JP2008510719A5 - - Google Patents

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Publication number
JP2008510719A5
JP2008510719A5 JP2007528037A JP2007528037A JP2008510719A5 JP 2008510719 A5 JP2008510719 A5 JP 2008510719A5 JP 2007528037 A JP2007528037 A JP 2007528037A JP 2007528037 A JP2007528037 A JP 2007528037A JP 2008510719 A5 JP2008510719 A5 JP 2008510719A5
Authority
JP
Japan
Prior art keywords
cancer
piperidin
methyl
pharmaceutically acceptable
ylmethoxy
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
JP2007528037A
Other languages
English (en)
Japanese (ja)
Other versions
JP2008510719A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/029518 external-priority patent/WO2006021002A2/en
Publication of JP2008510719A publication Critical patent/JP2008510719A/ja
Publication of JP2008510719A5 publication Critical patent/JP2008510719A5/ja
Pending legal-status Critical Current

Links

JP2007528037A 2004-08-19 2005-08-18 Chk1の阻害に有用な化合物 Pending JP2008510719A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US60296804P 2004-08-19 2004-08-19
PCT/US2005/029518 WO2006021002A2 (en) 2004-08-19 2005-08-18 Compounds useful for inhibiting chk1

Publications (2)

Publication Number Publication Date
JP2008510719A JP2008510719A (ja) 2008-04-10
JP2008510719A5 true JP2008510719A5 (enExample) 2008-10-02

Family

ID=35744692

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007528037A Pending JP2008510719A (ja) 2004-08-19 2005-08-18 Chk1の阻害に有用な化合物

Country Status (10)

Country Link
US (1) US20080318974A1 (enExample)
EP (1) EP1778648A2 (enExample)
JP (1) JP2008510719A (enExample)
KR (1) KR20070054205A (enExample)
CN (1) CN101115727A (enExample)
AU (1) AU2005272586A1 (enExample)
BR (1) BRPI0514466A (enExample)
CA (1) CA2577880A1 (enExample)
MX (1) MX2007002040A (enExample)
WO (1) WO2006021002A2 (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201008005D0 (en) 2010-05-13 2010-06-30 Sentinel Oncology Ltd Pharmaceutical compounds
GB201119799D0 (en) 2011-11-16 2011-12-28 Sentinel Oncology Ltd Pharmaceutical compounds
GB201402277D0 (en) 2014-02-10 2014-03-26 Sentinel Oncology Ltd Pharmaceutical compounds
PE20170268A1 (es) 2014-06-19 2017-04-21 Ariad Pharma Inc Compuestos de heteroarilo para la inhibicion de cinasa
CN104628659A (zh) * 2015-01-27 2015-05-20 广西师范大学 具有抗肿瘤作用的吡嗪-芳基脲衍生物及其制备方法与应用
ES2997263T3 (en) 2016-01-11 2025-02-14 Celator Pharmaceuticals Inc Inhibiting ataxia telangiectasia and rad3-related protein (atr)
DK3411036T3 (da) 2016-02-04 2022-01-17 Pharmaengine Inc 3,5-disubstituerede pyrazoler, der er nyttige som checkpoint-kinase 1 (chk1)-hæmmere, samt fremstilling og anvendelse deraf
AU2018243667A1 (en) 2017-03-31 2019-10-17 Seagen Inc. Combinations of Chk1- and Wee1 - inhibitors
KR20200144579A (ko) 2018-05-14 2020-12-29 어리어드 파마슈티칼스, 인코포레이티드 피리미딘 유도체의 약학 염 및 장애의 치료 방법
CN112457306A (zh) 2019-09-06 2021-03-09 上海瑛派药业有限公司 3,5-二取代吡唑化合物作为激酶抑制剂及其应用
ES3014705T3 (en) * 2019-11-29 2025-04-24 Novaonco Js Therapeutics Co Ltd Diazaindole derivative and use thereof as chk1 inhibitor
WO2021119236A1 (en) 2019-12-10 2021-06-17 Seagen Inc. Preparation of a chk1 inhibitor compound
GB202107932D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd Preparation of a CHK1 Inhibitor Compound
GB202107924D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd A pharmaceutical salt

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL254871A (enExample) * 1959-08-14
CH493480A (de) * 1969-01-31 1970-07-15 Agripat Sa Verfahren zur Herstellung von neuen O,N-Diphenyl-carbaminsäureestern
US4071524A (en) * 1976-11-08 1978-01-31 Riker Laboratories, Inc. Derivatives of urea
EP1449834A3 (en) * 1997-12-22 2004-12-22 Bayer Corporation Inhibition of raf kinase using symmetrical and unsymmetrical substituted diphenyl ureas
UA76977C2 (en) * 2001-03-02 2006-10-16 Icos Corp Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
JP4901102B2 (ja) * 2002-05-03 2012-03-21 エクセリクシス, インク. プロテインキナーゼモジュレーターおよびその使用方法
CA2539320A1 (en) * 2003-09-17 2005-03-31 Icos Corporation Use of chk1 inhibitors to control cell proliferation
BRPI0512593A (pt) * 2004-06-25 2008-03-25 Icos Corp composto ou um sal ou pró-droga ou solvato farmaceuticamente aceitável do mesmo, composição, e, métodos de inibir a quinase 1 de ponto de verificação em uma célula, de sensibilizar células em um indivìduo e de inibir a proliferação de célula aberrante
CN101010316A (zh) * 2004-07-02 2007-08-01 艾科斯有限公司 用于抑制chk1的化合物

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