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
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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

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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 (https=) 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 (https=)
JP (1) JP5595727B2 (https=)
KR (1) KR101448052B1 (https=)
CN (2) CN101610768B (https=)
AU (1) AU2007240400B2 (https=)
BR (1) BRPI0710542B8 (https=)
CA (1) CA2649755C (https=)
CO (1) CO6382175A2 (https=)
CR (1) CR10450A (https=)
EA (1) EA016611B1 (https=)
EC (1) ECSP088842A (https=)
ES (2) ES2458291T3 (https=)
GT (1) GT200800225A (https=)
IL (1) IL194846A (https=)
MX (1) MX2008013528A (https=)
MY (1) MY147226A (https=)
NO (1) NO342001B1 (https=)
NZ (1) NZ572200A (https=)
SG (1) SG171592A1 (https=)
WO (1) WO2007124369A2 (https=)
ZA (1) ZA200809874B (https=)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103717591B (zh) 2011-07-27 2016-08-24 Ab科学有限公司 作为选择性蛋白激酶(c-kit)抑制剂的噁唑和噻唑衍生物
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
JP6330040B2 (ja) 2013-07-22 2018-05-23 イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd 1−(ピペラジン−1−イル)−2−([1,2,4]トリアゾール−1−イル)−エタノン誘導体
AR103399A1 (es) 2015-01-15 2017-05-10 Actelion Pharmaceuticals Ltd Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3
PL3245203T3 (pl) 2015-01-15 2019-05-31 Idorsia Pharmaceuticals Ltd Pochodne hydroksyalkilopiperazyny jako modulatory receptora 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
EA202192575A1 (ru) 2019-03-21 2022-01-14 Онксео Соединения dbait в сочетании с ингибиторами киназ для лечения рака
CN114761006A (zh) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) 对激酶抑制剂产生耐药性的癌症的治疗方法
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
PT627940E (pt) 1992-03-05 2003-07-31 Univ Texas Utilizacao de imunoconjugados para o diagnostico e/ou terapia de tumores vascularizados
US6342219B1 (en) 1999-04-28 2002-01-29 Board Of Regents, The University Of Texas System Antibody compositions for 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
MXPA05001277A (es) * 2002-08-02 2005-10-06 Ab Science 2-(3-aminoaril)amino-4-aril-tiazoles y su uso como inhibidores del c-kit.
EP1684750B1 (en) * 2003-10-23 2010-04-28 AB Science 2-aminoaryloxazole compounds as tyrosine kinase inhibitors
GB0326601D0 (en) * 2003-11-14 2003-12-17 Novartis Ag Organic compounds
CA2554925A1 (en) * 2004-01-30 2005-08-11 Ab Science 2-(3-substituted-aryl)amino-4-aryl-thiazoles as tyrosine kinase inhibitors
PT1807077T (pt) * 2004-10-22 2017-01-06 Janssen Pharmaceutica Nv Inibidores de quinase c-fms
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
AU2006304897B2 (en) * 2005-10-18 2012-07-12 Janssen Pharmaceutica N.V. Method of inhibiting FLT3 kinase
WO2007124319A1 (en) * 2006-04-20 2007-11-01 Janssen Pharmaceutica N.V. Inhibitors of c-fms kinase
JP2009534380A (ja) * 2006-04-20 2009-09-24 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 c−fmsキナーゼインヒビター
PL2021335T3 (pl) * 2006-04-20 2011-10-31 Janssen Pharmaceutica Nv Związki heterocykliczne jako inhibitory kinazy C-FMS

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