JP2002532490A5 - - Google Patents
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- JP2002532490A5 JP2002532490A5 JP2000588166A JP2000588166A JP2002532490A5 JP 2002532490 A5 JP2002532490 A5 JP 2002532490A5 JP 2000588166 A JP2000588166 A JP 2000588166A JP 2000588166 A JP2000588166 A JP 2000588166A JP 2002532490 A5 JP2002532490 A5 JP 2002532490A5
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- JP
- Japan
- Prior art keywords
- substituted
- lower alkyl
- dihydro
- methylene
- cycloalkyl
- 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.)
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- 125000000217 alkyl group Chemical group 0.000 description 104
- 125000000623 heterocyclic group Chemical group 0.000 description 66
- 125000000753 cycloalkyl group Chemical group 0.000 description 60
- 229910052736 halogen Inorganic materials 0.000 description 28
- 125000001072 heteroaryl group Chemical group 0.000 description 28
- 229910052739 hydrogen Inorganic materials 0.000 description 24
- 239000001257 hydrogen Substances 0.000 description 24
- 125000003118 aryl group Chemical group 0.000 description 22
- 150000002367 halogens Chemical class 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 18
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 13
- -1 4-chloro-2-methylsulfanylmethoxy-phenyl Chemical group 0.000 description 8
- 125000005553 heteroaryloxy group Chemical group 0.000 description 7
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 125000004104 aryloxy group Chemical group 0.000 description 6
- 125000005843 halogen group Chemical group 0.000 description 6
- 150000002431 hydrogen Chemical class 0.000 description 6
- 125000003107 substituted aryl group Chemical group 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 3
- CNELYFGFVRCQQO-ATVHPVEESA-N (3z)-3-(1h-pyrrol-2-ylmethylidene)-5-(2-thiophen-2-ylethynyl)-1h-indol-2-one Chemical compound O=C1NC2=CC=C(C#CC=3SC=CC=3)C=C2\C1=C\C1=CC=CN1 CNELYFGFVRCQQO-ATVHPVEESA-N 0.000 description 2
- YJCIDAJKFWKYCS-OWBHPGMISA-N (3z)-4-[3-hydroxy-3-(3-methoxythiophen-2-yl)prop-1-ynyl]-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C4=C(C=CS4)OC)C=CC=C3NC\2=O)=C1OC YJCIDAJKFWKYCS-OWBHPGMISA-N 0.000 description 2
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 description 2
- 125000004404 heteroalkyl group Chemical group 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- LLTZGYZYWGAACV-HKVBYMSFSA-N (3z)-1-[(e)-2-phenylethenyl]-3-(1h-pyrrol-2-ylmethylidene)indol-2-one Chemical compound C12=CC=CC=C2\C(=C\C=2NC=CC=2)C(=O)N1\C=C\C1=CC=CC=C1 LLTZGYZYWGAACV-HKVBYMSFSA-N 0.000 description 1
- ZTAYJHNUGMKDAC-TVYBWHDCSA-N (3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1-[(e)-2-phenylethenyl]indol-2-one Chemical compound C1=CNC(\C=C/2C3=CC=CC=C3N(\C=C\C=3C=CC=CC=3)C\2=O)=C1OC ZTAYJHNUGMKDAC-TVYBWHDCSA-N 0.000 description 1
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- CIBQBCXWQYRSFJ-SDXDJHTJSA-N (3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-4-(3-phenoxyprop-1-ynyl)-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CCOC=4C=CC=CC=4)C=CC=C3NC\2=O)=C1OC CIBQBCXWQYRSFJ-SDXDJHTJSA-N 0.000 description 1
- HHYIPICNMBTBHU-PTNGSMBKSA-N (3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-5-nitro-4-(2-pyridin-3-ylethynyl)-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC=4C=NC=CC=4)C(=CC=C3NC\2=O)[N+]([O-])=O)=C1OC HHYIPICNMBTBHU-PTNGSMBKSA-N 0.000 description 1
- XWDAYWGNKHFMGK-GDNBJRDFSA-N (3z)-3-[(5-methyl-1h-imidazol-4-yl)methylidene]-5-(2-trimethylsilylethynyl)-1h-indol-2-one Chemical compound N1=CNC(\C=C/2C3=CC(=CC=C3NC\2=O)C#C[Si](C)(C)C)=C1C XWDAYWGNKHFMGK-GDNBJRDFSA-N 0.000 description 1
- POLVGKSHMPRQIF-SDXDJHTJSA-N (3z)-4-(3-hydroxy-3-phenylbut-1-ynyl)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(C)(O)C=4C=CC=CC=4)C=CC=C3NC\2=O)=C1OC POLVGKSHMPRQIF-SDXDJHTJSA-N 0.000 description 1
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- PXCCQARRVLKNIM-SQFISAMPSA-N (3z)-4-(3-hydroxy-3-pyridin-2-ylprop-1-ynyl)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C=4N=CC=CC=4)C=CC=C3NC\2=O)=C1OC PXCCQARRVLKNIM-SQFISAMPSA-N 0.000 description 1
- GIGNTIVPOROLOI-VBKFSLOCSA-N (3z)-4-(3-hydroxy-3-pyridin-3-ylprop-1-ynyl)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C=4C=NC=CC=4)C=CC=C3NC\2=O)=C1OC GIGNTIVPOROLOI-VBKFSLOCSA-N 0.000 description 1
- RGVWLPQHWJEXQI-OWBHPGMISA-N (3z)-4-(3-hydroxy-3-thiophen-2-ylprop-1-ynyl)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C=4SC=CC=4)C=CC=C3NC\2=O)=C1OC RGVWLPQHWJEXQI-OWBHPGMISA-N 0.000 description 1
- MUMWQVXWSSNTMM-PTNGSMBKSA-N (3z)-4-(3-hydroxy-3-thiophen-3-ylprop-1-ynyl)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C4=CSC=C4)C=CC=C3NC\2=O)=C1OC MUMWQVXWSSNTMM-PTNGSMBKSA-N 0.000 description 1
- WPAMZQZOUUBLDX-HNMBUVAWSA-N (3z)-4-[(e)-2-(2-chlorophenyl)ethenyl]-3-(1h-pyrrol-2-ylmethylidene)-1h-indol-2-one Chemical compound ClC1=CC=CC=C1\C=C\C1=CC=CC(NC\2=O)=C1C/2=C/C1=CC=CN1 WPAMZQZOUUBLDX-HNMBUVAWSA-N 0.000 description 1
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- DTCDOONGFRBLDF-PAAQWSFZSA-N (3z)-4-[(e)-2-(4-methoxyphenyl)ethenyl]-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=C(\C=C\C=4C=CC(OC)=CC=4)C=CC=C3NC\2=O)=C1OC DTCDOONGFRBLDF-PAAQWSFZSA-N 0.000 description 1
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- GZSXMGUALNRWHL-XFXZXTDPSA-N (3z)-5-ethynyl-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-1h-indol-2-one Chemical compound C1=CNC(\C=C/2C3=CC(=CC=C3NC\2=O)C#C)=C1OC GZSXMGUALNRWHL-XFXZXTDPSA-N 0.000 description 1
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- RSEGQJSFDGPSHB-LGMDPLHJSA-N 2-[4-[1-hydroxy-3-[(3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-2-oxo-1h-indol-4-yl]prop-2-ynyl]-2-methoxyphenoxy]acetic acid Chemical compound C1=CNC(\C=C/2C3=C(C#CC(O)C=4C=C(OC)C(OCC(O)=O)=CC=4)C=CC=C3NC\2=O)=C1OC RSEGQJSFDGPSHB-LGMDPLHJSA-N 0.000 description 1
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- 239000004480 active ingredient Substances 0.000 description 1
- 125000004367 cycloalkylaryl group Chemical group 0.000 description 1
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- 208000027866 inflammatory disease Diseases 0.000 description 1
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- 238000000034 method Methods 0.000 description 1
- FAFVKKUTZMVGHK-JXAWBTAJSA-N methyl 2-[4-[1-hydroxy-3-[(3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-2-oxo-1h-indol-4-yl]prop-2-ynyl]-2-methoxyphenoxy]acetate Chemical compound C1=C(OC)C(OCC(=O)OC)=CC=C1C(O)C#CC1=CC=CC(NC\2=O)=C1C/2=C/C1=C(OC)C=CN1 FAFVKKUTZMVGHK-JXAWBTAJSA-N 0.000 description 1
- RZTFYTLJOXSQKQ-PAAQWSFZSA-N methyl 4-[(e)-2-[(3z)-3-[(3-methoxy-1h-pyrrol-2-yl)methylidene]-2-oxo-1h-indol-4-yl]ethenyl]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1\C=C\C1=CC=CC(NC\2=O)=C1C/2=C/C1=C(OC)C=CN1 RZTFYTLJOXSQKQ-PAAQWSFZSA-N 0.000 description 1
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- 239000000203 mixture Substances 0.000 description 1
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Applications Claiming Priority (5)
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| US11258998P | 1998-12-17 | 1998-12-17 | |
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| US60/141,482 | 1999-06-29 | ||
| PCT/EP1999/009578 WO2000035906A2 (en) | 1998-12-17 | 1999-12-07 | 4- and 5-alkynyloxindoles and 4- and 5-alkenyloxindoles |
Publications (2)
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| JP2002532490A JP2002532490A (ja) | 2002-10-02 |
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| EP (1) | EP1149092B1 (https=) |
| JP (1) | JP2002532490A (https=) |
| KR (1) | KR20010087421A (https=) |
| CN (1) | CN1147486C (https=) |
| AT (1) | ATE253062T1 (https=) |
| AU (1) | AU771599B2 (https=) |
| BR (1) | BR9916272A (https=) |
| CA (1) | CA2354510A1 (https=) |
| DE (1) | DE69912479T2 (https=) |
| DK (1) | DK1149092T3 (https=) |
| ES (1) | ES2209527T3 (https=) |
| PT (1) | PT1149092E (https=) |
| TR (1) | TR200101747T2 (https=) |
| WO (1) | WO2000035906A2 (https=) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US6569868B2 (en) | 1998-04-16 | 2003-05-27 | Sugen, Inc. | 2-indolinone derivatives as modulators of protein kinase activity |
| MY128450A (en) | 2000-05-24 | 2007-02-28 | Upjohn Co | 1-(pyrrolidin-1-ylmethyl)-3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives |
| JP2003535847A (ja) | 2000-06-02 | 2003-12-02 | スージェン・インコーポレーテッド | 蛋白質キナーゼ／ホスファターゼ阻害剤としてのインドリノン誘導体 |
| WO2002002551A1 (en) * | 2000-06-30 | 2002-01-10 | Sugen, Inc. | 4-heteroaryl-3-heteroarylidenyl-2-indolinones and their use as protein kinase inhibitors |
| CN1300116C (zh) | 2001-04-16 | 2007-02-14 | 卫材株式会社 | 1h－吲唑化合物 |
| US7018999B2 (en) | 2001-05-16 | 2006-03-28 | Cephalon, Inc. | Methods for the treatment and prevention of pain |
| US6599902B2 (en) | 2001-05-30 | 2003-07-29 | Sugen, Inc. | 5-aralkysufonyl-3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives as kinase inhibitors |
| JP4414219B2 (ja) | 2001-07-23 | 2010-02-10 | メルク セローノ ソシエテ アノニム | Ｃ−ｊｕｎ−ｎ−末端キナーゼ（ｊｎｋ）インヒビターとしてのアリールスルホンアミド誘導体 |
| EP1434585A1 (en) * | 2001-10-12 | 2004-07-07 | Warner-Lambert Company LLC | Alkyne matrix metalloproteinase inhibitors |
| US6962922B2 (en) | 2001-10-12 | 2005-11-08 | Warner-Lambert Company Llc | Alkynylated quinazoline compounds |
| ATE465153T1 (de) | 2002-02-28 | 2010-05-15 | Eisai R&D Man Co Ltd | Neue indazolverbindungen mit kondensiertem ring |
| US6894057B2 (en) | 2002-03-08 | 2005-05-17 | Warner-Lambert Company | Oxo-azabicyclic compounds |
| US6747147B2 (en) | 2002-03-08 | 2004-06-08 | Warner-Lambert Company | Oxo-azabicyclic compounds |
| US7429609B2 (en) | 2002-05-31 | 2008-09-30 | Eisai R & D Management Co., Ltd. | Pyrazole compound and medicinal composition containing the same |
| WO2003106455A1 (en) | 2002-06-14 | 2003-12-24 | Applied Research Systems Ars Holding N.V. | Azole methylidene cyanide derivatives and their use as protein kinase modulators |
| RU2006117635A (ru) | 2003-10-24 | 2007-12-10 | Шеринг Акциенгезельшафт (De) | Производные индолинона и их применение для лечения патологических состояний, таких как злокачественное новообразование |
| DE102004012070A1 (de) * | 2004-03-12 | 2005-09-29 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue cycloalkyl-haltige 5-Acylindolinone, deren Herstellung und deren Verwendung als Arzneimittel |
| US7803824B2 (en) | 2004-10-29 | 2010-09-28 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases to treat glaucoma |
| US20060094753A1 (en) | 2004-10-29 | 2006-05-04 | Alcon, Inc. | Use of inhibitors of Jun N-terminal kinases for the treatment of glaucomatous retinopathy and ocular diseases |
| WO2006090698A1 (ja) * | 2005-02-22 | 2006-08-31 | Ono Pharmaceutical Co., Ltd. | キナーゼ阻害薬およびその用途 |
| BRPI0613042A2 (pt) | 2005-07-15 | 2010-12-14 | Serono Lab | inibidores de jnk para o tratamento de endometriose |
| KR20080044836A (ko) | 2005-07-15 | 2008-05-21 | 라보라뚜와르 세로노 에스. 에이. | 자궁내막증 치료용 ｊｎｋ 억제제 |
| CN1939922B (zh) * | 2005-09-27 | 2010-10-13 | 天津和美生物技术有限公司 | 可抑制细胞释放肿瘤坏死因子的5H-噻吩[3，4-c]吡咯-4，6-二酮衍生物 |
| US7968572B2 (en) | 2005-10-03 | 2011-06-28 | Ono Pharmaceuticals Co., Ltd. | Nitrogen-containing heterocyclic compound and pharmaceutical application thereof |
| FR2962729B1 (fr) | 2010-07-13 | 2012-09-21 | Arkema France | Molecules porteuses de groupes associatifs |
| FR2962733B1 (fr) | 2010-07-13 | 2012-08-17 | Michelin Soc Tech | Polymere greffe par des molecules associatives azotees. |
| US20140205537A1 (en) * | 2011-06-24 | 2014-07-24 | Zenobia Therapeutics, Inc. | Lrrk2 inhibitors |
| CN214057141U (zh) | 2019-11-27 | 2021-08-27 | 财团法人工业技术研究院 | 发电感测传输装置 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9501567D0 (en) * | 1995-01-26 | 1995-03-15 | Pharmacia Spa | Hydrosoluble 3-arylidene-2-oxindole derivatives as tyrosine kinase inhibitors |
| GB9507298D0 (en) * | 1995-04-07 | 1995-05-31 | Pharmacia Spa | Substituted indolylmethylene-oxindale analogues as tyrosine kinase inhibitors |
| US5880141A (en) * | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| GB9610964D0 (en) * | 1996-05-24 | 1996-07-31 | Pharmacia & Upjohn Spa | Substituted tetralylmethylen-oxindole analogues as tyrosine kinase inhibitors |
| DE69734521T9 (de) * | 1996-08-23 | 2006-12-07 | Sugen, Inc., South San Francisco | Kombinatorische indolinonbibliotheken und verwandte produkte und verfahren zur behandlung von erkrankungen |
| JP2002511852A (ja) * | 1997-05-07 | 2002-04-16 | スージェン・インコーポレーテッド | 蛋白質キナーゼ活性の調節剤としての２−インドリノン誘導体 |
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1999
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- 1999-12-07 WO PCT/EP1999/009578 patent/WO2000035906A2/en not_active Ceased
- 1999-12-07 JP JP2000588166A patent/JP2002532490A/ja active Pending
- 1999-12-07 DK DK99957341T patent/DK1149092T3/da active
- 1999-12-07 CA CA002354510A patent/CA2354510A1/en not_active Abandoned
- 1999-12-07 CN CNB998146994A patent/CN1147486C/zh not_active Expired - Fee Related
- 1999-12-07 KR KR1020017007552A patent/KR20010087421A/ko not_active Ceased
- 1999-12-07 PT PT99957341T patent/PT1149092E/pt unknown
- 1999-12-07 TR TR2001/01747T patent/TR200101747T2/xx unknown
- 1999-12-07 AT AT99957341T patent/ATE253062T1/de not_active IP Right Cessation
- 1999-12-07 ES ES99957341T patent/ES2209527T3/es not_active Expired - Lifetime
- 1999-12-07 AU AU15076/00A patent/AU771599B2/en not_active Ceased
- 1999-12-07 EP EP99957341A patent/EP1149092B1/en not_active Expired - Lifetime
- 1999-12-07 DE DE69912479T patent/DE69912479T2/de not_active Expired - Fee Related
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