JP2005508337A5 - - Google Patents

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Publication number
JP2005508337A5
JP2005508337A5 JP2003530699A JP2003530699A JP2005508337A5 JP 2005508337 A5 JP2005508337 A5 JP 2005508337A5 JP 2003530699 A JP2003530699 A JP 2003530699A JP 2003530699 A JP2003530699 A JP 2003530699A JP 2005508337 A5 JP2005508337 A5 JP 2005508337A5
Authority
JP
Japan
Prior art keywords
hydrogen
alkyl
compound
halogen
physiologically functional
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
JP2003530699A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005508337A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2002/030150 external-priority patent/WO2003027111A1/en
Publication of JP2005508337A publication Critical patent/JP2005508337A/ja
Publication of JP2005508337A5 publication Critical patent/JP2005508337A5/ja
Pending legal-status Critical Current

Links

JP2003530699A 2001-09-27 2002-09-24 化合物 Pending JP2005508337A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32601201P 2001-09-27 2001-09-27
PCT/US2002/030150 WO2003027111A1 (en) 2001-09-27 2002-09-24 Chemical compounds

Publications (2)

Publication Number Publication Date
JP2005508337A JP2005508337A (ja) 2005-03-31
JP2005508337A5 true JP2005508337A5 (enExample) 2005-12-22

Family

ID=23270442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003530699A Pending JP2005508337A (ja) 2001-09-27 2002-09-24 化合物

Country Status (7)

Country Link
US (2) US7015231B2 (enExample)
EP (1) EP1430053B1 (enExample)
JP (1) JP2005508337A (enExample)
AT (1) ATE343575T1 (enExample)
DE (1) DE60215682T2 (enExample)
ES (1) ES2275021T3 (enExample)
WO (1) WO2003027111A1 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002020513A1 (en) 2000-09-01 2002-03-14 Glaxo Group Limited Oxindole derivatives
JP2004517049A (ja) 2000-09-01 2004-06-10 グラクソ グループ リミテッド チロシンキナーゼ阻害剤としての置換オキシインドール誘導体
DE60215682T2 (de) * 2001-09-27 2007-09-06 Smithkline Beecham Corp. AZAOXOINDOL DERIVATE ALS Trk PROTEIN KINASE HEMMSTOFFE ZUR BEHANDLUNG VON KREBS UND CHRONISCHEM SCHMERZ
SI1846394T1 (sl) 2005-02-04 2012-06-29 Astrazeneca Ab Pirazolilaminopiridinski derivati uporabni kot kinazni inhibitorji
RU2405780C2 (ru) 2005-02-16 2010-12-10 Астразенека Аб Химические соединения
WO2006087538A1 (en) * 2005-02-16 2006-08-24 Astrazeneca Ab Chemical compounds
WO2007049041A1 (en) 2005-10-28 2007-05-03 Astrazeneca Ab 4- (3-aminopyrazole) pyrimidine derivatives for use as tyrosine kinase inhibitors in the treatment of cancer
US7514435B2 (en) 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
KR20090004976A (ko) 2006-04-19 2009-01-12 아스테라스 세이야쿠 가부시키가이샤 아졸카르복사미드 유도체
CN101835764B (zh) 2007-10-24 2012-09-19 安斯泰来制药有限公司 唑甲酰胺化合物或其盐
EP2292089A1 (en) 2008-01-11 2011-03-09 Astellas Pharma Inc. Model animal having both pain in testis or testis-related discomfort actions and frequent urination
WO2010077680A2 (en) * 2008-12-08 2010-07-08 Vm Discovery Inc. Compositions of protein receptor tyrosine kinase inhibitors
ES2496093T3 (es) * 2010-04-15 2014-09-18 Merck Patent Gmbh Proceso para la preparación de hidroquinonas
US8999992B2 (en) 2013-03-15 2015-04-07 Vm Pharma Llc Crystalline forms of tryosine kinase inhibitors and their salts
CN103804273B (zh) * 2014-01-27 2016-06-15 贵州大学 氧化吲哚与茚三酮双季碳拼接衍生物及其制备方法
TWI672141B (zh) 2014-02-20 2019-09-21 美商醫科泰生技 投予ros1突變癌細胞之分子
WO2016043975A1 (en) 2014-09-17 2016-03-24 Vm Pharma Llc Crystalline forms of tyrosine kinase inhibitors and their salts
CN107207471B (zh) 2014-12-02 2020-06-26 伊尼塔公司 用于治疗神经母细胞瘤的组合
BR112018012255A2 (pt) 2015-12-18 2018-12-04 Ignyta Inc método para tratar câncer
CA3069339A1 (en) 2017-07-19 2019-01-24 Ignyta, Inc. Pharmaceutical compositions comprising entrectinib
JP7311498B2 (ja) 2017-10-17 2023-07-19 イグナイタ インコーポレイテッド 薬学的組成物および剤形
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
EP4054579A1 (en) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) 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 (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9423997D0 (en) * 1994-11-28 1995-01-11 Erba Carlo Spa Substituted 3-arylidene-7-azaoxindole compounds and process for their preparation
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
GB9721437D0 (en) * 1997-10-10 1997-12-10 Glaxo Group Ltd Heteroaromatic compounds and their use in medicine
AU5468499A (en) 1998-08-04 2000-02-28 Sugen, Inc. 3-methylidenyl-2-indolinone modulators of protein kinase
DE60215682T2 (de) * 2001-09-27 2007-09-06 Smithkline Beecham Corp. AZAOXOINDOL DERIVATE ALS Trk PROTEIN KINASE HEMMSTOFFE ZUR BEHANDLUNG VON KREBS UND CHRONISCHEM SCHMERZ

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