UA80393C2 - Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці - Google Patents

Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці Download PDF

Info

Publication number: UA80393C2
Authority: UA; Ukraine
Prior art keywords: sodium; acid; composition according; droplets; excipients
Prior art date: 2000-12-07

Application number

UA2003076286A

Other languages

English (en)

Russian (ru)

Ukrainian (uk)

Inventor

Ранго Дітріх

Рудольф Ліндер

Хартмут Ней

Original Assignee

Алтана Фарма Аг

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.)

2000-12-07

Filing date

2001-06-12

Publication date

2007-09-25

2001-06-12 Application filed by Алтана Фарма Аг filed Critical Алтана Фарма Аг

2007-09-25 Publication of UA80393C2 publication Critical patent/UA80393C2/uk

Links

239000011159 matrix material Substances 0.000 title claims abstract description 27
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239000000825 pharmaceutical preparation Substances 0.000 title 1
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239000000546 pharmaceutical excipient Substances 0.000 claims abstract description 53
150000002191 fatty alcohols Chemical class 0.000 claims abstract description 24
235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 22
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UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 18
239000002552 dosage form Substances 0.000 claims abstract 7
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BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 52
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VUPBDWQPEOWRQP-RTUCOMKBSA-N [(2R,3S,4S,5R,6R)-2-[(2R,3S,4S,5S,6S)-2-[(1S,2S)-3-[[(2R,3S)-5-[[(2S,3R)-1-[[2-[4-[4-[[4-amino-6-[3-(4-aminobutylamino)propylamino]-6-oxohexyl]carbamoyl]-1,3-thiazol-2-yl]-1,3-thiazol-2-yl]-1-[(2S,3R,4R,5S,6S)-5-amino-3,4-dihydroxy-6-methyloxan-2-yl]oxy-2-hydroxyethyl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-3-hydroxy-5-oxopentan-2-yl]amino]-2-[[6-amino-2-[(1S)-3-amino-1-[[(2S)-2,3-diamino-3-oxopropyl]amino]-3-oxopropyl]-5-methylpyrimidine-4-carbonyl]amino]-1-(1H-imidazol-5-yl)-3-oxopropoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] carbamate Chemical compound C[C@@H](O)[C@H](NC(=O)C[C@H](O)[C@@H](C)NC(=O)[C@@H](NC(=O)c1nc(nc(N)c1C)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@H](O[C@@H]1O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](OC(N)=O)[C@@H]1O)c1cnc[nH]1)C(=O)NC(O[C@@H]1O[C@@H](C)[C@@H](N)[C@@H](O)[C@H]1O)C(O)c1nc(cs1)-c1nc(cs1)C(=O)NCCCC(N)CC(=O)NCCCNCCCCN VUPBDWQPEOWRQP-RTUCOMKBSA-N 0.000 description 1
NNZPUHNTEVTLKH-VIXFLFLMSA-N [(2e,6e)-3,7,11-trimethyldodeca-2,6,10-trienyl] (3e,7e)-4,8,12-trimethyltrideca-3,7,11-trienoate Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\COC(=O)C\C=C(/C)CC\C=C(/C)CCC=C(C)C NNZPUHNTEVTLKH-VIXFLFLMSA-N 0.000 description 1
UFUVLHLTWXBHGZ-MGZQPHGTSA-N [(2r,3r,4s,5r,6r)-6-[(1s,2s)-2-chloro-1-[[(2s,4r)-1-methyl-4-propylpyrrolidine-2-carbonyl]amino]propyl]-4,5-dihydroxy-2-methylsulfanyloxan-3-yl] dihydrogen phosphate Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H](SC)O1 UFUVLHLTWXBHGZ-MGZQPHGTSA-N 0.000 description 1
JDYLJSDIEBHXPO-ALNZGLKXSA-N [(2r,3r,4s,6r)-3-[(2s,4s,5r,6r)-4-acetyloxy-5-[(2s,4s,5r,6r)-4,5-diacetyloxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-[[(3s,5r,8r,9s,10s,13r,14s,16s,17r)-16-acetyloxy-14-hydroxy-10,13-dimethyl-17-(5-oxo-2h-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17 Chemical compound O([C@H]1[C@@H](OC(C)=O)C[C@@H](O[C@@H]1C)O[C@H]1[C@@H](OC(C)=O)C[C@@H](O[C@@H]1C)O[C@@H]1C[C@@H]2[C@]([C@@H]3[C@H]([C@]4(C[C@@H]([C@@H]([C@@]4(C)CC3)C=3COC(=O)C=3)OC(C)=O)O)CC2)(C)CC1)[C@H]1C[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](C)O1 JDYLJSDIEBHXPO-ALNZGLKXSA-N 0.000 description 1
SPKNARKFCOPTSY-XWPZMVOTSA-N [(2r,3s)-2-[(2s,3r)-3-methyloxiran-2-yl]-6-oxo-2,3-dihydropyran-3-yl] acetate Chemical compound C[C@H]1O[C@@H]1[C@H]1[C@@H](OC(C)=O)C=CC(=O)O1 SPKNARKFCOPTSY-XWPZMVOTSA-N 0.000 description 1
VZPXFHVJUUSVLH-VNJAQMQMSA-N [(2r,3s)-4-(dimethylamino)-3-methyl-1,2-diphenylbutan-2-yl] propanoate;naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21.C([C@@](OC(=O)CC)([C@@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 VZPXFHVJUUSVLH-VNJAQMQMSA-N 0.000 description 1
XIRGHRXBGGPPKY-OTPQUNEMSA-N [(2r,3s,4r,6s)-6-[(2'r,3's,3ar,4r,4'r,6s,7ar)-6-[(2s,3r,4r,5s,6r)-2-[(2r,3s,4s,5s,6s)-6-[(2r,3as,3'ar,6'r,7r,7's,7ar,7'ar)-7'-acetyl-7'-hydroxy-6'-methyl-7-(2-methylpropanoyloxy)spiro[4,6,7,7a-tetrahydro-3ah-[1,3]dioxolo[4,5-c]pyran-2,4'-6,7a-dihydro-3ah- Chemical compound O([C@H]1[C@H](O)C[C@@H](O[C@@H]1C)O[C@H]1[C@H](O)CC2(O[C@]3(C)C[C@@H](O[C@H](C)[C@H]3O2)O[C@H]2[C@@H](OC)[C@@H](C)O[C@H]([C@@H]2O)O[C@H]2[C@H](O)[C@H](OC)[C@H](OC3[C@@H]([C@@H]4O[C@]5(O[C@H]4CO3)[C@@H]3OCO[C@H]3[C@@](O)([C@@H](C)O5)C(C)=O)OC(=O)C(C)C)O[C@@H]2COC)O[C@@H]1C)C(=O)C1=C(C)C(Cl)=C(O)C(Cl)=C1OC XIRGHRXBGGPPKY-OTPQUNEMSA-N 0.000 description 1
IUSFTUWHKCSCDY-QTKZZPNDSA-N [(2s,3s)-5-[2-(dimethylamino)ethyl]-2-(4-methoxyphenyl)-4-oxo-2,3-dihydro-1,5-benzothiazepin-3-yl] acetate;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.C1=CC(OC)=CC=C1[C@H]1[C@@H](OC(C)=O)C(=O)N(CCN(C)C)C2=CC=CC=C2S1 IUSFTUWHKCSCDY-QTKZZPNDSA-N 0.000 description 1
AYSBIMSATXNCSF-VFEFFJNBSA-N [(3S,5S,8R,9S,10S,13R,14S,17S)-17-[(1S)-1-acetyloxyethyl]-3-(dimethylamino)-10-methyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-13-yl]methyl acetate Chemical compound C[C@H](OC(C)=O)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3CC[C@]12COC(C)=O)N(C)C AYSBIMSATXNCSF-VFEFFJNBSA-N 0.000 description 1
ZSYULWHBPBAOKV-TXEJJXNPSA-N [(3ar,6as)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]pyrrol-5-yl]-phenylmethanone Chemical compound C([C@H]1COC[C@H]1C1)N1C(=O)C1=CC=CC=C1 ZSYULWHBPBAOKV-TXEJJXNPSA-N 0.000 description 1
YYBNDIVPHIWTPK-KYJQVDHRSA-N [(3as,8bs)-3,4,8b-trimethyl-1,2,3,3a-tetrahydropyrrolo[2,3-b]indol-3-ium-7-yl] n-methylcarbamate;sulfate Chemical compound [O-]S([O-])(=O)=O.C12=CC(OC(=O)NC)=CC=C2N(C)[C@@H]2[C@@]1(C)CC[NH+]2C.C12=CC(OC(=O)NC)=CC=C2N(C)[C@@H]2[C@@]1(C)CC[NH+]2C YYBNDIVPHIWTPK-KYJQVDHRSA-N 0.000 description 1
MDJOZYCYNUJABP-HKUYNNGSSA-N [(3r)-1-azabicyclo[2.2.2]octan-3-yl] (2r)-3-hydroxy-2-imidazol-1-yl-2-phenylpropanoate Chemical compound C1([C@](C(=O)O[C@@H]2C3CCN(CC3)C2)(CO)N2C=NC=C2)=CC=CC=C1 MDJOZYCYNUJABP-HKUYNNGSSA-N 0.000 description 1
WTIJXIZOODAMJT-WBACWINTSA-N [(3r,4s,5r,6s)-5-hydroxy-6-[4-hydroxy-3-[[5-[[4-hydroxy-7-[(2s,3r,4s,5r)-3-hydroxy-5-methoxy-6,6-dimethyl-4-(5-methyl-1h-pyrrole-2-carbonyl)oxyoxan-2-yl]oxy-8-methyl-2-oxochromen-3-yl]carbamoyl]-4-methyl-1h-pyrrole-3-carbonyl]amino]-8-methyl-2-oxochromen- Chemical compound O([C@@H]1[C@H](C(O[C@H](OC=2C(=C3OC(=O)C(NC(=O)C=4C(=C(C(=O)NC=5C(OC6=C(C)C(O[C@@H]7[C@@H]([C@H](OC(=O)C=8NC(C)=CC=8)[C@@H](OC)C(C)(C)O7)O)=CC=C6C=5O)=O)NC=4)C)=C(O)C3=CC=2)C)[C@@H]1O)(C)C)OC)C(=O)C1=CC=C(C)N1 WTIJXIZOODAMJT-WBACWINTSA-N 0.000 description 1
KSCZWFXQKITHSL-OKCNGXCSSA-N [(3s,8r,9s,10r,13s,14s,17r)-17-acetyl-17-acetyloxy-6-chloro-10,13-dimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate Chemical compound C1C[C@]2(C)[C@](C(C)=O)(OC(C)=O)CC[C@H]2[C@@H]2C=C(Cl)C3=C[C@@H](OC(=O)C)CC[C@]3(C)[C@H]21 KSCZWFXQKITHSL-OKCNGXCSSA-N 0.000 description 1
FYTLCZSXKONUTF-OIELIUQCSA-N [(5s,8r,9s,10s,13s,14s,17s)-2,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] acetate Chemical compound C([C@@H]1CC2)C(=O)C(C)=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](OC(=O)C)[C@@]2(C)CC1 FYTLCZSXKONUTF-OIELIUQCSA-N 0.000 description 1
FFVXQGMUHIJQAO-KXUCESEGSA-N [(6s,6ar,9r,10ar)-9-hydroxy-6-methyl-3-(5-phenylpentan-2-yloxy)-5,6,6a,7,8,9,10,10a-octahydrophenanthridin-1-yl] acetate Chemical compound C=1([C@@H]2C[C@H](O)CC[C@H]2[C@H](C)NC=1C=1)C(OC(C)=O)=CC=1OC(C)CCCC1=CC=CC=C1 FFVXQGMUHIJQAO-KXUCESEGSA-N 0.000 description 1
QRRVOCXLQYLNEC-PPJDWOAVSA-N [(6s,8s,9s,10r,11s,13s,14s,17r)-17-(2-acetyloxyacetyl)-11-hydroxy-6,10,13-trimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1h-cyclopenta[a]phenanthren-17-yl] butanoate Chemical compound C1([C@@H](C)C2)=CC(=O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@@](C(=O)COC(C)=O)(OC(=O)CCC)[C@@]2(C)C[C@@H]1O QRRVOCXLQYLNEC-PPJDWOAVSA-N 0.000 description 1
JXWVQHSDWAODPY-HHJIKABBSA-N [(6s,8s,9s,10r,11s,13s,14s,17r)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-17-yl] pentanoate Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@@](C(=O)CO)(OC(=O)CCCC)[C@@]2(C)C[C@@H]1O JXWVQHSDWAODPY-HHJIKABBSA-N 0.000 description 1
ZWBTYMGEBZUQTK-PVLSIAFMSA-N [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-1'-(2-methylpropyl)-6,23-dioxospiro[8,33-dioxa-24,27,29-triazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(32),2,4,9,19,21,24,26,30-nonaene-28,4'-piperidine]-13-yl] acetate Chemical compound CO[C@H]1\C=C\O[C@@]2(C)Oc3c(C2=O)c2c4NC5(CCN(CC(C)C)CC5)N=c4c(=NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(O)c2c(O)c3C ZWBTYMGEBZUQTK-PVLSIAFMSA-N 0.000 description 1
VRJOZKQKYDFLGF-UHFFFAOYSA-N [(8-methyl-8-azabicyclo[3.2.1]octan-3-ylidene)amino] 3,4,5-trimethoxybenzoate Chemical compound COC1=C(OC)C(OC)=CC(C(=O)ON=C2CC3CCC(N3C)C2)=C1 VRJOZKQKYDFLGF-UHFFFAOYSA-N 0.000 description 1
IWSXBCZCPVUWHT-VIFKTUCRSA-N [(8r,9s,10r,11s,13s,14s,17r)-17-acetyl-11,13-dimethyl-3-oxo-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl] acetate Chemical compound O=C1CC[C@@H]2[C@H]3[C@@H](C)C[C@]4(C)[C@](C(C)=O)(OC(C)=O)CC[C@H]4[C@@H]3CCC2=C1 IWSXBCZCPVUWHT-VIFKTUCRSA-N 0.000 description 1
WWSKHPDYSWDMNC-YRNSVOBJSA-N [(8r,9s,10r,13s,14s,16r,17r)-17-acetyl-6-chloro-10,13,16-trimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1h-cyclopenta[a]phenanthren-17-yl] acetate Chemical compound C1=C(Cl)C2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(C)=O)(OC(C)=O)[C@@]1(C)CC2 WWSKHPDYSWDMNC-YRNSVOBJSA-N 0.000 description 1
PSJMYDLEWUWIAN-KYPKCDLESA-N [(8r,9s,10r,13s,14s,17r)-17-acetyl-6-chloro-13-methyl-3-oxo-1,2,8,9,10,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-17-yl] acetate Chemical compound C1=C(Cl)C2=CC(=O)CC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 PSJMYDLEWUWIAN-KYPKCDLESA-N 0.000 description 1
AHMMSNQYOPMLSX-CNQKSJKFSA-N [(8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] undec-10-enoate Chemical compound O=C1C=C[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)OC(=O)CCCCCCCCC=C)[C@@H]4[C@@H]3CCC2=C1 AHMMSNQYOPMLSX-CNQKSJKFSA-N 0.000 description 1
OVTRPNSKIPQZEC-NJLPOHDGSA-N [(8s,9r,10s,11s,13s,14s,16r,17r)-17-(2-acetyloxyacetyl)-9-chloro-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] butanoate Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(Cl)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COC(C)=O)(OC(=O)CCC)[C@@]1(C)C[C@@H]2O OVTRPNSKIPQZEC-NJLPOHDGSA-N 0.000 description 1
CDKNUFNIFGPFSF-AYVLZSQQSA-N [(8s,9s,10r,11s,13s,14s,17r)-11-hydroxy-10,13-dimethyl-3-oxo-17-(2-propanoylsulfanylacetyl)-2,6,7,8,9,11,12,14,15,16-decahydro-1h-cyclopenta[a]phenanthren-17-yl] butanoate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)CSC(=O)CC)(OC(=O)CCC)[C@@]1(C)C[C@@H]2O CDKNUFNIFGPFSF-AYVLZSQQSA-N 0.000 description 1
AEVUURWLDCELOV-AYVPJYCDSA-N [(9s,13s,14s,17s)-17-(furan-3-yl)-17-hydroxy-13-methyl-9,11,12,14,15,16-hexahydro-6h-cyclopenta[a]phenanthren-3-yl] acetate Chemical compound C=1([C@]2(O)CC[C@@H]3[C@]2(C)CC[C@@H]2C4=CC=C(C=C4CC=C23)OC(=O)C)C=COC=1 AEVUURWLDCELOV-AYVPJYCDSA-N 0.000 description 1
QNBVYCDYFJUNLO-UHDJGPCESA-N [(e)-(1-methylpyridin-2-ylidene)methyl]-oxoazanium;iodide Chemical compound [I-].CN1C=CC=C\C1=C/[NH+]=O QNBVYCDYFJUNLO-UHDJGPCESA-N 0.000 description 1
XPHBRTNHVJSEQD-ATJXCDBQSA-N [(z)-[3-(diethylamino)-1-phenylpropylidene]amino] n-(4-methoxyphenyl)carbamate Chemical compound C=1C=CC=CC=1C(/CCN(CC)CC)=N\OC(=O)NC1=CC=C(OC)C=C1 XPHBRTNHVJSEQD-ATJXCDBQSA-N 0.000 description 1
QJGVXJYGDBSPSJ-UHFFFAOYSA-N [1-(6,7-dimethoxyphthalazin-1-yl)piperidin-4-yl] n-ethylcarbamate Chemical compound C1CC(OC(=O)NCC)CCN1C1=NN=CC2=CC(OC)=C(OC)C=C12 QJGVXJYGDBSPSJ-UHFFFAOYSA-N 0.000 description 1
KMLCRELJHYKIIL-UHFFFAOYSA-N [1-(azanidylmethyl)cyclohexyl]methylazanide;platinum(2+);sulfuric acid Chemical compound [Pt+2].OS(O)(=O)=O.[NH-]CC1(C[NH-])CCCCC1 KMLCRELJHYKIIL-UHFFFAOYSA-N 0.000 description 1
AVXDZNOJIVOGRR-UHFFFAOYSA-N [2-(diethylamino)-1-phenylethyl] benzoate Chemical compound C=1C=CC=CC=1C(CN(CC)CC)OC(=O)C1=CC=CC=C1 AVXDZNOJIVOGRR-UHFFFAOYSA-N 0.000 description 1
ODEDPKNSRBCSDO-UHFFFAOYSA-N [2-(hexadecylsulfanylmethyl)-3-methoxypropyl] 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCCSCC(COC)COP([O-])(=O)OCC[N+](C)(C)C ODEDPKNSRBCSDO-UHFFFAOYSA-N 0.000 description 1
ICKMASVVMCGZLR-UHFFFAOYSA-N [2-[(4-chlorophenyl)carbamoyl]-4,6-diiodophenyl] acetate Chemical compound CC(=O)OC1=C(I)C=C(I)C=C1C(=O)NC1=CC=C(Cl)C=C1 ICKMASVVMCGZLR-UHFFFAOYSA-N 0.000 description 1
UWGRWFCLGQWKPR-GSTUPEFVSA-N [2-[(6s,8s,9r,10s,11s,13s,14s,16r,17s)-6,9-difluoro-11-hydroxy-10,13,16-trimethyl-3-oxo-7,8,11,12,14,15,16,17-octahydro-6h-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] 2,2-dimethylpropanoate Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@@H](C)[C@H](C(=O)COC(=O)C(C)(C)C)[C@@]2(C)C[C@@H]1O UWGRWFCLGQWKPR-GSTUPEFVSA-N 0.000 description 1
DPHFJXVKASDMBW-RQRKFSSASA-N [2-[(8s,9r,10s,11s,13s,14s,16r,17r)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate;hydrate Chemical compound O.C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@@H](C)[C@@](C(=O)COC(C)=O)(O)[C@@]1(C)C[C@@H]2O DPHFJXVKASDMBW-RQRKFSSASA-N 0.000 description 1
UYVYDRXVNVNQEA-BJTOFBPUSA-N [2-[(8s,9r,10s,11s,13s,14s,16s,17r)-9-chloro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl]-2-oxoethyl] 4-(acetamidomethyl)cyclohexane-1-carboxylate Chemical compound O=C([C@]1(O)[C@@]2(C)C[C@H](O)[C@]3(Cl)[C@@]4(C)C=CC(=O)C=C4CC[C@H]3[C@@H]2C[C@@H]1C)COC(=O)C1CCC(CNC(C)=O)CC1 UYVYDRXVNVNQEA-BJTOFBPUSA-N 0.000 description 1
HLAFSNJRKZLMPT-UHFFFAOYSA-N [2-[2-(aminomethyl)phenyl]sulfanylphenyl]methanol Chemical compound NCC1=CC=CC=C1SC1=CC=CC=C1CO HLAFSNJRKZLMPT-UHFFFAOYSA-N 0.000 description 1
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LMOINURANNBYCM-UHFFFAOYSA-N metaproterenol Chemical compound CC(C)NCC(O)C1=CC(O)=CC(O)=C1 LMOINURANNBYCM-UHFFFAOYSA-N 0.000 description 1
229960003663 metaraminol Drugs 0.000 description 1
229960000509 metaxalone Drugs 0.000 description 1
YEOTYALSMRNXLJ-UHFFFAOYSA-N metazosin Chemical compound C1CN(C(=O)C(C)OC)CCN1C1=NC(N)=C(C=C(OC)C(OC)=C2)C2=N1 YEOTYALSMRNXLJ-UHFFFAOYSA-N 0.000 description 1
229950006294 meteneprost Drugs 0.000 description 1
229960004650 metergoline Drugs 0.000 description 1
WZHJKEUHNJHDLS-QTGUNEKASA-N metergoline Chemical compound C([C@H]1CN([C@H]2[C@@H](C=3C=CC=C4N(C)C=C(C=34)C2)C1)C)NC(=O)OCC1=CC=CC=C1 WZHJKEUHNJHDLS-QTGUNEKASA-N 0.000 description 1
JHPHVAVFUYTVCL-UHFFFAOYSA-M methacholine chloride Chemical compound [Cl-].C[N+](C)(C)CC(C)OC(C)=O JHPHVAVFUYTVCL-UHFFFAOYSA-M 0.000 description 1
229960002931 methacholine chloride Drugs 0.000 description 1
229960001797 methadone Drugs 0.000 description 1
TWXDDNPPQUTEOV-FVGYRXGTSA-N methamphetamine hydrochloride Chemical compound Cl.CN[C@@H](C)CC1=CC=CC=C1 TWXDDNPPQUTEOV-FVGYRXGTSA-N 0.000 description 1
229960002532 methamphetamine hydrochloride Drugs 0.000 description 1
KPQJSSLKKBKWEW-RKDOVGOJSA-N methanesulfonic acid;5-nitro-2-[(2r)-1-[2-[[(2r)-2-(5-nitro-1,3-dioxobenzo[de]isoquinolin-2-yl)propyl]amino]ethylamino]propan-2-yl]benzo[de]isoquinoline-1,3-dione Chemical compound CS(O)(=O)=O.CS(O)(=O)=O.[O-][N+](=O)C1=CC(C(N([C@@H](CNCCNC[C@@H](C)N2C(C=3C=C(C=C4C=CC=C(C=34)C2=O)[N+]([O-])=O)=O)C)C2=O)=O)=C3C2=CC=CC3=C1 KPQJSSLKKBKWEW-RKDOVGOJSA-N 0.000 description 1
OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
229960002803 methaqualone Drugs 0.000 description 1
NRZPASQBOYNGHR-HWROMZCQSA-M methicillin sodium monohydrate Chemical compound O.[Na+].COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C([O-])=O)C(C)(C)S[C@@H]21 NRZPASQBOYNGHR-HWROMZCQSA-M 0.000 description 1
PMRYVIKBURPHAH-UHFFFAOYSA-N methimazole Chemical compound CN1C=CNC1=S PMRYVIKBURPHAH-UHFFFAOYSA-N 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
229950008237 methitural Drugs 0.000 description 1
229960002330 methocarbamol Drugs 0.000 description 1
229960002683 methohexital Drugs 0.000 description 1
229960000485 methotrexate Drugs 0.000 description 1
DASQOOZCTWOQPA-GXKRWWSZSA-L methotrexate disodium Chemical compound [Na+].[Na+].C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC([O-])=O)C([O-])=O)C=C1 DASQOOZCTWOQPA-GXKRWWSZSA-L 0.000 description 1
QTQPGZVDUCMVLK-ZXFNITATSA-N methoxymethyl (2s,5r,6r)-6-[(4r)-2,2-dimethyl-5-oxo-4-phenylimidazolidin-1-yl]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate Chemical compound C1([C@@H]2C(=O)N(C(N2)(C)C)[C@H]2[C@@H]3N(C2=O)[C@H](C(S3)(C)C)C(=O)OCOC)=CC=CC=C1 QTQPGZVDUCMVLK-ZXFNITATSA-N 0.000 description 1
ALPPGSBMHVCELA-WHUUVLPESA-N methyl (19E,21E,23E,25E,27E,29E,31E)-33-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-17-[7-(4-aminophenyl)-5-hydroxy-7-oxoheptan-2-yl]-1,3,5,7,9,13,37-heptahydroxy-18-methyl-11,15-dioxo-16,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylate methyl (19E,21E,23E,25E,27E,29E,31E)-33-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-1,3,5,7,9,13,37-heptahydroxy-17-[5-hydroxy-7-[4-(methylamino)phenyl]-7-oxoheptan-2-yl]-18-methyl-11,15-dioxo-16,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylate Chemical compound CC1\C=C\C=C\C=C\C=C\C=C\C=C\C=C\C(O[C@H]2[C@H]([C@@H](N)[C@H](O)[C@@H](C)O2)O)CC(O2)C(C(=O)OC)C(O)CC2(O)CC(O)CC(O)CC(O)CC(O)CC(=O)CC(O)CC(=O)OC1C(C)CCC(O)CC(=O)C1=CC=C(N)C=C1.C1=CC(NC)=CC=C1C(=O)CC(O)CCC(C)C1C(C)/C=C/C=C/C=C/C=C/C=C/C=C/C=C/C(O[C@H]2[C@H]([C@@H](N)[C@H](O)[C@@H](C)O2)O)CC(O2)C(C(=O)OC)C(O)CC2(O)CC(O)CC(O)CC(O)CC(O)CC(=O)CC(O)CC(=O)O1 ALPPGSBMHVCELA-WHUUVLPESA-N 0.000 description 1
ZHAGGRWTJXROKV-HJOGWXRNSA-N methyl (2s)-2-[[(2s)-2-[[(2s)-2-acetamido-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-3-(1h-imidazol-5-yl)propanoate Chemical compound C([C@@H](C(=O)OC)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CC=1C=CC=CC=1)NC(C)=O)C1=CNC=N1 ZHAGGRWTJXROKV-HJOGWXRNSA-N 0.000 description 1
CBKLICUQYUTWQL-XWGBWKJCSA-N methyl (3s,4r)-3-methyl-1-(2-phenylethyl)-4-(n-propanoylanilino)piperidine-4-carboxylate;oxalic acid Chemical compound OC(=O)C(O)=O.CCC(=O)N([C@]1([C@H](CN(CCC=2C=CC=CC=2)CC1)C)C(=O)OC)C1=CC=CC=C1 CBKLICUQYUTWQL-XWGBWKJCSA-N 0.000 description 1
QQCOAAFKJZXJFP-GANRVJIKSA-N methyl (Z)-7-[(1S,2S,3S,5R)-3,5-dihydroxy-2-[(E,3R)-3-hydroxy-3-methyloct-1-enyl]cyclopentyl]hept-5-enoate Chemical group CCCCC[C@@](C)(O)\C=C\[C@@H]1[C@@H](O)C[C@@H](O)[C@H]1C\C=C/CCCC(=O)OC QQCOAAFKJZXJFP-GANRVJIKSA-N 0.000 description 1
ZZVPHCPLTZTOBC-BZXXIRPUSA-N methyl (e)-7-[(1r,2r,3r)-2-[(1e,5e)-6-(cyclopenten-1-yl)-4-hydroxy-4-methylhexa-1,5-dienyl]-3-hydroxy-5-oxocyclopentyl]hept-4-enoate Chemical compound O[C@@H]1CC(=O)[C@H](CC/C=C/CCC(=O)OC)[C@H]1\C=C\CC(C)(O)\C=C\C1=CCCC1 ZZVPHCPLTZTOBC-BZXXIRPUSA-N 0.000 description 1
CIBHDGPIOICRGX-ZQCHCGQNSA-N methyl (z)-7-[(1r,2r,3r)-3-hydroxy-2-[(e)-4-hydroxy-4-methyloct-1-enyl]-5-oxocyclopentyl]hept-4-enoate Chemical compound CCCCC(C)(O)C\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CC\C=C/CCC(=O)OC CIBHDGPIOICRGX-ZQCHCGQNSA-N 0.000 description 1
VKQFCGNPDRICFG-UHFFFAOYSA-N methyl 2-methylpropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OCC(C)C)C1C1=CC=CC=C1[N+]([O-])=O VKQFCGNPDRICFG-UHFFFAOYSA-N 0.000 description 1
YFEDJMLMWJSRJJ-UHFFFAOYSA-N methyl 3-amino-2-(5-methoxy-1h-indol-3-yl)propanoate Chemical compound C1=C(OC)C=C2C(C(CN)C(=O)OC)=CNC2=C1 YFEDJMLMWJSRJJ-UHFFFAOYSA-N 0.000 description 1
VSIUFPQOEIKNCY-UHFFFAOYSA-N methyl 4-oxo-6,7-di(propan-2-yloxy)-1h-quinoline-3-carboxylate Chemical compound CC(C)OC1=C(OC(C)C)C=C2C(=O)C(C(=O)OC)=CNC2=C1 VSIUFPQOEIKNCY-UHFFFAOYSA-N 0.000 description 1
ASSMECARUIRCML-UHFFFAOYSA-N methyl 6-methyl-2-[(3-methylpyridin-2-yl)methylsulfinyl]-1h-benzimidazole-5-carboxylate Chemical compound N1C=2C=C(C)C(C(=O)OC)=CC=2N=C1S(=O)CC1=NC=CC=C1C ASSMECARUIRCML-UHFFFAOYSA-N 0.000 description 1
NMYCTBARPUAEQN-UHFFFAOYSA-N methyl 7-(diethylamino)-4-oxo-6-propyl-1h-quinoline-3-carboxylate Chemical compound N1C=C(C(=O)OC)C(=O)C2=C1C=C(N(CC)CC)C(CCC)=C2 NMYCTBARPUAEQN-UHFFFAOYSA-N 0.000 description 1
OJLOPKGSLYJEMD-URPKTTJQSA-N methyl 7-[(1r,2r,3r)-3-hydroxy-2-[(1e)-4-hydroxy-4-methyloct-1-en-1-yl]-5-oxocyclopentyl]heptanoate Chemical compound CCCCC(C)(O)C\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(=O)OC OJLOPKGSLYJEMD-URPKTTJQSA-N 0.000 description 1
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Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
- A61K9/2081—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets with microcapsules or coated microparticles according to A61K9/50
- 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
- A61K31/435—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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- 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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Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Medicinal Chemistry (AREA)
Epidemiology (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Biophysics (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Molecular Biology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Immunology (AREA)
Pulmonology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)

UA2003076286A 2000-12-07 2001-06-12 Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці UA80393C2 (uk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP00126847		2000-12-07
PCT/EP2001/014307 WO2002045693A1 (en)	2000-12-07	2001-12-06	Pharmaceutical preparation comprising an active dispersed on a matrix

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UA80393C2 true UA80393C2 (uk)	2007-09-25

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Country Status (28)

Country	Link
US (2)	US7175854B2 (de)
EP (1)	EP1341527B1 (de)
JP (1)	JP4950409B2 (de)
KR (1)	KR20030072557A (de)
CN (2)	CN101810592A (de)
AT (1)	ATE519481T1 (de)
AU (2)	AU2002216073B2 (de)
BR (1)	BR0115987A (de)
CA (1)	CA2430828C (de)
CY (1)	CY1112333T1 (de)
CZ (1)	CZ20031881A3 (de)
DK (1)	DK1341527T3 (de)
EA (1)	EA007151B1 (de)
EE (1)	EE05256B1 (de)
ES (1)	ES2371060T3 (de)
HR (1)	HRP20030493B1 (de)
HU (1)	HUP0400566A3 (de)
IL (2)	IL155964A0 (de)
MX (1)	MXPA03005092A (de)
NO (1)	NO333722B1 (de)
NZ (1)	NZ526015A (de)
PL (1)	PL206595B1 (de)
PT (1)	PT1341527E (de)
SG (1)	SG148028A1 (de)
SI (1)	SI1341527T1 (de)
UA (1)	UA80393C2 (de)
WO (1)	WO2002045693A1 (de)
ZA (1)	ZA200305114B (de)

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FR2754177B1 (fr) *	1996-10-07	1999-08-06	Sanofi Sa	Microspheres pharmaceutiques d'acide valproique pour administration orale
UA80393C2 (uk) *	2000-12-07	2007-09-25	Алтана Фарма Аг	Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці
SI1341524T1 (sl) *	2000-12-07	2012-02-29	Nycomed Gmbh	Farmacevtski pripravek v obliki paste, ki obsega kislinsko labilno učinkovino
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2001
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- 2001-12-06 MX MXPA03005092A patent/MXPA03005092A/es active IP Right Grant
- 2001-12-06 AT AT01999359T patent/ATE519481T1/de active
- 2001-12-06 EE EEP200300235A patent/EE05256B1/xx not_active IP Right Cessation
- 2001-12-06 CZ CZ20031881A patent/CZ20031881A3/cs unknown
- 2001-12-06 SG SG200503573-8A patent/SG148028A1/en unknown
- 2001-12-06 PL PL362323A patent/PL206595B1/pl unknown
- 2001-12-06 CA CA2430828A patent/CA2430828C/en not_active Expired - Fee Related
- 2001-12-06 SI SI200131002T patent/SI1341527T1/sl unknown
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- 2001-12-06 CN CN201010149221A patent/CN101810592A/zh active Pending
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- 2001-12-06 EP EP01999359A patent/EP1341527B1/de not_active Expired - Lifetime
- 2001-12-06 HU HU0400566A patent/HUP0400566A3/hu not_active Application Discontinuation
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- 2001-12-06 US US10/433,398 patent/US7175854B2/en not_active Expired - Fee Related
- 2001-12-06 KR KR10-2003-7007647A patent/KR20030072557A/ko not_active Ceased
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- 2003-06-06 NO NO20032593A patent/NO333722B1/no not_active IP Right Cessation
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Also Published As

Publication number	Publication date
NO333722B1 (no)	2013-09-02
BR0115987A (pt)	2003-12-23
HRP20030493A2 (en)	2005-06-30
KR20030072557A (ko)	2003-09-15
EA007151B1 (ru)	2006-08-25
EP1341527A1 (de)	2003-09-10
PT1341527E (pt)	2011-10-04
AU2002216073B2 (en)	2006-11-23
EP1341527B1 (de)	2011-08-10
AU1607302A (en)	2002-06-18
WO2002045693A1 (en)	2002-06-13
ZA200305114B (en)	2004-05-12
HRP20030493B1 (hr)	2011-10-31
NO20032593L (no)	2003-08-05
CN1523980A (zh)	2004-08-25
DK1341527T3 (da)	2011-10-24
CA2430828A1 (en)	2002-06-13
ES2371060T3 (es)	2011-12-27
ATE519481T1 (de)	2011-08-15
MXPA03005092A (es)	2003-09-05
JP2004514736A (ja)	2004-05-20
PL362323A1 (en)	2004-10-18
EA200300634A1 (ru)	2003-12-25
CZ20031881A3 (en)	2004-04-14
US20040058896A1 (en)	2004-03-25
PL206595B1 (pl)	2010-08-31
NO20032593D0 (no)	2003-06-06
JP4950409B2 (ja)	2012-06-13
EE200300235A (et)	2003-08-15
US7175854B2 (en)	2007-02-13
IL155964A (en)	2012-06-28
IL155964A0 (en)	2003-12-23
NZ526015A (en)	2006-03-31
SG148028A1 (en)	2008-12-31
US20070122474A1 (en)	2007-05-31
HUP0400566A3 (en)	2012-09-28
CA2430828C (en)	2010-11-09
SI1341527T1 (sl)	2011-12-30
CY1112333T1 (el)	2015-12-09
CN101810592A (zh)	2010-08-25
US7951398B2 (en)	2011-05-31
HUP0400566A2 (hu)	2004-06-28
EE05256B1 (et)	2010-02-15

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KR20220126287A (ko)	2022-09-15	멀티모달 조성물 및 치료 방법
DE10061137A1 (de)	2002-06-20	Neue pharmazeutische Zubereitung