JP2010507578A5 - - Google Patents

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Publication number
JP2010507578A5
JP2010507578A5 JP2009533541A JP2009533541A JP2010507578A5 JP 2010507578 A5 JP2010507578 A5 JP 2010507578A5 JP 2009533541 A JP2009533541 A JP 2009533541A JP 2009533541 A JP2009533541 A JP 2009533541A JP 2010507578 A5 JP2010507578 A5 JP 2010507578A5
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JP
Japan
Prior art keywords
cancer
receptor tyrosine
tyrosine kinase
kinase
leukemia
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
JP2009533541A
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English (en)
Japanese (ja)
Other versions
JP2010507578A (ja
JP5378222B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/081841 external-priority patent/WO2008051808A2/en
Publication of JP2010507578A publication Critical patent/JP2010507578A/ja
Publication of JP2010507578A5 publication Critical patent/JP2010507578A5/ja
Application granted granted Critical
Publication of JP5378222B2 publication Critical patent/JP5378222B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2009533541A 2006-10-23 2007-10-18 タンパク質キナーゼ調節物質としての二環式トリアゾール Expired - Fee Related JP5378222B2 (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US86255206P 2006-10-23 2006-10-23
US60/862,552 2006-10-23
US87030906P 2006-12-15 2006-12-15
US60/870,309 2006-12-15
US91376607P 2007-04-24 2007-04-24
US60/913,766 2007-04-24
US95284007P 2007-07-30 2007-07-30
US60/952,840 2007-07-30
PCT/US2007/081841 WO2008051808A2 (en) 2006-10-23 2007-10-18 Bicyclic triazoles as protein kinase modulators

Publications (3)

Publication Number Publication Date
JP2010507578A JP2010507578A (ja) 2010-03-11
JP2010507578A5 true JP2010507578A5 (enExample) 2010-12-02
JP5378222B2 JP5378222B2 (ja) 2013-12-25

Family

ID=38956385

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009533541A Expired - Fee Related JP5378222B2 (ja) 2006-10-23 2007-10-18 タンパク質キナーゼ調節物質としての二環式トリアゾール

Country Status (25)

Country Link
US (1) US8507489B2 (enExample)
EP (1) EP2084162B1 (enExample)
JP (1) JP5378222B2 (enExample)
KR (1) KR20090071612A (enExample)
AR (1) AR063520A1 (enExample)
AU (1) AU2007309149C1 (enExample)
BR (1) BRPI0717320A2 (enExample)
CA (1) CA2667428A1 (enExample)
CO (1) CO6190620A2 (enExample)
CR (1) CR10803A (enExample)
DK (1) DK2084162T3 (enExample)
EA (1) EA200970403A1 (enExample)
ES (1) ES2393130T3 (enExample)
IL (1) IL197958A0 (enExample)
MA (1) MA30871B1 (enExample)
MX (1) MX2009004059A (enExample)
NO (1) NO20091618L (enExample)
NZ (1) NZ575336A (enExample)
PE (1) PE20080893A1 (enExample)
PL (1) PL2084162T3 (enExample)
PT (1) PT2084162E (enExample)
SV (1) SV2009003235A (enExample)
TN (1) TN2009000142A1 (enExample)
TW (1) TW200835492A (enExample)
WO (1) WO2008051808A2 (enExample)

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TWI365185B (en) 2008-07-24 2012-06-01 Lilly Co Eli Amidophenoxyindazoles useful as inhibitors of c-met
UY32049A (es) 2008-08-14 2010-03-26 Takeda Pharmaceutical Inhibidores de cmet
EP2165710A1 (en) * 2008-09-19 2010-03-24 Institut Curie Tyrosine kinase receptor Tyro3 as a therapeutic target in the treatment of a bladder tumor
JP2012509342A (ja) 2008-11-20 2012-04-19 オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド 置換ピロロ[2,3−b]−ピリジンおよび−ピラジン
FR2941950B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941949B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-o-cycloalkyl ou 6-nh-cycloalkyl- triazolopyridazine-sulfanyl)benzothiazoles et benzimidazoles preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941951B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-nh-substitue-triazolopyridazine-sulfanyl) benzothiazoles et benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
FR2941952B1 (fr) * 2009-02-06 2011-04-01 Sanofi Aventis Derives de 6-(6-substitue-triazolopyridazine-sulfanyl) 5-fluoro-benzothiazoles et 5-fluoro-benzimidazoles : preparation, application comme medicaments et utilisation comme inhibiteurs de met.
KR20120089643A (ko) 2009-08-12 2012-08-13 노파르티스 아게 헤테로시클릭 히드라존 화합물, 및 암 및 염증을 치료하기 위한 그의 용도
JP5775871B2 (ja) 2009-08-20 2015-09-09 ノバルティス アーゲー ヘテロ環式オキシム化合物
EP2719699B1 (en) 2009-12-31 2015-07-08 Hutchison Medipharma Limited Certain triazolopyrazines, compositions thereof and methods of use therefor
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
US20130072495A1 (en) 2010-05-14 2013-03-21 OSI Pharmaceuticals, LLC Fused bicyclic kinase inhibitors
AR085183A1 (es) 2010-07-30 2013-09-18 Lilly Co Eli Compuesto 6-(1-metil-1h-pirazol-4-il)-3-(2-metil-2h-indazol-5-iltio)-[1,2,4]triazol[4,3-b]piridazina, composicion farmaceutica que lo comprende y uso para preparar un medicamento util para tratar cancer
UY33549A (es) * 2010-08-10 2012-01-31 Glaxo Group Ltd Quinolil aminas como agentes inhibidores de las quinasas
WO2012042421A1 (en) 2010-09-29 2012-04-05 Pfizer Inc. Method of treating abnormal cell growth
CN102532141A (zh) 2010-12-08 2012-07-04 中国科学院上海药物研究所 [1,2,4]三唑并[4,3-b][1,2,4]三嗪类化合物、其制备方法和用途
US8765760B2 (en) 2011-01-11 2014-07-01 Sunovion Pharmaceuticals, Inc. [1,2,4] triazol [1,5-a] pyrazines useful as inhibitors of phosphodiesterases
EP2673277A1 (en) * 2011-02-10 2013-12-18 Novartis AG [1, 2, 4]triazolo [4, 3 -b]pyridazine compounds as inhibitors of the c-met tyrosine kinase
CN103459396B (zh) * 2011-02-10 2015-08-19 诺瓦提斯公司 作为c-Met酪氨酸激酶抑制剂的[1,2,4]三唑并[4,3-b]哒嗪化合物
JP2014513724A (ja) 2011-05-16 2014-06-05 オーエスアイ・ファーマシューティカルズ,エルエルシー 融合二環キナーゼ阻害剤
US9062045B2 (en) * 2011-09-15 2015-06-23 Novartis Ag Triazolopyridine compounds
CN103958509B (zh) * 2011-09-15 2015-12-23 诺华股份有限公司 作为酪氨酸激酶抑制剂的6-取代的3-(喹啉-6-基硫代)-[1,2,4]三唑并[4,3-a]吡啶化合物
ES2894830T3 (es) 2012-04-03 2022-02-16 Novartis Ag Productos combinados con inhibidores de tirosina·cinasa y su uso
WO2013151913A1 (en) 2012-04-03 2013-10-10 Novartis Ag Tyrosine kinase inhibitor combinations and their use
CN103122000B (zh) * 2012-09-03 2013-12-25 中美冠科生物技术(太仓)有限公司 用作抗肿瘤药物的高选择性的c-Met激酶抑制剂
WO2014089904A1 (en) * 2012-12-10 2014-06-19 Abbvie Inc. Triazinone compounds
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US9364405B2 (en) 2013-03-13 2016-06-14 Avon Products, Inc. Tyrosinase inhibitors
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JPS60194443A (ja) * 1984-03-16 1985-10-02 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
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WO2002083139A1 (en) 2001-04-10 2002-10-24 Merck & Co., Inc. Inhibitors of akt activity
US20030229453A1 (en) 2002-04-09 2003-12-11 Antonysamy Stephen Suresh Crystals and structures of PAK4KD kinase PAK4KD
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CA2573573A1 (en) * 2004-07-27 2006-02-09 Sgx Pharmaceuticals, Inc. Fused ring heterocycle kinase modulators
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BRPI0519508A2 (pt) 2004-12-27 2009-03-17 Alcon Inc análogos de aminopirazina para tratamento de glaucoma e outras doenças ou condições mediadas por rho cinase

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