JP2009534418A5 - - Google Patents

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Publication number
JP2009534418A5
JP2009534418A5 JP2009506778A JP2009506778A JP2009534418A5 JP 2009534418 A5 JP2009534418 A5 JP 2009534418A5 JP 2009506778 A JP2009506778 A JP 2009506778A JP 2009506778 A JP2009506778 A JP 2009506778A JP 2009534418 A5 JP2009534418 A5 JP 2009534418A5
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JP
Japan
Prior art keywords
absent
hydrogen
alkyl
membered ring
hydroxyalkyl
Prior art date
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Granted
Application number
JP2009506778A
Other languages
English (en)
Japanese (ja)
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JP2009534418A (ja
JP5595727B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2007/066985 external-priority patent/WO2007124369A2/en
Publication of JP2009534418A publication Critical patent/JP2009534418A/ja
Publication of JP2009534418A5 publication Critical patent/JP2009534418A5/ja
Application granted granted Critical
Publication of JP5595727B2 publication Critical patent/JP5595727B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2009506778A 2006-04-20 2007-04-19 C−kitキナーゼ阻害法 Expired - Fee Related JP5595727B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US79347106P 2006-04-20 2006-04-20
US60/793,471 2006-04-20
PCT/US2007/066985 WO2007124369A2 (en) 2006-04-20 2007-04-19 Method of inhibiting c kit kinase

Publications (3)

Publication Number Publication Date
JP2009534418A JP2009534418A (ja) 2009-09-24
JP2009534418A5 true JP2009534418A5 (cg-RX-API-DMAC7.html) 2014-08-14
JP5595727B2 JP5595727B2 (ja) 2014-09-24

Family

ID=38625740

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009506778A Expired - Fee Related JP5595727B2 (ja) 2006-04-20 2007-04-19 C−kitキナーゼ阻害法

Country Status (21)

Country Link
EP (2) EP2015748B1 (cg-RX-API-DMAC7.html)
JP (1) JP5595727B2 (cg-RX-API-DMAC7.html)
KR (1) KR101448052B1 (cg-RX-API-DMAC7.html)
CN (2) CN101610768B (cg-RX-API-DMAC7.html)
AU (1) AU2007240400B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0710542B8 (cg-RX-API-DMAC7.html)
CA (1) CA2649755C (cg-RX-API-DMAC7.html)
CO (1) CO6382175A2 (cg-RX-API-DMAC7.html)
CR (1) CR10450A (cg-RX-API-DMAC7.html)
EA (1) EA016611B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP088842A (cg-RX-API-DMAC7.html)
ES (2) ES2458291T3 (cg-RX-API-DMAC7.html)
GT (1) GT200800225A (cg-RX-API-DMAC7.html)
IL (1) IL194846A (cg-RX-API-DMAC7.html)
MX (1) MX2008013528A (cg-RX-API-DMAC7.html)
MY (1) MY147226A (cg-RX-API-DMAC7.html)
NO (1) NO342001B1 (cg-RX-API-DMAC7.html)
NZ (1) NZ572200A (cg-RX-API-DMAC7.html)
SG (1) SG171592A1 (cg-RX-API-DMAC7.html)
WO (1) WO2007124369A2 (cg-RX-API-DMAC7.html)
ZA (1) ZA200809874B (cg-RX-API-DMAC7.html)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101924247B1 (ko) 2011-07-27 2019-02-22 에이비 사이언스 선택적 프로테인 키나제 저해제로서 옥사졸 및 티아졸 유도체
CN104370880A (zh) * 2013-01-24 2015-02-25 韩冰 一类蛋白酶抑制剂及其制备方法和用途
US10259807B2 (en) 2013-07-22 2019-04-16 Idorsia Pharmaceuticals Ltd. 1-(piperazin-1-yl)-2-([1,2,4]triazol-1-yl)-ethanone derivatives
CA2972952C (en) 2015-01-15 2021-01-05 Idorsia Pharmaceuticals Ltd Hydroxyalkyl-piperazine derivatives as cxcr3 receptor modulators
AR103399A1 (es) 2015-01-15 2017-05-10 Actelion Pharmaceuticals Ltd Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3
CN105753770A (zh) * 2015-05-27 2016-07-13 上海佐林生物医药有限公司 蛋白激酶抑制剂制备方法、中间体、制备方法及应用
CN114364798A (zh) 2019-03-21 2022-04-15 欧恩科斯欧公司 用于治疗癌症的Dbait分子与激酶抑制剂的组合
US20220401436A1 (en) 2019-11-08 2022-12-22 INSERM (Institute National de la Santé et de la Recherche Médicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69332948T2 (de) 1992-03-05 2003-11-27 Board Of Regents, The University Of Texas System Verwendung von Immunokonjugate zur Diagnose und/oder Therapie der vaskularisierten Tumoren
WO2000064946A2 (en) 1999-04-28 2000-11-02 Board Of Regents, The University Of Texas System Compositions and methods for cancer treatment by selectively inhibiting vegf
DE19962924A1 (de) 1999-12-24 2001-07-05 Bayer Ag Substituierte Oxazolidinone und ihre Verwendung
ITMI992711A1 (it) * 1999-12-27 2001-06-27 Novartis Ag Composti organici
ATE375342T1 (de) * 2002-08-02 2007-10-15 Ab Science 2-(3-aminoaryl)amino-4-aryl-thiazole und ihre verwendung als c-kit inhibitoren
ATE465731T1 (de) * 2003-10-23 2010-05-15 Ab Science 2-aminoaryloxazol-verbindungen als tyrosinkinase- hemmer
GB0326601D0 (en) * 2003-11-14 2003-12-17 Novartis Ag Organic compounds
AU2005209485A1 (en) * 2004-01-30 2005-08-11 Ab Science 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors
MX2007004784A (es) * 2004-10-22 2007-09-11 Johnson & Johnson Inhibidores de la c-fms cinasa.
US20060281788A1 (en) * 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor
JP2009511628A (ja) * 2005-10-18 2009-03-19 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ Flt3キナーゼの阻害方法
CA2649736C (en) * 2006-04-20 2013-11-26 Janssen Pharmaceutica N.V. Heterocyclic compounds as inhibitors of c-fms kinase
CN101466686A (zh) * 2006-04-20 2009-06-24 詹森药业有限公司 C-fms激酶抑制剂
CA2649924C (en) * 2006-04-20 2014-08-19 Janssen Pharmaceutica N.V. Inhibitors of c-fms kinase

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