JP2015501784A5 - - Google Patents

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Publication number
JP2015501784A5
JP2015501784A5 JP2014540115A JP2014540115A JP2015501784A5 JP 2015501784 A5 JP2015501784 A5 JP 2015501784A5 JP 2014540115 A JP2014540115 A JP 2014540115A JP 2014540115 A JP2014540115 A JP 2014540115A JP 2015501784 A5 JP2015501784 A5 JP 2015501784A5
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JP
Japan
Prior art keywords
alkyl
disease
methyl
cycloalkyl
syndrome
Prior art date
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JP2014540115A
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English (en)
Japanese (ja)
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JP2015501784A (ja
JP6005753B2 (ja
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Priority claimed from PCT/US2012/063235 external-priority patent/WO2013067296A1/en
Publication of JP2015501784A publication Critical patent/JP2015501784A/ja
Publication of JP2015501784A5 publication Critical patent/JP2015501784A5/ja
Application granted granted Critical
Publication of JP6005753B2 publication Critical patent/JP6005753B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2014540115A 2011-11-04 2012-11-02 治療の方法 Expired - Fee Related JP6005753B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161555650P 2011-11-04 2011-11-04
US61/555,650 2011-11-04
PCT/US2012/063235 WO2013067296A1 (en) 2011-11-04 2012-11-02 Method of treatment

Publications (3)

Publication Number Publication Date
JP2015501784A JP2015501784A (ja) 2015-01-19
JP2015501784A5 true JP2015501784A5 (enExample) 2015-12-24
JP6005753B2 JP6005753B2 (ja) 2016-10-12

Family

ID=48192800

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014540115A Expired - Fee Related JP6005753B2 (ja) 2011-11-04 2012-11-02 治療の方法

Country Status (11)

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US (2) US9242962B2 (enExample)
EP (1) EP2773754B1 (enExample)
JP (1) JP6005753B2 (enExample)
KR (1) KR20140095073A (enExample)
CN (1) CN104039956A (enExample)
AU (1) AU2012332297B2 (enExample)
BR (1) BR112014010803A2 (enExample)
CA (1) CA2854447A1 (enExample)
ES (1) ES2600161T3 (enExample)
RU (1) RU2621148C2 (enExample)
WO (1) WO2013067296A1 (enExample)

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EP2935264B1 (en) 2012-12-21 2017-10-18 Epizyme, Inc. 1,4-pyridone bicyclic heteroaryl compounds
US9045477B2 (en) 2013-03-15 2015-06-02 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
EP2970305B1 (en) 2013-03-15 2017-02-22 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
EP3033334A1 (en) 2013-08-15 2016-06-22 Constellation Pharmaceuticals, Inc. Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof
US9822103B2 (en) 2013-11-22 2017-11-21 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
US20160340674A1 (en) * 2014-02-10 2016-11-24 University Of Rochester Compositions and Methods to Inhibit EZH2 for the Treatment of Cardiovascular Diseases
WO2015132765A1 (en) * 2014-03-07 2015-09-11 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
SMT202000123T1 (it) * 2014-03-17 2020-05-08 Daiichi Sankyo Co Ltd Derivati 1,3-benzodiossolici come inibitori di ezh1 e/o di ezh2
US20170334891A1 (en) * 2014-10-28 2017-11-23 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
US20190000860A1 (en) * 2014-11-06 2019-01-03 Dana-Farber Cancer Institute, Inc. Use of compositions modulating chromatin structure for graft versus host disease (gvhd)
EP3885343A1 (en) 2014-11-06 2021-09-29 Dana-Farber Cancer Institute, Inc. Indole compounds as ezh2 inhibitors and uses thereof
TW201636344A (zh) 2014-12-05 2016-10-16 美國禮來大藥廠 Ezh2抑制劑
WO2017023671A1 (en) * 2015-08-03 2017-02-09 Constellation Pharmaceuticals, Inc. Ezh2 inhibitors and modulation of regulatory t-cell function
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US10577350B2 (en) 2015-08-28 2020-03-03 Constellation Pharmaceuticals, Inc. Crystalline forms of (R)-N-((4-methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide
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CA3018270A1 (en) 2016-04-22 2017-10-26 Dana-Farber Cancer Institute, Inc. Ezh2 inhibitors and uses thereof
CN109790166A (zh) * 2016-06-20 2019-05-21 诺华股份有限公司 咪唑并吡啶化合物用于治疗癌症
MA46199A (fr) * 2016-09-07 2019-07-17 Shanghai Haihe Pharmaceutical Co Ltd Composé cyclique aromatique de pyrido à cinq éléments, son procédé de préparation et son utilisation
WO2018075598A1 (en) 2016-10-19 2018-04-26 Constellation Pharmaceuticals, Inc. Synthesis of inhibitors of ezh2
WO2018137639A1 (zh) * 2017-01-25 2018-08-02 恩瑞生物医药科技(上海)有限公司 一种组蛋白甲基转移酶ezh2抑制剂、其制备方法及其医药用途
EP3823671B1 (en) 2018-07-09 2024-02-07 Fondation Asile Des Aveugles Inhibition of prc2 subunits to treat eye disorders
TWI837231B (zh) 2018-11-29 2024-04-01 日商第一三共股份有限公司 含有ezh1/2雙重抑制劑之醫藥組合及其用途
US20220016111A1 (en) * 2018-12-21 2022-01-20 The Walter And Eliza Hall Institute Of Medical Research Methods of Treating Inflammation
CN113773304B (zh) * 2019-02-25 2023-03-10 江苏豪森药业集团有限公司 抗耐药抗肿瘤egfr抑制剂的制备方法
CN111961034A (zh) * 2019-05-20 2020-11-20 浙江同源康医药股份有限公司 用作ret激酶抑制剂的化合物及其应用
WO2021021986A1 (en) * 2019-07-31 2021-02-04 Ribon Therapeutics, Inc. Heterobicyclic amides as inhibitors of cd38
CN114555112A (zh) 2019-08-22 2022-05-27 朱诺治疗学股份有限公司 T细胞疗法和zeste增强子同源物2(ezh2)抑制剂的组合疗法及相关方法
CA3165891A1 (en) * 2019-12-25 2021-07-01 Nippon Shinyaku Co., Ltd. Prophylactic and/or therapeutic agent for chronic prostatitis/chronic pelvic pain syndrome
CR20230323A (es) 2021-01-29 2023-10-02 Boehringer Ingelheim Int Quinolinas y azaquinolinas como inhibidores de cd38

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EP3323820B1 (en) * 2011-02-28 2023-05-10 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds

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