JP2008510719A5 - - Google Patents

Download PDF

Info

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)
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

Claims (4)

  1. 式:
    Figure 2008510719
    [式中、
    およびX は−N(H)−であり;
    YはOであり;
    WはCF で置換されているピラジニルであり;
    はOR 11 であり;
    およびR はヒドロであり;
    10 はCF またはCH であり;
    11 はピペリジン−3−イルまたは1−メチル−ピペリジン−3−イルで置換されているCH である]
    で示される化合物またはその薬学的に許容可能な塩。
  2. 請求項1記載の化合物またはその薬学的に許容可能な塩を薬学的に許容可能な希釈剤または担体とともに含む、医薬組成物。
  3. 請求項1記載の化合物またはその薬学的に許容可能な塩を含む、直腸癌、頭部および頸部癌、膵臓癌、乳癌、胃癌、膀胱癌、外陰部癌、白血病、リンパ腫、黒色腫、腎細胞癌腫、卵巣癌、脳腫瘍、骨肉腫、および肺癌からなるグループから選択される癌の治療剤
  4. 1-[2-(ピペリジン-3-イルメトキシ)-5-トリフルオロメチル-フェニル]-3-(5-トリフルオロメチルピラジン-2-イル)ウレア塩酸塩;
    1-[5-メチル-2-(ピペリジン-3-イルメトキシ)フェニル]-3-(5-トリフルオロメチル-ピラジン-2-イル)ウレア塩酸塩;および
    1-[5-メチル-2-(1-メチル-ピペリジン-3-イルメトキシ)フェニル]-3-(5-トリフルオロメチル-ピラジン-2-イル)ウレアからなるグループから選択される化合物。
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 (ja) 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 (ja)
EP (1) EP1778648A2 (ja)
JP (1) JP2008510719A (ja)
KR (1) KR20070054205A (ja)
CN (1) CN101115727A (ja)
AU (1) AU2005272586A1 (ja)
BR (1) BRPI0514466A (ja)
CA (1) CA2577880A1 (ja)
MX (1) MX2007002040A (ja)
WO (1) WO2006021002A2 (ja)

Families Citing this family (12)

* 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
DK3157916T3 (en) 2014-06-19 2019-03-18 Ariad Pharma Inc HETEROARYL COMPOUNDS FOR CHINESE INHIBITION
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
US10570119B2 (en) 2016-01-11 2020-02-25 Merrimack Pharmaceuticals, Inc. Inhibiting ataxia telangiectasia and Rad3-related protein (ATR)
SI3411036T1 (sl) 2016-02-04 2022-03-31 Pharmaengine, Inc. 3,5-disubstituirani pirazoli, uporabni kot kontrolne točke inhibitorjev kinaze 1 (CHK1), ter njihovi pripravki in uporaba
KR20190130621A (ko) 2017-03-31 2019-11-22 시애틀 지네틱스, 인크. Chk1 저해제와 wee1 저해제의 조합물
JP7260718B2 (ja) * 2019-11-29 2023-04-18 メッドシャイン ディスカバリー インコーポレイテッド ジアザインドール誘導体及びそのChk1阻害剤としての使用
WO2021119236A1 (en) 2019-12-10 2021-06-17 Seagen Inc. Preparation of a chk1 inhibitor compound
GB202107924D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd A pharmaceutical salt
GB202107932D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd Preparation of a CHK1 Inhibitor Compound

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL254871A (ja) * 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
TR200002616T2 (tr) * 1997-12-22 2000-11-21 Bayer Corporation Simetrik ve simetrik olmayan sübstitüe edilmiş difenil üreler kullanılarak raf kinazın inhibe edilmesi
UA76977C2 (en) * 2001-03-02 2006-10-16 Icos Corp Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
CA2484209C (en) * 2002-05-03 2013-06-11 Exelixis, Inc. Protein kinase modulators and methods of use
CA2539320A1 (en) * 2003-09-17 2005-03-31 Icos Corporation Use of chk1 inhibitors to control cell proliferation
WO2006012308A1 (en) * 2004-06-25 2006-02-02 Icos Corporation Bisarylurea derivatives useful for inhibiting chk1
KR20070043996A (ko) * 2004-07-02 2007-04-26 이코스 코포레이션 Chk1의 억제에 유용한 화합물

Similar Documents

Publication Publication Date Title
JP2008510719A5 (ja)
JP2018138577A5 (ja)
JP2007511504A5 (ja)
JP2006524222A5 (ja)
JP2008535903A5 (ja)
JP2018507877A5 (ja)
JP2010506950A5 (ja)
JP2007529534A5 (ja)
JP2014508811A5 (ja)
JP2012508252A5 (ja)
JP2006505543A5 (ja)
JP2015510886A5 (ja)
JP2009503110A5 (ja)
JP2008519049A5 (ja)
JP2011504903A5 (ja)
JP2011524422A5 (ja)
JP2005518382A5 (ja)
JP2005504039A5 (ja)
JP2007528883A5 (ja)
JP2012510502A5 (ja)
JP2010511721A5 (ja)
JP2011526913A5 (ja) キナゾリン化合物及び同化合物を含む治療薬
JP2009514899A5 (ja)
JP2012509352A5 (ja)
JP2012526766A5 (ja)