JP2010524937A5 - - Google Patents

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Publication number
JP2010524937A5
JP2010524937A5 JP2010504069A JP2010504069A JP2010524937A5 JP 2010524937 A5 JP2010524937 A5 JP 2010524937A5 JP 2010504069 A JP2010504069 A JP 2010504069A JP 2010504069 A JP2010504069 A JP 2010504069A JP 2010524937 A5 JP2010524937 A5 JP 2010524937A5
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JP
Japan
Prior art keywords
cancer
methyl
composition
pharmaceutically acceptable
triazol
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.)
Granted
Application number
JP2010504069A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010524937A (ja
JP5498936B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/004862 external-priority patent/WO2008130552A1/en
Publication of JP2010524937A publication Critical patent/JP2010524937A/ja
Publication of JP2010524937A5 publication Critical patent/JP2010524937A5/ja
Application granted granted Critical
Publication of JP5498936B2 publication Critical patent/JP5498936B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2010504069A 2007-04-18 2008-04-15 Smoアンタゴニストであるトリアゾール誘導体 Active JP5498936B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US92501807P 2007-04-18 2007-04-18
US60/925,018 2007-04-18
PCT/US2008/004862 WO2008130552A1 (en) 2007-04-18 2008-04-15 Triazole derivatives which are smo antagonists

Publications (3)

Publication Number Publication Date
JP2010524937A JP2010524937A (ja) 2010-07-22
JP2010524937A5 true JP2010524937A5 (https=) 2011-05-19
JP5498936B2 JP5498936B2 (ja) 2014-05-21

Family

ID=39433852

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010504069A Active JP5498936B2 (ja) 2007-04-18 2008-04-15 Smoアンタゴニストであるトリアゾール誘導体

Country Status (12)

Country Link
US (1) US7691887B2 (https=)
EP (1) EP2136803B1 (https=)
JP (1) JP5498936B2 (https=)
CN (1) CN101663033B (https=)
AR (1) AR066063A1 (https=)
AT (1) ATE555785T1 (https=)
AU (1) AU2008241527B2 (https=)
CA (1) CA2683946C (https=)
CL (1) CL2008001074A1 (https=)
PE (1) PE20090806A1 (https=)
TW (1) TW200901987A (https=)
WO (1) WO2008130552A1 (https=)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI433674B (zh) 2006-12-28 2014-04-11 Infinity Discovery Inc 環杷明(cyclopamine)類似物類
US20100297118A1 (en) * 2007-12-27 2010-11-25 Macdougall John Therapeutic Cancer Treatments
PE20091180A1 (es) * 2007-12-27 2009-08-26 Infinity Pharmaceuticals Inc Tratamientos terapeuticos contra el cancer
CA2710858A1 (en) 2007-12-27 2009-07-09 Infinity Pharmaceuticals, Inc. Methods for stereoselective reduction
GB0813740D0 (en) * 2008-07-28 2008-09-03 Angeletti P Ist Richerche Biologica Therapeutic compounds
AU2009286528B2 (en) * 2008-08-29 2014-07-17 Msd Italia S.R.L. Saturated bicyclic heterocyclic derivatives as Smo antagonists
AU2010279325B2 (en) 2009-08-05 2016-10-20 Infinity Pharmaceuticals, Inc. Enzymatic transamination of cyclopamine analogs
EP2502078A1 (en) * 2009-11-20 2012-09-26 Infinity Pharmaceuticals, Inc. Methods and compositions for treating hedgehog-associated cancers
US9394313B2 (en) 2010-09-14 2016-07-19 Infinity Pharmaceuticals, Inc. Transfer hydrogenation of cyclopamine analogs
KR20160061911A (ko) 2013-04-08 2016-06-01 데니스 엠. 브라운 최적하 투여된 화학 화합물의 치료 효과
CN104324039A (zh) * 2014-10-20 2015-02-04 付茜 一种治疗人身体表面脂肪瘤的药剂及使用方法
PL3302428T3 (pl) 2015-06-04 2026-04-13 Sol-Gel Technologies Ltd. Preparaty do zastosowania miejscowego do dostarczania związków inhibitora hedgehog i ich zastosowanie
CN108623446A (zh) * 2017-03-24 2018-10-09 北京艾德旺科技发展有限公司 一种合成3,3-二氟环丁烷甲酸的方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7291626B1 (en) 1998-04-09 2007-11-06 John Hopkins University School Of Medicine Inhibitors of hedgehog signaling pathways, compositions and uses related thereto
AU2003207717B9 (en) 2002-02-01 2009-05-07 Merck & Co., Inc. 11-beta-hydroxysteroid dehydrogenase 1 inhibitors useful for the treatment of diabetes, obesity and dyslipidemia
JO2397B1 (en) 2002-12-20 2007-06-17 ميرك شارب اند دوم كوربوريشن Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors
CN1795181A (zh) 2003-05-29 2006-06-28 麦克公司 用作11β-羟基类固醇脱氢酶-1抑制剂的三唑衍生物
WO2005033288A2 (en) 2003-09-29 2005-04-14 The Johns Hopkins University Hedgehog pathway antagonists
PL1745041T3 (pl) 2004-04-30 2012-11-30 Genentech Inc Inhibitory chinoksalinowe szlaku sygnałowego hedgehog
JP2008509146A (ja) 2004-08-06 2008-03-27 メルク エンド カムパニー インコーポレーテッド 11−ベータ−ヒドロキシステロイドデヒドロゲナーゼ−1の阻害剤としてのスルホニル化合物
AU2005280112B2 (en) 2004-08-27 2012-07-19 Infinity Pharmaceuticals, Inc. Cyclopamine analogues and methods of use thereof
ES2377430T3 (es) 2004-09-02 2012-03-27 Genentech, Inc. Inhibidores piridílicos de la señalización de hedgehog
CA2583812A1 (en) 2004-10-28 2006-05-11 Irm Llc Compounds and compositions as hedgehog pathway modulators
EP1807074B1 (en) 2004-11-03 2013-10-23 Curis, Inc. Mediators of hedgehog signaling pathways, compositions and uses related thereto
US7981910B2 (en) * 2005-10-20 2011-07-19 Merck Sharp & Dohme Corp. Triazole derivatives as inhibitors of 11-β-hydroxysteroid dehydrogenase-1

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