JP2011506494A5 - - Google Patents

Download PDF

Info

Publication number
JP2011506494A5
JP2011506494A5 JP2010538297A JP2010538297A JP2011506494A5 JP 2011506494 A5 JP2011506494 A5 JP 2011506494A5 JP 2010538297 A JP2010538297 A JP 2010538297A JP 2010538297 A JP2010538297 A JP 2010538297A JP 2011506494 A5 JP2011506494 A5 JP 2011506494A5
Authority
JP
Japan
Prior art keywords
alkyl
group
optionally substituted
phenyl
halogen
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.)
Withdrawn
Application number
JP2010538297A
Other languages
English (en)
Japanese (ja)
Other versions
JP2011506494A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/CA2008/002227 external-priority patent/WO2009079767A1/en
Publication of JP2011506494A publication Critical patent/JP2011506494A/ja
Publication of JP2011506494A5 publication Critical patent/JP2011506494A5/ja
Withdrawn legal-status Critical Current

Links

JP2010538297A 2007-12-21 2008-12-19 癌の治療に有用なキナーゼ阻害剤としてのインダゾリル、ベンズイミダゾリル、ベンゾトリアゾリル置換インドルモン誘導体 Withdrawn JP2011506494A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US886507P 2007-12-21 2007-12-21
US13171708P 2008-06-11 2008-06-11
PCT/CA2008/002227 WO2009079767A1 (en) 2007-12-21 2008-12-19 Indazolyl, benzimidazolyl, benzotriazolyl substituted indolinone derivatives as kinase inhibitors useful in the treatment of cancer

Publications (2)

Publication Number Publication Date
JP2011506494A JP2011506494A (ja) 2011-03-03
JP2011506494A5 true JP2011506494A5 (cg-RX-API-DMAC7.html) 2012-02-16

Family

ID=40800609

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010538297A Withdrawn JP2011506494A (ja) 2007-12-21 2008-12-19 癌の治療に有用なキナーゼ阻害剤としてのインダゾリル、ベンズイミダゾリル、ベンゾトリアゾリル置換インドルモン誘導体

Country Status (7)

Country Link
US (1) US8765748B2 (cg-RX-API-DMAC7.html)
EP (1) EP2235004A4 (cg-RX-API-DMAC7.html)
JP (1) JP2011506494A (cg-RX-API-DMAC7.html)
CN (1) CN101970426A (cg-RX-API-DMAC7.html)
AU (1) AU2008340991B2 (cg-RX-API-DMAC7.html)
CA (1) CA2709536C (cg-RX-API-DMAC7.html)
WO (1) WO2009079767A1 (cg-RX-API-DMAC7.html)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2008340991B2 (en) 2007-12-21 2012-02-23 University Health Network Indazolyl, benzimidazolyl, benzotriazolyl substituted indolinone derivatives as kinase inhibitors useful in the treatment of cancer
US8481525B2 (en) 2009-04-06 2013-07-09 University Of Health Network Kinase inhibitors and method of treating cancer with same
AU2011238384B2 (en) 2010-04-06 2015-02-19 University Health Network Kinase inhibitors and method of treating cancer with same
US8933070B2 (en) 2010-07-02 2015-01-13 University Health Network Methods of targeting PTEN mutant diseases and compositions therefor
WO2012048411A1 (en) * 2010-10-13 2012-04-19 University Health Network Plk-4 inhibitors and method of treating cancer with same
CN102295640B (zh) * 2011-06-29 2013-09-18 南京工业大学 3-杂环席夫碱-5-氟-吲哚-2-酮类化合物及其制备方法和应用
CN103006642B (zh) * 2013-01-04 2014-10-22 中国药科大学 一类炔亚甲基吲哚-2-酮类衍生物的用途
BR112016006930A2 (pt) 2013-10-04 2017-08-01 Bayer Cropscience Ag uso de diidrooxindolilsulfonamidas substituídas, ou dos sais destas, para o aumento da tolerância ao estresse de plantas
EP3057593B1 (en) 2013-10-18 2021-12-08 University Health Network Treatment for pancreatic cancer
TWI659952B (zh) 2013-10-18 2019-05-21 健康網路大學 Plk-4抑制劑之鹽和結晶形式
WO2015164956A1 (en) * 2014-04-29 2015-11-05 The University Of British Columbia Benzisothiazole derivative compounds as therapeutics and methods for their use
HUE057289T2 (hu) 2016-08-31 2022-05-28 Jiangsu Hengrui Medicine Co Oxopikolinamid-származék, annak elõállítási módszere és gyógyszerészeti felhasználása
CN106916143B (zh) * 2017-03-14 2019-09-27 哈尔滨医科大学 一种预防和治疗冠心病的药物及其应用
US12325700B2 (en) 2019-04-24 2025-06-10 University Health Network Crystal form S4 of the PLK4 inhibitor (1R,2S)-(e)-2-(3-(4-((cis-2,6-dimethylmorpholino)methyl)styryl)-1 h-imidazol-6-yl)-5′-methoxyspiro[cyclopropane-1,3′-indolin]-2′-one fumarate
TW202300485A (zh) * 2021-03-02 2023-01-01 大陸商上海齊魯製藥研究中心有限公司 Plk4抑制劑及其用途
JP7717842B2 (ja) 2021-05-11 2025-08-04 オリック ファーマシューティカルズ,インク. ポロ様キナーゼ4阻害剤
CR20250419A (es) 2023-04-06 2025-10-07 Pfizer Compuestos de derivados de ácido indazol propiónico sustituidos y usos de estos
ES3022196A1 (es) * 2023-11-27 2025-05-28 Univ Madrid Complutense Derivados de 2-indolinona y usos de los mismos

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1326A (en) * 1839-09-17 Improvement in the mode of setting and arranging sugar-kettles
DE3310891A1 (de) * 1983-03-25 1984-09-27 Boehringer Mannheim Gmbh, 6800 Mannheim Neue indolinon-(2)-derivate, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und zwischenprodukte
US5182397A (en) * 1990-05-31 1993-01-26 American Cyanamid Company Aryloxyspiroalkylindolinone herbicides
GB9507298D0 (en) 1995-04-07 1995-05-31 Pharmacia Spa Substituted indolylmethylene-oxindale analogues as tyrosine kinase inhibitors
US5880141A (en) 1995-06-07 1999-03-09 Sugen, Inc. Benzylidene-Z-indoline compounds for the treatment of disease
ATE308520T1 (de) * 1996-08-23 2005-11-15 Sugen Inc Kombinatorische bibliotheken von indolinone und verwandte produkte und verfahren zur behandlung von krankheiten
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
US6133305A (en) * 1997-09-26 2000-10-17 Sugen, Inc. 3-(substituted)-2-indolinones compounds and use thereof as inhibitors of protein kinase activity
CA2383623A1 (en) * 1998-08-04 2000-02-17 Sugen, Inc. 3-methylidenyl-2-indolinone modulators of protein kinase
WO2000056709A1 (en) 1999-03-24 2000-09-28 Sugen, Inc. Indolinone compounds as kinase inhibitors
US7148249B2 (en) * 2002-09-12 2006-12-12 Boehringer Ingelheim Pharma Gmbh & Co. Kg Indolinones substituted by heterocycles, the preparation thereof and their use as medicaments
AU2003286604A1 (en) * 2002-10-21 2004-05-13 Irm Llc Oxindoles with anti-hiv activity
WO2005058309A1 (en) 2003-12-16 2005-06-30 Leo Pharma A/S Novel therapeutic use of indolinone derivatives
US7309787B2 (en) 2005-07-13 2007-12-18 Allergan, Inc. Kinase inhibitors
US20070135509A1 (en) * 2005-12-09 2007-06-14 Blackburn Thomas P Indolone compounds useful to treat cognitive impairment
CA2690567A1 (en) 2007-06-12 2008-12-18 Boehringer Ingelheim International Gmbh 3-hetrocyclylidene-indolinone derivatives as inhibitors of specific cell cycle kinases
AU2008340991B2 (en) 2007-12-21 2012-02-23 University Health Network Indazolyl, benzimidazolyl, benzotriazolyl substituted indolinone derivatives as kinase inhibitors useful in the treatment of cancer
EP2108641A1 (en) 2008-04-11 2009-10-14 Laboratorios Almirall, S.A. New substituted spiro[cycloalkyl-1,3'-indo]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors
EP2113503A1 (en) 2008-04-28 2009-11-04 Laboratorios Almirall, S.A. New substituted indolin-2-one derivatives and their use as p39 mitogen-activated kinase inhibitors
US8481525B2 (en) 2009-04-06 2013-07-09 University Of Health Network Kinase inhibitors and method of treating cancer with same
AU2011238384B2 (en) * 2010-04-06 2015-02-19 University Health Network Kinase inhibitors and method of treating cancer with same

Similar Documents

Publication Publication Date Title
JP2011506494A5 (cg-RX-API-DMAC7.html)
RU2477723C2 (ru) Ингибиторы протеинкиназ (варианты), их применение для лечения онкологических заболеваний и фармацевтическая композиция на их основе
JP2013523652A5 (cg-RX-API-DMAC7.html)
NZ590268A (en) 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
JP2020517616A5 (cg-RX-API-DMAC7.html)
CA2443950A1 (en) Inhibition of raf kinase using quinolyl, isoquinolyl or pyridyl ureas
HRP20161498T1 (hr) Inhibitori kinaza i njihova upotreba u liječenju raka
JP2012522729A5 (cg-RX-API-DMAC7.html)
JP2013525458A5 (cg-RX-API-DMAC7.html)
NO20071234L (no) Forbindelser som potensierer glutamatreseptor og anvendelse derav innen medisin
JP2017526675A (ja) ヒストンデメチラーゼを阻害するための化合物および方法
TW200643015A (en) 2-(4-oxo-4H-quinazolin-3-yl)acetamide derivatives
JP2014517017A5 (ja) 化合物、その医薬組成物、及び癌治療用の阻害薬としてのその使用
JP2011529500A5 (cg-RX-API-DMAC7.html)
JP2009515988A5 (cg-RX-API-DMAC7.html)
HRP20080064T3 (hr) Predlijekovi piperazina i protuvirusna sredstva supstituiranog piperidina
RU2017139564A (ru) 5-ароматическое алкинилзамещенное бензамидное соединение и способ его получения, фармацевтическая композиция и их применение
RU2015121424A (ru) Комбинированная терапия
HRP20120202T1 (hr) AMIDOFENOKSIINDAZOLI, KORISNI KAO INHIBITORI c-MET
ME02675B (me) Novi derivati cikloheksilamina sa aktivnostima beta2 adrenergijskog agonista i m3 muscarinskog antagonista
JP2017514855A5 (cg-RX-API-DMAC7.html)
JP2014524441A5 (cg-RX-API-DMAC7.html)
RU2014141674A (ru) 3,5-диаминопиразоловые ингибиторы киназы
JP2017504595A5 (cg-RX-API-DMAC7.html)
AR087212A1 (es) ANTAGONISTAS DE CRTh2