AU2001242669A1 - Pharmaceutical compositions of glycogen phosphorylase inhibitors - Google Patents

Pharmaceutical compositions of glycogen phosphorylase inhibitors

Info

Publication number: AU2001242669A1
Authority: AU; Australia
Prior art keywords: alkyl; composition; cellulose acetate; hydroxy; strand
Prior art date: 2000-03-16
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

Application number

AU2001242669A

Other languages

English (en)

Inventor

Dwayne Thomas Friesen

Dennis Jay Hoover

Douglas Alan Lorenz

James Alan Schriver Nightingale

Ravi Mysore Shanker

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Pfizer Products Inc

Original Assignee

Pfizer Products Inc

Priority date (The priority date 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 date listed.)

2000-03-16

Filing date

2001-03-16

Publication date

2001-09-24

2001-03-16 Application filed by Pfizer Products Inc filed Critical Pfizer Products Inc

2001-09-24 Publication of AU2001242669A1 publication Critical patent/AU2001242669A1/en

Status Abandoned legal-status Critical Current

Links

102000007390 Glycogen Phosphorylase Human genes 0.000 title claims description 37
108010046163 Glycogen Phosphorylase Proteins 0.000 title claims description 37
239000008194 pharmaceutical composition Substances 0.000 title claims description 15
239000003112 inhibitor Substances 0.000 title description 21
ROJNYKZWTOHRNU-UHFFFAOYSA-N 2-chloro-4,5-difluoro-n-[[2-methoxy-5-(methylcarbamoylamino)phenyl]carbamoyl]benzamide Chemical compound CNC(=O)NC1=CC=C(OC)C(NC(=O)NC(=O)C=2C(=CC(F)=C(F)C=2)Cl)=C1 ROJNYKZWTOHRNU-UHFFFAOYSA-N 0.000 claims description 280
229920000642 polymer Polymers 0.000 claims description 267
239000000203 mixture Substances 0.000 claims description 254
125000000217 alkyl group Chemical group 0.000 claims description 244
-1 trifuloromethyl Chemical group 0.000 claims description 174
125000003545 alkoxy group Chemical group 0.000 claims description 71
238000000034 method Methods 0.000 claims description 68
229920002301 cellulose acetate Polymers 0.000 claims description 58
125000005843 halogen group Chemical group 0.000 claims description 57
239000002904 solvent Substances 0.000 claims description 56
239000006185 dispersion Substances 0.000 claims description 53
150000001875 compounds Chemical class 0.000 claims description 48
125000001424 substituent group Chemical group 0.000 claims description 45
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 44
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 42
FUQOTYRCMBZFOL-UHFFFAOYSA-N 5-chloro-1H-indole-2-carboxylic acid Chemical group ClC1=CC=C2NC(C(=O)O)=CC2=C1 FUQOTYRCMBZFOL-UHFFFAOYSA-N 0.000 claims description 34
229910052799 carbon Inorganic materials 0.000 claims description 34
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 33
229940081735 acetylcellulose Drugs 0.000 claims description 32
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 30
229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 29
235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 29
125000004093 cyano group Chemical group *C#N 0.000 claims description 28
229910052739 hydrogen Inorganic materials 0.000 claims description 28
239000001863 hydroxypropyl cellulose Substances 0.000 claims description 28
206010012601 diabetes mellitus Diseases 0.000 claims description 27
125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 26
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 25
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 24
229910052757 nitrogen Inorganic materials 0.000 claims description 24
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 23
239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 21
238000001694 spray drying Methods 0.000 claims description 21
GAMPNQJDUFQVQO-UHFFFAOYSA-N acetic acid;phthalic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O GAMPNQJDUFQVQO-UHFFFAOYSA-N 0.000 claims description 20
125000003282 alkyl amino group Chemical group 0.000 claims description 20
239000007787 solid Substances 0.000 claims description 20
125000005591 trimellitate group Chemical group 0.000 claims description 20
208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 20
239000001257 hydrogen Substances 0.000 claims description 19
230000002209 hydrophobic effect Effects 0.000 claims description 18
125000003118 aryl group Chemical group 0.000 claims description 17
239000000651 prodrug Substances 0.000 claims description 17
229940002612 prodrug Drugs 0.000 claims description 17
150000003839 salts Chemical class 0.000 claims description 17
125000000623 heterocyclic group Chemical group 0.000 claims description 16
229920000609 methyl cellulose Polymers 0.000 claims description 16
235000010981 methylcellulose Nutrition 0.000 claims description 16
239000001923 methylcellulose Substances 0.000 claims description 16
229920000623 Cellulose acetate phthalate Polymers 0.000 claims description 15
239000007864 aqueous solution Substances 0.000 claims description 15
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
229940081734 cellulose acetate phthalate Drugs 0.000 claims description 15
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 15
229920003132 hydroxypropyl methylcellulose phthalate Polymers 0.000 claims description 15
229940031704 hydroxypropyl methylcellulose phthalate Drugs 0.000 claims description 15
238000001727 in vivo Methods 0.000 claims description 15
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
125000004076 pyridyl group Chemical group 0.000 claims description 14
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 13
230000002708 enhancing effect Effects 0.000 claims description 13
125000001475 halogen functional group Chemical group 0.000 claims description 13
239000006069 physical mixture Substances 0.000 claims description 13
IYKJEILNJZQJPU-UHFFFAOYSA-N acetic acid;butanedioic acid Chemical compound CC(O)=O.OC(=O)CCC(O)=O IYKJEILNJZQJPU-UHFFFAOYSA-N 0.000 claims description 12
125000001153 fluoro group Chemical group F* 0.000 claims description 12
125000002541 furyl group Chemical group 0.000 claims description 12
125000002883 imidazolyl group Chemical group 0.000 claims description 12
125000001786 isothiazolyl group Chemical group 0.000 claims description 12
125000000842 isoxazolyl group Chemical group 0.000 claims description 12
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 12
125000002971 oxazolyl group Chemical group 0.000 claims description 12
125000003373 pyrazinyl group Chemical group 0.000 claims description 12
125000003226 pyrazolyl group Chemical group 0.000 claims description 12
125000002098 pyridazinyl group Chemical group 0.000 claims description 12
125000000714 pyrimidinyl group Chemical group 0.000 claims description 12
125000000168 pyrrolyl group Chemical group 0.000 claims description 12
125000000335 thiazolyl group Chemical group 0.000 claims description 12
125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 claims description 11
201000001320 Atherosclerosis Diseases 0.000 claims description 11
229920000639 hydroxypropylmethylcellulose acetate succinate Polymers 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
238000012545 processing Methods 0.000 claims description 11
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 10
206010020772 Hypertension Diseases 0.000 claims description 10
125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 10
125000005842 heteroatom Chemical group 0.000 claims description 10
208000028867 ischemia Diseases 0.000 claims description 10
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims description 10
208000002177 Cataract Diseases 0.000 claims description 9
229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 claims description 9
208000035150 Hypercholesterolemia Diseases 0.000 claims description 9
208000031226 Hyperlipidaemia Diseases 0.000 claims description 9
206010022489 Insulin Resistance Diseases 0.000 claims description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
201000001421 hyperglycemia Diseases 0.000 claims description 9
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 9
229910052717 sulfur Inorganic materials 0.000 claims description 9
208000007342 Diabetic Nephropathies Diseases 0.000 claims description 8
208000032131 Diabetic Neuropathies Diseases 0.000 claims description 8
239000001856 Ethyl cellulose Substances 0.000 claims description 8
241001465754 Metazoa Species 0.000 claims description 8
125000000676 alkoxyimino group Chemical group 0.000 claims description 8
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 8
229920006218 cellulose propionate Polymers 0.000 claims description 8
208000033679 diabetic kidney disease Diseases 0.000 claims description 8
235000019325 ethyl cellulose Nutrition 0.000 claims description 8
229920001249 ethyl cellulose Polymers 0.000 claims description 8
125000001072 heteroaryl group Chemical group 0.000 claims description 8
125000002757 morpholinyl group Chemical group 0.000 claims description 8
125000004043 oxo group Chemical group O=* 0.000 claims description 8
UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 8
125000004193 piperazinyl group Chemical group 0.000 claims description 8
125000003386 piperidinyl group Chemical group 0.000 claims description 8
125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims description 8
125000003072 pyrazolidinyl group Chemical group 0.000 claims description 8
125000002755 pyrazolinyl group Chemical group 0.000 claims description 8
125000000719 pyrrolidinyl group Chemical group 0.000 claims description 8
206010012689 Diabetic retinopathy Diseases 0.000 claims description 7
241000282414 Homo sapiens Species 0.000 claims description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 7
125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 6
SOGNHUJSAKAIRG-UHFFFAOYSA-N 2-chloro-6h-thieno[2,3-b]pyrrole-5-carboxylic acid Chemical group C1=C(Cl)SC2=C1C=C(C(=O)O)N2 SOGNHUJSAKAIRG-UHFFFAOYSA-N 0.000 claims description 6
239000004354 Hydroxyethyl cellulose Substances 0.000 claims description 6
229920000663 Hydroxyethyl cellulose Polymers 0.000 claims description 6
ZNPLZHBZUSCANM-UHFFFAOYSA-N acetic acid;benzene-1,3-dicarboxylic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CC(C(O)=O)=C1 ZNPLZHBZUSCANM-UHFFFAOYSA-N 0.000 claims description 6
PLEULVPCZZDBNB-UHFFFAOYSA-N acetic acid;butanedioic acid;phthalic acid Chemical compound CC(O)=O.OC(=O)CCC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O PLEULVPCZZDBNB-UHFFFAOYSA-N 0.000 claims description 6
FMTQGBMMIVVKSN-UHFFFAOYSA-N acetic acid;terephthalic acid Chemical compound CC(O)=O.OC(=O)C1=CC=C(C(O)=O)C=C1 FMTQGBMMIVVKSN-UHFFFAOYSA-N 0.000 claims description 6
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
235000019447 hydroxyethyl cellulose Nutrition 0.000 claims description 6
230000005764 inhibitory process Effects 0.000 claims description 6
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
125000000304 alkynyl group Chemical group 0.000 claims description 5
125000001589 carboacyl group Chemical group 0.000 claims description 5
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 5
238000000338 in vitro Methods 0.000 claims description 5
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 5
229960004889 salicylic acid Drugs 0.000 claims description 5
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 4
125000006529 (C3-C6) alkyl group Chemical group 0.000 claims description 4
VMJNTFXCTXAXTC-UHFFFAOYSA-N 2,2-difluoro-1,3-benzodioxole-5-carbonitrile Chemical group C1=C(C#N)C=C2OC(F)(F)OC2=C1 VMJNTFXCTXAXTC-UHFFFAOYSA-N 0.000 claims description 4
ZNNQGSGPVUYWOS-UHFFFAOYSA-N 2-(3-hydroxypropoxy)benzoic acid Chemical compound OCCCOC1=CC=CC=C1C(O)=O ZNNQGSGPVUYWOS-UHFFFAOYSA-N 0.000 claims description 4
OEXIDSNKGPWFGB-UHFFFAOYSA-N 2-ethyl-3-(3-hydroxypropyl)benzoic acid Chemical compound CCC1=C(CCCO)C=CC=C1C(O)=O OEXIDSNKGPWFGB-UHFFFAOYSA-N 0.000 claims description 4
CGMMPMYKMDITEA-UHFFFAOYSA-N 2-ethylbenzoic acid Chemical compound CCC1=CC=CC=C1C(O)=O CGMMPMYKMDITEA-UHFFFAOYSA-N 0.000 claims description 4
RESGCFMULOVHHB-UHFFFAOYSA-N 2-ethylpyridine-3-carboxylic acid Chemical compound CCC1=NC=CC=C1C(O)=O RESGCFMULOVHHB-UHFFFAOYSA-N 0.000 claims description 4
NMGBFVPQUCLJGM-UHFFFAOYSA-N 3-ethylphthalic acid Chemical compound CCC1=CC=CC(C(O)=O)=C1C(O)=O NMGBFVPQUCLJGM-UHFFFAOYSA-N 0.000 claims description 4
VFTOHJFKIJLYKN-UHFFFAOYSA-N 7-nitro-9h-fluoren-2-ol Chemical group [O-][N+](=O)C1=CC=C2C3=CC=C(O)C=C3CC2=C1 VFTOHJFKIJLYKN-UHFFFAOYSA-N 0.000 claims description 4
DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 claims description 4
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims description 4
206010067584 Type 1 diabetes mellitus Diseases 0.000 claims description 4
CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 claims description 4
GZRANGIRVYGSDJ-UHFFFAOYSA-N acetic acid;pyridine-2,3-dicarboxylic acid Chemical compound CC(O)=O.OC(=O)C1=CC=CN=C1C(O)=O GZRANGIRVYGSDJ-UHFFFAOYSA-N 0.000 claims description 4
125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 4
VHEMBTYWURNBQQ-UHFFFAOYSA-N butanoic acid;phthalic acid Chemical compound CCCC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O VHEMBTYWURNBQQ-UHFFFAOYSA-N 0.000 claims description 4
125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims description 4
239000001768 carboxy methyl cellulose Substances 0.000 claims description 4
229920001727 cellulose butyrate Polymers 0.000 claims description 4
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 4
208000031225 myocardial ischemia Diseases 0.000 claims description 4
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 4
230000002441 reversible effect Effects 0.000 claims description 4
125000001544 thienyl group Chemical group 0.000 claims description 4
229920002554 vinyl polymer Polymers 0.000 claims description 4
INTNEELQXPKMNM-UHFFFAOYSA-N 3-ethylpyridine-2-carboxylic acid Chemical compound CCC1=CC=CN=C1C(O)=O INTNEELQXPKMNM-UHFFFAOYSA-N 0.000 claims description 3
XULPAMMHMRIVOO-UHFFFAOYSA-N 5-acetyl-n-[3-[(4-bromophenyl)carbamoyl]phenyl]-1-methyl-2-oxo-3h-indole-3-carboxamide Chemical compound C12=CC(C(C)=O)=CC=C2N(C)C(=O)C1C(=O)NC(C=1)=CC=CC=1C(=O)NC1=CC=C(Br)C=C1 XULPAMMHMRIVOO-UHFFFAOYSA-N 0.000 claims description 3
QUWRSNVQONCPEX-UHFFFAOYSA-N 5-chloro-n-[2-oxo-2-(1-oxo-1,3-thiazolidin-3-yl)ethyl]-1h-indole-2-carboxamide Chemical compound C=1C2=CC(Cl)=CC=C2NC=1C(=O)NCC(=O)N1CCS(=O)C1 QUWRSNVQONCPEX-UHFFFAOYSA-N 0.000 claims description 3
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 3
229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
SIOXPEMLGUPBBT-UHFFFAOYSA-N Picolinic acid Natural products OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims description 3
125000003342 alkenyl group Chemical group 0.000 claims description 3
235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 3
210000001035 gastrointestinal tract Anatomy 0.000 claims description 3
230000002401 inhibitory effect Effects 0.000 claims description 3
229960002900 methylcellulose Drugs 0.000 claims description 3
208000035408 type 1 diabetes mellitus 1 Diseases 0.000 claims description 3
125000005988 1,1-dioxo-thiomorpholinyl group Chemical group 0.000 claims description 2
125000004317 1,3,5-triazin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=N1 0.000 claims description 2
125000005987 1-oxo-thiomorpholinyl group Chemical group 0.000 claims description 2
RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 2
125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims description 2
CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 claims description 2
WAAVFJWSRFFSSW-BETUJISGSA-N 5-chloro-n-[2-[(3s,4r)-3,4-dihydroxypyrrolidin-1-yl]-2-oxoethyl]-1h-indole-2-carboxamide Chemical group C1[C@@H](O)[C@@H](O)CN1C(=O)CNC(=O)C1=CC2=CC(Cl)=CC=C2N1 WAAVFJWSRFFSSW-BETUJISGSA-N 0.000 claims description 2
208000035143 Bacterial infection Diseases 0.000 claims description 2
208000032781 Diabetic cardiomyopathy Diseases 0.000 claims description 2
XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims description 2
208000022362 bacterial infectious disease Diseases 0.000 claims description 2
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 2
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 2
125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
VYGAQHDGEYQIJU-UHFFFAOYSA-N butanedioic acid;phthalic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)C1=CC=CC=C1C(O)=O VYGAQHDGEYQIJU-UHFFFAOYSA-N 0.000 claims description 2
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical group C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims description 2
239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
229920003064 carboxyethyl cellulose Polymers 0.000 claims description 2
229910021419 crystalline silicon Inorganic materials 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
229920013819 hydroxyethyl ethylcellulose Polymers 0.000 claims description 2
125000001041 indolyl group Chemical group 0.000 claims description 2
DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 claims description 2
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
229940081066 picolinic acid Drugs 0.000 claims description 2
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
125000004568 thiomorpholinyl group Chemical group 0.000 claims description 2
230000004614 tumor growth Effects 0.000 claims description 2
229920006163 vinyl copolymer Polymers 0.000 claims description 2
HSHXDCVZWHOWCS-UHFFFAOYSA-N N'-hexadecylthiophene-2-carbohydrazide Chemical group CCCCCCCCCCCCCCCCNNC(=O)c1cccs1 HSHXDCVZWHOWCS-UHFFFAOYSA-N 0.000 claims 6
125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 2
VFFMCGXIWQUAEL-UHFFFAOYSA-N 5-acetyl-1-ethyl-2-oxo-n-[3-(phenylcarbamoyl)phenyl]-3h-indole-3-carboxamide Chemical group C12=CC(C(C)=O)=CC=C2N(CC)C(=O)C1C(=O)NC(C=1)=CC=CC=1C(=O)NC1=CC=CC=C1 VFFMCGXIWQUAEL-UHFFFAOYSA-N 0.000 claims 2
125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
KFPUKDCJSXIZJN-OEEJBDNKSA-N 5-chloro-N-[2-[(3R,4S)-3,4-dihydroxypyrrolidin-1-yl]-2-oxoethyl]-1H-indole-2-carboxamide 5-chloro-1H-indole-2-carboxylic acid Chemical group ClC=1C=C2C=C(NC2=CC1)C(=O)O.O[C@@H]1CN(C[C@@H]1O)C(CNC(=O)C=1NC2=CC=C(C=C2C1)Cl)=O KFPUKDCJSXIZJN-OEEJBDNKSA-N 0.000 claims 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
208000006575 hypertriglyceridemia Diseases 0.000 claims 1
125000003107 substituted aryl group Chemical group 0.000 claims 1
229940079593 drug Drugs 0.000 description 133
239000003814 drug Substances 0.000 description 133
239000000243 solution Substances 0.000 description 65
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 53
239000002552 dosage form Substances 0.000 description 48
238000012360 testing method Methods 0.000 description 45
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 44
238000010922 spray-dried dispersion Methods 0.000 description 41
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 38
239000003826 tablet Substances 0.000 description 35
230000008569 process Effects 0.000 description 32
239000000463 material Substances 0.000 description 27
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 26
238000007922 dissolution test Methods 0.000 description 25
238000002156 mixing Methods 0.000 description 24
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Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
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Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Epidemiology (AREA)
Diabetes (AREA)
Heart & Thoracic Surgery (AREA)
Cardiology (AREA)
Obesity (AREA)
Hematology (AREA)
Gastroenterology & Hepatology (AREA)
Urology & Nephrology (AREA)
Communicable Diseases (AREA)
Oncology (AREA)
Vascular Medicine (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Endocrinology (AREA)
Emergency Medicine (AREA)
Immunology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Plural Heterocyclic Compounds (AREA)
Indole Compounds (AREA)

AU2001242669A 2000-03-16 2001-03-16 Pharmaceutical compositions of glycogen phosphorylase inhibitors Abandoned AU2001242669A1 (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US18994200P	2000-03-16	2000-03-16
US60189942		2000-03-16
PCT/IB2001/000394 WO2001068055A1 (en)	2000-03-16	2001-03-16	Pharmaceutical compositions of glycogen phosphorylase inhibitors

Publications (1)

Publication Number	Publication Date
AU2001242669A1 true AU2001242669A1 (en)	2001-09-24

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ID=22699402

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AU2001242669A Abandoned AU2001242669A1 (en)	2000-03-16	2001-03-16	Pharmaceutical compositions of glycogen phosphorylase inhibitors

Country Status (32)

Country	Link
US (1)	US20010053778A1 (es)
EP (1)	EP1263414A1 (es)
JP (1)	JP2003526654A (es)
KR (1)	KR20020081445A (es)
CN (1)	CN1418089A (es)
AP (1)	AP2002002621A0 (es)
AR (1)	AR027656A1 (es)
AU (1)	AU2001242669A1 (es)
BG (1)	BG107037A (es)
BR (1)	BR0109189A (es)
CA (1)	CA2403241A1 (es)
CO (1)	CO5280087A1 (es)
CZ (1)	CZ20022955A3 (es)
EA (1)	EA200200858A1 (es)
EE (1)	EE200200530A (es)
HU (1)	HUP0204583A2 (es)
IL (1)	IL151320A0 (es)
IS (1)	IS6508A (es)
MA (1)	MA26882A1 (es)
MX (1)	MXPA02009097A (es)
NO (1)	NO20024386L (es)
OA (1)	OA12232A (es)
PA (1)	PA8513601A1 (es)
PE (1)	PE20011184A1 (es)
PL (1)	PL360780A1 (es)
SK (1)	SK12622002A3 (es)
SV (1)	SV2002000343A (es)
TN (1)	TNSN01040A1 (es)
TR (1)	TR200202184T2 (es)
WO (1)	WO2001068055A1 (es)
YU (1)	YU67202A (es)
ZA (1)	ZA200207290B (es)

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EP1269994A3 (en)	2001-06-22	2003-02-12	Pfizer Products Inc.	Pharmaceutical compositions comprising drug and concentration-enhancing polymers
PT1404300E (pt)	2001-06-22	2009-11-09	Bend Res Inc	Composições farmacêuticas de dispersões de fármacos e polímeros neutros
AU2002309172A1 (en) *	2001-06-22	2003-01-08	Pfizer Products Inc.	Pharmaceutical compositions containing polymer and drug assemblies
ES2878403T3 (es)	2002-02-01	2021-11-18	Bend Res Inc	Método para preparar dispersiones de fármacos amorfas sólidas homogéneas secadas mediante pulverización utilizando aparatos de secado por pulverización modificados
DE60320940D1 (de)	2002-02-01	2008-06-26	Pfizer Prod Inc	Pharmazeutische zusammensetzungen amorpher dispersionen von wirkstoffen und lipophiler mikrophasenbildender materialien
RU2288703C2 (ru)	2002-02-01	2006-12-10	Пфайзер Продактс Инк.	Способ создания однородных высушенных распылением твердых аморфных лекарственных дисперсных систем с использованием распыляющих напорных форсунок (варианты) и продукт
GB0205165D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
GB0205175D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
GB0205166D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
GB0205170D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
GB0205162D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
GB0205176D0 (en)	2002-03-06	2002-04-17	Astrazeneca Ab	Chemical compounds
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CL2004001884A1 (es)	2003-08-04	2005-06-03	Pfizer Prod Inc	Procedimiento de secado por pulverizacion para la formacion de dispersiones solidas amorfas de un farmaco y polimeros.
WO2005011635A2 (en) *	2003-08-04	2005-02-10	Pfizer Products Inc.	Pharmaceutical compositions of adsorbates of amorphous drugs and lipophilic microphase-forming materials
US7390503B1 (en)	2003-08-22	2008-06-24	Barr Laboratories, Inc.	Ondansetron orally disintegrating tablets
CA2548376A1 (en) *	2003-12-31	2005-07-21	Pfizer Products Inc.	Solid compositions of low-solubility drugs and poloxamers
WO2005085245A1 (en)	2004-03-08	2005-09-15	Prosidion Limited	Pyrrolopyridine-2-carboxylic acid hydrazides
US20090298745A1 (en) *	2004-12-02	2009-12-03	Gerard Hugh Thomas	Treatment of Diabetes with Glycogen Phosphorylase Inhibitors
DE102005026755A1 (de) *	2005-06-09	2006-12-14	Basf Ag	Herstellung von festen Lösungen schwerlöslicher Wirkstoffe durch Kurzzeitüberhitzung und schnelle Trocknung
CN107602710A (zh)	2012-08-24	2018-01-19	陶氏环球技术有限责任公司	新的具有高分子量和均匀性的酯化纤维素醚
US20140179749A1 (en)	2012-09-11	2014-06-26	Bend Research	Formulations of enzalutamide
CA3128535C (en)	2013-07-19	2024-10-15	Siga Technologies, Inc.	PREPARATION OF AMORPHIC TECOVIRIMAT
CN103709171B (zh) *	2014-01-20	2015-09-16	武汉大学	具有哒嗪并[3,4-b]吲哚骨架结构的衍生物及其合成方法
US12133911B2 (en)	2015-06-09	2024-11-05	Capsugel Belgium Nv	Formulations to achieve rapid dissolution of drug from spray-dried dispersions in capsules
CN112442022B (zh) *	2019-09-02	2022-05-20	承德医学院	苯并嗪-4-酮类化合物、其制备方法及医药用途
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CA2342471C (en) *	1995-06-06	2002-10-29	Judith L. Treadway	Heterocyclecarbonylmethyl amine intermediates
PT901786E (pt) *	1997-08-11	2007-08-07	Pfizer Prod Inc	Disperções farmacêuticas sólidas com biodisponibilidade melhorada
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2001
- 2001-03-14 PE PE2001000246A patent/PE20011184A1/es not_active Application Discontinuation
- 2001-03-14 AR ARP010101185A patent/AR027656A1/es not_active Application Discontinuation
- 2001-03-14 US US09/805,828 patent/US20010053778A1/en not_active Abandoned
- 2001-03-15 SV SV2001000343A patent/SV2002000343A/es not_active Application Discontinuation
- 2001-03-15 TN TNTNSN01040A patent/TNSN01040A1/fr unknown
- 2001-03-16 HU HU0204583A patent/HUP0204583A2/hu unknown
- 2001-03-16 EA EA200200858A patent/EA200200858A1/ru unknown
- 2001-03-16 IL IL15132001A patent/IL151320A0/xx unknown
- 2001-03-16 AP APAP/P/2002/002621A patent/AP2002002621A0/en unknown
- 2001-03-16 CN CN01806619A patent/CN1418089A/zh active Pending
- 2001-03-16 PA PA20018513601A patent/PA8513601A1/es unknown
- 2001-03-16 JP JP2001566619A patent/JP2003526654A/ja active Pending
- 2001-03-16 OA OA1200200290A patent/OA12232A/en unknown
- 2001-03-16 TR TR2002/02184T patent/TR200202184T2/xx unknown
- 2001-03-16 AU AU2001242669A patent/AU2001242669A1/en not_active Abandoned
- 2001-03-16 CA CA002403241A patent/CA2403241A1/en not_active Abandoned
- 2001-03-16 KR KR1020027012009A patent/KR20020081445A/ko not_active Ceased
- 2001-03-16 EP EP01915586A patent/EP1263414A1/en not_active Withdrawn
- 2001-03-16 SK SK1262-2002A patent/SK12622002A3/sk unknown
- 2001-03-16 CO CO01021769A patent/CO5280087A1/es not_active Application Discontinuation
- 2001-03-16 YU YU67202A patent/YU67202A/sh unknown
- 2001-03-16 EE EEP200200530A patent/EE200200530A/xx unknown
- 2001-03-16 PL PL36078001A patent/PL360780A1/xx not_active Application Discontinuation
- 2001-03-16 BR BR0109189-1A patent/BR0109189A/pt not_active Application Discontinuation
- 2001-03-16 WO PCT/IB2001/000394 patent/WO2001068055A1/en not_active Ceased
- 2001-03-16 CZ CZ20022955A patent/CZ20022955A3/cs unknown
- 2001-03-16 MX MXPA02009097A patent/MXPA02009097A/es unknown
2002
- 2002-08-16 IS IS6508A patent/IS6508A/is unknown
- 2002-08-26 BG BG107037A patent/BG107037A/bg unknown
- 2002-09-11 ZA ZA200207290A patent/ZA200207290B/xx unknown
- 2002-09-11 MA MA26810A patent/MA26882A1/fr unknown
- 2002-09-13 NO NO20024386A patent/NO20024386L/no not_active Application Discontinuation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2002302903B9 (en) *	2001-06-22	2003-01-08	Pfizer Products Inc.	Pharmaceutical compositions of adsorbates of amorphous drug
AU2002302903B2 (en) *	2001-06-22	2007-05-17	Pfizer Products Inc.	Pharmaceutical compositions of adsorbates of amorphous drug

Also Published As

Publication number	Publication date
PL360780A1 (en)	2004-09-20
HUP0204583A2 (hu)	2003-04-28
TNSN01040A1 (fr)	2005-11-10
IL151320A0 (en)	2003-04-10
CN1418089A (zh)	2003-05-14
BG107037A (bg)	2003-04-30
AP2002002621A0 (en)	2002-09-30
MXPA02009097A (es)	2003-03-12
ZA200207290B (en)	2003-09-11
CA2403241A1 (en)	2001-09-20
NO20024386D0 (no)	2002-09-13
TR200202184T2 (tr)	2003-01-21
SV2002000343A (es)	2002-07-03
MA26882A1 (fr)	2004-12-20
US20010053778A1 (en)	2001-12-20
PE20011184A1 (es)	2001-11-15
EA200200858A1 (ru)	2003-02-27
CZ20022955A3 (cs)	2003-09-17
EE200200530A (et)	2004-04-15
IS6508A (is)	2002-08-16
SK12622002A3 (sk)	2004-02-03
AR027656A1 (es)	2003-04-09
OA12232A (en)	2006-05-10
PA8513601A1 (es)	2004-08-31
WO2001068055A1 (en)	2001-09-20
YU67202A (sh)	2006-01-16
BR0109189A (pt)	2003-05-27
EP1263414A1 (en)	2002-12-11
KR20020081445A (ko)	2002-10-26
JP2003526654A (ja)	2003-09-09
NO20024386L (no)	2002-11-13
CO5280087A1 (es)	2003-05-30

Publication	Publication Date	Title
US20010053778A1 (en)	2001-12-20	Pharmaceutical compositions of glycogen phosphorylase inhibitors
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