JP2005529155A5 - - Google Patents
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- Publication number
- JP2005529155A5 JP2005529155A5 JP2004506758A JP2004506758A JP2005529155A5 JP 2005529155 A5 JP2005529155 A5 JP 2005529155A5 JP 2004506758 A JP2004506758 A JP 2004506758A JP 2004506758 A JP2004506758 A JP 2004506758A JP 2005529155 A5 JP2005529155 A5 JP 2005529155A5
- Authority
- JP
- Japan
- Prior art keywords
- dimethylcarbamoyloxyphenyl
- ylamino
- pyrimidin
- diethylamino
- propionic acid
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 19
- 150000003839 salts Chemical class 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 125000001309 chloro group Chemical group Cl* 0.000 claims 6
- 125000001153 fluoro group Chemical group F* 0.000 claims 6
- 201000010099 disease Diseases 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- -1 4-fluorobenzenesulfonyl Chemical group 0.000 claims 4
- 102000006495 integrins Human genes 0.000 claims 4
- 108010044426 integrins Proteins 0.000 claims 4
- 230000001404 mediated effect Effects 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 208000027866 inflammatory disease Diseases 0.000 claims 2
- XCHMCUCXTAVCLX-UHFFFAOYSA-N 2-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound OC(=O)C(C)C1=CC=C(OC(=O)N(C)C)C=C1 XCHMCUCXTAVCLX-UHFFFAOYSA-N 0.000 claims 1
- UEHGISKTKRLKLO-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(2,4-difluorophenyl)sulfonyl-prop-2-ynylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(CC#C)S(=O)(=O)C1=CC=C(F)C=C1F UEHGISKTKRLKLO-UHFFFAOYSA-N 0.000 claims 1
- YQPPFPAOQXSSBY-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(2,4-difluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=C(F)C=C1F YQPPFPAOQXSSBY-UHFFFAOYSA-N 0.000 claims 1
- QNBPSKYQBURTTK-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(2-fluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=CC=C1F QNBPSKYQBURTTK-UHFFFAOYSA-N 0.000 claims 1
- XGZSKLPECGWKPZ-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(3,4-difluorophenyl)sulfonyl-propan-2-ylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(C(C)C)S(=O)(=O)C1=CC=C(F)C(F)=C1 XGZSKLPECGWKPZ-UHFFFAOYSA-N 0.000 claims 1
- QKAALEADKHAZAF-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(3,4-difluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=C(F)C(F)=C1 QKAALEADKHAZAF-UHFFFAOYSA-N 0.000 claims 1
- NADHCGMMZGXNJU-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(3,5-difluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC(F)=CC(F)=C1 NADHCGMMZGXNJU-UHFFFAOYSA-N 0.000 claims 1
- PFFXAHQMJBDKHJ-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(3-fluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=CC(F)=C1 PFFXAHQMJBDKHJ-UHFFFAOYSA-N 0.000 claims 1
- CFDKPPWKFDOSSA-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(4-fluorophenyl)sulfonyl-(2-methylpropyl)amino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(CC(C)C)S(=O)(=O)C1=CC=C(F)C=C1 CFDKPPWKFDOSSA-UHFFFAOYSA-N 0.000 claims 1
- JODSWHRKWYEUDL-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(4-fluorophenyl)sulfonyl-prop-2-ynylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(CC#C)S(=O)(=O)C1=CC=C(F)C=C1 JODSWHRKWYEUDL-UHFFFAOYSA-N 0.000 claims 1
- RAPVDKCWUQBKGG-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(4-fluorophenyl)sulfonyl-propan-2-ylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(C(C)C)S(=O)(=O)C1=CC=C(F)C=C1 RAPVDKCWUQBKGG-UHFFFAOYSA-N 0.000 claims 1
- WWBYAPLJMTZOTK-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[(4-fluorophenyl)sulfonylmethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=C(F)C=C1 WWBYAPLJMTZOTK-UHFFFAOYSA-N 0.000 claims 1
- AIGZEIASVOBQCI-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[2-(2,3-difluorophenyl)sulfonylethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC=CC(F)=C1F AIGZEIASVOBQCI-UHFFFAOYSA-N 0.000 claims 1
- PQYHPONWVXTFQW-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[2-(2,4-difluorophenyl)sulfonylethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC=C(F)C=C1F PQYHPONWVXTFQW-UHFFFAOYSA-N 0.000 claims 1
- KBVXEABVOVICFP-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[2-(3,4-difluorophenyl)sulfonylethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC=C(F)C(F)=C1 KBVXEABVOVICFP-UHFFFAOYSA-N 0.000 claims 1
- FQXLXEDBFFIHNX-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[2-(3,5-difluorophenyl)sulfonylethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC(F)=CC(F)=C1 FQXLXEDBFFIHNX-UHFFFAOYSA-N 0.000 claims 1
- KGSLYLUBNSUZQN-UHFFFAOYSA-N 2-[[2-(diethylamino)-5-[2-(4-fluorophenyl)sulfonylethylamino]pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC=C(F)C=C1 KGSLYLUBNSUZQN-UHFFFAOYSA-N 0.000 claims 1
- XCPNGIQSOZEOOZ-UHFFFAOYSA-N 2-[[5-(benzenesulfonylmethylamino)-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=CC=C1 XCPNGIQSOZEOOZ-UHFFFAOYSA-N 0.000 claims 1
- BMCDGJILQKTGDV-UHFFFAOYSA-N 2-[[5-[(3,4-dichlorophenyl)sulfonylmethylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=C(Cl)C(Cl)=C1 BMCDGJILQKTGDV-UHFFFAOYSA-N 0.000 claims 1
- FPIRQHBDFYJJDM-UHFFFAOYSA-N 2-[[5-[(3,5-dichlorophenyl)sulfonylmethylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC(Cl)=CC(Cl)=C1 FPIRQHBDFYJJDM-UHFFFAOYSA-N 0.000 claims 1
- BBTTXCPSXDESDD-UHFFFAOYSA-N 2-[[5-[(4-chlorophenyl)sulfonyl-propan-2-ylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(C(C)C)S(=O)(=O)C1=CC=C(Cl)C=C1 BBTTXCPSXDESDD-UHFFFAOYSA-N 0.000 claims 1
- IQIAJOUTZIBYET-UHFFFAOYSA-N 2-[[5-[(4-chlorophenyl)sulfonylmethylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCS(=O)(=O)C1=CC=C(Cl)C=C1 IQIAJOUTZIBYET-UHFFFAOYSA-N 0.000 claims 1
- MAZNQIVGHXAJRX-UHFFFAOYSA-N 2-[[5-[2-(3,5-dichlorophenyl)sulfonylethylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC(Cl)=CC(Cl)=C1 MAZNQIVGHXAJRX-UHFFFAOYSA-N 0.000 claims 1
- QBKUKQMAGFTCQA-UHFFFAOYSA-N 2-[[5-[2-(4-chlorophenyl)sulfonylethylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1NCCS(=O)(=O)C1=CC=C(Cl)C=C1 QBKUKQMAGFTCQA-UHFFFAOYSA-N 0.000 claims 1
- IKXAHYJACJXEFL-UHFFFAOYSA-N 2-[[5-[butyl-(4-fluorophenyl)sulfonylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(F)C=CC=1S(=O)(=O)N(CCCC)C1=CN=C(N(CC)CC)N=C1NC(C(O)=O)CC1=CC=C(OC(=O)N(C)C)C=C1 IKXAHYJACJXEFL-UHFFFAOYSA-N 0.000 claims 1
- MIOUNZYFTCIBLP-UHFFFAOYSA-N 2-[[5-[cyclopropylmethyl-(4-fluorophenyl)sulfonylamino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(dimethylcarbamoyloxy)phenyl]propanoic acid Chemical compound C=1C=C(OC(=O)N(C)C)C=CC=1CC(C(O)=O)NC1=NC(N(CC)CC)=NC=C1N(S(=O)(=O)C=1C=CC(F)=CC=1)CC1CC1 MIOUNZYFTCIBLP-UHFFFAOYSA-N 0.000 claims 1
- 125000006325 2-propenyl amino group Chemical group [H]C([H])=C([H])C([H])([H])N([H])* 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38324402P | 2002-05-24 | 2002-05-24 | |
| PCT/US2003/017150 WO2003099231A2 (en) | 2002-05-24 | 2003-05-27 | Heteroaryl compounds which inhibit leukocyte adhesion mediated by alpha-4 integrins |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005529155A JP2005529155A (ja) | 2005-09-29 |
| JP2005529155A5 true JP2005529155A5 (enExample) | 2006-07-13 |
| JP4413135B2 JP4413135B2 (ja) | 2010-02-10 |
Family
ID=29584533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004506758A Expired - Fee Related JP4413135B2 (ja) | 2002-05-24 | 2003-05-27 | α４インテグリンによって媒介される白血球接着を阻害するヘテロアリール化合物 |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7335663B2 (enExample) |
| EP (1) | EP1507533B1 (enExample) |
| JP (1) | JP4413135B2 (enExample) |
| CN (1) | CN1311829C (enExample) |
| AT (1) | ATE464298T1 (enExample) |
| AU (1) | AU2003237302B8 (enExample) |
| BR (1) | BR0309619A (enExample) |
| CA (1) | CA2480756A1 (enExample) |
| DE (1) | DE60332109D1 (enExample) |
| EA (1) | EA008180B1 (enExample) |
| IL (1) | IL164323A (enExample) |
| MX (1) | MXPA04011657A (enExample) |
| NO (1) | NO20045276L (enExample) |
| NZ (1) | NZ535723A (enExample) |
| TW (1) | TW200307671A (enExample) |
| WO (1) | WO2003099231A2 (enExample) |
| ZA (1) | ZA200407944B (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HK1045157A1 (zh) * | 1999-01-22 | 2002-11-15 | 依兰制药公司 | 抑制vla-4介导的白细胞粘着的化合物 |
| US20050074451A1 (en) * | 2003-06-25 | 2005-04-07 | Elan Pharmaceuticals, Inc. | Methods and compositions for treating rheumatoid arthritis |
| JP2007528397A (ja) * | 2004-03-10 | 2007-10-11 | メルク エンド カムパニー インコーポレーテッド | Ｖｌａ−４アンタゴニスト |
| CA2573245C (en) * | 2004-07-08 | 2013-10-01 | Elan Pharmaceuticals, Inc. | Multivalent vla-4 antagonists comprising polymer moieties |
| WO2006023396A2 (en) * | 2004-08-16 | 2006-03-02 | Merck & Co., Inc. | Vla-4 antagonists |
| ZA200803016B (en) * | 2005-09-29 | 2009-10-28 | Elan Pharmaceuticals Inc Wyeth | Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| ATE493405T1 (de) * | 2005-09-29 | 2011-01-15 | Elan Pharm Inc | Pyrimidinylamidverbindungen, die die durch vla-4 vermittelte leukozytenadhäsion inhibieren |
| EA017110B1 (ru) * | 2006-02-27 | 2012-09-28 | Элан Фамэсьютикэлс, Инк. | ПИРИМИДИНИЛСУЛЬФОНАМИДНЫЕ СОЕДИНЕНИЯ (ВАРИАНТЫ), СПОСОБ ПОЛУЧЕНИЯ ПИРИМИДИНИЛСУЛЬФОНАМИДНЫХ СОЕДИНЕНИЙ (ВАРИАНТЫ), ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СПОСОБ ЛЕЧЕНИЯ ЗАБОЛЕВАНИЯ, ОПОСРЕДОВАННОГО ИНТЕГРИНОМ α4, СПОСОБ СНИЖЕНИЯ И/ИЛИ ПРЕДУПРЕЖДЕНИЯ ВОСПАЛИТЕЛЬНОГО КОМПОНЕНТА ЗАБОЛЕВАНИЯ ИЛИ АУТОИММУННОГО ОТВЕТА |
| US8410115B2 (en) * | 2006-02-28 | 2013-04-02 | Elan Pharmaceuticals, Inc. | Methods of treating inflammatory and autoimmune diseases with alpha-4 inhibitory compounds |
| HUE047230T2 (hu) | 2006-02-28 | 2020-04-28 | Biogen Ma Inc | Gyulladásos és autoimmun betegségek natalizumabbal való kezelésének módszerei |
| KR20080104343A (ko) * | 2006-03-03 | 2008-12-02 | 엘란 파마슈티칼스, 인크. | 나탈리주마브로 염증 및 자가면역 질환을 치료하는 방법 |
| CA2708262A1 (en) * | 2007-12-07 | 2009-06-18 | Elan Pharmaceuticals, Inc. | Methods and compositions for treating liquid tumors |
| SG10201401836RA (en) * | 2009-04-27 | 2014-10-30 | Elan Pharm Inc | Pyridinone antagonists of alpha-4 integrins |
| BR112012017014B1 (pt) | 2010-01-11 | 2021-07-20 | Biogen Ma Inc | Métodos para detecção de anticorpos de vírus jc |
| US11287423B2 (en) | 2010-01-11 | 2022-03-29 | Biogen Ma Inc. | Assay for JC virus antibodies |
| US8343706B2 (en) | 2010-01-25 | 2013-01-01 | International Business Machines Corporation | Fluorine-free fused ring heteroaromatic photoacid generators and resist compositions containing the same |
| HUE061244T2 (hu) | 2011-05-31 | 2023-06-28 | Biogen Ma Inc | A PML kockázat értékelésének módszere |
| EP3004334A4 (en) | 2013-05-28 | 2016-12-21 | Biogen Ma Inc | METHOD FOR ASSESSING A PML RISK |
| EP3810085A1 (en) | 2018-06-20 | 2021-04-28 | Progenity, Inc. | Treatment of a disease of the gastrointestinal tract with an integrin inhibitor |
| ES2987796T3 (es) | 2018-10-30 | 2024-11-18 | Gilead Sciences Inc | Derivados de N-benzoil-fenilalanina como inhibidores de la integrina alfa4beta7 para el tratamiento de enfermedades inflamatorias |
| DK3873884T3 (da) | 2018-10-30 | 2025-02-17 | Gilead Sciences Inc | 3-(quinolin-8-yl)-1,4-dihydropyrido[3,4-d]pyrimidin-2,4-dion-derivater som alpha4beta7-integrinhæmmere til behandling af inflammatoriske sygdomme |
| WO2020092394A1 (en) | 2018-10-30 | 2020-05-07 | Gilead Sciences, Inc. | Imidazopyridine derivatives as alpha4beta7 integrin inhibitors |
| WO2020092401A1 (en) | 2018-10-30 | 2020-05-07 | Gilead Sciences, Inc. | COMPOUNDS FOR INHIBITION OF ALPHA 4β7 INTEGRIN |
| CN111197057B (zh) * | 2018-11-19 | 2024-04-19 | 中国科学院分子细胞科学卓越创新中心 | 调控免疫细胞迁移的组合物和方法 |
| AU2020329207B2 (en) | 2019-08-14 | 2024-02-29 | Gilead Sciences, Inc. | Compounds for inhibition of alpha 4 beta 7 integrin |
Family Cites Families (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2525656A1 (de) | 1974-06-19 | 1976-01-15 | Sandoz Ag | Verfahren zur herstellung neuer heterocyclischer verbindungen |
| US4046876A (en) * | 1974-11-08 | 1977-09-06 | Mitsubishi Chemical Industries Limited | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4096255A (en) * | 1974-11-08 | 1978-06-20 | Mitsubishi Chemical Industries Limited | N2 -naphthalenesulfonyl-L-argininamides, and pharmaceutical salts, compositions and methods |
| US4073914A (en) * | 1974-11-08 | 1978-02-14 | Mitsubishi Chemical Industries Limited | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4055651A (en) * | 1974-11-08 | 1977-10-25 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4041156A (en) * | 1974-11-08 | 1977-08-09 | Mitsubishi Chemical Industries Limited | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4018915A (en) * | 1976-01-05 | 1977-04-19 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4070457A (en) * | 1974-11-08 | 1978-01-24 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4055636A (en) * | 1974-11-08 | 1977-10-25 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4104392A (en) * | 1974-11-08 | 1978-08-01 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof, and antithrombotic compositions and methods employing them |
| JPS5727454B2 (enExample) * | 1975-02-21 | 1982-06-10 | ||
| CA1102316A (en) | 1975-12-09 | 1981-06-02 | Shosuke Okamoto | N su2 xx-arylsulfonyl-l-argininamides and the pharmaceutically acceptable salts thereof |
| US4036955A (en) * | 1976-07-22 | 1977-07-19 | Mitsubishi Chemical Industries Ltd. | N2 -naphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| US4018913A (en) * | 1976-01-14 | 1977-04-19 | Mitsubishi Chemical Industries Ltd. | N2 -alkoxynaphthalenesulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof |
| DE2742173A1 (de) * | 1977-09-20 | 1979-03-29 | Bayer Ag | Phenoxy-pyridinyl(pyrimidinyl)-alkanole, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide |
| US4235871A (en) * | 1978-02-24 | 1980-11-25 | Papahadjopoulos Demetrios P | Method of encapsulating biologically active materials in lipid vesicles |
| IT1211096B (it) * | 1981-08-20 | 1989-09-29 | Lpb Ist Farm | Pirimidine e s.triazinici adattivita' ipolipidemizzante. |
| US4672065A (en) * | 1982-11-19 | 1987-06-09 | Chevron Research Company | N-substituted phenoxyacetamide fungicides |
| US4501728A (en) * | 1983-01-06 | 1985-02-26 | Technology Unlimited, Inc. | Masking of liposomes from RES recognition |
| US4565814A (en) | 1983-01-28 | 1986-01-21 | Sanofi | Pyridazine derivatives having a psychotropic action and compositions |
| JPS59212480A (ja) | 1983-05-17 | 1984-12-01 | Nippon Soda Co Ltd | ピリダジン誘導体及び除草剤 |
| DE3322720A1 (de) * | 1983-06-24 | 1985-01-03 | Chemische Werke Hüls AG, 4370 Marl | Verwendung von in 2-stellung mit (substituierten) aminogruppen substituierten 4-dl-alkylester-(alpha)-alaninyl-6-chlor-s-triazinen als herbizide, insbesondere gegen flughafer |
| US4505910A (en) * | 1983-06-30 | 1985-03-19 | American Home Products Corporation | Amino-pyrimidine derivatives, compositions and use |
| NZ210669A (en) | 1983-12-27 | 1988-05-30 | Syntex Inc | Benzoxazin-4-one derivatives and pharmaceutical compositions |
| PH22520A (en) * | 1984-11-12 | 1988-10-17 | Yamanouchi Pharma Co Ltd | Heterocyclic compounds having 4-lover alkyl-3-hydroxy-2-lower alkyl phenoxy-lower alkylene-y-group, and process of producing them |
| US4959364A (en) * | 1985-02-04 | 1990-09-25 | G. D. Searle & Co. | Method of treating inflammation, allergy, asthma and proliferative skin disease using heterocyclic amides |
| US5023252A (en) * | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US4837028A (en) * | 1986-12-24 | 1989-06-06 | Liposome Technology, Inc. | Liposomes with enhanced circulation time |
| JPH0784424B2 (ja) | 1987-04-15 | 1995-09-13 | 味の素株式会社 | チロシン誘導体及びその用途 |
| EP0330506A3 (en) | 1988-02-26 | 1990-06-20 | Dana Farber Cancer Institute | Vla proteins |
| DE3904931A1 (de) * | 1989-02-17 | 1990-08-23 | Bayer Ag | Pyridyl-substituierte acrylsaeureester |
| US5030644A (en) * | 1989-07-31 | 1991-07-09 | Merck & Co., Inc. | Imidazole compounds and their use as transglutaminase inhibitors |
| US5260210A (en) | 1989-09-27 | 1993-11-09 | Rubin Lee L | Blood-brain barrier model |
| US4992439A (en) * | 1990-02-13 | 1991-02-12 | Bristol-Myers Squibb Company | Pyridazine carboxylic acids and esters |
| FR2679903B1 (fr) | 1991-08-02 | 1993-12-03 | Elf Sanofi | Derives de la n-sulfonyl indoline portant une fonction amidique, leur preparation, les compositions pharmaceutiques en contenant. |
| NZ239846A (en) * | 1990-09-27 | 1994-11-25 | Merck & Co Inc | Sulphonamide derivatives and pharmaceutical compositions thereof |
| DE4108029A1 (de) * | 1991-03-13 | 1992-09-17 | Bayer Ag | Triazinyl-substituierte acrylsaeureester |
| WO1992016549A1 (de) | 1991-03-18 | 1992-10-01 | Pentapharm Ag | Para-substituierte phenylalanin-derivate |
| IT1247509B (it) * | 1991-04-19 | 1994-12-17 | Univ Cagliari | Composti di sintesi atti all'impiego nella terapia delle infezioni da rhinovirus |
| US5296486A (en) | 1991-09-24 | 1994-03-22 | Boehringer Ingelheim Pharmaceuticals, Inc. | Leukotriene biosynthesis inhibitors |
| AU3420693A (en) | 1991-12-24 | 1993-07-28 | Fred Hutchinson Cancer Research Center | Competitive inhibition of high-avidity alpha4-beta1 receptor using tripeptide ldv |
| BR9306058A (pt) * | 1992-03-11 | 1997-11-18 | Narhex Ltd | Derivados de amina de hidrocarbonetos oxo- e hidroxi- substituidos |
| DE4227748A1 (de) * | 1992-08-21 | 1994-02-24 | Bayer Ag | Pyridyloxy-acrylsäureester |
| JP2848232B2 (ja) * | 1993-02-19 | 1999-01-20 | 武田薬品工業株式会社 | アルデヒド誘導体 |
| US5770573A (en) * | 1993-12-06 | 1998-06-23 | Cytel Corporation | CS-1 peptidomimetics, compositions and methods of using the same |
| TW574214B (en) * | 1994-06-08 | 2004-02-01 | Pfizer | Corticotropin releasing factor antagonists |
| US5510332A (en) * | 1994-07-07 | 1996-04-23 | Texas Biotechnology Corporation | Process to inhibit binding of the integrin α4 62 1 to VCAM-1 or fibronectin and linear peptides therefor |
| EP0769958B1 (en) | 1994-07-11 | 2003-04-16 | Athena Neurosciences, Inc. | Inhibitors of leukocyte adhesion |
| US6306840B1 (en) | 1995-01-23 | 2001-10-23 | Biogen, Inc. | Cell adhesion inhibitors |
| IL117659A (en) | 1995-04-13 | 2000-12-06 | Dainippon Pharmaceutical Co | Substituted 2-phenyl pyrimidino amino acetamide derivative process for preparing the same and a pharmaceutical composition containing same |
| MX9801716A (es) * | 1995-08-30 | 1998-05-31 | Searle & Co | Derivados de meta-guanidina, urea, tiourea o acido aminobenzoico azaciclico, como antagonistas de integrina. |
| PT765879E (pt) * | 1995-09-29 | 2001-05-31 | Sankyo Co | Derivados 13-substituidos de milbemicina-5-oxima sua preparacao e utilizacao contra insectos e outras pragas |
| DE19536891A1 (de) | 1995-10-04 | 1997-04-10 | Basf Ag | Neue Aminosäurederivate, ihre Herstellung und Verwendung |
| DE19548709A1 (de) | 1995-12-23 | 1997-07-03 | Merck Patent Gmbh | Tyrosinderivate |
| US6211333B1 (en) | 1996-06-21 | 2001-04-03 | Takeda Chemical Industries, Ltd. | Method for producing peptides and their salts which have an agonist activity of luteinizing hormone releasing hormones secreted from the hypothalamus |
| EP0907637A1 (de) | 1996-06-28 | 1999-04-14 | MERCK PATENT GmbH | Phenylalanin-derivate als integrin-inhibitoren |
| DE19629817A1 (de) * | 1996-07-24 | 1998-01-29 | Hoechst Ag | Neue Imino-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten |
| DE19647317A1 (de) * | 1996-11-15 | 1998-05-20 | Hoechst Schering Agrevo Gmbh | Substituierte Stickstoff-Heterocyclen, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel |
| DE19647381A1 (de) * | 1996-11-15 | 1998-05-20 | Hoechst Ag | Neue Heterocyclen als Inhibitoren der Leukozytenadhäsion und VLA-4-Antagonisten |
| NZ334950A (en) | 1996-11-22 | 2001-03-30 | Lilly Co Eli | N-(aryl/heteroarylacetyl) amino acid esters and pharmaceutical compositions comprising same; useful for inhibiting beta-amyloid peptide release and/or its synthesis |
| AU6264898A (en) | 1997-02-04 | 1998-08-25 | Versicor Inc | Solid phase and combinatorial library syntheses of 3,1-benzoxazine-4-ones |
| DE19713000A1 (de) | 1997-03-27 | 1998-10-01 | Merck Patent Gmbh | Adhäsionsrezeptor-Antagonisten |
| EP1001764A4 (en) | 1997-05-29 | 2005-08-24 | Merck & Co Inc | HETEROCYCLIC AMIDE COMPOUNDS AS INHIBITORS OF CELL ADHESION |
| ATE318841T1 (de) | 1997-05-29 | 2006-03-15 | Merck & Co Inc | Biarylalkansäuren in der verwendung als zelladhäsionsinhibitoren |
| IL133640A0 (en) | 1997-07-31 | 2001-04-30 | Elan Pharm Inc | Substituted phenylalanine type compounds which inhibit leukocyte adhesion mediated by vla-4 |
| IL133641A0 (en) | 1997-07-31 | 2001-04-30 | Elan Pharm Inc | Compounds which inhibit leukocyte adhesion mediated by vla-4 |
| AR016133A1 (es) | 1997-07-31 | 2001-06-20 | Wyeth Corp | Compuesto de carbamiloxi que inhiben la adhesion de leucocitos mediada por vla-4, compuestos que son prodrogas de dichos compuestos, composicionfarmaceutica, metodo para fijar vla-4 a una muestra biologica, metodo para el tratamiento de una condicion inflamatoria |
| PL338373A1 (en) | 1997-07-31 | 2000-10-23 | Elan Pharm Inc | Dipeptide and its affinite compounds inhibiting adhesion of leucocytes occurring through mediation of vla-4 |
| ATE260243T1 (de) | 1997-08-22 | 2004-03-15 | Hoffmann La Roche | N-aroylphenylalaninderivate |
| KR100554815B1 (ko) | 1997-08-22 | 2006-02-22 | 에프. 호프만-라 로슈 아게 | 엔-아로일페닐알라닌 유도체 |
| CN1294576A (zh) | 1998-01-23 | 2001-05-09 | 诺瓦提斯公司 | Vla－4拮抗剂 |
| US6329372B1 (en) | 1998-01-27 | 2001-12-11 | Celltech Therapeutics Limited | Phenylalanine derivatives |
| KR20010042614A (ko) | 1998-04-10 | 2001-05-25 | 윌리암스 로저 에이 | 비트로넥틴 길항제로서 복소환식 글리실 베타-알라닌 유도체 |
| HUP0101419A3 (en) | 1998-04-16 | 2002-08-28 | Texas Biotechnology Corp Houst | Compounds that inhibit the binding of integrins to their receptors and pharmaceutical compositions containing them |
| GB9821061D0 (en) | 1998-09-28 | 1998-11-18 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9825652D0 (en) | 1998-11-23 | 1999-01-13 | Celltech Therapeutics Ltd | Chemical compounds |
| HK1045157A1 (zh) * | 1999-01-22 | 2002-11-15 | 依兰制药公司 | 抑制vla-4介导的白细胞粘着的化合物 |
| WO2000043369A1 (en) | 1999-01-22 | 2000-07-27 | Elan Pharmaceuticals, Inc. | Compounds which inhibit leukocyte adhesion mediated by vla-4 |
-
2003
- 2003-05-26 TW TW092114184A patent/TW200307671A/zh unknown
- 2003-05-27 NZ NZ535723A patent/NZ535723A/en unknown
- 2003-05-27 CA CA002480756A patent/CA2480756A1/en not_active Abandoned
- 2003-05-27 DE DE60332109T patent/DE60332109D1/de not_active Expired - Lifetime
- 2003-05-27 AT AT03736768T patent/ATE464298T1/de not_active IP Right Cessation
- 2003-05-27 BR BR0309619-0A patent/BR0309619A/pt not_active IP Right Cessation
- 2003-05-27 AU AU2003237302A patent/AU2003237302B8/en not_active Ceased
- 2003-05-27 MX MXPA04011657A patent/MXPA04011657A/es active IP Right Grant
- 2003-05-27 EP EP03736768A patent/EP1507533B1/en not_active Expired - Lifetime
- 2003-05-27 US US10/494,788 patent/US7335663B2/en not_active Expired - Fee Related
- 2003-05-27 JP JP2004506758A patent/JP4413135B2/ja not_active Expired - Fee Related
- 2003-05-27 CN CNB038112582A patent/CN1311829C/zh not_active Expired - Fee Related
- 2003-05-27 US US10/447,208 patent/US7008949B2/en not_active Expired - Fee Related
- 2003-05-27 WO PCT/US2003/017150 patent/WO2003099231A2/en not_active Ceased
- 2003-05-27 EA EA200401561A patent/EA008180B1/ru not_active IP Right Cessation
-
2004
- 2004-09-28 IL IL164323A patent/IL164323A/en not_active IP Right Cessation
- 2004-10-01 ZA ZA200407944A patent/ZA200407944B/en unknown
- 2004-12-01 NO NO20045276A patent/NO20045276L/no not_active Application Discontinuation
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