JP2005535586A5 - - Google Patents

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Publication number
JP2005535586A5
JP2005535586A5 JP2004501387A JP2004501387A JP2005535586A5 JP 2005535586 A5 JP2005535586 A5 JP 2005535586A5 JP 2004501387 A JP2004501387 A JP 2004501387A JP 2004501387 A JP2004501387 A JP 2004501387A JP 2005535586 A5 JP2005535586 A5 JP 2005535586A5
Authority
JP
Japan
Prior art keywords
alkyl
optionally substituted
hydrogen
cycloalkyl
compound
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.)
Pending
Application number
JP2004501387A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005535586A (ja
Filing date
Publication date
Priority claimed from GBGB0209891.1A external-priority patent/GB0209891D0/en
Application filed filed Critical
Publication of JP2005535586A publication Critical patent/JP2005535586A/ja
Publication of JP2005535586A5 publication Critical patent/JP2005535586A5/ja
Pending legal-status Critical Current

Links

JP2004501387A 2002-04-30 2003-04-29 p38キナーゼ阻害剤としてのヘテロアリール置換ビフェニル誘導体 Pending JP2005535586A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0209891.1A GB0209891D0 (en) 2002-04-30 2002-04-30 Novel compounds
PCT/GB2003/001834 WO2003093248A1 (en) 2002-04-30 2003-04-29 Heteroaryl substituted biphenyl derivatives as p38 kinase inhibitors

Publications (2)

Publication Number Publication Date
JP2005535586A JP2005535586A (ja) 2005-11-24
JP2005535586A5 true JP2005535586A5 (US20040106767A1-20040603-C00005.png) 2006-06-08

Family

ID=9935812

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004501387A Pending JP2005535586A (ja) 2002-04-30 2003-04-29 p38キナーゼ阻害剤としてのヘテロアリール置換ビフェニル誘導体

Country Status (9)

Country Link
US (1) US7425555B2 (US20040106767A1-20040603-C00005.png)
EP (1) EP1499600B1 (US20040106767A1-20040603-C00005.png)
JP (1) JP2005535586A (US20040106767A1-20040603-C00005.png)
AT (1) ATE368034T1 (US20040106767A1-20040603-C00005.png)
AU (1) AU2003226572A1 (US20040106767A1-20040603-C00005.png)
DE (1) DE60315146T2 (US20040106767A1-20040603-C00005.png)
ES (1) ES2290486T3 (US20040106767A1-20040603-C00005.png)
GB (1) GB0209891D0 (US20040106767A1-20040603-C00005.png)
WO (1) WO2003093248A1 (US20040106767A1-20040603-C00005.png)

Families Citing this family (42)

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GB0124931D0 (en) * 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124936D0 (en) * 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124934D0 (en) * 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
DK1474395T3 (da) 2002-02-12 2008-02-11 Smithkline Beecham Corp Nicotinamidderivater, der er nyttige som p38-inhibitorer
GB0209891D0 (en) 2002-04-30 2002-06-05 Glaxo Group Ltd Novel compounds
GB0217757D0 (en) 2002-07-31 2002-09-11 Glaxo Group Ltd Novel compounds
GB0308185D0 (en) * 2003-04-09 2003-05-14 Smithkline Beecham Corp Novel compounds
GB0308186D0 (en) 2003-04-09 2003-05-14 Smithkline Beecham Corp Novel compounds
GB0308201D0 (en) 2003-04-09 2003-05-14 Smithkline Beecham Corp Novel compounds
ES2315703T3 (es) * 2003-07-25 2009-04-01 Novartis Ag Inhibidores de la quinasa p-38.
GB0318814D0 (en) 2003-08-11 2003-09-10 Smithkline Beecham Corp Novel compounds
GB0402140D0 (en) * 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
GB0402143D0 (en) * 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
GB0402137D0 (en) * 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
GB0402138D0 (en) * 2004-01-30 2004-03-03 Smithkline Beecham Corp Novel compounds
US7683097B2 (en) * 2004-05-27 2010-03-23 Propharmacon Inc. Topoisomerase inhibitors
US20080051416A1 (en) * 2004-10-05 2008-02-28 Smithkline Beecham Corporation Novel Compounds
EP1802606B1 (en) * 2004-10-19 2011-03-16 Compass Pharmaceuticals LLC Arylcarboxamides and their use as anti-tumor agents
US7968574B2 (en) 2004-12-28 2011-06-28 Kinex Pharmaceuticals, Llc Biaryl compositions and methods for modulating a kinase cascade
KR101478933B1 (ko) 2004-12-28 2015-01-02 키넥스 파마슈티컬즈, 엘엘씨 세포 증식 질환의 치료를 위한 조성물 및 방법
GB0512429D0 (en) * 2005-06-17 2005-07-27 Smithkline Beecham Corp Novel compound
CA2621364A1 (en) * 2005-09-16 2007-03-22 Arrow Therapeutics Limited Biphenyl derivatives and their use in treating hepatitis c
GB0612026D0 (en) 2006-06-16 2006-07-26 Smithkline Beecham Corp New use
CN101595084B (zh) 2006-06-29 2013-01-02 金克斯医药品有限公司 用于调整激酶级联的二芳基组合物和方法
PT2511301T (pt) 2006-08-04 2018-03-08 Medimmune Ltd Anticorpos humanos para erbb2
US7935697B2 (en) 2006-12-28 2011-05-03 Kinex Pharmaceuticals, Llc Compositions for modulating a kinase cascade and methods of use thereof
US7939529B2 (en) 2007-05-17 2011-05-10 Kinex Pharmaceuticals, Llc Process for the preparation of compositions for modulating a kinase cascade and methods of use thereof
US8124605B2 (en) 2007-07-06 2012-02-28 Kinex Pharmaceuticals, Llc Compositions and methods for modulating a kinase cascade
EP2217229B1 (en) * 2007-10-20 2020-10-14 Athenex, Inc. Pharmaceutical compositions for modulating a kinase cascade and methods of use thereof
TWI490214B (zh) 2008-05-30 2015-07-01 艾德克 上野股份有限公司 苯或噻吩衍生物及該等作為vap-1抑制劑之用途
JP2011526620A (ja) * 2008-07-04 2011-10-13 アンスティトゥート・ナシオナル・ドゥ・ラ・サンテ・エ・ドゥ・ラ・ルシャルシュ・メディカル・(インセルム) プロテアソームモジュレーターとしての窒素複素環誘導体
CN102905700A (zh) 2010-04-16 2013-01-30 金克斯医药品有限公司 用于预防和治疗癌症的组合物以及方法
RU2538964C1 (ru) 2010-12-17 2015-01-10 Мицубиси Танабе Фарма Корпорейшн Соединение с последовательной арициклической структурой, обладающее активностью ингибирования ацилкофермента а: диацилглицеринацилтрансферазы (dgat1)
ES2690315T3 (es) 2012-06-15 2018-11-20 Mitsubishi Tanabe Pharma Corporation Compuestos de imidazol y triazol como inhibidores de DGAT-1
WO2014036426A1 (en) 2012-08-30 2014-03-06 Kinex Pharmaceuticals, Llc N-(3-fluorobenzyl)-2-(5-(4-morpholinophenyl)pyridin-2-yl) acetamide as protein|tyrosine kinase modulators
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
EP3070085B1 (en) * 2013-02-04 2019-01-09 Janssen Pharmaceutica NV Flap modulators
US20190060286A1 (en) 2016-02-29 2019-02-28 University Of Florida Research Foundation, Incorpo Chemotherapeutic Methods
US10342786B2 (en) 2017-10-05 2019-07-09 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
WO2019071147A1 (en) 2017-10-05 2019-04-11 Fulcrum Therapeutics, Inc. INHIBITORS OF KINASE P38 REDUCING EXPRESSION OF DUX4 GENE AND DOWNSTREAM GENES FOR THE TREATMENT OF FSHD
CA3094324A1 (en) 2018-03-26 2019-10-03 Clear Creek Bio, Inc. Compositions and methods for inhibiting dihydroorotate dehydrogenase
US12076315B2 (en) 2020-03-20 2024-09-03 Clear Creek Bio, Inc. Stable polymorphic compositions of brequinar sodium and methods of use and manufacture thereof

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TW240217B (US20040106767A1-20040603-C00005.png) * 1992-12-30 1995-02-11 Glaxo Group Ltd
AU1108395A (en) * 1993-12-07 1995-06-27 Smithkline Beecham Plc Heterocyclic biphenylylamides useful as 5ht1d antagonists
ES2179254T3 (es) * 1996-11-04 2003-01-16 Bayer Cropscience Sa 1-poliarilpirazoles plaguicidas.
PE20020506A1 (es) * 2000-08-22 2002-07-09 Glaxo Group Ltd Derivados de pirazol fusionados como inhibidores de la proteina cinasa
GB0119863D0 (en) * 2001-08-14 2001-10-10 Cancer Res Campaign Tech DNA-PK inhibitors
GB0124939D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124931D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124934D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124932D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124938D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124936D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124933D0 (en) * 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124928D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
GB0124941D0 (en) 2001-10-17 2001-12-05 Glaxo Group Ltd Chemical compounds
DK1474395T3 (da) 2002-02-12 2008-02-11 Smithkline Beecham Corp Nicotinamidderivater, der er nyttige som p38-inhibitorer
GB0209891D0 (en) 2002-04-30 2002-06-05 Glaxo Group Ltd Novel compounds
GB0217757D0 (en) 2002-07-31 2002-09-11 Glaxo Group Ltd Novel compounds

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