AR056884A1 - Compuestos biciclicos fusionados inhibidores de mtor - Google Patents
Compuestos biciclicos fusionados inhibidores de mtorInfo
- Publication number
- AR056884A1 AR056884A1 ARP060105058A ARP060105058A AR056884A1 AR 056884 A1 AR056884 A1 AR 056884A1 AR P060105058 A ARP060105058 A AR P060105058A AR P060105058 A ARP060105058 A AR P060105058A AR 056884 A1 AR056884 A1 AR 056884A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- aryl
- optionally substituted
- nr313c
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 101150097381 Mtor gene Proteins 0.000 title 1
- 102100023085 Serine/threonine-protein kinase mTOR Human genes 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 100
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 13
- 125000001072 heteroaryl group Chemical group 0.000 abstract 11
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 7
- -1 3-indolyl Chemical group 0.000 abstract 6
- 125000004043 oxo group Chemical group O=* 0.000 abstract 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 abstract 1
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 abstract 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 1
- 125000005015 aryl alkynyl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000004475 heteroaralkyl group Chemical group 0.000 abstract 1
- 229940124302 mTOR inhibitor Drugs 0.000 abstract 1
- 239000003628 mammalian target of rapamycin inhibitor Substances 0.000 abstract 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/06—1,2,4-Triazines
- C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
- C07D253/07—1,2,4-Triazines having 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Transplantation (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Son inhibidores de mTOR y son utiles en el tratamiento del cáncer. Reivindicacion 1: Un compuesto representado por la formula (1), o una sal aceptable para uso farmacéutico del mismo, donde, X1, y X2 son cada uno independientemente N o C-(E1)aa; X5 es N, C-(E1)aa, o N-(E1)aa; X3, X4, X6, y X7 son cada uno independientemente N o C; donde al menos uno de X3, X4, X5, X6 y X7 es independientemente N o N-(E1)aa; es alquilo C0-10, cicloalquilo C3-10, aminometilcicloalquilo C3-10, bicicloalquilo C5- 10, arilo, heteroarilo, aralquilo, heteroaralquilo, heterociclilo o heterobicicloalquilo, cualquiera de los cuales se sustituye opcionalmente con uno o más sustituyentes G11 independientes; Q1 es A(R1)mB(W)n o B(G11)nA(Y)m; A y B son respectivamente, anillos aromáticos o heteroaromáticos de 5 y 6 miembros, fusionados para formar un sistema heteroaromático de 9 miembros con la salvedad de 5-benzo[b]furilo y 3-indolilo; y con la salvedad de 2-indolilo, 2-benzoxazol, 2-benzotiazol, 2-benzimidazolilo, 4-aminopirrolpirimidin-5-ilo, 4-aminopirrolpirimidin-6-ilo y derivados de 7-deaza-7-adenosinilo cuando X1 y X5 son CH, X3, X6 y X7 son C, y X2 y X4 son N; o Q1 es A(R1)mA(Y)m, donde cada A es el mismo anillo o un anillo diferente aromático o heteroaromático de 5 miembros y los dos se fusionan para formar un sistema heteroaromático de 8 miembros; R1 es independientemente, hidrogeno, -N(alquil C0-8)(alquilo C0-8), hidroxilo, halogeno, oxo, arilo (sustituido opcionalmente por 1 o más grupos R31), hetarilo (sustituido opcionalmente por 1 o más grupos R31), alquilo C1-6, -alquil C0-8-cicloalquilo C3-8, -alquil C0-8-NR311S(O)0-2R321, -alquil C0-8-NR311S(O)0-2NR321R331, -alquil C0-8-S(O)0-2NR311R321, -alquil C0-8-NR311COR321, - alquil C0-8-NR311CO2R321, -alquil C0-8-NR311CONR321R331, -alquil C0-8-CONR311R321, -alquil C0-8CON(R311)S(O)0-2R321, -alquil C0-8-CO2R311, -alquil C0-8-S(O)0-2R311, -alquil C0-8-O-alquilo C1-8, -alquil C0-8-O-alquil C0-8-cicloalquilo C3-8, -alquil C0-8-O-alquilheterociclilo C0-8, -alquil C0-8-O-alquilarilo C0-8, -alquil C0-8-arilo, -alquil C0-8-hetarilo, -alquil C0-8-heterociclilo, -alquil C0-8-O-alquilhetarilo C0-8, -alquil C0-8-S-alquilo C0-8, -alquil C0-8-S-alquil C0-8-cicloalquilo C3-8, - alquil C0-8-S-alquilheterociclilo C0-8, -alquil C0-8-S-alquilarilo C0-8, -alquil C0-8-S-alquilhetarilo C0-8, -alquil C0-8-N(R311)-alquilo C0-8, -alquil C0-8-N(R311)-alquil C0-8-cicloalquilo C3-8, -alquil C0-8-N(R311)-alquilheterociclilo C0-8, - alquil C0-8-N(R311)-alquilarilo C0-8, -alquil C0-8-N(R311)-alquilhetarilo C0-8, -alquil C0-8-NR311R321, -alquenilo C2-8, -alquinilo C2-8, NO2, CN, CF3, OCF3, OCHF2 siempre que Q1 no sea N-metil-2-indolilo, N(fenilsulfonil)-2-indolilo o N-ter- butoxicarbonilo; W es independientemente hidrogeno, -N(alquil C0-8)(alquilo C0-8), hidroxilo, halogeno, oxo, arilo (sustituido opcionalmente por 1 o más grupos R31), hetarilo (sustituido opcionalmente por 1 o más grupos R31), alquilo C1-6, -alquil C0-8-cicloalquilo C3-8, -alquil C0-8-NR312S(O)0-2R322, -alquil C0-8-NR311S(O)0-2NR321R331, -alquil C0-8-NR311CO2R321, -alquil C0-8-CON(R311)S(O)0-2R321, -alquil C0-8-S(O)0-2NR312R322, -alquil C0-8-NR312COR322, -alquil C0-8-NR312CONR322R332, -alquil C0-8-CONR312R322, -alquil C0-8-CO2R312, -alquil C0-8-S(O)0-2R312, -alquil C0-8-O-alquilo C1-8, -alquil C0-8-O-alquilciclilo C0-8, -alquil C0-8-O-alquilheterocicloalquilo C0-8, -alquil C0-8-O-alquilarilo C0-8, -alquilarilo C0-8, -alquilhetarilo C0-8, -alquilheterociclilo C0-8, -O-arilo, -alquil C0-8-O-alquilhetarilo C0-8, -alquil C0-8-S-alquilo C0-8, -alquil C0-8-S-alquil C0-8-cicloalquilo C3-8, -alquil C0-8-S-alquiIheterocicIoaIquilo C0-8, -alquil C0-8-S-alquilarilo C0-8, -alquil C0-8-S- alquilhetarilo C0-8, -alquil C0-8-N(R312)-alquilo C0-8, -alquil C0-8-N(R312)-alquil C0-8-cicloalquilo C3-8, -alquil C0-8-N(R312)-alquilheterocicloalquilo C0-8, -alquil C0-8-N(R312)-alquilarilo C0-8, -alquil C0-8-N(R312)-alquilhetarilo C0-8, alquil C0-8-NR312R322, -alquenilo C2-8, -alquinilo C2-8, NO2, CN, CF3, OCF3, OCHF2 siempre que no sea 4-benciloxi-2-indolilo; Y es independientemente hidrogeno, -N(alquil C0-8)(alquilo C0-8), hidroxilo, halogeno, oxo, arilo (sustituido opcionalmente por 1 o más grupos R31), hetarilo (sustituido opcionalmente por 1 o más grupos R31), alquilo C0-6, -alquil C0-8-cicloalquilo C3-8, -alquil C0-8-NR311S(O)0-2R321, -alquil C0-8-NR311S(O)0-2NR321R331, -alquil C0-8-NR311CO2R321, -alquil C0-8-CON(R311)S(O)0- 2R321, -alquil C0-8-S(O)0-2NR311R321, -alquil C0-8-NR311COR321, -alquil C0-8-NR311CONR321R331, -alquil C0-8-CONR311R321, -alquil C0-8-CO2R311, -alquil C0-8-S(O)0-2R311, -alquil C0-8-O-alquilo C1-8, -alquil C0-8-O-alquil C0-8-cicloalquilo C3-8, - alquil C0-8-O-alquilheterocicloalquilo C0-8, -alquil C0-8-O-alquilarilo C0-8, -alquilarilo C0-8, -alquilhetarilo C0-8, -alquilheterociclilo C0-8, -alquil C0-8-O-alquilhetarilo C0-8, -alquil C0-8-S-alquilo C0-8, -alquil C0-8-S-alquil C0-8- cicloalquilo C3-8, -alquil C0-8-S-alquilheterocicloalquilo C0-8, -alquil C0-8-S-alquilarilo C0-8, -alquil C0-8-S-alquilhetarilo C0-8, -alquil C0-8-N(R311)-alquilo C0-8, -alquil C0-8-N(R311)-alquil C0-8-cicloalquilo C3-8, -alquil C0-8-N(R311)- alquilheterocicloalquilo C0-8, -alquil C0-8-N(R311)-alquilarilo C0-8, -alquil C0-8N(R311)-alquilhetarilo C0-8, -alquil C0-8-NR311R321, -alquenilo C2-8, -alquinilo C2-8, NO2, CN, CF3, OCF3, OCHF2 siempre que no sea 2-carboxi-5- benzo[b]tiofenilo; G11 es halo, oxo, -CF3, -OCF3, -OR312, -NR312R322, -C(O)R312, -(O)cicloalquilo C3-8, -CO2-cicloalquilo C3-8, -CO2R312, -C(=O)NR312R322, -NO2, -CN, -S(O)0-2R312, -SO2NR312R322, NR312(C=O)R322, NR312C(=O)OR322, NR312C(=O)NR322R332, NR312S(O)0-2R322, - C(=S)OR312, -C(=O)SR312, -NR312C(=NR322)NR332R341, -NR312C(=NR322)OR332, -NR312C(=NR322)SR332, -OC(=O)OR312, -OC(=O)NR312R322, -OC(=O)SR312, -SC(=O)OR312, -SC(=O)NR312R322, -P(O)OR312OR322, alquilideno C1-10, alquilo C0-10, alquenilo C2-10, alquinilo C2-10, -alcoxi C1-10-alquilo C1-10, -alcoxi C1-10-alquenilo C2-10, -alcoxi C1-10-alquinilo C2-10, -alquiltio C1-10-alquilo C1-10, -alquiltio C1-10-alquenilo C2-10, -alquiltio C1-10-alquinilo C2-10, cicloalquilo C3-8, cicloalquenilo C3-8, - cicloalquil C3-8-alquilo C1-10, -cicloalquenil C3-8-alquilo C1-10, -cicloalquil C3-8-alquenilo C2-10, -cicloalquenil C3-8-alquenilo C2-10, -cicloalquil C3-8-alquinilo C2-10, -cicloalquenil C3-8-alquinilo C2-10, -heterociclil-alquilo C0-10, - heterociclil-alquenilo C2-10 o -heterociclil-alquinilo C2-10, cualquiera de los cuales está sustituido opcionalmente por uno o más sustituyentes independientes halo, oxo, -CF3, -OCF3, -OR313, -NR313R323, -C(O)R313, -CO2R313, -C(=O)NR313R323, -NO2, - CN, -S(O)0-2R313, -SO2NR313R323, -NR313C(=O)R323, -NR313C(=O)OR323, -NR313C(=O)NR323R333, -NR313S(O)0-2R323, -C(=S)OR313, -C(=O)SR313, -NR313C(=NR323)NR333R342, -NR313C(=NR323)OR333, -NR313C(=NR323)SR333, -OC(=O)OR333, -OC(=O)NR313R323, - OC(=O)SR313, -SC(=O)OR313, -P(O)OR313OR323 o -SC(=O)R313R323; o G11 es aril-alquilo C0-10, aril-alquenilo C2-10, aril-alquinilo C2-10, hetarilalquilo C0-10, hetaril-alquenilo C2-10, o hetaril-alquinilo C2-10, donde el punto de union es desde la izquierda o la derecha segun lo escrito, donde cualquiera de los cuales está sustituido opcionalmente por uno o más sustituyentes independientes halo, -CF3, -OCF3, -OR313, -NR313R323, -C(O)R313, -CO2R313, -C(=O)NR313R323, -NO2, -CN, -S(O)0-2R313, - SO2NR313R323, -NR313C(=O)R323, -NR313C(=O)OR323, -NR313C(=O)NR323R333, -NR313S(O)0-2R323, -C(S)OR313, -C(O)SR313, -NR323C(=NR313)NR333R342, -NR313C(=NR323)OR333, -NR313C(=NR323)SR333, -OC(=O)OR313, -OC(=O)NR313R323, -OC(=O)SR313, -P(O)OR313OR323, o - SC(=O)NR313R323 siempre que G11 no sea N-CH2CO2H cuando R3 es 4-piperidinilo; R31, R32, R33, R311, R321, R331, R312, R322, R332, R341, R313, R323, R333, y R342, en cada caso, es independientemente alquilo C0-8 sustituido opcionalmente por un sustituyente arilo, heterociclilo o hetarilo o alquilo C0-8 sustituido opcionalmente por 1-6 sustituyentes independientes halo, -CON(alquil C0-8)(alquilo C0-8), -CO(alquilo C0-8), -O-alquilo C0-8, -O-arilo, -O-hetarilo, -O-heterociclilo, -S(O)0- 2arilo, -S(O)0-2hetarilo, -S(O)0-2heterociclilo, -S(O)0-2alquilo C0-8, -N(alquil C0-8)(alquilo C0-8), -N(alquil C0-8)CON(alquil C0-8)(alquilo C0-8), -N(alquil C0-8)CO(alquilo C1-8), -N(alquil C0-8)CO(cicloalquilo C3-8), -N(alquil C0-8)CO2(alquilo C1- 8), S(O)1-2N(alquil C0-8)(alquilo C0-8), -NR11S(O)1-2(alquilo C0-8), -CON(cicloalquil C3-8)(cicloalquilo C3-8), -CON(alquil C0-8)(cicloalquilo C3-8), -N(cicloalquil C3-8)CON(alquil C0-8)(alquilo C0-8), -N(cicloalquil C3-8)CON(cicloalquil C3- 8)(alquilo C0-8), -N(alquil C0-8)CON(cicloalquil C3-8)(alquilo C0-8), -N(alquil C0-8)CO2(cicloalquilo C3-8), -N(cicloalquil C3-8)CO2(cicloalquilo C3-8), S(O)1-2N(alquil C0-8)(cicloalquilo C3-8), -NR11S(O)1-2(cicloalquilo C3-8), alquenilo C2-8, alquinilo C2-8, CN, CF3, OH, o arilo sustituido opcionalmente; de manera que uno de los anteriores grupos arilo, heterociclilo, hetarilo, alquilo o cicloalquilo se pueden sustituir opcional e independientemente por -N(alquil C0-8)(alquilo C0-8), hidroxilo, halogeno, oxo, arilo, hetarilo, alquilo C0-6, -alquilciclilo C0-8, -alquil C0-8-N(alquil C0-8)-S(O)0-2-(alquilo C0-8), -alquil C0-8-S(O)0-2-N(alquil C0-8)(alquilo C0-8), -alquil C0-8-N(alquil C0-8)CO(alquilo C0-8), -alquil C0-8-N(alquil C0-8)CO-N(alquil C0-8)(alquilo C0-8), -alquil C0-8-CO-N(alquil C0-8)(alquilo C0-8), -alquil C1-8-CO2-(alquilo C0-8), -alquil C0-8-S(O)0-2-(alquilo C0-8), -alquil C0-8-O-alquilo C1-8, -alquil C0-8-O-alquilciclilo C0-8, -alquil C0-8-O- alquilheterociclilo C0-8, -alquil C0-8-O-alquilarilo C0-8, -alquil C0-8-O-alquilhetarilo C0-8, -alquil C0-8-S-alquilo C0-8, -alquil C0-8-S-alquilciclilo C0-8, -alquil C0-8-S-alquilheterociclilo C0-8, -alquil C0-8-S-alquilarilo C0-8, -alquil C0-8-S- alquilhetarilo C0-8, -alquil C0-8-N(alquil C0-8)-alquilo C0-8, -alquil C0-8N(alquil C0-8)-alquilciclilo C0-8, -alquil C0-8-N(alquil C0-8)-alquilheterocicl
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- 2006-11-15 PL PL11155270T patent/PL2385053T3/pl unknown
- 2006-11-15 AT AT06837752T patent/ATE507227T1/de active
- 2006-11-15 CN CN201210369830.2A patent/CN102936250B/zh not_active Expired - Fee Related
- 2006-11-15 WO PCT/US2006/044461 patent/WO2007061737A2/en not_active Ceased
- 2006-11-15 US US11/599,663 patent/US7700594B2/en active Active
- 2006-11-15 MY MYPI20081660A patent/MY148491A/en unknown
- 2006-11-15 SI SI200631064T patent/SI1951724T1/sl unknown
- 2006-11-15 DE DE602006021608T patent/DE602006021608D1/de active Active
- 2006-11-15 NZ NZ569050A patent/NZ569050A/en not_active IP Right Cessation
- 2006-11-15 BR BRPI0618622-0A patent/BRPI0618622A2/pt not_active IP Right Cessation
- 2006-11-16 TW TW095142464A patent/TWI382028B/zh not_active IP Right Cessation
- 2006-11-17 AR ARP060105058A patent/AR056884A1/es not_active Application Discontinuation
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2008
- 2008-05-16 ZA ZA200804237A patent/ZA200804237B/xx unknown
- 2008-05-18 IL IL191532A patent/IL191532A0/en unknown
- 2008-12-02 US US12/326,536 patent/US7923555B2/en active Active
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2009
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- 2009-11-20 US US12/622,545 patent/US7943767B2/en active Active
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2011
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2013
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