JP2009528296A5 - - Google Patents
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- Publication number
- JP2009528296A5 JP2009528296A5 JP2008556582A JP2008556582A JP2009528296A5 JP 2009528296 A5 JP2009528296 A5 JP 2009528296A5 JP 2008556582 A JP2008556582 A JP 2008556582A JP 2008556582 A JP2008556582 A JP 2008556582A JP 2009528296 A5 JP2009528296 A5 JP 2009528296A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- alkyl
- ylamino
- pyrimidin
- 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
Links
- 150000001875 compounds Chemical class 0.000 claims description 41
- -1 propargyl compound Chemical class 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000006239 protecting group Chemical group 0.000 claims description 5
- 150000003935 benzaldehydes Chemical class 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims description 2
- 238000006722 reduction reaction Methods 0.000 claims description 2
- 238000006268 reductive amination reaction Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 150000002148 esters Chemical class 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- JJOWVQRSSFANTK-QHCPKHFHSA-N (2s)-2-[[2-(diethylamino)-5-[ethyl(2-methylpropylsulfonyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(CC)S(=O)(=O)CC(C)C)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 JJOWVQRSSFANTK-QHCPKHFHSA-N 0.000 claims 1
- LLYUGVGQHYKTPB-NRFANRHFSA-N (2s)-2-[[2-(diethylamino)-5-[ethyl(3,3,3-trifluoropropylsulfonyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(CC)S(=O)(=O)CCC(F)(F)F)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 LLYUGVGQHYKTPB-NRFANRHFSA-N 0.000 claims 1
- WQRWVWWUVJMCFW-FQEVSTJZSA-N (2s)-2-[[2-(diethylamino)-5-[ethyl(methylsulfonyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(CC)S(C)(=O)=O)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 WQRWVWWUVJMCFW-FQEVSTJZSA-N 0.000 claims 1
- GWHSRLXGMCCAIN-QFIPXVFZSA-N (2s)-2-[[2-(diethylamino)-5-[ethyl(propylsulfonyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCCS(=O)(=O)N(CC)C1=CN=C(N(CC)CC)N=C1N[C@H](C(O)=O)CC(C=C1)=CC=C1OC(=O)N1CCCC1 GWHSRLXGMCCAIN-QFIPXVFZSA-N 0.000 claims 1
- DFGIRJIXSZXHRL-IBGZPJMESA-N (2s)-2-[[2-(diethylamino)-5-[methyl(methylsulfonyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(C)S(C)(=O)=O)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 DFGIRJIXSZXHRL-IBGZPJMESA-N 0.000 claims 1
- GDLQGBLMGXDNRQ-NRFANRHFSA-N (2s)-2-[[2-(diethylamino)-5-[methylsulfonyl(prop-2-ynyl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(CC#C)S(C)(=O)=O)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 GDLQGBLMGXDNRQ-NRFANRHFSA-N 0.000 claims 1
- SDRNIMLNYYTUKR-NRFANRHFSA-N (2s)-2-[[2-(diethylamino)-5-[methylsulfonyl(propan-2-yl)amino]pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(C(C)C)S(C)(=O)=O)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 SDRNIMLNYYTUKR-NRFANRHFSA-N 0.000 claims 1
- UIUBHENCCNLCKN-QFIPXVFZSA-N (2s)-2-[[5-[3-chloropropylsulfonyl(ethyl)amino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(CC)S(=O)(=O)CCCCl)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 UIUBHENCCNLCKN-QFIPXVFZSA-N 0.000 claims 1
- MJWZBNGONSQHGU-NRFANRHFSA-N (2s)-2-[[5-[3-chloropropylsulfonyl(methyl)amino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCN(CC)C1=NC=C(N(C)S(=O)(=O)CCCCl)C(N[C@@H](CC=2C=CC(OC(=O)N3CCCC3)=CC=2)C(O)=O)=N1 MJWZBNGONSQHGU-NRFANRHFSA-N 0.000 claims 1
- SWLRXLYNAHKZOI-QHCPKHFHSA-N (2s)-2-[[5-[butylsulfonyl(ethyl)amino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound CCCCS(=O)(=O)N(CC)C1=CN=C(N(CC)CC)N=C1N[C@H](C(O)=O)CC(C=C1)=CC=C1OC(=O)N1CCCC1 SWLRXLYNAHKZOI-QHCPKHFHSA-N 0.000 claims 1
- UJURHSUDCZMQEN-QHCPKHFHSA-N (2s)-2-[[5-[cyclopentyl(methylsulfonyl)amino]-2-(diethylamino)pyrimidin-4-yl]amino]-3-[4-(pyrrolidine-1-carbonyloxy)phenyl]propanoic acid Chemical compound N([C@@H](CC=1C=CC(OC(=O)N2CCCC2)=CC=1)C(O)=O)C1=NC(N(CC)CC)=NC=C1N(S(C)(=O)=O)C1CCCC1 UJURHSUDCZMQEN-QHCPKHFHSA-N 0.000 claims 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 claims 1
- 208000011231 Crohn disease Diseases 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 230000006472 autoimmune response Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000002757 inflammatory effect Effects 0.000 claims 1
- 102000006495 integrins Human genes 0.000 claims 1
- 108010044426 integrins Proteins 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 201000006417 multiple sclerosis Diseases 0.000 claims 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 150000003461 sulfonyl halides Chemical class 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 0 CCN(CC)C(C)N=CC(N(*)S(*)(=O)=O)=C(N)N[C@@](CC(C=CC=C)=C*(C)C(N1CCCC1)=O)C(O)=O Chemical compound CCN(CC)C(C)N=CC(N(*)S(*)(=O)=O)=C(N)N[C@@](CC(C=CC=C)=C*(C)C(N1CCCC1)=O)C(O)=O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77759506P | 2006-02-27 | 2006-02-27 | |
| US60/777,595 | 2006-02-27 | ||
| PCT/US2007/062824 WO2007101165A1 (en) | 2006-02-27 | 2007-02-26 | Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009528296A JP2009528296A (ja) | 2009-08-06 |
| JP2009528296A5 true JP2009528296A5 (enExample) | 2011-04-07 |
| JP5135235B2 JP5135235B2 (ja) | 2013-02-06 |
Family
ID=38215011
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008556582A Expired - Fee Related JP5135235B2 (ja) | 2006-02-27 | 2007-02-26 | Ｖａｌ−４によって媒介される白血球の接着を阻害するピリミジニルスルホンアミド化合物 |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7579466B2 (enExample) |
| EP (1) | EP1996559A1 (enExample) |
| JP (1) | JP5135235B2 (enExample) |
| KR (1) | KR20080100271A (enExample) |
| CN (1) | CN101389611B (enExample) |
| AR (1) | AR059671A1 (enExample) |
| AU (1) | AU2007220068B2 (enExample) |
| BR (1) | BRPI0708331A2 (enExample) |
| CA (1) | CA2643838A1 (enExample) |
| EA (1) | EA017110B1 (enExample) |
| EC (1) | ECSP088701A (enExample) |
| IL (1) | IL193425A (enExample) |
| MA (1) | MA30318B1 (enExample) |
| MX (1) | MX2008010988A (enExample) |
| MY (1) | MY151045A (enExample) |
| NO (1) | NO20083743L (enExample) |
| NZ (1) | NZ570679A (enExample) |
| TW (1) | TWI389904B (enExample) |
| WO (1) | WO2007101165A1 (enExample) |
| ZA (1) | ZA200807188B (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EA006301B1 (ru) * | 1999-01-22 | 2005-10-27 | Элан Фармасьютикалз, Инк. | Ацильные производные, используемые для лечения опосредованных vla-4 расстройств |
| BRPI0511479C1 (pt) * | 2004-05-27 | 2021-05-25 | Crucell Holland Bv | molécula de ligação tendo atividade neutralizadora do vìrus da raiva, variante funcional de uma molécula de ligação, imunoconjugado, molécula de ácido nucléico, vetor, hospedeiro, método para produzir uma molécula de ligação ou uma variante funcional, composição farmacêutica, uso de uma molécula de ligação, uma variante funcional, um imunoconjugado como, ou uma composição, kit, método para identificar uma molécula de ligação ou uma molécula de ácido nucléico, e, coleção de moléculas de ligação humanas na superfìcie de pacotes genéticos replicáveis |
| AU2006297220B8 (en) * | 2005-09-29 | 2013-01-31 | Elan Pharmaceuticals, Inc. | Pyrimidinyl amide compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| US7727996B2 (en) * | 2005-09-29 | 2010-06-01 | Elan Pharmaceuticals, Inc. | Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4 |
| CA2643838A1 (en) * | 2006-02-27 | 2007-09-07 | Elan Pharmaceuticals, Inc. | Pyrimidinyl sulfonamide compounds which inhibit leukocyte adhesion mediated by vla-4 |
| JP2009531304A (ja) | 2006-02-28 | 2009-09-03 | エラン ファーマシューティカルズ，インコーポレイテッド | α−４阻害剤化合物を用いて炎症性疾患および自己免疫疾患を治療する方法 |
| WO2007100770A2 (en) | 2006-02-28 | 2007-09-07 | Elan Pharmaceuticals, Inc. | Methods of treating inflammatory and autoimmune diseases with natalizumab |
| WO2007103112A2 (en) | 2006-03-03 | 2007-09-13 | Elan Pharmaceuticals, Inc. | Methods of treating inflammatory and autoimmune diseases with natalizumab |
| JP2011506322A (ja) * | 2007-12-07 | 2011-03-03 | エラン ファーマシューティカルズ，インコーポレイテッド | 液性腫瘍を治療するための方法および組成物 |
| SG10201401836RA (en) * | 2009-04-27 | 2014-10-30 | Elan Pharm Inc | Pyridinone antagonists of alpha-4 integrins |
| WO2011020874A1 (en) | 2009-08-20 | 2011-02-24 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Vla-4 as a biomarker for prognosis and target for therapy in duchenne muscular dystrophy |
| SMT201800148T1 (it) | 2010-01-11 | 2018-05-02 | Biogen Ma Inc | Saggio per anticorpi del virus jc |
| US11287423B2 (en) | 2010-01-11 | 2022-03-29 | Biogen Ma Inc. | Assay for JC virus antibodies |
| KR102039751B1 (ko) | 2011-05-31 | 2019-11-01 | 바이오젠 엠에이 인코포레이티드 | Pml의 위험을 판단하는 방법 |
| EP3004334A4 (en) | 2013-05-28 | 2016-12-21 | Biogen Ma Inc | METHOD FOR ASSESSING A PML RISK |
| WO2018106959A1 (en) | 2016-12-07 | 2018-06-14 | Progenity Inc. | Gastrointestinal tract detection methods, devices and systems |
| EP3554539B9 (en) | 2016-12-14 | 2023-10-04 | Biora Therapeutics, Inc. | Treatment of a disease of the gastrointestinal tract with an integrin inhibitor |
| WO2019246455A1 (en) | 2018-06-20 | 2019-12-26 | Progenity, Inc. | Treatment of a disease of the gastrointestinal tract with an integrin inhibitor |
| ES3013256T3 (en) | 2018-10-30 | 2025-04-11 | Gilead Sciences Inc | Imidazo[1,2-a]pyridine derivatives as alpha4beta7 integrin inhibitors for the treatment of inflammatory diseases |
| KR102652797B1 (ko) | 2018-10-30 | 2024-04-02 | 길리애드 사이언시즈, 인코포레이티드 | 알파4베타7 인테그린의 억제를 위한 화합물 |
| EP3873605B1 (en) | 2018-10-30 | 2024-10-23 | Gilead Sciences, Inc. | Compounds for inhibition of alpha4beta7 integrin |
| JP7192139B2 (ja) | 2018-10-30 | 2022-12-19 | ギリアード サイエンシーズ， インコーポレイテッド | α４β７インテグリン阻害剤としてのキノリン誘導体 |
| WO2020106750A1 (en) | 2018-11-19 | 2020-05-28 | Progenity, Inc. | Methods and devices for treating a disease with biotherapeutics |
| EP4013499A1 (en) | 2019-08-14 | 2022-06-22 | Gilead Sciences, Inc. | Compounds for inhibition of alpha 4 beta 7 integrin |
| EP3870261B1 (en) | 2019-12-13 | 2024-01-31 | Biora Therapeutics, Inc. | Ingestible device for delivery of therapeutic agent to the gastrointestinal tract |
| EP4284947A1 (en) | 2021-01-29 | 2023-12-06 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Methods of assessing the risk of developing progressive multifocal leukoencephalopathy in patients treated with vla-4 antagonists |
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-
2007
- 2007-02-26 CA CA002643838A patent/CA2643838A1/en not_active Abandoned
- 2007-02-26 MX MX2008010988A patent/MX2008010988A/es active IP Right Grant
- 2007-02-26 WO PCT/US2007/062824 patent/WO2007101165A1/en not_active Ceased
- 2007-02-26 EA EA200801906A patent/EA017110B1/ru not_active IP Right Cessation
- 2007-02-26 AU AU2007220068A patent/AU2007220068B2/en not_active Ceased
- 2007-02-26 TW TW096106544A patent/TWI389904B/zh not_active IP Right Cessation
- 2007-02-26 EP EP07757498A patent/EP1996559A1/en not_active Withdrawn
- 2007-02-26 MY MYPI20083293 patent/MY151045A/en unknown
- 2007-02-26 NZ NZ570679A patent/NZ570679A/en not_active IP Right Cessation
- 2007-02-26 US US11/679,042 patent/US7579466B2/en not_active Expired - Fee Related
- 2007-02-26 JP JP2008556582A patent/JP5135235B2/ja not_active Expired - Fee Related
- 2007-02-26 BR BRPI0708331-9A patent/BRPI0708331A2/pt not_active IP Right Cessation
- 2007-02-26 KR KR1020087023333A patent/KR20080100271A/ko not_active Ceased
- 2007-02-26 CN CN2007800065837A patent/CN101389611B/zh not_active Expired - Fee Related
- 2007-02-27 AR ARP070100812A patent/AR059671A1/es not_active Application Discontinuation
-
2008
- 2008-08-13 IL IL193425A patent/IL193425A/en not_active IP Right Cessation
- 2008-08-22 ZA ZA2008/07188A patent/ZA200807188B/en unknown
- 2008-08-27 EC EC2008008701A patent/ECSP088701A/es unknown
- 2008-08-29 NO NO20083743A patent/NO20083743L/no not_active Application Discontinuation
- 2008-09-11 MA MA31231A patent/MA30318B1/fr unknown
-
2009
- 2009-07-17 US US12/505,383 patent/US7820687B2/en not_active Expired - Fee Related
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