JP2010536876A5 - - Google Patents

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Publication number
JP2010536876A5
JP2010536876A5 JP2010522030A JP2010522030A JP2010536876A5 JP 2010536876 A5 JP2010536876 A5 JP 2010536876A5 JP 2010522030 A JP2010522030 A JP 2010522030A JP 2010522030 A JP2010522030 A JP 2010522030A JP 2010536876 A5 JP2010536876 A5 JP 2010536876A5
Authority
JP
Japan
Prior art keywords
dihydro
pyrrolo
compound
composition
cancer
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Withdrawn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
JP2010522030A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010536876A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/073873 external-priority patent/WO2009026446A2/en
Publication of JP2010536876A publication Critical patent/JP2010536876A/ja
Publication of JP2010536876A5 publication Critical patent/JP2010536876A5/ja
Withdrawn legal-status Critical Current

Links

JP2010522030A 2007-08-21 2008-08-21 Hdacインヒビター Withdrawn JP2010536876A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US96558407P 2007-08-21 2007-08-21
PCT/US2008/073873 WO2009026446A2 (en) 2007-08-21 2008-08-21 Hdac inhibitors

Publications (2)

Publication Number Publication Date
JP2010536876A JP2010536876A (ja) 2010-12-02
JP2010536876A5 true JP2010536876A5 (https=) 2012-09-13

Family

ID=39828970

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010522030A Withdrawn JP2010536876A (ja) 2007-08-21 2008-08-21 Hdacインヒビター

Country Status (6)

Country Link
US (1) US20100261710A1 (https=)
EP (1) EP2190845A2 (https=)
JP (1) JP2010536876A (https=)
CN (1) CN101835778A (https=)
CA (1) CA2695452A1 (https=)
WO (1) WO2009026446A2 (https=)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5688367B2 (ja) 2008-08-29 2015-03-25 トポターゲット・アクティーゼルスカブTopoTarget A/S 新規なウレアおよびチオウレア誘導体
WO2011082266A2 (en) 2009-12-30 2011-07-07 Arqule, Inc. Substituted heterocyclic compounds
US8546588B2 (en) 2010-02-26 2013-10-01 Millennium Pharmaceuticals, Inc. Substituted hydroxamic acids and uses thereof
WO2011106632A1 (en) * 2010-02-26 2011-09-01 Millennium Pharmaceuticals, Inc. Substituted hydroxamic acids and uses thereof
WO2013041407A1 (en) * 2011-09-19 2013-03-28 Cellzome Ag Hydroxamic acids as hdac6 inhibitors
JP6272773B2 (ja) * 2011-11-29 2018-01-31 ナンジン アルゲン ファルマ カンパニー リミテッドNanjing Allgen Pharma Co. Ltd. Hdac6阻害剤・抗腫瘍剤用複素環アミド化合物
WO2013154870A1 (en) 2012-04-10 2013-10-17 Annji Pharmaceutical Co., Ltd. Histone deacetylases (hdacs) inhibitors
US20150141470A1 (en) 2012-05-08 2015-05-21 The Broad Institute, Inc. Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy
US9878986B2 (en) 2013-04-29 2018-01-30 Chong Kun Dang Pharmaceutical Corp. Compounds for selective histone deacetylase inhibitors, and pharmaceutical composition comprising the same
CN110621317B (zh) 2017-05-16 2023-05-12 安基生技新药股份有限公司 组蛋白去乙酰化酶(hdacs)抑制剂
CN113121527B (zh) * 2019-12-31 2024-09-06 上海辉启生物医药科技有限公司 三环类化合物及其用途
JP2023530788A (ja) 2020-06-08 2023-07-19 アンジー ファーマシューティカル カンパニー リミテッド 選択的hdac6阻害剤として有用なキナゾリン誘導体
CN119143740B (zh) * 2024-08-15 2025-11-14 杭州科兴生物化工有限公司 一种苯并噻吩类衍生物及其制备方法与应用

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1335898B1 (en) * 2000-09-29 2005-11-23 TopoTarget UK Limited Carbamic acid compounds comprising an amide linkage as hdac inhibitors
AR035417A1 (es) * 2001-01-27 2004-05-26 Hoffmann La Roche Derivados triciclicos de lactama y sultama, procesos para su elaboracion, medicamentos que los contienen, y el uso de dichos compuestos en la preparacion de medicamentos
EP1644323B1 (en) * 2003-07-07 2015-03-18 Georgetown University Histone deacetylase inhibitors and methods of use thereof
ITFI20050041A1 (it) * 2005-03-15 2006-09-16 Menarini Internat Operations Luxembourg Sa Idrossammati come inibitori dell'istone deacelitasi, loro preparazione e formulazioni farmaceutiche che li contengono

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