JP2016503009A5 - - Google Patents

Download PDF

Info

Publication number
JP2016503009A5
JP2016503009A5 JP2015547522A JP2015547522A JP2016503009A5 JP 2016503009 A5 JP2016503009 A5 JP 2016503009A5 JP 2015547522 A JP2015547522 A JP 2015547522A JP 2015547522 A JP2015547522 A JP 2015547522A JP 2016503009 A5 JP2016503009 A5 JP 2016503009A5
Authority
JP
Japan
Prior art keywords
alkyl
methyl
alkoxy
heterocycloalkyl
cycloalkyl
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
JP2015547522A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016503009A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2013/074558 external-priority patent/WO2014107277A1/en
Publication of JP2016503009A publication Critical patent/JP2016503009A/ja
Publication of JP2016503009A5 publication Critical patent/JP2016503009A5/ja
Pending legal-status Critical Current

Links

JP2015547522A 2012-12-13 2013-12-12 Zesteホモログ2エンハンサー阻害剤 Pending JP2016503009A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201261736645P 2012-12-13 2012-12-13
US61/736,645 2012-12-13
US201361777443P 2013-03-12 2013-03-12
US61/777,443 2013-03-12
PCT/US2013/074558 WO2014107277A1 (en) 2012-12-13 2013-12-12 Enhancer of zeste homolog 2 inhibitors

Publications (2)

Publication Number Publication Date
JP2016503009A JP2016503009A (ja) 2016-02-01
JP2016503009A5 true JP2016503009A5 (enExample) 2017-01-05

Family

ID=51062419

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015547522A Pending JP2016503009A (ja) 2012-12-13 2013-12-12 Zesteホモログ2エンハンサー阻害剤

Country Status (10)

Country Link
US (1) US9382234B2 (enExample)
EP (1) EP2931707A4 (enExample)
JP (1) JP2016503009A (enExample)
KR (1) KR20150095779A (enExample)
CN (1) CN104968646B (enExample)
AU (1) AU2013371541B2 (enExample)
BR (1) BR112015014090A2 (enExample)
CA (1) CA2894657A1 (enExample)
RU (1) RU2015127822A (enExample)
WO (1) WO2014107277A1 (enExample)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2894216A1 (en) * 2012-12-21 2014-06-26 Epizyme, Inc. 1,4-pyridone compounds
EP2935264B1 (en) 2012-12-21 2017-10-18 Epizyme, Inc. 1,4-pyridone bicyclic heteroaryl compounds
CN105473580A (zh) 2013-07-10 2016-04-06 葛兰素史密斯克莱知识产权(第2号)有限公司 Zeste同源物增强子2抑制剂
TW201636344A (zh) 2014-12-05 2016-10-16 美國禮來大藥廠 Ezh2抑制劑
WO2016101956A2 (en) 2014-12-23 2016-06-30 University Of Copenhagen Treatment of cancer by inhibiting ezh2 activity
UY36758A (es) * 2015-06-30 2016-12-30 Glaxosmithkline Ip No 2 Ltd Inhibidores del potenciador del homólogo zeste 2
TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
CA3018270A1 (en) * 2016-04-22 2017-10-26 Dana-Farber Cancer Institute, Inc. Ezh2 inhibitors and uses thereof
WO2018086592A1 (zh) 2016-11-11 2018-05-17 上海海雁医药科技有限公司 4,5,6-三取代吲唑类衍生物、其制法与医药上的用途
US10266542B2 (en) 2017-03-15 2019-04-23 Mirati Therapeutics, Inc. EZH2 inhibitors
WO2019152419A1 (en) 2018-01-31 2019-08-08 Mirati Therapeutics, Inc Prc2 inhibitors
CN120097995A (zh) 2018-05-21 2025-06-06 星座制药公司 甲基修饰酶的调节剂、其组合物和用途
EP3823671B1 (en) 2018-07-09 2024-02-07 Fondation Asile Des Aveugles Inhibition of prc2 subunits to treat eye disorders
CN109801676B (zh) * 2019-02-26 2021-01-01 北京深度制耀科技有限公司 一种用于评价化合物对基因通路活化作用的方法及装置
EP3959214A1 (en) 2019-04-22 2022-03-02 Mirati Therapeutics, Inc. Naphthyridine derivatives as prc2 inhibitors
CA3142711A1 (en) 2019-06-05 2020-12-10 Mirati Therapeutics, Inc. Imidazo[1,2-c]pyrimidine derivatives as prc2 inhibitors for treating cancer
BR112022001154A2 (pt) * 2019-07-24 2022-06-07 Constellation Pharmaceuticals Inc Terapias de inibição de ezh2 para o tratamento de cânceres
CN110950834A (zh) * 2019-11-26 2020-04-03 济南大学 新型eed-ezh2相互作用小分子抑制剂的确定和评价

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4038396A (en) * 1975-02-24 1977-07-26 Merck & Co., Inc. Anti-inflammatory oxazole[4,5-b]pyridines
US6559145B2 (en) 2000-07-12 2003-05-06 Pharmacia & Upjohn Company Heterocycle carboxamides as antiviral agents
WO2003088903A2 (en) 2002-04-17 2003-10-30 Cytokinetics, Inc. Compounds, compositions, and methods
TW200410921A (en) * 2002-11-25 2004-07-01 Hoffmann La Roche Mandelic acid derivatives
CN101023057A (zh) * 2004-05-06 2007-08-22 赛特凯恩蒂克公司 某些化学品、组合物及方法
US7618981B2 (en) * 2004-05-06 2009-11-17 Cytokinetics, Inc. Imidazopyridinyl-benzamide anti-cancer agents
MX2012012966A (es) * 2010-05-07 2013-01-22 Glaxosmithkline Llc Indoles.
TW201733984A (zh) 2011-04-13 2017-10-01 雅酶股份有限公司 經取代之苯化合物
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
SG10201608579UA (en) 2012-04-13 2016-12-29 Epizyme Inc Combination therapy for treating cancer
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
JP6461802B2 (ja) 2012-10-15 2019-01-30 エピザイム,インコーポレイティド 置換ベンゼン化合物
EP3022184B1 (en) 2013-07-19 2017-09-27 Epizyme, Inc. Substituted benzene compounds

Similar Documents

Publication Publication Date Title
JP2016503009A5 (enExample)
RU2015127822A (ru) Ингибиторы энхансера гомолога 2 белка zeste
JP2016517878A5 (enExample)
JP2014521653A5 (enExample)
ES2923875T3 (es) Moduladores de la vía integrada del estrés
CN101142198B (zh) 用于治疗疾病的异*唑坎布雷它斯丁衍生物
JP2019505541A5 (enExample)
JP2017530999A5 (enExample)
JP2014511869A5 (enExample)
JP2014526549A5 (enExample)
RU2017116598A (ru) Соединения и композиции для модуляции киназной активности мутантов egfr
RU2014105624A (ru) Соединения индазола, способ их применения и фармацевтическая композиция
JP2016516043A5 (enExample)
JP2010526129A5 (enExample)
RU2012116877A (ru) Соединения 2-пиридона, применяемые в качестве ингибиторов нейтрофильной эластазы
RU2021133444A (ru) Производные бензимидазола в качестве модуляторов ror-гамма
JP2015524472A5 (enExample)
RU2017116197A (ru) 2-амино-3,5-дифтор-3,6-диметил-6-фенил-3,4,5,6-тетрагидропиридины как ингибиторы васе1 для лечения болезни альцгеймера
JP2010538076A5 (enExample)
JP2014528464A5 (enExample)
RU2008135690A (ru) Соединения и композиции в качестве ингибиторов протеинкиназы
JP2017532360A5 (enExample)
JP2014520809A5 (enExample)
JP2016540811A5 (enExample)
RU2017120217A (ru) 2-амино-5,5-дифтор-6-(фторметил)-6-фенил-3,4,5,6-тетрагидпропиридины в качестве ингибиторов bace1