749, CH3, CH3, H, n-Pen, H), (M-11750, CH3, CH3, H, n-Pen, Cl), (M-11751, CH3, CH3, H, n-Pen, F), (M-11752, CH3, CH3, H, n-Pen, CF3), (M-11753, CH3, CH3, H, n-Pen, Br), (M-11754, CH3, CH3, H, n-Pen, CH3), (M-11755, CH3, CH3, H, c-Pen, H), (M-11756, CH3, CH3, H, c-Pen, Cl), (M-11757, CH3, CH3, H, c-Pen, F), (M-11758, CH3, CH3, H, c-Pen, CF3), (M-11759, CH3, CH3, H, c-Pen, Br), (M-11760, CH3, CH3, H, c-Pen, CH3), (M-11761, CH3, CH3, H, n-Hex, H), (M-11762, CH3, CH3, H, n-Hex, Cl), (M-11763, CH3, CH3, H, n-Hex, F), (M-11764, CH3, CH3, H, n-Hex, CF3), (M-11765, CH3, CH3, H, n-Hex, Br), (M-11766, CH3, CH3, H, n-Hex, CH3), (M-11767, CH3, CH3, H, c-Hex, H), (M-11768, CH3, CH3, H, c-Hex, Cl), (M-11769, CH3, CH3, H, c-Hex, F), (M-11770, CH3, CH3, H, c-Hex, CF3), (M-11771, CH3, CH3, H, c-Hex, Br), (M-11772, CH3, CH3, H, c-Hex, CH3), (M-11773, CH3, CH3, H, OH, H), (M-11774, CH3, CH3, H, OH, Cl), (M-11775, CH3, CH3, H, OH, F), (M-11776, CH3, CH3, H, OH, CF3), (M-11777, CH3, CH3, H, OH, Br), (M-11778, CH3, CH3, H, OH, CH3), (M-11779, CH3, CH3, H, EtO, H), (M-11780, CH3, CH3, H, EtO, Cl), (M-11781, CH3, CH3, H, EtO, F), (M-11782, CH3, CH3, H, EtO, CF3), (M-11783, CH3, CH3, H, EtO, Br), (M-11784, CH3, CH3, H, EtO, CH3), (M-11785, CH3, CH3, H, n-PrO, H), (M-11786, CH3, CH3, H, n-PrO, Cl), (M-11787, CH3, CH3, H, n-PrO, F), (M-11788, CH3, CH3, H, n-PrO, CF3), (M-11789, CH3, CH3, H, n-PrO, Br), (M-11790, CH3, CH3, H, n-PrO, CH3), (M-11791, CH3, CH3, H, PhO, H), (M-11792, CH3, CH3, H, PhO, Cl), (M-11793, CH3, CH3, H, PhO, F), (M-11794, CH3, CH3, H, PhO, CF3), (M-11795, CH3, CH3, H, PhO, Br), (M-11796, CH3, CH3, H, PhO, CH3), (M-11797, CH3, CH3, H, BnO, H), (M-11798, CH3, CH3, H, BnO, Cl), (M-11799, CH3, CH3, H, BnO, F), (M-11800, CH3, CH3, H, BnO, CF3), (M-11801, CH3, CH3, H, BnO, Br), (M-11802, CH3, CH3, H, BnO, CH3), (M-11803, CH3, CH3, H, PhCH2CH2O, H), (M-11804, CH3, CH3, H, PhCH2CH2O, Cl), (M-11805, CH3, CH3, H, PhCH2CH2O, F), (M-11806, CH3, CH3, H, PhCH2CH2O, CF3), (M-11807, CH3, CH3, H, PhCH2CH2O, Br), (M-11808, CH3, CH3, H, PhCH2CH2O, CH3), (M-11809, CH3, CH3, H, CF3O, H), (M-11810, CH3, CH3, H, CF3O, Cl), (M-11811, CH3, CH3, H, CF3O, E), (M-11812, CH3, CH3, H, CF3O, CF3), (M-11813, CH3, CH3, H, CF3O, Br), (M-11814, CH3, CH3, H, CF3O, CH3), (M-11815, CH3, CH3, H, Ph, H), (M-11816, CH3, CH3, H, Ph, Cl), (M-11817, CH3, CH3, H, Ph, F), (M-11818, CH3, CH3, H, Ph, CF3), (M-11819, CH3, CH3, H, Ph, Br), (M-11820, CH3, CH3, H, Ph, CH3), (M-11821, CH3, CH3, H, 4-F-Ph, H), (M-11822, CH3, CH3, H, 4-F-Ph, Cl), (M-11823, CH3, CH3, H, 4-F-Ph, F), (M-11824, CH3, CH3, H, 4-F-Ph, CF3), (M-11825, CH3, CH3, H, 4-F-Ph, Br), (M-11826, CH3, CH3, H, 4-F-Ph, CH3), (M-11827, CH3, CH3, H, 4-CF3-Ph, H), (M-11828, CH3, CH3, H, 4-CF3-Ph, Cl), (M-11829, CH3, CH3, H, 4-CF3-Ph, F), (M-11830, CH3, CH3, H, 4-CF3-Ph, CF3), (M-11831, CH3, CH3, H, 4-CF3-Ph, Br), (M-11832, CH3, CH3, H, 4-CF3-Ph, CH3), (M-11833, CH3, CH3, H, 4-(Me)2N-Ph, H), (M-11834, CH3, CH3, H, 4-(Me)2N-Ph, Cl), (M-11835, CH3, CH3, H, 4-(Me)2N-Ph, F), (M-11836, CH3, CH3, H, 4-(Me)2N-Ph, CF3), (M-11837, CH3, CH3, H, 4-(Me)2N-Ph, Br), (M-11838, CH3, CH3, H, 4-(Me)2N-Ph, CH3), (M-11839, CH3, CH3, H, 4-OH-Ph, H), (M-11840, CH3, CH3, H, 4-OH-Ph, Cl), (M-11841, CH3, CH3, H, 4-OH-Ph, F), (M-11842, CH3, CH3, H, 4-OH-Ph, CF3), (M-11843, CH3, CH3, H, 4-OH-Ph, Br), (M-11844, CH3, CH3, H, 4-OH-Ph, CH3), (M-11845, CH3, CH3, H, 3,4-di-F-Ph, H), (M-11846, CH3, CH3, H, 3,4-di-F-Ph, Cl), (M-11847, CH3, CH3, H, 3,4-di-F-Ph, F), (M-11848, CH3, CH3, H, 3,4-di-F-Ph, CF3), (M-11849, CH3, CH3, H, 3,4-di-F-Ph, Br), (M-11850, CH3, CH3, H, 3,4-di-F-Ph, CH3), (M-11851, CH3, CH3, H, 4-COOH-Ph, H), (M-11852, CH3, CH3, H, 4-COOH-Ph, Cl), (M-11853, CH3, CH3, H, 4-COOH-Ph, F), (M-11854, CH3, CH3, H, 4-COOH-Ph, CF3), (M-11855, CH3, CH3, H, 4-COOH-Ph, Br), (M-11856, CH3, CH3, H, 4-COOH-Ph, CH3), (M-11857, CH3, CH3, H, Bn, H), (M-11858, CH3, CH3, H, Bn, Cl), (M-11859, CH3, CH3, H, Bn, F), (M-11860, CH3, CH3, H, Bn, CF3), (M-11861, CH3, CH3, H, Bn, Br), (M-11862, CH3, CH3, H, Bn, CH3), (M-11863, CH3, CH3, H, 4-F-Bn, H), (M-11864, CH3, CH3, H, 4-F-Bn, Cl), (M-11865, CH3, CH3, H, 4-F-Bn, F), (M-11866, CH3, CH3, H, 4-F-Bn, CF3), (M-11867, CH3, CH3, H, 4-F-Bn, Br), (M-11868, CH3, CH3, H, 4-F-Bn, CH3), (M-11869, CH3, CH3, H, 2-Py, H), (M-11870, CH3, CH3, H, 2-Py, Cl), (M-11871, CH3, CH3, H, 2-Py, F), (M-11872, CH3, CH3, H, 2-Py, CF3), (M-11873, CH3, CH3, H, 2-Py, Br), (M-11874, CH3, CH3, H, 2-Py, CH3), (M-11875, CH3, CH3, H, 3-Py, H), (M-11876, CH3, CH3, H, 3-Py, Cl), (M-11877, CH3, CH3, H, 3-Py, F), (M-11878, CH3, CH3, H, 3-Py, CF3), (M-11879, CH3, CH3, H, 3-Py, Br), (M-11880, CH3, CH3, H, 3-Py, CH3), (M-11881, CH3, CH3, H, 4-Py, H), (M-11882, CH3, CH3, H, 4-Py, Cl), (M-11883, CH3, CH3, H, 4-Py, F), (M-11884, CH3, CH3, H, 4-Py, CF3), (M-11885, CH3, CH3, H, 4-Py, Br), (M-11886, CH3, CH3, H, 4-Py, CH3), (M-11887, CH3, CH3, H, 2-Th, H), (M-11888, CH3, CH3, H, 2-Th, Cl), (M-11889, CH3, CH3, H, 2-Th, F), (M-11890, CH3, CH3, H, 2-Th, CF3), (M-11891, CH3, CH3, H, 2-Th, Br), (M-11892, CH3, CH3, H, 2-Th, CH3), (M-11893, CH3, CH3, H, 3-Th, H), (M-11894, CH3, CH3, H, 3-Th, Cl), (M-11895, CH3, CH3, H, 3-Th, F), (M-11896, CH3, CH3, H, 3-Th, CF3), (M-11897, CH3, CH3, H, 3-Th, Br), (M-11898, CH3, CH3, H, 3-Th, CH3), (M-11899, CH3, CH3, H, pyrrazol-2-yl, H), (M-11900, CH2, CH3, H, pyrrazol-2-yl, Cl), (M-11901, CH3, CH3, H, pyrrazol-2-yl, F), (M-11902, CH3, CH3, H, pyrrazol-2-yl, CF3), (M-11903, CH3, CH3, H, pyrrazol-2-yl, Br), (M-11904, CH3, CH3, H, pyrrazol-2-yl, CH3), (M-11905, CH3, CH3, H, pyrrazol-3-yl, H), (M-11906, CH3, CH3, H, pyrrazol-3-yl, Cl), (M-11907, CH3, CH3, H, pyrrazol-3-yl, F), (M-11908, CH3, CH3, H, pyrrazol-3-yl, CF3), (M-11909, CH3, CH3, H, pyrrazol-3-yl, Br), (M-11910, CH3, CH3, H, pyrrazol-3-yl, CH3), (M-11911, CH3, CH3, H, pyrimidin-2-yl, H), (M-11912, CH3, CH3, H, pyrimidin-2-yl, Cl), (M-11913, CH3, CH3, H, pyrimidin-2-yl, F), (M-11914, CH3, CH3, H, pyrimidin-2-yl, CF3), (M-11915, CH3, CH3, H, pyrimidin-2-yl, Br), (M-11916, CH3, CH3, H, pyrimidin-2-yl, CH3), (M-11917, CH3, CH3, H, pyrimidin-4-yl, H), (M-11918, CH3, CH3, H, pyrimidin-4-yl, Cl), (M-11919, CH3, CH3, H, pyrimidin-4-yl, F), (M-11920, CH3, CH3, H, pyrimidin-4-yl, CF3), (M-11921, CH3, CH3, H, pyrimidin-4-yl, Br), (M-11922, CH3, CH3, H, pyrimidin-4-yl, CH3), (M-11923, CH3, CH3, H, pyrimidin-5-yl, H), (M-11924, CH3, CH3, H, pyrimidin-5-yl, Cl), (M-11925, CH3, CH3, H, pyrimidin-5-yl, F), (M-11926, CH3, CH3, H, pyrimidin-5-yl, CF3), (M-11927, CH3, CH3, H, pyrimidin-5-yl, Br), (M-11928, CH3, CH3, H, pyrimidin-5-yl, CH3), (M-11929, CH3, CH3, H, HOOCCH2CH2CH2, H), (M-11930, CH3, CH3, H, HOOCCH2CH2CH2, Cl), (M-11931, CH3, CH3, H, HOOCCH2CH2CH2, F), (M-11932, CH3, CH3, H, HOOCCH2CH2CH2, CF3), (M-11933, CH3, CH3, H, HOOCCH2CH2CH2, Br), (M-11934, CH3, CH3, H, HOOCCH2CH2CH2, CH3), (M-11935, CH3, CH3, H, HOOCCH2CH2CH2CH2, H), (M-11936, CH3, CH3, H, HOOCCH2CH2CH2CH2, Cl), (M-11937, CH3, CH3, H, HOOCCH2CH2CH2CH2, F), (M-11938, CH3, CH3, H, HOOCCH2CH2CH2CH2, CF3), (M-11939, CH3, CH3, H, HOOCCH2CH2CH2CH2, Br), (M-11940, CH3, CH3, H, HOOCCH2CH2CH2CH2, CH3), (M-11941, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, H), (M-11942, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, Cl), (M-11943, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, F), (M-11944, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, CF3), (M-11945, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, Br), (M-11946, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2, CH3), (M-11947, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-11948, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-11949, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-11950, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-11951, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-11952, CH3, CH3, H, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-11953, CH3, CH3, H, MeOCH2, H), (M-11954, CH3, CH3, H, MeOCH2, Cl), (M-11955, CH3, CH3, H, MeOCH2, F), (M-11956, CH3, CH3, H, MeOCH2, CF3), (M-11957, CH3, CH3, H, MeOCH2, Br), (M-11958, CH3, CH3, H, MeOCH2, CH3), (M-11959, CH3, CH3, H, EtOCH2, H), (M-11960, CH3, CH3, H, EtOCH2, Cl), (M-11961, CH3, CH3, H, EtOCH2, F), (M-11962, CH3, CH3, H, EtOCH2, CF3), (M-11963, CH3, CH3, H, EtOCH2, Br), (M-11964, CH3, CH3, H, EtOCH2, CH3), (M-11965, CH3, CH3, H, EtOCH2CH2, H), (M-11966, CH3, CH3, H, EtOCH2CH2, Cl), (M-11967, CH3, CH3, H, EtOCH2CH2, F), (M-11968, CH3, CH3, H, EtOCH2CH2, CF3), (M-11969, CH3, CH3, H, EtOCH2CH2, Br), (M-11970, CH3, CH3, H, EtOCH2CH2, CH3), (M-11971, CH3, CH3, H, MeOCH2CH2OCH2CH2, H), (M-11972, CH3, CH3, H, MeOCH2CH2OCH2CH2, Cl), (M-11973, CH3, CH3, H, MeOCH2CH2OCH2CH2, F), (M-11974, CH3, CH3, H, MeOCH2CH2OCH2CH2, CF3), (M-11975, CH3, CH3, H, MeOCH2CH2OCH2CH2, Br), (M-110976, CH3, CH3, H, MeOCH2CH2OCH2CH2, CH3), (M-11977, CH3, CH3, H, MeOCH2CH2, H), (M-11978, CH3, CH3, H, MeOCH2CH2, Cl), (M-11979, CH3, CH3, H, MeOCH2CH2, F), (M-11980, CH3, CH3, H, MeOCH2CH2, CF3), (M-11981, CH3, CH3, H, MeOCH2CH2, Br), (M-11982, CH3, CH3, H, MeOCH2CH2, CH3), (M-11983, CH3, CH3, H, HOCH2, H), (M-11984, CH3, CH3, H, HOCH2, Cl), (M-11985, CH3, CH3, H, HOCH2, F), (M-11986, CH3, CH3, H, HOCH2, CF3), (M-11987, CH3, CH3, H, HOCH2, Br), (M-11988, CH3, CH3, H, HOCH2, CH3), (M-11989, CH3, CH3, H, HOCH2CH2, H), (M-11990, CH3, CH3, H, HOCH2CH2, Cl), (M-11991, CH3, CH3, H, HOCH2CH2, F), (M-11992, CH3, CH3, H, HOCH2CH2, CF3), (M-11993, CH3, CH3, H, HOCH2CH2, Br), (M-11994, CH3, CH3, H, HOCH2CH2, CH3), (M-11995, CH3, CH3, H, HOCH2CH2CH2, H), (M-11996, CH3, CH3, H, HOCH2CH2CH2, Cl), (M-11997, CH3, CH3, H, HOCH2CH2CH2, F), (M-11998, CH3, CH3, H, HOCH2CH2CH2, CF3), (M-11999, CH3, CH3, H, HOCH2CH2CH2, Br), (M-12000, CH3, CH3, H, HOCH2CH2CH2, CH3), (M-12001, CH3, CH3, H, HOCH2CH2CH2CH2, H), (M-12002, CH3, CH3, H, HOCH2CH2CH2CH2, Cl), (M-12003, CH3, CH3, H, HOCH2CH2CH2CH2, F), (M-12004, CH3, CH3, H, HOCH2CH2CH2CH2, CF3), (M-12005, CH3, H, HOCH2CH2CH2CH2, Br), (M-12006, CH3, CH3, H, HOCH2CH2CH2CH2, CH3), (M-12007, CH3, CH3, H, HOCH2CH2CH2CH2CH2, H), (M-12008, CH3, CH3, H, HOCH2CH2CH2CH2CH2, Cl), (M-12009, CH3, CH3, H, HOCH2CH2CH2CH2CH2, F), (M-12010, CH3, CH3, H, HOCH2CH2CH2CH2CH2, CF3), (M-12011, CH3, CH3, H, HOCH2CH2CH2CH2CH2, Br), (M-12012, CH3, CH3, H, HOCH2CH2CH2CH2CH2, CH3), (M-12013, CH3, CH3, H, HOCH2CH2OCH2CH2, H), (M-12014, CH3, CH3, H, HOCH2CH2OCH2CH2, Cl), (M-12015, CH3, CH3, H, HOCH2CH2OCH2CH2, F), (M-12016, CH3, CH3, H, HOCH2CH2OCH2CH2, CF3), (M-12017, CH3, CH3, H, HOCH2CH2OCH2CH2, Br), (M-12018, CH3, CH3, H, HOCH2CH2OCH2CH2, CH3), (M-12019, CH3, CH3, H, (Me)2N, H), (M-12020, CH3, CH3, H, (Me)2N, Cl), (M-12021, CH3, CH3, H, (Me)2N, F), (M-12022, CH3, CH3, H, (Me)2N, CF3), (M-12023, CH3, CH3, H, (Me)2N, Br), (M-12024, CH3, CH3, H, (Me)2N, CH3), (M-12025, CH3, CH3, H, piperidin-4-yl-methyl, H), (M-12026, CH3, CH3, H, piperidin-4-yl-methyl, Cl), (M-12027, CH3, CH3, H, piperidin-4-yl-methyl, F), (M-12028, CH3, CH3, H, piperidin-4-yl-methyl, CF3), (M-12029, CH3, CH3, H, piperidin-4-yl-methyl, Br), (M-12030, CH3, CH3, H, piperidin-4-yl-methyl, CH3), (M-12031, CH3, CH3, H, cyclohexylmethyl, H), (M-12032, CH3, CH3, H, cyclohexylmethyl, Cl), (M-12033, CH3, CH3, H, cyclohexylmethyl, F), (M-12034, CH3, CH3, H, cyclohexylmethyl, CF3), (M-12035, CH3, CH3, H, cyclohexylmethyl, Br), (M-12036, CH3, CH3, H, cyclohexylmethyl, CH3), (M-12037, CH3, CH3, F, H, H), (M-12038, CH3, CH3, F, H, Cl), (M-12039, CH3, CH3, F, H, F), (M-12040, CH3, CH3, F, H, CF3), (M-12041, CH3, CH3, F, H, Br), (M-12042, CH3, CH3, F, H, CH3), (M-12043, CH3, CH3, F, F, H), (M-12044, CH3, CH3, F, F, Cl), (M-12045, CH3, CH3, F, F, F), (M-12046, CH3, CH3, F, F, CF3), (M-12047, CH3, CH3, F, F, Br), (M-12048, CH3, CH3, F, F, CH3), (M-12049, CH3, CH3, F, Cl, H), (M-12050, CH3, CH3, F, Cl, Cl), (M-12051, CH3, CH3, F, Cl, F), (M-12052, CH3, CH3, F, Cl, CF3), (M-12053, CH3, CH3, F, Cl, Br), (M-12054, CH3, CH3, F, Cl, CH3), (M-12055, CH3, CH3, F, CH3, H), (M-12056, CH3, CH3, F, CH3, Cl), (M-12057, CH3, CH3, F, CH3, F), (M-12058, CH3, CH3, F, CH3, CF3), (M-12059, CH3, CH3, F, CH3, Br), (M-12060, CH3, CH3, F, CH3, CH3), (M-12061, CH3, CH3, F, Et, H), (M-12062, CH3, CH3, F, Et, Cl), (M-12063, CH3, CH3, F, Et, F), (M-12064, CH3, CH3, F, Et, CF3), (M-12065, CH3, CH3, F, Et, Br), (M-12066, CH3, CH3, F, Et, CH3), (M-12067, CH3, CH3, F, n-Pr, H), (M-12068, CH3, CH3, F, n-Pr, Cl), (M-12069, CH3, CH3, F, n-Pr, F), (M-12070, CH3, CH3, F, n-Pr, CF3), (M-12071, CH3, CH3, F, n-Pr, Br), (M-12072, CH3, CH3, F, n-Pr, CH3), (M-12073, CH3, CH3, F, c-Pr, H), (M-12074, CH3, CH3, F, c-Pr, Cl), (M-12075, CH3, CH3, F, c-Pr, F), (M-12076, CH3, CH3, F, c-Pr, CF3), (M-12077, CH3, CH3, F, c-Pr, Br), (M-12078, CH3, CH3, F, c-Pr, CH3), (M-12079, CH3, CH3, F, i-Pr, H), (M-12080, CH3, CH3, F, i-Pr, Cl), (M-12081, CH3, CH3, F, i-Pr, F), (M-12082, CH3, CH3, F, i-Pr, CF3), (M-12083, CH3, CH3, F, i-Pr, Br), (M-12084, CH3, CH3, F, i-Pr, CH3), (M-12085, CH3, CH3, F, n-Bu, H), (M-12086, CH3, CH3, F, n-Bu, Cl), (M-12087, CH3, CH3, F, n-Bu, F), (M-12088, CH3, CH3, F, n-Bu, CF3), (M-12089, CH3, CH3, F, n-Bu, Br), (M-12090, CH3, CH3, F, n-Bu, CH3), (M-12091, CH3, CH3, F, i-Bu, H), (M-12092, CH3, CH3, F, i-Bu, Cl), (M-12093, CH3, CH3, F, i-Bu, F), (M-12094, CH3, CH3, F, i-Bu, CF3), (M-12095, CH3, CH3, F, i-Bu, Br), (M-12096, CH3, CH3, F, i-Bu, CH3), (M-12097, CH3, CH3, F, sec-Bu, H), (M-12098, CH3, CH3, F, sec-Bu, Cl), (M-12099, CH3, CH3, F, sec-Bu, F), (M-12100, CH3, CH3, F, sec-Bu, CF3), (M-12101, CH3, CH3, F, sec-Bu, Br), (M-12102, CH3, CH3, F, sec-Bn, CH3), (M-12103, CH3, CH3, F, n-Pen, H), (M-12104, CH3, CH3, F, n-Pen, Cl), (M-12105, CH3, CH3, F, n-Pen, F), (M-12106, CH3, CH3, F, n-Pen, CF3), (M-12107, CH3, CH3, F, n-Pen, Br), (M-12108, CH3, CH3, F, n-Pen, CH3), (M-12109, CH3, CH3, F, c-Pen, H), (M-12110, CH3, CH3, F, c-Pen, Cl), (M-12111, CH3, CH3, F, c-Pen, F), (M-12112, CH3, CH3, F, c-Pen, CF3), (M-12113, CH3, CH3, F, c-Pen, Br), (M-12114, CH3, CH3, F, c-Pen, CH3), (M-12115, CH3, CH3, F, n-Hex, H), (M-12116, CH3, CH3, F, n-Hex, Cl), (M-12117, CH3, CH3, F, n-Hex, F), (M-12118, CH3, CH3, F, n-Hex, CF3), (M-12119, CH3, CH3, F, n-Hex, Br), (M-12120, CH3, CH3, F, n-Hex, CH3), (M-12121, CH3, CH3, F, c-Hex, H), (M-12122, CH3, CH3, F, c-Hex, Cl), (M-12123, CH3, CH3, F, c-Hex, F), (M-12124, CH3, CH3, F, c-Hex, CF3), (M-12125, CH3, CH3, F, c-Hex, Br), (M-12126, CH3, CH3, F, c-Hex, CH3), (M-12127, CH3, CH3, F, OH, H), (M-12128, CH3, CH3, F, OH, Cl), (M-12129, CH3, CH3, F, OH, F), (M-12130, CH3, CH3, F, OH, CF3), (M-12131, CH3, CH3, F, OH, Br), (M-12132, CH3, CH3, F, OH, CH3), (M-12133, CH3, CH3, F, EtO, H), (M-12134, CPIs, CH3, F, EtO, Cl), (M-12135, CH3, CH3, F, EtO, F), (M-12136, CH3, CH3, F, EtO, CF3), (M-12137, CH3, CH3, F, EtO, Br), (M-12138, CH3, CH3, F, EtO, CH3), (M-12139, CH3, CH3, F, n-PrO, H), (M-12140, CH3, CH3, F, n-PrO, Cl), (M-12141, CH3, CH3, F, n-PrO, F), (M-12142, CH3, CH3, F, n-PrO, CF3), (M-12143, CH3, CH3, F, n-PrO, Br), (M-12144, CH3, CH3, F, n-PrO, CH3), (M-12145, CH3, CH3, F, PhO, H), (M-12146, CH3, CH3, F, PhO, Cl), (M-12147, CH3, CH3, F, PhO, F), (M-12148, CH3, CH3, F, PhO, CF3), (M-12149, CH3, CH3, F, PhO, Br), (M-12150, CH3, CH3, F, PhO, CH3), (M-12151, CH3, CH3, F, BnO, H), (M-12152, CH3, CH3(F, BnO, Cl), (M-12153, CH3, CH3, F, BnO, F), (M-12154, CH3, CH3, F, BnO, CF3), (M-12155, CH3, CH3, F, BnO, Br), (M-12156, CH3, CH3, F, BnO, CH3), (M-12157, CH3, CH3, F, PhCH2CH2O, H), (M-12158, CH3, CH3, F, PhCH2CH2O, Cl), (M-12159, CH3, CH3, F, PhCH2CH2O, F), (M-12160, CH3, CH3, F, PhCH2CH2O, CF3), (M-12161, CH3, CH3, F, PhCH2CH2O, Br), (M-12162, CH3, CH3, F, PhCH2CH2O, CH3), (M-12163, CH3, CH3, F, CF3O, H), (M-12164, CH3, CH3, F, CF3O, Cl), (M-12165, CH3, CH3, F, CF3O, F), (M-12166, CH3, CH3, F, CF30, CF3), (M-12167, CH3, CH3, F, CF3O, Br), (M-12168, CH3, CH3, F, CF3O, CH3), (M-12169, CH3, CH3, F, Ph, H), (M-12170, CH3, CH3, F, Ph, Cl), (M-12171, CH3, CH3, F, Ph, F), (M-12172, CH3, CH3, F, Ph, CF3), (M-12173, CH3, CH3, F, Ph, Br), (M-12174, CH3, CH3, F, Ph, CH3), (M-12175, CH3, CH3, F, 4-F-Ph, H), (M-12176, CH3, CH3, F, 4-F-Ph, Cl), (M-12177, CH3, CH3, F, 4-F-Ph, F), (M-12178, CH3, CH3, F, 4-F-Ph, CF3), (M-12179, CH3, CH3, F, 4-F-Ph, Br), (M-12180, CH3, CH3, F, 4-F-Ph, CH3), (M-12181, CH3, CH3, F, 4-CF3-Ph, H), (M-12182, CH3, CH3, F, 4-CF3-Ph, Cl), (M-12183, CH3, CH3, F, 4-CF3-Ph, F), (M-12184, CH3, CH3, F, 4-CF3-Ph, CF3), (M-12185, CH3, CH3, F, 4-CF3-Ph, Br), (M-12186, CH3, CH3, F, 4-CF3-Ph, CH3), (M-12187, CH3, CH3, F, 4-(Me)2N-Ph, H), (M-12188, CH3, CH3, F, 4-(Me)2N-Ph, Cl), (M-12189, CH3, CH3, F, 4-(Me)2N-Ph, F), (M-12190, CH3, CH3, F, 4-(Me)2N-Ph, CF3), (M-12191, CH3, CH3, F, 4-(Me)2N-Ph, Br), (M-12192, CH3, CH3, F, 4-(Me)2N-Ph, CH3), (M-12193, CH3, CH3, F, 4-OH-Ph, H), (M-12194, CH3, CH3, F, 4-OH-Ph, Cl), (M-12195, CH3, CH3, F, 4-OH-Ph, F), (M-12196, CH3, CH3, F, 4-OH-Ph, CF3), (M-12197, CH3, CH3, F, 4-OH-Ph, Br), (M-12198, CH3, CH3, F, 4-OH-Ph, CH3), (M-12199, CH3, CH3, F, 3,4-di-F-Ph, H), (M-12200, CH3, CH3, F, 3,4-di-F-Ph, Cl), (M-12201, CH3, CH3, F, 3,4-di-F-Ph, F), (M-12202, CH3, CH3, F, 3,4-di-F-Ph, CF3), (M-12203, CH3, CH3, F, 3,4-di-F-Ph, Br), (M-12204, CH3, CH3, F, 3,4-di-F-Ph, CH3), (M-12205, CH3, CH3, F, 4-COOH-Ph, H), (M-12206, CH3, CH3, F, 4-COOH-Ph, Cl), (M-12207, CH3, CH3, F, 4-COOH-Ph, F), (M-12208, CH3, CH3, F, 4-COOH-Ph, CF3), (M-12209, CH3, CH3, F, 4-COOH-Ph, Br), (M-12210, CH3, CH3, F, 4-COOH-Ph, CH3), (M-12211, CH3, CH3, F, Bn, H), (M-12212, CH3, CH3, F, Bn, Cl), (M-12213, CH3, CH3, F, Bn, F), (M-12214, CH3, CH3, F, Bn, CF3), (M-12215, CH3, CH3, F, Bn, Br), (M-12216, CH3, CH3, F, Bn, CH3), (M-12217, CH3, CH3, F, 4-F-Bn, H), (M-12218, CH3, CH3, F, 4-F-Bn, Cl), (M-12219, CH3, CH3, F, 4-F-Bn, F), (M-12220, CH3, CH3, F, 4-F-Bn, CF3), (M-12221, CH3, CH3, F, 4-F-Bn, Br), (M-12222, CH3, CH3, F, 4-F-Bn, CH3), (M-12223, CH3, CH3, F, 2-Py, H), (M-12224, CH3, CH3, F, 2-Py, Cl), (M-12225, CH3, CH3, F, 2-Py, F), (M-12226, CH3, CH3, F, 2-Py, CF3), (M-12227, CH3, CH3, F, 2-Py, Br), (M-12228, CH3, CH3, F, 2-Py, CH3), (M-12229, CH3, CH3, F, 3-Py, H), (M-12230, CH3, CH3, F, 3-Py, Cl), (M-12231, CH3, CH3, F, 3-Py, F), (M-12232, CH3, CH3, F, 3-Py, CF3), (M-12233, CH3, CH3, F, 3-Py, Br), (M-12234, CH3, CH3, F, 3-Py, CH3), (M-12235, CH3, CH3, F, 4-Py, H), (M-12236, CH3, CH3, F, 4-Py, Cl), (M-12237, CH3, CH3, F, 4-Py, F), (M-12238, CH3, CH3, F, 4-Py, CF3), (M-12239, CH3, CH3, F, 4-Py, Br), (M-12240, CH3, CH3, F, 4-Py, CH3), (M-12241, CH3, CH3, F, 2-Th, H), (M-12242, CH3, CH3, F, 2-Th, Cl), (M-12243, CH3, CH3, F, 2-Th, F), (M-12244, CH3, CH3, F, 2-Th, CF3), (M-12245, CH3, CH3, F, 2-Th, Br), (M-12246, CH3, CH3, F, 2-Th, CH3), (M-12247, CH3, CH3, F, 3-Th, H), (M-12248, CH3, CH3, F, 3-Th, Cl), (M-12249, CH3, CH3, F, 3-Th, F), (M-12250, CH3, CH3, F, 3-Th, CF3), (M-12251, CH3, CH3, F, 3-Th, Br), (M-12252, CH3, CH3, F, 3-Th, CH3), (M-12253, CH3, CH3, F, pyrrazol-2-yl, H), (M-12254, CH3, CH3, F, pyrrazol-2-yl, Cl), (M-12255, CH3, CH3, F, pyrrazol-2-yl, F), (M-12256, CH3, CH3, F, pyrrazol-2-yl, CF3), (M-12257, CH3, CH3, F, pyrrazol-2-yl, Br), (M-12258, CH3, CH3, F, pyrrazol-2-yl, CH3), (M-12259, CH3, CH3, F, pyrrazol-3-yl, H), (M-12260, CH3, CH3, F, pyrrazol-3-yl, Cl), (M-12261, CH3, CH3, F, pyrrazol-3-yl, F), (M-12262, CH3, CH3, F, pyrrazol-3-yl, CF3), (M-12263, CH3, CH3, F, pyrrazol-3-yl, Br), (M-12264, CH3, CH3, F, pyrrazol-3-yl, CH3), (M-12265, CH3, CH3, F, pyrimidin-2-yl, H), (M-12266, CH3, CH3, F, pyrimidin-2-yl, Cl), (M-12267, CH3, CH3, F, pyrimidin-2-yl, F), (M-12268, CH3, CH3, F, pyrimidin-2-yl, CF3), (M-12269, CH3, CH3, F, pyrimidin-2-yl, Br), (M-12270, CH3, CH3, F, pyrimidin-2-yl, CH3), (M-12271, CH3, CH3, F, pyrimidin-4-yl, H), (M-12272, CH3, CH3, F, pyrimidin-4-yl, Cl), (M-12273, CH3, CH3, F, pyrimidin-4-yl, F), (M-12274, CH3, CH3, F, pyrimidin-4-yl, CF3), (M-12275, CH3, CH3, F, pyrimidin-4-yl, Br), (M-12276, CH3, CH3, F, pyrimidin-4-yl, CH3), (M-12277, CH3, CH3, F, pyrimidin-5-yl, H), (M-12278, CH3, CH3, F, pyrimidin-5-yl, Cl), (M-12279, CH3, CH3, F, pyrimidin-5-yl, F), (M-12280, CH3, CH3, F, pyrimidin-5-yl, CF3), (M-12281, CH3, CH3, F, pyrimidin-5-yl, Br), (M-12282, CH3, CH3, F, pyrimidin-5-yl, CH3), (M-12283, CH3, CH3, F, HOOCCH2CH2CH3, H), (M-12284, CH3, CH3, F, HOOCCH3CH2CH3, Cl), (M-12285, CH3, CH3, F, HOOCCH3CH2CH2, F), (M-12286, CH3, CH3, F, HOOCCH3CH2CH2, CF3), (M-12287, CH3, CH3, F, HOOCCH2CH2CH2, Br), (M-12288, CH3, CH3, F, HOOCCH2CH2CH2, CH3), (M-12289, CH3, CH3, F, HOOCCH2CH2CH2CH2, H), (M-12290, CH3, CH3, F, HOOCCH2CH2CH2CH2, Cl), (M-12291, CH3, CH3, F, HOOCCH2CH2CH2CH2, F), (M-12292, CH3, CH3, F, HOOCCH2CH2CH2CH2, CF3), (M-12293, CH3, CH3, F, HOOCCH2CH2CH2CH2, Br), (M-12294, CH3, CH3, F, HOOCCH2CH2CH2CH2, CH3), (M-12295, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2, H), (M-12296, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2, Cl), (M-12297, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2, F), (M-12298, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH3, CF3), (M-12299, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2, Br), (M-12300, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH3, CH3), (M-12301, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-12302, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2Cl), (M-12303, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-12304, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-12305, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-12306, CH3, CH3, F, (Me)2NCOCH2CH2CH2CH2CH2, CH3), (M-12307, CH3, CH3, F, MeOCH2, H), (M-12308, CH3, CH3, F, MeOCH2, Cl), (M-12309, CH3, CH3, F, MeOCH2, F), (M-12310, CH3, CH3, F, MeOCH2, CF3), (M-12311, CH3, CH3, F, MeOCH2, Br), (M-12312, CH3, CH3, F, MeOCH2, CH3), (M-12313, CH3, CH3, F, EtOCH2, H), (M-12314, CH3, CH3, F, EtOCH2, Cl), (M-12315, CH3, CH3, F, EtOCH2, F), (M-12316, CH3, CH3, F, EtOCH2, CF3), (M-12317, CH3, CH3, F, EtOCH2, Br), (M-12318, CH3, CH3, F, EtOCH2, CH3), (M-12319, CH3, CH3, F, EtOCH2CH2, H), (M-12320, CH3, CH3, F, EtOCH2CH2, Cl), (M-12321, CH3, CH3, F, EtOCH2CH2, F), (M-12322, CH3, CH3, F, EtOCH2CH2, CF3), (M-12323, CH3, CH3, F, EtOCH2CH2, Br), (M-12324, CH3, CH3, F, EtOCH2CH2, CH3), (M-12325, CH3, CH3, F, MeOCH2CH2OCH2CH2, H), (M-12326, CH3, CH3, F, MeOCH2CH2OCH2CH2, Cl), (M-12327, CH3, CH3, F, MeOCH2CH2OCH2CH2, F), (M-12328, CH3, CH3, F, MeOCH2CH2OCH2CH2, CF3), (M-12329, CH3, CH3, F, MeOCH2CH2OCH2CH2, Br), (M-12330, CH3, CH3, F, MeOCH2CH2OCH2CH2, CH3), (M-12331, CH3, CH3, F, MeOCH2CH2, H), (M-12332, CH3, CH3, F, MeOCH2CH2, Cl), (M-12333, CH3, CH3, F, MeOCH2CH2, F), (M-12334, CH3, CH3, F, MeOCH2CH2, CF3), (M-12335, CH3, CH3, F, MeOCH2CH2, Br), (M-12336, CH3, CH3, F, MeOCH2CH2, CH3), (M-12337, CH3, CH3, F, HOCH2, H), (M-12338, CH3, CH3, F, HOCH2, Cl), (M-12339, CH3, CH3, F, HOCH2, F), (M-12340, CH3, CH3, F, HOCH2, CF3), (M-12341, CH3, CH3, F, HOCH2, Br), (M-12342, CH3, CH3, F, HOCH2, CH3), (M-12343, CH3, CH3, F, HOCH2CH2, H), (M-12344, CH3, CH3, F, HOCH2CH2, Cl), (M-12345, CH3, CH3, F, HOCH2CH2, F), (M-12346, CH3, CH3, F, HOCH2CH2, CF3), (M-12347, CH3, CH3, F, HOCH2CH2, Br), (M-12348, CH3, CH3, F, HOCH2CH2, CH3), (M-12349, CH3, CH3, F, HOCH2CH2CH2, H), (M-12350, CH3, CH3, F, HOCH2CH2CH2, Cl), (M-12351, CH3, CH3, F, HOCH2CH2CH3, F), (M-12352, CH3, CH3, F, HOCH2CH2CH2, CF3), (M-12353, CH3, CH3, F, HOCH2CH2CH2, Br), (M-12354, CH3, CH3, F, HOCH2CH2CH2, CH3), (M-12355, CH3, CH3, F, HOCH2CH2CH2CH2, H), (M-12356, CH3, CH3, F, HOCH2CH2CH2CH2, Cl), (M-12357, CH3, CH3, F, HOCH2CH2CH2CH2, F), (M-12358, CH3, CH3, F, HOCH2CH2CH2CH2, CF3), (M-12359, CH3, CH3, F, HOCH2CH2CH2CH2, Br), (M-12360, CH3, CH3, F, HOCH2CH2CH2CH2, CH3), (M-12361, CH3, CH3, F, HOCH2CH2CH2CH2CH2, H), (M-12362, CH3, CH3, F, HOCH2CH2CH2CH2CH2Cl), (M-12363, CH3, CH3, F, HOCH2CH2CH2CH2CH2, F), (M-12364, CH3, CH3, F, HOCH2CH2CH2CH2CH2CF3), (M-12365, CH3, CH3, F, HOCH2CH2CH2CH3CH3, Br), (M-12366, CH3, CH3, F, HOCH2CH2CH3CH2CH2, CH3), (M-12367, CH3, CH3, F, HOCH2CH2OCH2CH2, H), (M-12368, CH3, CH3, F, HOCH2CH2OCH2CH2, Cl), (M-12369, CH3, CH3, F, HOCH2CH2OCH2CH2, F), (M-12370, CH3, CH3, F, HOCH2CH2OCH2CH2, CF3), (M-12371, CH3, CH3, F, HOCH2CH2OCH2CH2, Br), (M-12372, CH3, CH3, F, HOCH2CH2OCH2CH2, CH3), (M-12373, CH3, CH3, F, (Me)2N, H), (M-12374, CH3, CH3, F, (Me)2N, Cl), (M-12375, CH3, CH3, F, (Me)2N, F), (M-12376, CH3, CH3, F, (Me)2N, CF3), (M-12377, CH3, CH3, F, (Me)2N, Br), (M-12378, CH3, CH3, F, (Me)2N, CH3), (M-12379, CH3, CH3, F, piperidin-4-yl-methyl, H), (M-12380, CH3, CH3, F, piperidin-4-yl-methyl, Cl), (M-12381, CH3, CH3, F, piperidin-4-yl-methyl, F), (M-12382, CH3, CH3, F, piperidin-4-yl-methyl, CF3), (M-12383, CH3, CH3, F, piperidin-4-yl-methyl, Br), (M-12384, CH3, CH3, F, piperidin-4-yl-methyl, CH3), (M-12385, CH3, CH3, F, cyclohexylmethyl, H), (M-12386, CH3, CH3, F, cyclohexylmethyl, Cl), (M-12387, CH3, CH3, F, cyclohexylmethyl, F), (M-12388, CH3, CH3, F, cyclohexylmethyl, CF3), (M-12389, CH3, CH3, F, cyclohexylmethyl, Br), (M-12390, CH3, CH3, F, cyclohexylmethyl, CH3), (M-12391, CH3, CH3, Cl, H, H), (M-12392, CH3, CH3, Cl, H, Cl), (M-12393, CH3, CH3, Cl, H, F), (M-12394, CH3, CH3, Cl, H, CF3), (M-12395, CH3, CH3, Cl, H, Br), (M-12396, CH3, CH3, Cl, H, CH3), (M-12397, CH3, CH3, Cl, F, H), (M-12398, CH3, CH3, Cl, F, Cl), (M-12399, CH3, CH3, Cl, F, F), (M-12400, CH3, CH3, Cl, F, CF3), (M-12401, CH3, CH3, Cl, F, Br), (M-12402, CH3, CH3, Cl, F, CH3), (M-12403, CH3, CH3, Cl, Cl, H), (M-12404, CH3, CH3, Cl, Cl, Cl), (M-12405, CH3, CH3, Cl, Cl, F), (M-12406, CH3, CH3, Cl, Cl, CF3), (M-12407, CH3, CH3, Cl, Cl, Br), (M-12408, CH3, CH3, Cl, Cl, CH3), (M-12409, CH3, CH3, Cl, CH3, H), (M-12410, CH3, CH3, Cl, CH3, Cl), (M-12411, CH3, CH3, Cl, CH3, F), (M-12412, CH3, CH3, Cl, CH3, CF3), (M-12413, CH3, CH3, Cl, CH3, Br), (M-12414, CH3, CH3, Cl, CH3, CH3), (M-12415, CH3, CH3, Cl, Et, H), (M-12416, CH3, CH3, Cl, Et, Cl), (M-12417, CH3, CH3, Cl, Et, F), (M-12418, CH3, CH3, Cl, Et, CF3), (M-12419, CH3, CH3, Cl, Et, Br), (M-12420, CH3, CH3, Cl, Et, CH3), (M-12421, CH3, CH3, Cl, n-Pr, H), (M-12422, CH3, CH3, Cl, n-Pr, Cl), (M-12423, CH3, CH3, Cl, n-Pr, F), (M-12424, CH3, CH3, Cl, n-Pr, CF3), (M-12425, CH3, CH3, Cl, n-Pr, Br), (M-12426, CH3, CH3, Cl, n-Pr, CH3), (M-12427, CH3, CH3, Cl, c-Pr, H), (M-12428, CH3, CH3, Cl, c-Pr, Cl), (M-12429, CH3, CH3, Cl, c-Pr, F), (M-12430, CH3, CH3, Cl, c-Pr, CF3), (M-12431, CH3, CH3, Cl, c-Pr, Br), (M-12432, CH3, CH3, Cl, c-Pr, CH3), (M-12433, CH3, CH3, Cl, i-Pr, H), (M-12434, CH3, CH3, Cl, i-Pr, Cl), (M-12435, CH3, CH3, Cl, i-Pr, F), (M-12436, CH3, CH3, Cl, i-Pr, CF3), (M-12437, CH3, CH3, Cl, i-Pr, Br), (M-12438, CH3, CH3, Cl, i-Pr, CH3), (M-12439, CH3, CH3, Cl, n-Bu, H), (M-12440, CH3, CH3, Cl, n-Bu, Cl), (M-12441, CH3, CH3, Cl, n-Bu, F), (M-12442, CH3, CH3, Cl, n-Bu, CF3), (M-12443, CH3, CH3, Cl, n-Bu, Br), (M-12444, CH3, CH3, Cl, n-Bu, CH3), (M-12445, CH3, CH3, Cl, i-Bu, H), (M-12446, CH3, CH3, Cl, i-Bu, Cl), (M-12447, CH3, CH3, Cl, i-Bu, F), (M-12448, CH3, CH3, Cl, i-Bu, CF3), (M-12449, CH3, CH3, Cl, i-Bu, Br), (M-12450, CH3, CH3, Cl, i-Bn, CH3), (M-12451, CH3, CH3, Cl, sec-Bu, H), (M-12452, CH3, CH3, Cl, sec-Bu, Cl), (M-12453, CH3, CH3, Cl, sec-Bu, F), (M-12454, CH3, CH3, Cl, sec-Bu, CF3), (M-12455, CH3, CH3, Cl, sec-Bu, Br), (M-12456, CH3, CH3, Cl, sec-Bu, CH3), (M-12457, CH3, CH3, Cl, n-Pen, H), (M-12458, CH3, CH3, Cl, n-Pen, Cl), (M-12459, CH3, CH3, Cl, n-Pen, F), (M-12460, CH3, CH3, Cl, n-Pen, CF3), (M-12461, CH3, CH3, Cl, n-Pen, Br), (M-12462, CH3, CH3, Cl, n-Pen, CH3), (M-12463, CH3, CH3, Cl, c-Pen, H), (M-12464, CH3, CH3, Cl, c-Pen, Cl), (M-12465, CH3, CH3, Cl, c-Pen, F), (M-12466, CH3, CH3, Cl, c-Pen, CF3), (M-12467, CH3, CH3, Cl, c-Pen, Br), (M-12468, CH3, CH3, Cl, c-Pen, CH3), (M-12469, CH3, CH3, Cl, n-Hex, H), (M-12470, CH3, CH3, Cl, n-Hex, Cl), (M-12471, CH3, CH3, Cl, n-Hex, F), (M-12472, CH3, CH3, Cl, h-Hex, CF3), (M-12473, CH3, CH3, Cl, n-Hex, Br), (M-12474, CH3, CH3, Cl, n-Hex, CH3), (M-12475, CH3, CH3, Cl, c-Hex, H), (M-12476, CH3, CH3, Cl, c-Hex, Cl), (M-12477, CH3, CH3, Cl, c-Hex, F), (M-12478, CH3, CH3, Cl, c-Hex, CF3), (M-12479, CH3, CH3, Cl, c-Hex, Br), (M-12480, CH3, CH3, Cl, c-Hex, CH3), (M-12481, CH3, CH3, Cl, OH, H), (M-12482, CH3, CH3, Cl, OH, Cl), (M-12483, CH3, CH3, Cl, OH, F), (M-12484, CH3, CH3, Cl, OH, CF3), (M-12485, CH3, CH3, Cl, OH, Br), (M-12486, CH3, CH3, Cl, OH, CH3), (M-12487, CH3, CH3, Cl, EtO, H), (M-12488, CH3, CH3, Cl, EtO, Cl), (M-12489, CH3, CH3, Cl, EtO, F), (M-12490, CH3, CH3, Cl, EtO, CF3), (M-12491, CH3, CH3, Cl, EtO, Br), (M-12492, CH3, CH3, Cl, EtO, CH3), (M-12493, CH3, CH3, Cl, n-PrO, H), (M-12494, CH3, CH3, Cl, n-PrO, Cl), (M-12495, CH3, CH3, Cl, n-PrO, F), (M-12496, CH3, CH3, Cl, n-PrO, CF3), (M-12497, CH3, CH3, Cl, n-PrO, Br), (M-12498, CH3, CH3, Cl, n-PrO, CH3), (M-12499, CH3, CH3, Cl, PhO, H), (M-12500, CH3, CH3, Cl, PhO, Cl), (M-12501, CH3, CH3, Cl, PhO, F), (M-12502, CH3, CH3, Cl, PhO, CF3), (M-12503, CH3, CH3, Cl, PhO, Br), (M-12504, CH3, CH3, Cl, PhO, CH3), (M-12505, CH3, CH3) Cl, BnO, H), (M-12506, CH3, CH3, Cl, BnO, Cl), (M-12507, CH3, CH3, Cl, BnO, F), (M-12508, CH3, CH3, Cl, BnO, CF3), (M-12509, CH3, CH3, Cl, BnO, Br), (M-12510, CH3, CH3, Cl, BnO, CH3), (M-12511, CH3, CH3, Cl, PhCH2CH2O, H), (M-12512, CH3, CH3, Cl, PhCH2CH2O, Cl), (M-12513, CH3, CH3, Cl, PhCH2CH2O, F), (M-12514, CH3, CH3, Cl, PhCH2CH2O, CF3), (M-12515, CH3, CH3, Cl, PhCH2CH2O, Br), (M-12516, CH3, CH3, Cl, PhCH2CH2O, CH3), (M-12517, CH3, CH3, Cl, CF3O, H), (M-12518, CH3, CH3, Cl, CF3O, Cl), (M-12519, CH3, CH3, Cl, CF3O, F), (M-12520, CH3, CH3, Cl, CF3O, CF3), (M-12521, CH3, CH3, Cl, CF3O, Br), (M-12622, CH3, CH3, Cl, CF3O, CH3), (M-12523, CH3, CH3, Cl, Ph, H), (M-12524, CH3, CH3, Cl, Ph, Cl), (M-12525, CH3, CH3, Cl, Ph, F), (M-12526, CH3, CH3, Cl, Ph, CF3), (M-12527, CH3, CH3, Cl, Ph, Br), (M-12528, CH3, CH3, Cl, Ph, CH3), (M-12529, CH3, CH3, Cl, 4-F-Ph, H), (M-12530, CH3, CH3, Cl, 4-F-Ph, Cl), (M-12531, CH3, CH3, Cl, 4-F-Ph, F), (M-12632, CH3, CH3, Cl, 4-F-Ph, CF3), (M-12533, CH3, CH3, Cl, 4-F-Ph, Br), (M-12534, CH3, CH3, Cl, 4-F-Ph, CH3), (M-12535, CH3, CH3, Cl, 4-CF3-Ph, H), (M-12536, CH3, CH3, Cl, 4-CF3-Ph, Cl), (M-12537, CH3, CH3, Cl, 4-CF3-Ph, F), (M-12538, CH3, CH3, Cl, 4-CF3-Ph, CF3), (M-12539, CH3, CH3, Cl, 4-CF3-Ph, Br), (M-12540, CH3, CH3, Cl, 4-CF3-Ph, CH3), (M-12541, CH3, CH3, Cl, 4-(Me)2N-Ph, H), (M-12542, CH3, CH3, Cl, 4-(Me)2N-Ph, Cl), (M-12543, CH3, CH3, Cl, 4-(Me)2N-Ph, F), (M-12544, CH3, CH3, Cl, 4-(Me)2N-Ph, CF3), (M-12545, CH3, CH3, Cl, 4-(Me)2N-Ph, Br), (M-12546, CH3, CH3, Cl, 4-(Me)2N-Ph, CH3), (M-12547, CH3, CH3, Cl, 4-OH-Ph, H), (M-12548, CH3, CH3, Cl, 4-OH-Ph, Cl), (M-12549, CH3, CH3, Cl, 4-OH-Ph, F), (M-12550, CH3, CH3, Cl, 4-OH-Ph, CF3), (M-12551, CH3, CH3, Cl, 4-OH-Ph, Br), (M-12552, CH3, CH3, Cl, 4-OH-Ph, CH3), (M-12553, CH3, CH3, Cl, 3,4-di-F-Ph, H), (M-12554, CH3, CH3, Cl, 3,4-di-F-Ph, Cl), (M-12555, CH3, CH3, Cl, 3,4-di-F-Ph, F), (M-12556, CH3, CH3, Cl, 3,4-di-F-Ph, CF3), (M-12557, CH3, CH3, Cl, 3,4-di-F-Ph, Br), (M-12558, CH3, CH3, Cl, 3,4-di-F-Ph, CH3), (M-12559, CH3, CH3, Cl, 4-COOH-Ph, H), (M-12560, CH3, CH3, Cl, 4-COOH-Ph, Cl), (M-12561, CH3, CH3, Cl, 4-COOH-Ph, F), (M-12562, CH3, CH3, Cl, 4-COOH-Ph, CF3), (M-12563, CH3, CH3, Cl, 4-COOH-Ph, Br), (M-12564, CH3, CH3, Cl, 4-COOH-Ph, CH3), (M-12565, CH3, CH3, Cl, Bn, H), (M-12566, CH3, CH3, Cl, Bn, Cl), (M-12567, CH3, CH3, Cl, Bn, F), (M-12568, CH3, CH3, Cl, Bn, CF3), (M-12569, CH3, CH3, Cl, Bn, Br), (M-12570, CH3, CH3, Cl, Bn, CH3), (M-12571, CH3, CH3, Cl, 4-F-Bn, H), (M-12572, CH3, CH3, Cl, 4-F-Bn, Cl), (M-12573, CH3, CH3, Cl, 4-F-Bn, F), (M-12574, CH3, CH3, Cl, 4-F-Bn, CF3), (M-12575, CH3, CH3, Cl, 4-F-Bn, Br), (M-12576, CPU, CH3, Cl, 4-F-Bn, CH3), (M-12577, CH3, CH3, Cl, 2-Py, H), (M-12578, CH3, CH3, Cl, 2-Py, Cl), (M-12579, CH3, CH3, Cl, 2-Py, F), (M-12580, CH3, CH3, Cl, 2-Py, CF3), (M-12581, CH3, CH3, Cl, 2-Py, Br), (M-12582, CH3, CH3, Cl, 2-Py, CH3), (M-12583, CH3, CH3, Cl, 3-Py, H), (M-12584, CH3, CH3, Cl, 3-Py, Cl), (M-12585, CH3, CH3, Cl, 3-Py, F), (M-12586, CH3, CH3, Cl, 3-Py, CF3), (M-12587, CH3, CH3, Cl, 3-Py, Br), (M-12588, CH3, CH3, Cl, 3-Py, CH3), (M-12589, CH3, CH3, Cl, 4-Py, H), (M-12590, CH3, CH3, Cl, 4-Py, Cl), (M-12591, CH3, CH3, Cl, 4-Py, F), (M-12592, CH3, CH3, Cl, 4-Py, CF3), (M-12593, CH3, CH3, Cl, 4-Py, Br), (M-12594, CH3, CH3, Cl, 4-Py, CH3), (M-12595, CH3, CH3, Cl, 2-Th, H), (M-12596, CH3, CH3, Cl, 2-Th, Cl), (M-12597, CH3, CH3, Cl, 2-Th, F), (M-12598, CH3, CH3, Cl, 2-Th, CF3), (M-12599, CH3, CH3, Cl, 2-Th, Br), (M-12600, CH3, CH3, Cl, 2-Th, CH3), (M-12601, CH3, CH3, Cl, 3-Th, H), (M-12602, CH3, CH3, Cl, 3-Th, Cl), (M-12603, CH3, CH3, Cl, 3-Th, F), (M-12604, CH3, CH3, Cl, 3-Th, CF3), (M-12605, CH3, CH3, Cl, 3-Th, Br), (M-12606, CH3, CH3, Cl, 3-Th, CH3), (M-12607, CH3, CH3, Cl, pyrrazol-2-yl, H), (M-12608, CH3, CH3, Cl, pyrrazol-2-yl, Cl), (M-12609, CH3, CH3, Cl, pyrrazol-2-yl, F), (M-12610, CH3, CH3, Cl, pyrrazol-2-yl, CF3), (M-12611, CH3, CH3, Cl, pyrrazol-2-yl, Br), (M-12612, CH3, CH3, Cl, pyrrazol-2-yl, CH3), (M-12613, CH3, CH3, Cl, pyrrazol-3-yl, H), (M-12614, CH3, CH3, Cl, pyrrazol-3-yl, Cl), (M-12615, CH3, CH3, Cl, pyrrazol-3-yl, F), (M-12616, CH3, CH3, Cl, pyrrazol-3-yl, CF3), (M-12617, CH3, CH3, Cl, pyrrazol-3-yl, Br), (M-12618, CH3, CH3, Cl, pyrrazol-3-yl, CH3), (M-12619, CH3, CH3, Cl, pyrimidin-2-yl, H), (M-12620, CH3, CH3, Cl, pyrimidin-2-yl, Cl), (M-12621, CH3, CH3, Cl, pyrimidin-2-yl, F), (M-12622, CH3, CH3, Cl, pyrimidin-2-yl, CF3), (M-12623, CH3, CH3, Cl, pyrimidin-2-yl, Br), (M-12624, CH3, CH3, Cl, pyrimidin-2-yl, CH3), (M-12625, CH3, CH3, Cl, pyrimidin-4-yl, H), (M-12626, CH3, CH3, Cl, pyrimidin-4-yl, Cl), (M-12627, CH3, CH3, Cl, pyrimidin-4-yl, F), (M-12628, CH3, CH3, Cl, pyrimidin-4-yl, CF3), (M-12629, CH3, CH3, Cl, pyrimidin-4-yl, Br), (M-12630, CH3, CH3, Cl, pyrimidin-4-yl, CH3), (M-12631, CH3, CH3, Cl, pyrimidin-5-yl, H), (M-12632, CH3, CH3, Cl, pyrimidin-5-yl, Cl), (M-12633, CH3, CH3, Cl, pyrimidin-5-yl, F), (M-12634, CH3, CH3, Cl, pyrimidin-5-yl, CF3), (M-12635, CH3, CH3, Cl, pyrimidin-5-yl, Br), (M-12636, CH3, CH3, Cl, pyrimidin-5-yl, CH3), (M-12637, CH3, CH3, Cl, HOOCCH2CH2CH2, H), (M-12638, CH3, CH3, Cl, HOOCCH2CH2CH2, Cl), (M-12639, CH3, CH3, Cl, HOOCCH2CH2CH2, F), (M-12640, CH3, CH3, Cl, HOOCCH2CH2CH2, CF3), (M-12641, CH3, CH3, Cl, HOOCCH2CH2CH2, Br), (M-12642, CH3, CH3, Cl, HOOCCH2CH2CH2, CH3), (M-12643, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, H), (M-12644, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, Cl), (M-12645, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, F), (M-12646, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, CF3), (M-12647, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, Br), (M-12648, CH3, CH3, Cl, HOOCCH2CH2CH2CH2, CH3), (M-12649, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, H), (M-12650, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Cl), (M-12651, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, F), (M-12652, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CF3), (M-12653, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, Br), (M-12654, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2, CH3), (M-12655, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, H), (M-12656, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Cl), (M-12657, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, F), (M-12658, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, CF3), (M-12659, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2, Br), (M-12660, CH3, CH3, Cl, (Me)2NCOCH2CH2CH2CH2CH2CH3), (M-12661, CH3, CH3, Cl, MeOCH2, H), (M-12662, CH3, CH3, Cl, MeOCH2, Cl), (M-12663, CH3, CH3, Cl, MeOCH2, F), (M-12664, CH3, CH3, Cl, MeOCH2, CF3), (M-12665, CH3, CH3, Cl, MeOCH2, Br), (M-12666, CH3, CH3, Cl, MeOCH2, CH3), (M-12667, CH3, CH3, Cl, EtOCH2, H), (M-12668, CH3, CH3, Cl, EtOCH2, Cl), (M-12669, CH3, CH3, Cl, EtOCH2, F), (M-12670, CH3, CH3, Cl, EtOCH2, CF3), (M-12671, CH3, CH3, Cl, EtOCH2, Br), (M-12672, CH3, CH3, Cl, EtOCH2, CH3), (M-12673, CH3, CH3, Cl, EtOCH2CH2, H), (M-12674, CH3, CH3, Cl, EtOCH2CH2, Cl), (M-12675, CH3, CH3, Cl, EtOCH2CH2, F), (M-12676, CH3, CH3, Cl, EtOCH2CH2, CF3), (M-12677, CH3, CH3, Cl, EtOCH2CH2, Br), (M-12678, CH3, CH3, Cl, EtOCH2CH2, CH3), (M-12679, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, H), (M-12680, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, Cl), (M-12681, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, F), (M-12682, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, CF3), (M-12683, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, Br), (M-12684, CH3, CH3, Cl, MeOCH2CH2OCH2CH2, CH3), (M-12685, CH3, CH3, Cl, MeOCH2CH2, H), (M-12686, CH3, CH3, Cl, MeOCH2CH2, Cl), (M-12687, CH3, CH3, Cl, MeOCH2CH2, F), (M-12688, CH3, CH3, Cl, MeOCH2CH2, CF3), (M-12689, CH3, CH3, Cl, MeOCH2CH2, Br), (M-12690, CH3, CH3, Cl, MeOCH2CH2, CH3), (M-12691, CH3, CH3, Cl, HOCH2, H), (M-12692, CH3, CH3, Cl, HOCH2, Cl), (M-12693, CH3, CH3, Cl, HOCH2, F), (M-12694, CH3, CH3, Cl, HOCH2, CF3), (M-12695, CH3, CH3, Cl, HOCH2, Br), (M-12696, CH3, CH3, Cl, HOCH2, CH3), (M-12697, CH3, CH3, Cl, HOCH2CH2, H), (M-12698, CH3, CH3, Cl, HOCH2CH2, Cl), (M-12699, CH3, CH3, Cl, HOCH2CH2, F), (M-12700, CH3, CH3, Cl, HOCH2CH2, CF3), (M-12701, CH3, CH3, Cl, HOCH2CH2, Br), (M-12702, CH3, CH3, Cl, HOCH2CH2, CH3), (M-12703, CH3, CH3, Cl, HOCH2CH2CH2, H), (M-12704, CH3, CH3, Cl, HOCH2CH2CH2, Cl), (M-12705, CH3, CH3, Cl, HOCH2CH2CH2, F), (M-12706, CH3, CH3, Cl, HOCH2CH2CH2, CF3), (M-12707, CH3, CH3, Cl, HOCH2CH2CH2, Br), (M-12708, CH3, CH3, Cl, HOCH2CH2CH2, CH3), (M-12709, CH3, CH3, Cl, HOCH2CH2CH2CH2, H), (M-12710, CH3, CH3, Cl, HOCH2CH2CH2CH2, Cl), (M-12711, CH3, CH3, Cl, HOCH2CH2CH2CH2, F), (M-12712, CH3, CH3, Cl, HOCH2CH2CH2CH2, CF3), (M-12713, CH3, CH3, Cl, HOCH2CH2CH2CH2, Br), (M-12714, CH3, CH3, Cl, HOCH2CH2CH2CH2, CH3), (M-12715, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2H), (M-12716, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2Cl), (M-12717, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2, F), (M-12718, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2CF3), (M-12719, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2, Br), (M-12720, CH3, CH3, Cl, HOCH2CH2CH2CH2CH2CH3), (M-12721, CH3, CH3, Cl, HOCH2CH2OCH2CH2, H), (M-12722, CH3, CH3, Cl, HOCH2CH2OCH2CH2, Cl), (M-12723, CH3, CH3, Cl, HOCH2CH2OCH2CH2, F), (M-12724, CH3, CH3, Cl, HOCH2CH2OCH2CH2, CF3), (M-12725, CH3, CH3, Cl, HOCH2CH2OCH2CH2, Br), (M-12726, CH3, CH3, Cl, HOCH2CH2OCH2CH2, CH3), (M-12727, CH3, CH3, Cl, (Me)2N, H), (M-12728, CH3, CH3, Cl, (Me)2N, Cl), (M-12729, CH3, CH3, Cl, (Me)2N, F), (M-12730, CH3, CH3, Cl, (Me)2N, CF3), (M-12731, CH3, CH3, Cl, (Me)2N, Br), (M-12732, CH3, CH3, Cl, (Me)2N, CH3), (M-12733, CH3, CH3, Cl, piperidin-4-yl-methyl, H), (M-12734, CH3, CH3, Cl, piperidin-4-yl-methyl, Cl), (M-12735, CH3, CH3, Cl, piperidin-4-yl-methyl, F), (M-12736, CH3, CH3, Cl, piperidin-4-yl-methyl, CF3), (M-12737, CH3, CH3, Cl, piperidin-4-yl-methyl, Br), (M-12738, CH3, CH3, Cl, piperidin-4-yl-methyl, CH3), (M-12739, CH3, CH3, Cl, cyclohexylmethyl, H), (M-12740, CH3, CH3, Cl, cyclohexylmethyl, Cl), (M-12741, CH3, CH3, Cl, cyclohexylmethyl, F), (M-12742, CH3, CH3, Cl, cyclohexylmethyl, CF3), (M-12743, CH3, CH3, Cl, cyclohexylmethyl, Br), (M-12744, CH3, CH3, Cl, cyclohexylmethyl, CH3), (M-12745, H, H, H, CH3, H), (M-12746, H, H, H, CH3, Cl), (M-12747, H, H, H, CH3, F), (M-12748, H, H, H, CH3, CF3), (M-12749, H, H, H, CH3, Br), (M-12750, H, H, H, CF3, CH3), (M-12751, H, H, F, CF3, H), (M-12752, H, H, F, CF3, Cl), (M-12753, H, H, F, CF3, F), (M-12754, H, H, F, CF3, CF3), (M-12755, H, H, F, CF3, Br), (M-12756, H, H, F, CF3, CH3), (M-12757, H, H, Cl, CF3, H), (M-12758, H, H, Cl, CF3, Cl), (M-12759, H, H, Cl, CF3, F), (M-12760, H, H, Cl, CF3, CF3), (M-12761, H, H, Cl, CF3, Br), (M-12762, H, H, Cl, CF3, CH3), (M-12763, H, F, H, CF3, H), (M-12764, H, F, H, CF3, Cl), (M-12765, H, F, H, CF3, F), (M-12766, H, F, H, CF3, CF3), (M-12767, H, F, H, CF3, Br), (M-12768, H, F, H, CF3, CH3), (M-12769, H, F, F, CF3, H), (M-12770, H, F, F, CF3, Cl), (M-12771, H, F, F, CF3, F), (M-12772, H, F, F, CF3, CF3), (M-12773, H, F, F, CF3, Br), (M-12774, H, F, F, CF3, CH3), (M-12775, H, F, Cl, CF3, H), (M-12776, H, F, Cl, CF3, Cl), (M-12777, H, F, Cl, CF3, F), (M-12778, H, F, Cl, CF3, CF3), (M-12779, H, F, Cl, CF3, Br), (M-12780, H, F, Cl, CF3, CH3), (M-12781, H, CH3, H, CF3, H), (M-12782, H, CH3, H, CF3, Cl), (M-12783, H, CH3, H, CF3, F), (M-12784, H, CH3, H, CF3, CF3), (M-12785, H, CH3, H, CF3, Br), (M-12786, H, CH3, H, CF3, CH3), (M-12787, H, CH3, F, CF3, H), (M-12788, H, CH3, F, CF3, Cl), (M-12789, H, CH3, F, CF3, F), (M-12790, H, CH3, F, CF3, CF3), (M-12791, H, CH3, F, CF3, Br), (M-12792, H, CH3, F, CF3, CH3), (M-12793, H, CH3, Cl, CF3, H), (M-12794, H, CH3, Cl, CF3, Cl), (M-12795, H, CH3, Cl, CF3, F), (M-12796, H, CH3, Cl, CF3, CF3), (M-12797, H, CH3, Cl, CF3, Br), (M-12798, H, CH3, Cl, CF3, CH3), (M-12799, F, H, H, CF3, i-Pr), (M-12800, F, H, H, CF3, Cl), (M-12801, F, H, H, CF3, F), (M-12802, F, H, H, CF3, CF3), (M-12803, F, H, H, CF3, Br), (M-12804, F, H, H, CF3, CH3), (M-12805, F, H, F, CF3, H), (M-12806, F, H, F, CF3, Cl), (M-12807, F, H, F, CF3, F), (M-12808, F, H, F, CF3, CF3), (M-12809, F, H, F, CF3, Br), (M-12810, F, H, F, CF3, CH3), (M-12811, F, H, Cl, CF3, H), (M-12812, F, H, Cl, CF3, Cl), (M-12813, F, H, Cl, CF3, F), (M-12814, K, H, Cl, CF3, CF3), (M-12815, F, H, Cl, CF3, Br), (M-12816, F, H, Cl, CF3, CH3), (M-12817, F, F, H, CF3, H), (M-12818, F, F, H, CF3, Cl), (M-12819, F, F, H, CF3, F), (M-12820, F, F, H, CF3, CF3), (M-12821, F, F, H, CF3, Br), (M-12822, F, F, H, CF3, CH3), (M-12823, F, F, F, CF3, H), (M-12824, F, F, F, CF3, Cl), (M-12825, F, F, F, CF3, F), (M-12826, F, F, F, CF3, CF3), (M-12827, F, F, F, CF3, Br), (M-12828, V, F, F, CF3, CH3), (M-12829, F, F, Cl, CF3, H), (M-12830, F, F, Cl, CF3, Cl), (M-12831, F, F, Cl, CF3, F), (M-12832, F, F, Cl, CF3, CF3), (M-12833, F, F, Cl, CF3, Br), (M-12834, F, F, Cl, CF3, CH3), (M-12835, F, CH3, H, CF3, H), (M-12836, F, CH3, H, CF3, Cl), (M-12837, F, CH3, H, CF3, F), (M-12838, F, CH3, H, CF3, CF3), (M-12839, F, CH3, H, CF3, Br), (M-12840, F, CH3, H, CF3, CH3), (M-12841, F, CH3, F, CF3, H), (M-12842, F, CH3, F, CF3, Cl), (M-12843, F, CH3, F, CF3, F), (M-12844, F, CH3, F, CF3, CF3), (M-12845, F, CH3, F, CF3, Br), (M-12846, F, CH3, F, CF3, CH3), (M-12847, F, CH3, Cl, CF3, H), (M-12848, F, CH3, Cl, CF3, Cl), (M-12849, F, CH3, Cl, CF3, P), (M-12850, F, CH3, Cl, CF3, CF3), (M-12851, F, CH3, Cl, CF3, Br), (M-12852, F, CH3, Cl, CF3, CH3), (M-12853, Cl, H, H, CF3, i-Pr), (M-12854, Cl, H, H, CF3, Cl), (M-12855, Cl, H, H, CF3, F), (M-12856, Cl, H, H, CF3, CF3), (M-12867, Cl, H, H, CF3, Br), (M-12858, Cl, H, H, CF3, CH3), (M-12859, Cl, H, F, CF3, i-Pr), (M-12860, Cl, H, F, CF3, Cl), (M-12861, Cl, H, F, CF3, F), (M-12862, Cl, H, F, CF3, CF3), (M-12863, Cl, H, F, CF3, Br), (M-12864, Cl, H, F, CF3, CH3), (M-12865, Cl, H, Cl, CF3, H), (M-12866, Cl, H, Cl, CF3, Cl), (M-12867, Cl, Ft, Cl, CF3, F), (M-12868, Cl, H, Cl, CF3, CF3), (M-12869, Cl, H, Cl, CF3, Br), (M-12870, Cl, H, Cl, CF3, CH3), (M-12871, Cl, F, H, CF3, i-Pr), (M-12872, Cl, F, H, CF3, Cl), (M-12873, Cl, F, H, CF3, F), (M-12874, Cl, F, H, CF3, CF3), (M-12875, Cl, F, H, CF3, Br), (M-12876, Cl, F, H, CF3, CH3), (M-12877, Cl, F, F, CF3, H), (M-12878, Cl, F, F, CF3, Cl), (M-12879, Cl, F, F, CF3, F), (M-12880, Cl, F, F, CF3, CF3), (M-12881, Cl, F, F, CF3, Br), (M-12882, Cl, F, F, CF3, CH3), (M-12883, Cl, F, Cl, CF3, H), (M-12884, Cl, F, Cl, CF3, Cl), (M-12885, Cl, F, Cl, CF3, F), (M-12886, Cl, F, Cl, CF3, CF3), (M-12887, Cl, F, Cl, CF3, Br), (M-12888, Cl, F, Cl, CF3, CH3), (M-12889, Cl, CH3, H, CF3, i-Pr), (M-12890, Cl, CH3, H, CF3) Cl), M-12891, Cl, CH3, H, CF3, F), (M-12892, Cl, CH3, H, CF3, CF3), (M-12893, Cl, CH3, H, CF3, Br), (M-12894, Cl, CH3, H, CF3, CH3), (M-12895, Cl, CH3, F, CF3, i-Pr), (M-12896, Cl, CH3, F, CF3, Cl), (M-12897, Cl, CH3, F, CF3, F), (M-12898, Cl, CH3, F, CF3, CF3), (M-12899, Cl, CH3, F, CF3, Br), (M-12900, Cl, CH3, F, CF3, CH3), (M-12901, Cl, CH3, Cl, CF3, H), (M-12902, Cl, CH3, Cl, CF3, Cl), (M-12903, Cl, CH3, Cl, CF3, F), (M-12904, Cl, CH3, Cl, CF3, CF3), (M-12905, Cl, CH3, Cl, CF3, Br), (M-12906, Cl, CH3, Cl, CF3, CH3), (M-12907, CH3, H, H, CF3, i-Pr), (M-12908, CH3, H, H, CF3, Cl), (M-12909, CH3, H, H, CF3, F), (M-12910, CH3, H, H, CF3, CF3), (M-12911, CH3, H, H, CF3, Br), (M-12912, CH3, H, H, CF3, CH3), (M-12913, CH3, H, F, CF3, H), (M-12914, CH3, H, F, CF3, Cl), (M-12915, CH3, H, F, CF3, F), (M-12916, CH3, H, F, CF3, CF3), (M-12917, CH3, H, F, CF3, Br), (M-12918, CH3, H, F, CF3, CH3), (M-12919, CH3, H, Cl, CF3, H), (M-12920, CH3, H, Cl, CF3, Cl), (M-12921, CH3, H, Cl, CF3, F), (M-12922, CH3, H, Cl, CF3, CF3), (M-12923, CH3, H, Cl, CF3, Br), (M-12924, CH3, H, Cl, CF3, CH3), (M-12925, CH3, F, H, CF3, H), (M-12926, CH3, F, H, CF3, Cl), (M-12927, CH3, F, H, CF3, F), (M-12928, CH3, F, H, CF3, CF3), (M-12929, CH3, F, H, CF3, Br), (M-12930, CH3, F, H, CF3, CH3), (M-12931, CH3, F, F, CF3, H), (M-12932, CH3, F, F, CF3, Cl), (M-12933, CH3, F, F, CF3, F), (M-12934, CH3, F, F, CF3, CF3), (M-12935, CH3, F, F, CF3, Br), (M-12936, CH3, F, F, CF3, CH3), (M-12937, CH3, F, Cl, CF3, H), (M-12938, CH3, F, Cl, CF3, Cl), (M-12939, CH3, F, Cl, CF3, F), (M-12940, CH3, F, Cl, CF3, CF3), (M-12941, CH3, F, Cl, CF3, Br), (M-12942, CH3, F, Cl, CF3, CH3), (M-12943, CH3, CH3, H, CF3, H), (M-12944, CH3, CH3, H, CF3, Cl), (M-12945, CH3, CH3, H, CF3, F), (M-12946, CH3, CH3, H, CF3, CF3), (M-12947, CH3, CH3, H, CF3, Br), (M-12948, CH3, CH3, H, CF3, CH3), (M-12949, CH3, CH3, F, CF3, H), (M-12950, CH3, CH3, F, CF3, Cl), (M-12951, CH3, CH3, F, CF3, F), (M-12952, CH3, CH3, F, CF3, CF3), (M-12953, CH3, CH3, F, CF3, Br), (M-12954, CH3, CH3, F, CF3, CH3), (M-12955, CH3, CH3, Cl, CF3, H), (M-12956, CH3, CH3, Cl, CF3, Cl), (M-12957, CH3, CH3, Cl, CF3, F), (M-12958, CH3, CH3, Cl, CF3, CF3), (M-12959, CH3, CH3, Cl, CF3, Br), (M-12960, CH3, CH3, Cl, CF3, CH3),
- Human TPO (hTPO) and murine TPO (in TPO) were purchased from R&D Systems.
- We examined the ability of the compound in promoting differentiation of human hematopoietic progenitor cells into mature megakaryocytes. Human bone marrow cells (2.2×105 cells) were plated in 3-cm dishes and cultured in methylcellulose in Iscove's Modified Dulbccco's medium in the presence of 1% of the compound dissolved in 10% ethanol. After incubation at 37° C. for 7 days in the 5% CO2 incubator, the megakaryocyte colonies were counted. The results are shown in
FIG. 1 . - The TPO dependent BaF/hTPOR cell line which was established by introducing human TPO receptor (hTPOR) into BaF-B03 cells according to Collins et al (J. Cell. Physiol., 137:293-298 (1988)) was used to test the thrombopoietic activity of the present compound. The DNA sequences and encoded peptide sequences for human hTPOR have been described by Vigon et al (Proc. Natl. Acad. Sci. USA, 89:5640-5644 (1992)). TPO dose not have any ability to support proliferation of interleukin-3 dependent parental cell line BaF-B03. BAF/hTPOR cells were maintained in RPMI medium and WEHI-3B conditioned medium as a source of murine interleukin-3 (IL-3). These cells were washed and resuspended in RPMI medium without a source of murine IL-3 and seeded into each well of 96-well microtiter plates at a density of 5×104 cells per well in the absence or presence of various concentration of hTPO or the present compound. After incubation at 37° C. for 20 hours in the 5% CO2 incubator, 10% WST-1 reagent (Takara Biomedicals, Japan) was added to each wells and the cells were further incubated for 4 hours. The absorbance at 450 nm was measured and the results are shown in
FIG. 2 . Effect of the present compound on the growth of BAF/mTPOR cell line which was established by introducing murine TPO receptor (mTPOR) into BAF-B03 cells is shown inFIG. 3 . Table 8 exemplifies the ED50 for tested compounds of the present invention, wherein the ED50 is the half concentration of the concentration showing the maximum thrombopoietic activity. -
TABLE 33 Compound ED50 ED50 Compound ED50 ED50 No. (μM) No. (μM) No. (μM) No. (μM) A-1 0.117 A-54 0.065 B-6 0.084 G-5 0.260 A-2 0.066 A-55 0.037 B-7 0.059 G-6 0.370 A-3 0.218 A-56 0.066 B-8 0.378 G-7 0.400 A-4 0.124 A-57 0.019 B-9 0.082 G-8 0.360 A-5 0.984 A-58 0.497 B-11 0.236 H-7 0.038 A-6 0.248 A-59 0.164 B-12 0.207 H-8 0.250 A-8 0.529 A-60 0.023 B-13 0.213 J-11 0.311 A-9 0.504 A-61 0.207 B-14 0.305 J-12 0.107 A-10 0.365 A-62 0.101 B-15 0.197 J-13 0.116 A-11 0.0335 A-63 0.025 B-16 0.182 J-14 0.036 A-14 0.017 A-64 0.204 B-17 0.244 J-15 0.011 A-17 0.864 A-65 0.028 B-18 0.15 K-1 0.189 A-18 0.132 A-66 0.211 B-19 0.15 K-2 0.975 A-19 0.170 A-68 0.222 B-20 0.425 K-3 0.693 A-20 0.610 A-69 0.071 B-25 0.367 K-5 0.403 A-23 0.337 A-70 0.089 B-26 0.346 K-6 0.077 A-24 0.288 A-72 0.119 B-27 0.707 K-10 0.475 A-25 0.150 A-73 0.075 B-28 0.565 K-11 0.373 A-26 0.098 A-74 0.472 B-29 0.181 K-12 0.208 A-27 0.193 A-75 0.073 B-30 0.177 K-13 0.260 A-28 0.099 A-76 0.205 B-31 0.178 K-15 0.465 A-29 0.289 A-77 0.110 B-32 0.123 L-1 0.208 A-30 0.274 A-78 0.408 B-33 0.372 L-2 0.143 A-31 0.056 A-79 0.410 B-34 0.398 L-3 0.321 A-32 0.040 A-80 0.066 B-35 0.186 L-4 0.256 A-35 0.096 A-81 0.071 B-36 0.163 A-36 0.095 A-82 0.199 B-37 0.139 A-37 0.096 A-83 0.077 B-38 0.239 A-38 0.245 A-84 0.023 B-39 0.729 A-39 0.044 A-85 0.026 B-40 0.201 A-40 0.047 A-86 0.243 B-41 0.19 A-41 0.039 A-87 0.710 B-42 0.236 A-42 0.050 A-88 0.028 B-43 0.303 A-43 0.071 A-89 0.072 B-46 0.213 A-44 0.227 A-90 0.805 C-4 0.922 A-45 0.203 A-91 0.076 D-1 0.276 A-46 0.263 A-92 0.178 F-1 0.174 A-47 0.512 A-93 0.008 F-2 0.144 A-48 0.473 B-1 0.081 F-3 0.198 A-49 0.116 B-2 0.257 G-1 0.261 A-50 0.113 B-3 0.156 G-2 0.299 A-51 0.568 B-4 0.089 G-3 0.430 A-52 0.425 B-5 0.123 G-4 0.240 - As shown in
FIG. 1 , addition of the compounds of the present invention induced forming megakaryocyte colonies and the number of colonies increased depending on the concentration of the compounds. This result revealed that the compounds of the present invention induced the differentiation of human bone marrow cells and produced megakaryocytes having ability of producing platelet. - The compound supported the proliferation of TPO-dependent BaF/hTPOR in a dose-dependent manner as shown in
FIG. 2 . BaF/mTPOR expressing murine TPOR was not induced the proliferation by compounds as shown inFIG. 3 . These results suggest that the compound of the present invention exert the thrombopoietic activity by interacting with hTPOR because it is active only in cells expressing hTPOR. - Granules are prepared using the following ingredients.
-
Ingredients The compound represented by the Formula (I) 10 mg Lactose 700 mg Corn starch 274 mg HPC-L 16 mg 1000 mg - The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. They are mixed by a twin shell blender. An aqueous solution of HPC-L (low mucosity hydroxypropylcellulose) is added to the mixture and the resulting mixture is kneaded, granulated (by the extrusion with pore size 0.5 to 1 mm mesh), and dried. The dried granules thus obtained are sieved by a swing sieve (12/60 mesh) to yield the granules.
- Powders for filling capsules are prepared using the following ingredients.
-
Ingredients The compound represented by the formula (I) 10 mg Lactose 79 mg Corn starch 10 mg Magnesium stearate 1 mg 100 mg - The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. These ingredients and magnesium stearate are mixed by a twin shell blender. 100 mg of the 10-fold trituration is filled into a No. 5 hard gelatin capsule.
- Granules for filling capsules are prepared using the following ingredients
-
Ingredients The compound represented by the formula (I) 15 mg Lactose 90 mg Corn starch 42 mg HPC- L 3 mg 150 mg - The compound represented by the formula (I) and lactose are made pass through a 60 mesh sieve. Corn starch is made pass through a 120 mesh sieve. After mixing them, an aqueous solution of HPC-L is added to the mixture and the resulting mixture is kneaded, granulated, and dried. After the dried granules are lubricated, 150 mg of that are filled into a No. 4 hard gelatin capsule.
- Tablets are prepared using the following ingredients.
-
Ingredients The compound represented by the formula (I) 10 mg Lactose 90 mg Microcrystal cellulose 30 mg CMC- Na 15 mg Magnesium stearate 5 mg 150 mg - The compound represented by the formula (I), lactose, microcrystal cellulose, and CMC-Na (carboxymethylcellulose sodium salt) are made pass through a 60 mesh sieve and then mixed. The resulting mixture is mixed with magnesium stearate to obtain the mixed powder for the tablet formulation. The mixed powder is compressed to yield tablets of 150 mg.
- Intravenous formulations are prepared using the following ingredients.
-
Ingredients The compound represented by the formula (I) 100 mg Saturated fattyacid glyceride 1000 ml - Usually a solution of ingredients above described is administered intravenously to a patient by the speed of 1 ml/min.
- The compounds of the present invention have thrombopoietin receptor agonism and are useful as the treating or preventing agent for hemopathy accompanied with unusual count of platelet, for example, thrombocytopenia and the like
Claims (47)
1. A pharmaceutical composition exhibiting thrombopoietin receptor agonism which contains as an active ingredient a compound of the general formula (I):
X1—Y1-Z1-W1 (I)
X1—Y1-Z1-W1 (I)
wherein X1 is optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl;
Y1 is —NRACO—(CRCRD)0-2—, —NRACO—(CH2)0-2—V—, —NRACRC═CRD—, —V—(CH2)1-5—NRACO—(CH2)0-2—, —V—(CH2)1-5—CONRA—(CH2)0-2—, —CONRA—(CH2)0-2—, —(CH2)0-2—NRA—SO2—(CH2)0-2—, —(CH2)0-2—, SO2—NRA—(CH2)0-2—, —NRA—(CH2)0-2, —NRA—CO—NRA—, —NRA—CS—NRA—, —N═C(—SRA)—NRA, —NRACSNRACO—, —N═C(—SRA)—NRACO—, —NRA—(CH2)1-2—NRA—CO—, —NRACONRANRBCO—, or —N═C(—NRARA)—NRA—CO—,
wherein RA is each independently a hydrogen atom or lower alkyl; RB is a hydrogen atom or phenyl; RC and RD are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino; V is an oxygen atom or a sulfur atom;
Z1 is optionally substituted phenylene, optionally substituted monocyclic heteroarylene, optionally substituted monocyclic non-aromatic heterocycle-diyl, or optionally substituted monocyclic cycloalkane-diyl;
W1 is a group represented by the formula:
wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted nonaromatic heterocyclic group, or optionally substituted amino;
R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
A1 is a optionally substituted aryl or optionally substituted heteroaryl;
a broken line (---) represents the presence or absence of a bond,
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
2. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of claim 1 , wherein X1 is optionally substituted heteroaryl.
3. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of claim 1 , wherein X1 is a group represented by the formula:
5. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein Y1 is —NHCO—, —CONH—, —NHCH2—, —NHCO—CH═CH—, or —NHSO2—.
6. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein Y1 is —NHCO—.
7. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein Z1 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl.
8. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein R1 is a hydrogen atom or lower alkyl.
9. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein R2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino.
10. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein W1 is a group represented by the formula:
wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
a broken line (---) represents the presence or absence of a bond;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy.
11. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , wherein W1 is a group represented by the formula:
12. A pharmaceutical composition exhibiting thrombopoietin receptor agonism of any one of claims 1 to 4 , which is a platelet production modifier.
13. A pharmaceutical composition for platelet production modification, comprising at least one compound according to claim 1 and at least one of an excipient, binder, penetrant, disintegrator, or lubricant.
14. A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of claims 1 to 4 in a pharmaceutically effective amount.
15. A compound represented by the general formula (II):
X2—Y2-Z2-W2 (II)
X2—Y2-Z2-W2 (II)
wherein X2 is optionally substituted 5-member heteroaryl or optionally substituted pyridyl:
Y2 is —NRACO—(CRCRD)0-2—, —NRACO—(CH2)0-2—V—, —NRACO—CRC═CRD—, —V—(CH2)1-5—NRACO—(CH2)0-2—, —V—(CH2)1-5—CONRA—(CH2)0-2—, —CONRA—(CH2)0-2, —(CH2)0-2—NRASO2—(CH2)0-2—, —(CH2)0-2—SO2—NRA—(CH2)0-2—, —NRA—(CH2)0-2—, —NRA—CO—NRA—, —NRA—CS—NRA—, —N═C(—SRA)—NRA—, —NRACSNRA—CO—, —N═C(—SRA)—NRACO—, —NRA—(CH2)1-2—NRA—CO—, —NRACONRANRB—CO—, or —N═C(—NRARA)—NRA—CO—,
wherein RA is each independently a hydrogen atom or lower alkyl; RB is a hydrogen atom or phenyl; RC and RD are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroaryl-alkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino; V is an oxygen atom or a sulfur atom;
Z2 is optionally substituted phenylene, optionally substituted 2,5-pyridine-diyl, optionally substituted 2,5-thiophene-diyl, or optionally substituted 2,5-furan-diyl;
W2 is a group represented by the formula:
wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted nonaromaticheterocyclic group, or optionally substituted amino;
R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
A2 is a optionally substituted aryl or optionally substituted heteroaryl;
a broken line (---) represents the presence or absence of a bond,
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
16. A compound of claim 15 , wherein X2 is a group represented by the formula:
wherein R10 and R11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl,
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
17. A compound in of claim 15 or 16 , wherein X2 is a group represented by the formula:
wherein R16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted amino carbonyl;
R17, R18, R19, R20, R21, R22, and R23 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl;
substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromaticheterocyclic group, or heteroaryl; or
R16 and R17 taken together may form —CH2—, —CH2CH2—, —CH2CH2CH2—, —OCH2—, or —SCH2—;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
18. A compound of any one of claims 15 or 16 , wherein Y2 is —NHCO—;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
19. A compound of any one of claims 15 or 16 , wherein Z2 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
20. A compound of any one of claims 15 or 16 , wherein R1 is a hydrogen atom or lower alkyl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
21. A compound of any one of claims 15 or 16 , wherein R2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino;
its prodrug, or their pharmaceutically acceptable salts or solvates thereof.
22. A compound of any one of claims 15 or 16 , wherein W2 is a group represented by the formula:
23. A compound of any one of claims 15 or 16 , wherein W2 is a group represented by the formula:
wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
24. A compound of any one of claims 15 or 16 , wherein W2 is a group represented by the formula:
25. (canceled)
26. (canceled)
27. A compound represented by the general formula (IV-B):
wherein R28, R29, and R30 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, or heteroaryl;
substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, or heteroaryl;
R31 and R32 are each independently a hydrogen atom, lower alkyl, halogen atom, haro(lower)alkyl, lower alkyloxy, halo(lower)alkyloxy, or hydroxy;
W4 is a group represented by the formula:
wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group, each substituted by one or more substituent(s) selected
from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
R24 is a hydrogen atom or lower alkyl;
T is —CH2-, —CH2CH2-, —CH2CH2CH2-, —OCH2-, or —SCH2-;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
28. A pharmaceutical composition containing as the active ingredient a compound of any one of claims 15 or 27 .
29. A pharmaceutical composition containing as the active ingredient a compound of any one of claims 15 or 27 , which is exhibiting thrombopoietin receptor agonism.
30. A platelet production modifier which contains as the active ingredient a compound of any one of claims 15 or 27 .
31. A pharmaceutical composition for platelet production modification, comprising at least one compound according to any one of claims 15 or 27 and at least one of an excipient, binder, penetrant, disintegrator, or lubricant.
32. A method for modifying a platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of claims 15 or 27 in a pharmaceutically effective amount.
33. A compound represented by the general formula (II):
X2—Y2-Z2-W2 (II)
X2—Y2-Z2-W2 (II)
wherein X2 is optionally substituted 5-membered heteroaryl or optionally substituted pyridyl;
Y2 is —NRACO—(CRCRD)0-2—, —NRACO—(CH2)0-2—V—, —NRACO—CRC═CRD—, —V—(CH2)1-5—NRACO—(CH2)0-2—, —V—(CH2)1-5—CONRA—(CH2)0-2—, —CONRA—(CH2)0-2, —(CH2)0-2—NRASO2—(CH2)0-2—, —(CH2)0-2—SO2—NRA—(CH2)0-2—, —NRA—(CH2)0-2—, —NRA—CO—NRA—, —NRA—CS—NRA—, —N═C(—SRA)—NRA—, —NRACSNRACO—, —N═C(—SRA)—NRACO—, —NRA—(CH2)1-2—NRA—CO—, —NRACONRANRB—CO—, or —N═C(—NRARA)—NRA—CO—,
wherein RA is each independently a hydrogen atom or lower alkyl; RB is a hydrogen atom or phenyl; RC and RD are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino;
V is an oxygen atom or a sulfur atom;
Z2 is optionally substituted phenylene, optionally substituted 2,5-pyridine-diyl, optionally substituted 2,5-thiophene-diyl, or optionally substituted 2,5-furan-diyl;
W2 is a group represented by the formula:
wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted non-aromatic heterocyclic group, or optionally substituted amino; R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
A2 is optionally substituted aryl or optionally substituted heteroaryl;
a broken line (---) represents the presence or absence of a bond, provided that,
1) when X2 is thiazolyl optionally substituted with alkyl, or benzothiazolyl optionally substituted with alkoxyl or diethylamino; Z2 is 1,4-phenylene; and
W2 is a group represented by the formula:
R2 is not optionally substituted imidazolyl, optionally substituted triazolyl, or optionally substituted tetrazolyl,
2) when X2 is 2-pyridyl; Y2 is —NHCO—CH═CH—, or —NHCSNHCO—; Z2 is 1,4-phenylene; and W2 is a group represented by the formula:
R2 is not triazolyl,
3) when X2 is benzothiazolyl; Y2 is —NHCO—CH═CH—; Z2 is 1,4-phenylene; and
W2 is a group represented by the formula:
R2 is not 2-pyridyl or carboxymethyl,
4) when X2 is benzothiazolyl; Y2 is —NHCO—; and Z2 is 1,4-phenylene;
W2 is not a group represented by the formula:
5) when X2 is thiazolyl optionally substituted with methyl, t-butyl, or unsubstituted phenyl, or benzothiazolyl optionally substituted with alkyl or diethylaminoethyl; Z2 is optionally substituted phenylene; and W2 is —CH═O, Y2 is not —NHCO—(CH2)0-2—, —NHCO—CH═CH—, —NHCO—CH2—O—, or —NHCO—CH2—NMe-,
6) when Y2 is —NH—CH2—; Z2 is 1,4-phenylene; W2 is optionally substituted tetrazolyl wherein 2-position is substituted phenyl, X2 is not thiadiazolyl, thiazolyl, benzothiazolyl, oxadiazazolyl, imidazolyl, or oxazolyl,
7) when X2 is optionally substituted benzothiazolyl; Z2 is 1,4-phenylene; and
W2 is a group represented by the formula:
Y2 is not —NHCO—, —NH—CH2—, —NEt-CH2—, or —NH—
8) when X2 is optionally substituted benzothiazolyl; Y2 is —NH—; and Z2 is 1,4-phenylene; W2 is not —CH2COOH or —CH2COOEt,
9) when X2 is optionally substituted benzothiazolyl; Y2 is —NH—; and Z2 is 2,5-pyridinediyl;
W2 is not —COOH or —CONH2,
10) when X2 is optionally substituted benzothiazolyl;
Z2 is phenylene optionally substituted with methyl or chlorine atom; and W2 is —COOH, —COOEt, or —CONH2, Y2 is not —NH—, —NH—CH2—, —NH—CO—, or —NH—SO2—, its prodrug, or pharmaceutically acceptable salts or solvates thereof.
34. A compound of claim 33 wherein X2 is represented by the formula:
wherein R10 and R11 are each independently a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, optionally substituted aminocarbonyl, optionally substituted heteroaryl, or optionally substituted aryl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
35. A compound of claim 33 or 34 wherein X2 is represented by the formula:
wherein R16 is a hydrogen atom, optionally substituted lower alkyl, carboxy, lower alkyloxycarbonyl, halogen atom, or optionally substituted aminocarbonyl;
R17, R18, R19, R20, R21, R22, and R23 are each independently a hydrogen atom, optionally substituted lower alkyl by one or more substituent(s) selected from substituent group B, cycloalkyl, optionally substituted alkyoxy by one or more substituent(s) selected from substituent group B, alkylthio, halogen atom, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, optionally substituted heteroaryl by one or more substituent(s) selected from substituent group C, or optionally substituted nonaromatic heterocyclic group by one or more substituent(s) selected from substituent group C;
substituent group B consists of hydroxy, alkyloxy, halogen atom, carboxy, lower alkyloxycarbonyl, aryloxycarbonyl, optionally substituted amino, optionally substituted phenyl by one or more substituent(s) selected from substituent group C, non-aromatic heterocyclic group, and heteroaryl;
substituent group C consists of hydroxy, alkyl, halogen atom, halo(lower)alkyl, carboxy, lower alkyloxycarbonyl, alkyloxy, optionally substituted amino, non-aromatic heterocyclic group, and heteroaryl; or
R16 and R17 taken together may form —CH2—, —CH2CH2—, —CH2CH2CH2—, —OCH2—, or SCH2—;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
36. A compound of any one of claims 33 or 34 , wherein Y2 is —NHCO—;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
37. A compound of any one of claims 33 or 34 , wherein Z2 is 1,4-phenylene optionally substituted with halogen atom or lower alkyl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
38. A compound of any one of claims 33 or 34 , wherein R1 is a hydrogen atom or lower alkyl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
39. A compound of any one of claims 33 or 34 , wherein R2 is a hydrogen atom, lower alkyl, halogen atom, lower alkyloxy, lower alkylthio, or optionally substituted amino;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
40. A compound of any one of claims 33 or 34 , wherein W2 is a group represented by the formula:
wherein R1, R2, R3, R4, R7, and R8 are each independently a hydrogen atom, halogen atom, optionally substituted lower alkyl, optionally substituted lower alkyloxy, optionally substituted lower alkylthio, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted nonaromaticheterocyclic group, or optionally substituted amino;
R5, R6, and R9 are each independently a hydrogen atom, optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, or optionally substituted non-aromatic heterocyclic group;
A2 is a optionally substituted aryl or optionally substituted heteroaryl;
provided that R2 is not imidazolyl, triazolyl, or tetrazolyl;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
41. A compound of any one of claims 33 or 34 , wherein W2 is a group represented by the formula:
wherein R13 is a hydrogen atom, lower alkyl, lower alkyloxy, lower alkylthio, or halogen atom;
R14 and R15 are each independently a hydrogen atom, or optionally substituted lower alkyl, optionally substituted lower alkenyl, optionally substituted lower alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, or optionally substituted heteroarylalkyl, each substituted by one or more substituent(s) selected from substituent group A;
substituent group A consists of a halogen atom, halo(lower)alkyl, optionally substituted amino, carboxy, lower alkylthio, lower alkylsilyl, or lower alkyloxy;
its prodrug, or pharmaceutically acceptable salts or solvates thereof.
42. A compound of any one of claims 33 or 34 , wherein W2 is a group represented by the formula:
43. A pharmaceutical composition containing as an active ingredient a compound of any one of claims 33 or 34 .
44. A pharmaceutical composition containing as an active ingredient a compound of any one of claims 33 or 34 , which exhibits thrombopoietin receptor agonism.
45. A composition for use as a platelet production modifier which contains as an active ingredient a compound of any one of claims 33 or 34 .
46. A pharmaceutical composition for platelet production modification, comprising at least one compound according to claim 33 or 34 and at least one of an excipient, binder, penetrant, disintegrator, or lubricant.
47. A method for modifying the platelet production of a mammal, including a human, which comprises administration to said mammal of a compound of any one of claims 33 or 34 in a pharmaceutically effective amount.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/504,604 US20100022542A1 (en) | 2000-01-24 | 2009-07-16 | Compounds exhibiting thrombopoietin receptor agonism |
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000-13770 | 2000-01-24 | ||
| JP2000013770 | 2000-01-24 | ||
| JP2000030593 | 2000-02-08 | ||
| JP2000-30593 | 2000-02-08 | ||
| PCT/JP2001/000411 WO2001053267A1 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
| US10/169,362 US7582665B2 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
| US12/504,604 US20100022542A1 (en) | 2000-01-24 | 2009-07-16 | Compounds exhibiting thrombopoietin receptor agonism |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/169,362 Division US7582665B2 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
| PCT/JP2001/000411 Division WO2001053267A1 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20100022542A1 true US20100022542A1 (en) | 2010-01-28 |
Family
ID=26583969
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/169,362 Expired - Fee Related US7582665B2 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
| US12/504,604 Abandoned US20100022542A1 (en) | 2000-01-24 | 2009-07-16 | Compounds exhibiting thrombopoietin receptor agonism |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/169,362 Expired - Fee Related US7582665B2 (en) | 2000-01-24 | 2001-01-23 | Compounds exhibiting thrombopoietin receptor agonism |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US7582665B2 (en) |
| EP (1) | EP1253142A4 (en) |
| JP (2) | JP4136371B2 (en) |
| KR (2) | KR100563795B1 (en) |
| CN (1) | CN100491356C (en) |
| AU (1) | AU777777B2 (en) |
| CA (1) | CA2397018C (en) |
| TW (1) | TWI284639B (en) |
| WO (1) | WO2001053267A1 (en) |
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Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090318513A1 (en) * | 2003-08-12 | 2009-12-24 | Shionogi & Co., Ltd. | Compounds exhibiting thrombopoietin receptor agonism |
| US20100267783A1 (en) * | 2007-07-31 | 2010-10-21 | Masami Takayama | Pharmaceutical composition containing optically active compound having thrombopoietin receptor agonist activity, and intermediate therefor |
| US8530668B2 (en) * | 2007-07-31 | 2013-09-10 | Shionogi & Co., Ltd. | Pharmaceutical composition containing optically active compound having thrombopoietin receptor agonist activity, and intermediate therefor |
| US8889722B2 (en) | 2007-07-31 | 2014-11-18 | Shionogi & Co., Ltd. | Pharmaceutical composition containing optically active compound having thrombopoietin receptor agonist activity, and intermediate therefor |
| US8476249B2 (en) | 2009-05-07 | 2013-07-02 | Glaxosmithkline Llc | Method of treating thrombocytopenia |
| US11254767B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as an anti-fouling means |
| US11254768B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as an anti-infective means |
| US11254769B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as a barrier means |
| US11254770B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as a fertilizer means |
| US11254772B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as a treatment means |
| US11254771B1 (en) | 2013-10-28 | 2022-02-22 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as a photographic means |
| US11274175B1 (en) | 2013-10-28 | 2022-03-15 | Joseph Laurino | Conducting polymer, 1-octadecene, polymer with 2,5 furandione, metal salts used as a pesticide means |
Also Published As
| Publication number | Publication date |
|---|---|
| TWI284639B (en) | 2007-08-01 |
| CA2397018A1 (en) | 2001-07-26 |
| EP1253142A1 (en) | 2002-10-30 |
| US7582665B2 (en) | 2009-09-01 |
| US20030195231A1 (en) | 2003-10-16 |
| KR20030016219A (en) | 2003-02-26 |
| EP1253142A4 (en) | 2004-09-15 |
| AU2708901A (en) | 2001-07-31 |
| KR20050085991A (en) | 2005-08-29 |
| CN100491356C (en) | 2009-05-27 |
| CN1419547A (en) | 2003-05-21 |
| JP2008150386A (en) | 2008-07-03 |
| AU777777B2 (en) | 2004-10-28 |
| WO2001053267A1 (en) | 2001-07-26 |
| CA2397018C (en) | 2012-01-03 |
| JP4136371B2 (en) | 2008-08-20 |
| KR100563795B1 (en) | 2006-03-28 |
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