JP2008512359A5 - - Google Patents

Download PDF

Info

Publication number
JP2008512359A5
JP2008512359A5 JP2007528889A JP2007528889A JP2008512359A5 JP 2008512359 A5 JP2008512359 A5 JP 2008512359A5 JP 2007528889 A JP2007528889 A JP 2007528889A JP 2007528889 A JP2007528889 A JP 2007528889A JP 2008512359 A5 JP2008512359 A5 JP 2008512359A5
Authority
JP
Japan
Prior art keywords
group
phenyl
biphen
alkyl
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
JP2007528889A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008512359A (ja
JP5334414B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2005/054366 external-priority patent/WO2006027346A2/en
Publication of JP2008512359A publication Critical patent/JP2008512359A/ja
Publication of JP2008512359A5 publication Critical patent/JP2008512359A5/ja
Application granted granted Critical
Publication of JP5334414B2 publication Critical patent/JP5334414B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2007528889A 2004-09-06 2005-09-05 新規のピラゾロピリミジン Expired - Fee Related JP5334414B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04104283 2004-09-06
EP04104283.9 2004-09-06
PCT/EP2005/054366 WO2006027346A2 (en) 2004-09-06 2005-09-05 Novel pyrazolopyrimidines

Publications (3)

Publication Number Publication Date
JP2008512359A JP2008512359A (ja) 2008-04-24
JP2008512359A5 true JP2008512359A5 (enExample) 2013-06-06
JP5334414B2 JP5334414B2 (ja) 2013-11-06

Family

ID=34929540

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007528889A Expired - Fee Related JP5334414B2 (ja) 2004-09-06 2005-09-05 新規のピラゾロピリミジン

Country Status (8)

Country Link
US (1) US7745446B2 (enExample)
EP (1) EP1797096B1 (enExample)
JP (1) JP5334414B2 (enExample)
AT (1) ATE517901T1 (enExample)
AU (1) AU2005281704A1 (enExample)
CA (1) CA2578384A1 (enExample)
ES (1) ES2368930T3 (enExample)
WO (1) WO2006027346A2 (enExample)

Families Citing this family (32)

* 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
EP2298311B1 (en) 1999-01-13 2012-05-09 Bayer HealthCare LLC w-Carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
DK1478358T3 (da) 2002-02-11 2013-10-07 Bayer Healthcare Llc Sorafenibtosylat til behandling af sygdomme kendetegnet ved unormal angiogenese
EP1636585B2 (en) 2003-05-20 2012-06-13 Bayer HealthCare LLC Diaryl ureas with kinase inhibiting activity
PL1663978T3 (pl) 2003-07-23 2008-04-30 Bayer Healthcare Llc Fluoropodstawiony omega-karboksyarylodifenylomocznik do leczenia i profilaktyki chorób i stanów
JP2008545670A (ja) * 2005-05-27 2008-12-18 バイエル・ヘルスケア・アクチェンゲゼルシャフト 疾患を処置するためのジアリールウレア類を含む組合せ治療
US8168658B2 (en) 2006-02-28 2012-05-01 Merck Sharp & Dohme Corp. Inhibitors of histone deacetylase
US9539303B2 (en) 2006-04-24 2017-01-10 Celgene Corporation Treatment of Ras-expressing tumors
US8957027B2 (en) 2006-06-08 2015-02-17 Celgene Corporation Deacetylase inhibitor therapy
DE602007011628D1 (de) 2006-07-06 2011-02-10 Array Biopharma Inc Dihydrofuropyrimidine als akt-proteinkinaseinhibitoren
WO2008006039A1 (en) 2006-07-06 2008-01-10 Array Biopharma Inc. Dihydrothieno pyrimidines as akt protein kinase inhibitors
AU2007307489A1 (en) * 2006-10-06 2008-04-17 Takeda Pharmaceutical Company Limited Combination drug
EP2102230A2 (en) 2006-12-29 2009-09-23 Gloucester Pharmaceuticals, Inc. Purifiction of romidepsin
JP2010531358A (ja) 2007-06-27 2010-09-24 メルク・シャープ・エンド・ドーム・コーポレイション ヒストン脱アセチル化酵素阻害剤としてのピリジル及びピリミジニル誘導体
WO2009002495A1 (en) 2007-06-27 2008-12-31 Merck & Co., Inc. 4-carboxybenzylamino derivatives as histone deacetylase inhibitors
US20100136097A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Systems for modulating inflammation
US20100135908A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Delivery devices for modulating inflammation
US20100135983A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Anti-inflammatory compositions and methods
US20100136096A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Systems for modulating inflammation
US20100136094A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Systems for modulating inflammation
US20100136095A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Systems for modulating inflammation
US20100137246A1 (en) * 2008-12-02 2010-06-03 Searete Llc, A Limited Liability Corporation Of The State Of Delaware Anti-inflammatory compositions and methods
KR20120124428A (ko) * 2009-12-30 2012-11-13 아르퀼 인코포레이티드 치환된 피롤로-아미노피리미딘 화합물
CA2787714C (en) 2010-01-22 2019-04-09 Joaquin Pastor Fernandez Inhibitors of pi3 kinase
US20130131057A1 (en) 2010-05-13 2013-05-23 Centro Nacional De Investigaciones Oncologicas (Cnio New bicyclic compounds as pi3-k and mtor inhibitors
CN103108648A (zh) 2010-07-12 2013-05-15 细胞基因公司 罗米地辛固体形式及其用途
US8859502B2 (en) 2010-09-13 2014-10-14 Celgene Corporation Therapy for MLL-rearranged leukemia
UA113875C2 (uk) * 2012-04-24 2017-03-27 Новартіс Аг Спосіб лікування стероїдзалежних дерматозів
AU2013202506B2 (en) 2012-09-07 2015-06-18 Celgene Corporation Resistance biomarkers for hdac inhibitors
AU2013202507B9 (en) 2012-11-14 2015-08-13 Celgene Corporation Inhibition of drug resistant cancer cells
AU2014293013A1 (en) 2013-07-26 2016-03-17 Race Oncology Ltd. Combinatorial methods to improve the therapeutic benefit of bisantrene
NZ630311A (en) 2013-12-27 2016-03-31 Celgene Corp Romidepsin formulations and uses thereof

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5859205A (en) 1989-12-21 1999-01-12 Celltech Limited Humanised antibodies
EP0464533B1 (de) 1990-06-28 1998-07-29 Hoechst Aktiengesellschaft Fusionsproteine mit immunglobulinanteilen, ihre Herstellung und Verwendung
WO1994018215A1 (en) 1993-02-03 1994-08-18 Gensia, Inc. Adenosine kinase inhibitors comprising lyxofuranosyl derivatives
US6235741B1 (en) * 1997-05-30 2001-05-22 Merck & Co., Inc. Angiogenesis inhibitors
US6245759B1 (en) 1999-03-11 2001-06-12 Merck & Co., Inc. Tyrosine kinase inhibitors
WO2003033499A2 (en) 2001-10-15 2003-04-24 Gpc Biotech Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
US6960584B2 (en) 2001-04-10 2005-11-01 Merck & Co., Inc. Inhibitors of Akt activity
US7217710B2 (en) 2001-10-02 2007-05-15 Smithkline Beecham Corporation Substituted pyrazolopyrimidines
US20030199525A1 (en) 2002-03-21 2003-10-23 Hirst Gavin C. Kinase inhibitors
AU2003225933A1 (en) 2002-03-22 2003-10-13 Cellular Genomics, Inc. AN IMPROVED FORMULATION OF CERTAIN PYRAZOLO(3,4-d) PYRIMIDINES AS KINASE MODULATORS
ATE478872T1 (de) 2002-03-28 2010-09-15 Ustav Ex Botan Av Cr V V I I O Pyrazoloä4,3-düpyrimidine, verfahren zu ihrer herstellung und therapeutische anwendung
TW200400034A (en) 2002-05-20 2004-01-01 Bristol Myers Squibb Co Pyrazolo-pyrimidine aniline compounds useful as kinase inhibitors
US7181868B2 (en) 2002-06-26 2007-02-27 Nike, Incorporated Article of footwear having a sole with a flex control member
WO2004009597A2 (en) 2002-07-23 2004-01-29 Smithkline Beecham Corporation Pyrazolopyrimidines as protein kinase inhibitors
EP1534389A2 (en) 2002-07-23 2005-06-01 SmithKline Beecham Corporation Pyrazolopyrimidines as kinase inhibitors
JP2005536517A (ja) 2002-07-23 2005-12-02 スミスクライン ビーチャム コーポレーション キナーゼインヒビターとしてのピラゾロピリミジン
EP1545533A1 (en) 2002-09-04 2005-06-29 Schering Corporation Pyrazolopyrimidines as cyclin dependent kinase inhibitors
JP4881558B2 (ja) 2002-09-04 2012-02-22 シェーリング コーポレイション サイクリン依存性キナーゼインヒビターとしてのピラゾロピリミジン
KR20050057139A (ko) 2002-09-04 2005-06-16 쉐링 코포레이션 사이클린 의존성 키나제 억제제로서의 피라졸로피리미딘
DE60313872T2 (de) 2002-09-04 2008-01-17 Schering Corp. Pyrazoloä1,5-aüpyrimidine als hemmstoffe cyclin-abhängiger kinasen
WO2004030671A2 (en) 2002-10-02 2004-04-15 Merck Patent Gmbh Use of 4-amino-quinazolines as anti cancer agents
WO2004063195A1 (en) 2003-01-03 2004-07-29 Sloan-Kettering Institute For Cancer Research Pyridopyrimidine kinase inhibitors
WO2004087707A1 (en) * 2003-03-31 2004-10-14 Vernalis (Cambridge) Limited Pyrazolopyrimidine compounds and their use in medicine

Similar Documents

Publication Publication Date Title
ES2981592T3 (es) Derivados de 6-(4-amino-3-metil-2-oxa-8-azaespiro[4.5]decan-8-il)-3-(2,3-diclorofenil)-2-metilpirimidin-4(3H)-ona y compuestos relacionados como inhibidores de PTPN11 (SHP2) para tratar el cáncer
ES2925312T3 (es) Terapia combinada para el tratamiento del cáncer
ES2902501T3 (es) Métodos y composiciones para inhibir la interacción de menina con proteínas MLL
ES2977788T3 (es) Terapia combinada con un conjugado de anticuerpo anti-AXL y fármaco
JP2024516371A (ja) Egfr変異を有するがんを処置するためのアミノ置換ヘテロ環類
RS60236B1 (sr) Kombinovana terapija sa inhibitorom topoizomeraze
ES2823756T3 (es) Métodos para tratar el cáncer usando terapia de combinación de inhibidores de quinasa TOR
JP2019518741A5 (enExample)
JP2019530669A5 (enExample)
EA012837B1 (ru) Производные хиназолинона в качестве ингибиторов parp
HRP20120399T1 (hr) Novi sulfonilpiroli kao inhibitori hdac
CA2447021A1 (en) Pyridyl cyanoguanidine compounds
ES2979374T3 (es) Combinaciones farmacéuticas que comprenden un inhibidor de histona desacetilasa y un inhibidor de aurora quinasa y métodos de uso de las mismas
TW202237119A (zh) Alk﹘5抑制劑和彼之用途
JP2024516353A5 (enExample)
CA3201844A1 (en) Fap-activated radiotheranostics, and uses related thereto
AU2010319398B2 (en) Diazeniumdiolated compounds, pharmaceutical compositions, and method of treating cancer
JP2008534637A5 (enExample)
CN101484443A (zh) 放射线治疗增强剂
KR102823786B1 (ko) 조합 의약으로서 사용되는 ezh1/2 이중 저해제를 함유하는 의약 조성물
KR20160006669A (ko) 5-브로모-인디루빈
KR20110073486A (ko) 신장 세포 암종 치료용 3,3',4,4'-테트라하이드록시-2,2'-바이피리딘-n,n'-디옥시드
JP2010525046A (ja) 血液系腫瘍の治療のための方法
CN118488945A (zh) 磺酰胺核糖核苷酸还原酶(rnr)抑制剂及其用途
Di Maria et al. Applying molecular hybridization to design a new class of pyrazolo [3, 4-d] pyrimidines as Src inhibitors active in hepatocellular carcinoma