JP2008539215A5 - - Google Patents

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Publication number
JP2008539215A5
JP2008539215A5 JP2008508290A JP2008508290A JP2008539215A5 JP 2008539215 A5 JP2008539215 A5 JP 2008539215A5 JP 2008508290 A JP2008508290 A JP 2008508290A JP 2008508290 A JP2008508290 A JP 2008508290A JP 2008539215 A5 JP2008539215 A5 JP 2008539215A5
Authority
JP
Japan
Prior art keywords
alkyl
aryl
heteroaryl
optionally substituted
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.)
Granted
Application number
JP2008508290A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008539215A (ja
JP5243953B2 (ja
Filing date
Publication date
Priority claimed from GBGB0508471.0A external-priority patent/GB0508471D0/en
Application filed filed Critical
Publication of JP2008539215A publication Critical patent/JP2008539215A/ja
Publication of JP2008539215A5 publication Critical patent/JP2008539215A5/ja
Application granted granted Critical
Publication of JP5243953B2 publication Critical patent/JP5243953B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2008508290A 2005-04-26 2006-04-25 キナーゼ阻害剤としての縮合チアゾール誘導体 Active JP5243953B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0508471.0A GB0508471D0 (en) 2005-04-26 2005-04-26 Therapeutic agents
GB0508471.0 2005-04-26
PCT/GB2006/001505 WO2006114606A1 (en) 2005-04-26 2006-04-25 Fused thiazole derivatives as kinase inhibitors

Publications (3)

Publication Number Publication Date
JP2008539215A JP2008539215A (ja) 2008-11-13
JP2008539215A5 true JP2008539215A5 (enExample) 2012-08-30
JP5243953B2 JP5243953B2 (ja) 2013-07-24

Family

ID=34640185

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008508290A Active JP5243953B2 (ja) 2005-04-26 2006-04-25 キナーゼ阻害剤としての縮合チアゾール誘導体

Country Status (9)

Country Link
US (1) US7888344B2 (enExample)
EP (1) EP1881827B1 (enExample)
JP (1) JP5243953B2 (enExample)
AT (1) ATE526021T1 (enExample)
AU (1) AU2006239018B2 (enExample)
CA (1) CA2607426C (enExample)
ES (1) ES2373680T3 (enExample)
GB (1) GB0508471D0 (enExample)
WO (1) WO2006114606A1 (enExample)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2035436B1 (en) * 2006-06-26 2011-05-25 UCB Pharma S.A. Fused thiazole derivatives as kinase inhibitors
GB0620059D0 (en) 2006-10-10 2006-11-22 Ucb Sa Therapeutic agents
GB0620818D0 (en) * 2006-10-19 2006-11-29 Ucb Sa Therapeutic agents
WO2008060597A2 (en) 2006-11-15 2008-05-22 Vertex Pharmaceuticals Incorporated Compounds useful as protein kinase inhibitors
CN101616672A (zh) 2007-02-20 2009-12-30 诺瓦提斯公司 作为脂质激酶和mTOR双重抑制剂的咪唑并喹啉类
US7893060B2 (en) 2007-06-12 2011-02-22 F. Hoffmann-La Roche Ag Thiazolopyrimidines and their use as inhibitors of phosphatidylinositol-3 kinase
NZ581919A (en) 2007-06-26 2011-08-26 Ucb Pharma Sa Fused thiazole derivatives as kinase inhibitors
WO2009036768A2 (en) * 2007-09-19 2009-03-26 H. Lundbeck A/S Diagnosing potential weight gain in a subject
ES2399774T3 (es) 2007-09-24 2013-04-03 Genentech, Inc. Compuestos de tiazolopirimidina inhibidores de PI3K y métodos de uso
JP5348725B2 (ja) 2007-10-25 2013-11-20 ジェネンテック, インコーポレイテッド チエノピリミジン化合物の製造方法
GB0723747D0 (en) * 2007-12-04 2008-12-31 Ucb Pharma Sa Therapeutic agents
WO2009071895A1 (en) * 2007-12-04 2009-06-11 Ucb Pharma S.A. Fused thiazole and thiophene derivatives as kinase inhibitors
WO2009071890A1 (en) * 2007-12-04 2009-06-11 Ucb Pharma S.A. Tricyclic kinase inhibitors
US9029411B2 (en) 2008-01-25 2015-05-12 Millennium Pharmaceuticals, Inc. Thiophenes and uses thereof
WO2009120826A1 (en) * 2008-03-27 2009-10-01 Wyeth 2-aryl- and 2-heteroarylthiazolyl compounds, methods for their preparation and use thereof
GB0805818D0 (en) * 2008-03-31 2008-04-30 Ucb Pharma Sa Therapeutic agents
US8796314B2 (en) 2009-01-30 2014-08-05 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
EP2391619A1 (en) 2009-01-30 2011-12-07 Millennium Pharmaceuticals, Inc. Heteroaryls and their use as pi3k inhibitors
US9090601B2 (en) 2009-01-30 2015-07-28 Millennium Pharmaceuticals, Inc. Thiazole derivatives
US8410095B2 (en) 2009-05-20 2013-04-02 Glaxosmithkline Llc Thiazolopyrimidinone derivatives as PI3 kinase inhibitors
US8158625B2 (en) 2009-05-27 2012-04-17 Genentech, Inc. Bicyclic indole-pyrimidine PI3K inhibitor compounds selective for P110 delta, and methods of use
WO2010138589A1 (en) 2009-05-27 2010-12-02 Genentech, Inc. Bicyclic pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use
US9062038B2 (en) 2010-08-11 2015-06-23 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
SG10201506238SA (en) 2010-08-11 2015-09-29 Millennium Pharm Inc Heteroaryls And Uses Thereof
US8859768B2 (en) 2010-08-11 2014-10-14 Millennium Pharmaceuticals, Inc. Heteroaryls and uses thereof
PE20141044A1 (es) * 2010-10-13 2014-09-07 Millennium Pharm Inc Heteroarilos y sus usos
CA2828415A1 (en) 2011-03-10 2012-09-13 Lupin Limited Substituted morpholines as modulators for the calcium sensing receptor
SG10201707002VA (en) 2013-05-01 2017-10-30 Hoffmann La Roche Biheteroaryl compounds and uses thereof
WO2017156350A1 (en) 2016-03-09 2017-09-14 K-Gen, Inc. Methods of cancer treatment
CN107556199A (zh) * 2017-09-24 2018-01-09 杨子辉 一种3,4‑二氯‑2‑氨基‑5‑氟联苯的制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7091227B2 (en) * 2000-02-07 2006-08-15 Abbott Gmbh & Co. Kg Benzothiazole derivatives
WO2001083456A1 (en) * 2000-04-27 2001-11-08 Yamanouchi Pharmaceutical Co., Ltd. Condensed heteroaryl derivatives
US7176214B2 (en) * 2003-05-21 2007-02-13 Bristol-Myers Squibb Company Imidazo-fused oxazolo[4,5-β]pyridine and imidazo-fused thiazolo[4,5-β]pyridine based tricyclic compounds and pharmaceutical compositions comprising same

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