JP2007508238A5 - - Google Patents

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Publication number
JP2007508238A5
JP2007508238A5 JP2006518009A JP2006518009A JP2007508238A5 JP 2007508238 A5 JP2007508238 A5 JP 2007508238A5 JP 2006518009 A JP2006518009 A JP 2006518009A JP 2006518009 A JP2006518009 A JP 2006518009A JP 2007508238 A5 JP2007508238 A5 JP 2007508238A5
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JP
Japan
Prior art keywords
group
carbon atoms
chr
independently
disease
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
Application number
JP2006518009A
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English (en)
Japanese (ja)
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JP2007508238A (ja
JP4750701B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/EP2004/006573 external-priority patent/WO2005005389A2/en
Publication of JP2007508238A publication Critical patent/JP2007508238A/ja
Publication of JP2007508238A5 publication Critical patent/JP2007508238A5/ja
Application granted granted Critical
Publication of JP4750701B2 publication Critical patent/JP4750701B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2006518009A 2003-07-07 2004-06-18 マロンアミド誘導体 Expired - Fee Related JP4750701B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP03014556 2003-07-07
EP03014556.9 2003-07-07
PCT/EP2004/006573 WO2005005389A2 (en) 2003-07-07 2004-06-18 Malonamide derivatives

Publications (3)

Publication Number Publication Date
JP2007508238A JP2007508238A (ja) 2007-04-05
JP2007508238A5 true JP2007508238A5 (enExample) 2007-08-23
JP4750701B2 JP4750701B2 (ja) 2011-08-17

Family

ID=34042809

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006518009A Expired - Fee Related JP4750701B2 (ja) 2003-07-07 2004-06-18 マロンアミド誘導体

Country Status (7)

Country Link
US (1) US20070213374A1 (enExample)
EP (1) EP1641759B1 (enExample)
JP (1) JP4750701B2 (enExample)
AR (1) AR045033A1 (enExample)
AU (1) AU2004255566B2 (enExample)
CA (1) CA2531485C (enExample)
WO (1) WO2005005389A2 (enExample)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2319693C9 (ru) 1999-01-13 2008-08-20 Байер Копэрейшн Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты)
ATE538794T1 (de) 1999-01-13 2012-01-15 Bayer Healthcare Llc Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US7838541B2 (en) 2002-02-11 2010-11-23 Bayer Healthcare, Llc Aryl ureas with angiogenesis inhibiting activity
US20030216396A1 (en) 2002-02-11 2003-11-20 Bayer Corporation Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
WO2004113274A2 (en) 2003-05-20 2004-12-29 Bayer Pharmaceuticals Corporation Diaryl ureas with kinase inhibiting activity
RS52625B (sr) 2003-07-23 2013-06-28 Bayer Healthcare Llc Fluoro supstituisana omega-karboksiaril difenil urea za lečenje i prevenciju bolesti i stanja bolesti
EP2392565B1 (en) 2003-09-26 2014-03-19 Exelixis, Inc. c-Met modulators and methods of use
AU2005217325B2 (en) 2004-02-27 2007-11-29 Eisai R & D Management Co., Ltd. Novel pyridine derivative and pyrimidine derivative (1)
ES2359836T3 (es) * 2004-04-23 2011-05-27 Bristol-Myers Squibb Company Heterociclos monociclicos como inhibidores de quinasa.
US7459562B2 (en) * 2004-04-23 2008-12-02 Bristol-Myers Squibb Company Monocyclic heterocycles as kinase inhibitors
TW200538453A (en) 2004-04-26 2005-12-01 Bristol Myers Squibb Co Bicyclic heterocycles as kinase inhibitors
US7173031B2 (en) 2004-06-28 2007-02-06 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
US7432373B2 (en) 2004-06-28 2008-10-07 Bristol-Meyers Squibb Company Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors
US7439246B2 (en) 2004-06-28 2008-10-21 Bristol-Myers Squibb Company Fused heterocyclic kinase inhibitors
JP5368701B2 (ja) 2004-07-02 2013-12-18 エクセリクシス、インコーポレイテッド c−Metモジュレーター及び使用方法
US7470693B2 (en) 2005-04-21 2008-12-30 Bristol-Myers Squibb Company Oxalamide derivatives as kinase inhibitors
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
TWI377198B (en) 2005-08-24 2012-11-21 Eisai R&D Man Co Ltd Novel pyridine derivatives and pyrimidine derivatives (3)
CN101454311B (zh) 2006-08-23 2013-03-27 卫材R&D管理有限公司 苯氧基吡啶衍生物的盐和其结晶及其制备方法
US7790885B2 (en) 2006-08-31 2010-09-07 Eisai R&D Management Co., Ltd. Process for preparing phenoxypyridine derivatives
JP2009132660A (ja) 2007-11-30 2009-06-18 Eisai R & D Management Co Ltd 食道癌治療用組成物
RS52754B2 (sr) 2009-01-16 2022-08-31 Exelixis Inc Malat so n-(4- {[6,7-bis(metiloksi)hinolin-4-il]oksi}fenil-n'- (4-fluorofenil) ciklopropan-1,1-dikarboksamid-a, i njeni kristalni oblici za lečenje karcinoma
UA108618C2 (uk) 2009-08-07 2015-05-25 Застосування c-met-модуляторів в комбінації з темозоломідом та/або променевою терапією для лікування раку
TWI520962B (zh) * 2012-06-29 2016-02-11 As the c-Met tyrosine kinase inhibitors novel fused pyridine derivatives
US10519113B2 (en) * 2016-08-17 2019-12-31 Icahn School Of Medicine At Mount Sinai Kinase inhibitor compounds, compositions, and methods of treating cancer

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0156456B1 (en) * 1984-02-08 1989-11-15 Sawai Pharmaceutical Co., Ltd. [(1,3,-dioxo-1,3-propanediyl)diimino] bisbenzoic acid derivatives and their use
AU632288B2 (en) * 1988-09-12 1992-12-24 Pharmacia & Upjohn Company Novel cc-1065 analogs having two cpi subunits
JP2627238B2 (ja) * 1992-12-02 1997-07-02 富士写真フイルム株式会社 マロン酸ジアミド化合物の製造方法
JPH08295667A (ja) * 1995-04-27 1996-11-12 Takeda Chem Ind Ltd 複素環化合物、その製造法および剤
EP1047418B1 (en) * 1997-12-22 2005-07-27 Bayer Pharmaceuticals Corp. Inhibition of raf kinase using substituted heterocyclic ureas
JP4261639B2 (ja) * 1998-08-05 2009-04-30 日本曹達株式会社 フェニルイミダゾール系抗高脂血症薬
EP1127054A4 (en) * 1998-10-29 2006-11-02 Bristol Myers Squibb Co INHIBITORS OF IMPDH ENZYME
EP1140840B1 (en) * 1999-01-13 2006-03-22 Bayer Pharmaceuticals Corp. -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
JP3528152B2 (ja) 2000-01-17 2004-05-17 有限会社ひので屋 豆腐製造用撹拌器具
US6916846B2 (en) * 2000-05-12 2005-07-12 Merck & Co. Inc. Coumermycin analogs as chemical dimerizers of chimeric proteins
EP1339668A2 (en) * 2000-11-28 2003-09-03 Guilford Pharmaceuticals Inc. Bisubstituted carbocyclic cyclophilin binding compounds and theirus
DE10112771A1 (de) * 2001-03-16 2002-09-26 Merck Patent Gmbh Inhibitoren des Integrins alpha¶v¶beta¶6¶
EP2088141A3 (en) * 2001-06-22 2009-11-18 Kirin Pharma Kabushiki Kaisha Quinoline derivatives and quinazoline derivatives capable of inhibiting autophosphorylation of hepatocyte growth factor receptors, and pharmaceutical composition comprising the same
AU2003243921B2 (en) * 2002-06-27 2009-05-07 Novo Nordisk A/S Aryl carbonyl derivatives as therapeutic agents
US7476683B2 (en) * 2002-08-27 2009-01-13 Merck Patent Gmbh Glycinamide derivatives as raf-kinase inhibitors
EP1562905A2 (en) * 2002-10-24 2005-08-17 MERCK PATENT GmbH Methylene urea derivatives as raf-kinase inhibitors
JP2006514991A (ja) * 2002-12-27 2006-05-18 シエーリング アクチエンゲゼルシャフト 新規医薬組合せ

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