JP2009502921A5 - - Google Patents

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Publication number
JP2009502921A5
JP2009502921A5 JP2008523972A JP2008523972A JP2009502921A5 JP 2009502921 A5 JP2009502921 A5 JP 2009502921A5 JP 2008523972 A JP2008523972 A JP 2008523972A JP 2008523972 A JP2008523972 A JP 2008523972A JP 2009502921 A5 JP2009502921 A5 JP 2009502921A5
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JP
Japan
Prior art keywords
compound
independently
composition
cancer
substituted
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
JP2008523972A
Other languages
English (en)
Japanese (ja)
Other versions
JP2009502921A (ja
JP5255438B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2006/028149 external-priority patent/WO2007015923A2/en
Publication of JP2009502921A publication Critical patent/JP2009502921A/ja
Publication of JP2009502921A5 publication Critical patent/JP2009502921A5/ja
Application granted granted Critical
Publication of JP5255438B2 publication Critical patent/JP5255438B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2008523972A 2005-07-26 2006-07-21 プロテインキナーゼ阻害薬として有用なベンズイミダゾール Expired - Fee Related JP5255438B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US70239905P 2005-07-26 2005-07-26
US60/702,399 2005-07-26
PCT/US2006/028149 WO2007015923A2 (en) 2005-07-26 2006-07-21 Benzimidazoles useful as inhibitors of protein kinases

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2013025417A Division JP2013082757A (ja) 2005-07-26 2013-02-13 プロテインキナーゼ阻害薬として有用なベンズイミダゾール

Publications (3)

Publication Number Publication Date
JP2009502921A JP2009502921A (ja) 2009-01-29
JP2009502921A5 true JP2009502921A5 (https=) 2009-09-03
JP5255438B2 JP5255438B2 (ja) 2013-08-07

Family

ID=37680602

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2008523972A Expired - Fee Related JP5255438B2 (ja) 2005-07-26 2006-07-21 プロテインキナーゼ阻害薬として有用なベンズイミダゾール
JP2013025417A Withdrawn JP2013082757A (ja) 2005-07-26 2013-02-13 プロテインキナーゼ阻害薬として有用なベンズイミダゾール

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2013025417A Withdrawn JP2013082757A (ja) 2005-07-26 2013-02-13 プロテインキナーゼ阻害薬として有用なベンズイミダゾール

Country Status (17)

Country Link
US (1) US8076343B2 (https=)
EP (2) EP2336122B1 (https=)
JP (2) JP5255438B2 (https=)
KR (1) KR20080034483A (https=)
CN (1) CN101291927A (https=)
AT (1) ATE484501T1 (https=)
AU (1) AU2006276088A1 (https=)
CA (1) CA2616159A1 (https=)
DE (1) DE602006017574D1 (https=)
ES (1) ES2351357T3 (https=)
IL (1) IL188942A0 (https=)
NO (1) NO20080967L (https=)
NZ (1) NZ566021A (https=)
RU (1) RU2415853C2 (https=)
TW (1) TW200745088A (https=)
WO (1) WO2007015923A2 (https=)
ZA (1) ZA200800992B (https=)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105367503A (zh) 2007-10-19 2016-03-02 阿维拉制药公司 杂芳基化合物和其用途
US7989465B2 (en) 2007-10-19 2011-08-02 Avila Therapeutics, Inc. 4,6-disubstituted pyrimidines useful as kinase inhibitors
PT2300013T (pt) 2008-05-21 2017-10-31 Ariad Pharma Inc Derivados de fósforo como inibidores de cinases
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
US9834518B2 (en) 2011-05-04 2017-12-05 Ariad Pharmaceuticals, Inc. Compounds for inhibiting cell proliferation in EGFR-driven cancers
US20150166591A1 (en) 2012-05-05 2015-06-18 Ariad Pharmaceuticals, Inc. Methods and compositions for raf kinase mediated diseases
US9336046B2 (en) 2012-06-15 2016-05-10 International Business Machines Corporation Transaction abort processing
US9512136B2 (en) * 2012-11-26 2016-12-06 Universal Display Corporation Organic electroluminescent materials and devices
EP2976336A1 (en) * 2013-03-21 2016-01-27 Bayer Pharma Aktiengesellschaft 3-heteroaryl substituted indazoles
US9611283B1 (en) 2013-04-10 2017-04-04 Ariad Pharmaceuticals, Inc. Methods for inhibiting cell proliferation in ALK-driven cancers
WO2014170421A1 (en) * 2013-04-19 2014-10-23 F. Hoffmann-La Roche Ag Serine/threonine kinase inhibitors
ITUA20164278A1 (it) * 2016-06-10 2017-12-10 International Soc For Drug Development S R L COMPOSTI 2-OXO-1,2-DIIDROPIRIDIN-3-CARBOSSAMMIDE E LORO USO COME INIBITORI DUALI DI PDK1/AurA
US10793551B2 (en) 2017-10-19 2020-10-06 Effector Therapeutics Inc. Benzimidazole-indole inhibitors of Mnk1 and Mnk2
CN112552287B (zh) * 2020-12-16 2021-11-30 北京华氏精恒医药科技有限公司 一种吲哚类衍生物药物制剂及其制备方法
WO2023116888A1 (zh) * 2021-12-23 2023-06-29 杭州多域生物技术有限公司 一种五元并六元化合物、制备方法、药物组合物和应用

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4535350B2 (ja) * 1998-11-17 2010-09-01 クミアイ化学工業株式会社 ピリミジニルベンズイミダゾール誘導体及び農園芸用殺菌剤
CN1243002C (zh) 1998-11-17 2006-02-22 组合化学工业株式会社 嘧啶基苯并咪唑和三嗪基苯并咪唑衍生物及农业/园艺杀菌剂
WO2001025220A1 (en) 1999-10-07 2001-04-12 Amgen Inc. Triazine kinase inhibitors
EP1257546A1 (en) 2000-02-17 2002-11-20 Amgen Inc. Kinase inhibitors
EP1389617B1 (en) * 2001-04-27 2007-01-03 Zenyaku Kogyo Kabushiki Kaisha Heterocyclic compound and antitumor agent containing the same as active ingredient
FR2833948B1 (fr) * 2001-12-21 2004-02-06 Sod Conseils Rech Applic Nouveaux derives de benzimidazole et leur utilisation en tant que medicament
NZ537156A (en) * 2002-05-23 2007-06-29 Cytopia Pty Ltd Kinase inhibitors
CL2003002353A1 (es) * 2002-11-15 2005-02-04 Vertex Pharma Compuestos derivados de diaminotriazoles, inhibidores d ela proteina quinasa; composicion farmaceutica; procedimiento de preparacion; y su uso del compuesto en el tratamiento de enfermedades de desordenes alergicos, proliferacion, autoinmunes, condic
UA80767C2 (en) * 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
NZ546058A (en) * 2004-01-12 2010-09-30 Ym Biosciences Australia Pty Benzimidazole and other fused ring derivatives as selective janus kinase inhibitors

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