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
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Application number
JP2006518009A
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English (en)
Japanese (ja)
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JP4750701B2 (ja
JP2007508238A (ja
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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
EP03014556.9 2003-07-07
EP03014556 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
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
ME00275B (me) 1999-01-13 2011-02-10 Bayer Corp ω-KARBOKSIARIL SUPSTITUISANI DIFENIL KARBAMIDI KAO INHIBITORI RAF KINAZE
ES2384160T3 (es) 1999-01-13 2012-07-02 Bayer Healthcare Llc Difenil ureas sustituidas con omega-carboxi arilo como agentes inhibidores de la cinasa p38
US20030216396A1 (en) 2002-02-11 2003-11-20 Bayer Corporation Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
EP1478358B1 (en) 2002-02-11 2013-07-03 Bayer HealthCare LLC Sorafenib tosylate for the treatment of diseases characterized by abnormal angiogenesis
DK1626714T3 (da) 2003-05-20 2007-10-15 Bayer Pharmaceuticals Corp Dirarylurinstoffer mod sygdomme medieret af PDGFR
EA010485B1 (ru) 2003-07-23 2008-10-30 Байер Фамэсьютиклс Копэрейшн Производное n,n'-дифенилмочевины, фармацевтическая композиция (варианты) и способ лечения и предупреждения заболеваний и состояний с его использованием (варианты)
ES2436888T3 (es) 2003-09-26 2014-01-07 Exelixis, Inc Moduladores c-Met y métodos de uso
CN1906167A (zh) 2004-02-27 2007-01-31 卫材株式会社 新型吡啶衍生物及嘧啶衍生物(2)
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
US20050288290A1 (en) 2004-06-28 2005-12-29 Borzilleri Robert M Fused heterocyclic 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
EP1773826A4 (en) * 2004-07-02 2009-06-03 Exelixis Inc MODULATORS OF C-MET AND THEIR METHOD OF USE
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
BRPI0616799B8 (pt) 2005-08-24 2021-05-25 Eisai R&D Man Co Ltd derivado de piridina e derivado de pirimidina, composições farmacêuticas, usos, inibidores de angiogênese, contra receptor de fator de crescimento de hepatócito e contra metástase de câncer, e agente antitumor
KR101380444B1 (ko) 2006-08-23 2014-04-01 에자이 알앤드디 매니지먼트 가부시키가이샤 페녹시피리딘 유도체의 염 또는 그 결정 및 이들의 제조 방법
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
CA2995880C (en) 2009-01-16 2021-01-05 Exelixis, Inc. Processes for preparing n-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
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
CN110072526A (zh) * 2016-08-17 2019-07-30 西奈山伊坎医学院 治疗癌症的激酶抑制剂化合物、组合物和方法

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
KR0137959B1 (ko) * 1988-09-12 1998-05-15 로버트 에이. 아미테이지 2개의 cpi 소단위를 갖는 신규한 cc-1065 유사화합물
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
CN100360507C (zh) * 1997-12-22 2008-01-09 拜尔有限公司 用取代杂环脲抑制raf激酶
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
WO2002044126A2 (en) * 2000-11-28 2002-06-06 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¶
DE60233736D1 (de) 2001-06-22 2009-10-29 Kirin Pharma K K Chinolinderivat und chinazolinderivat, die die selbstphosphorylierung des hepatocytus-proliferator-rezeptors hemmen, und diese enthaltende medizinische zusammensetzung
KR101116627B1 (ko) * 2002-06-27 2012-10-09 노보 노르디스크 에이/에스 치료제로서 아릴 카르보닐 유도체
ATE402700T1 (de) * 2002-08-27 2008-08-15 Merck Patent Gmbh Glycinamid-derivate als raf-kinase-hemmer
MXPA05004206A (es) * 2002-10-24 2005-06-08 Merck Patent Gmbh Derivados de metilenurea.
WO2004058234A2 (en) * 2002-12-27 2004-07-15 Schering Aktiengesellschaft Pharmaceutical combinations of phthalazine vegf inhibitors and benzamide hdac inhibitors

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