KR20140095073A - 치료 방법 - Google Patents

치료 방법 Download PDF

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KR20140095073A
KR20140095073A KR1020147014677A KR20147014677A KR20140095073A KR 20140095073 A KR20140095073 A KR 20140095073A KR 1020147014677 A KR1020147014677 A KR 1020147014677A KR 20147014677 A KR20147014677 A KR 20147014677A KR 20140095073 A KR20140095073 A KR 20140095073A
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alkyl
methyl
indole
mmol
cycloalkyl
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Korean (ko)
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안나 케이. 바실
소렌 베인크
라빈더 쿠마르 프린자
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글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드
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Publication of KR20140095073A publication Critical patent/KR20140095073A/ko
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • C12N9/1007Methyltransferases (general) (2.1.1.)
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    • A61K31/404Indoles, e.g. pindolol
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  • Biotechnology (AREA)
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KR1020147014677A 2011-11-04 2012-11-02 치료 방법 Withdrawn KR20140095073A (ko)

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

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KR20140095073A true KR20140095073A (ko) 2014-07-31

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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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SMT202000123T1 (it) 2014-03-17 2020-05-08 Daiichi Sankyo Co Ltd Derivati 1,3-benzodiossolici come inibitori di ezh1 e/o di ezh2
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JP2017533922A (ja) * 2014-11-06 2017-11-16 ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド 移植片対宿主病(gvhd)のためのクロマチン構造を調節する組成物の使用
WO2016073956A1 (en) * 2014-11-06 2016-05-12 Dana-Farber Cancer Institute, Inc. Ezh2 inhibitors and uses thereof
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TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
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
CN105541801B (zh) * 2016-01-18 2018-07-17 常州大学 Ezh2甲基转移酶抑制剂gsk126的合成方法
EP3445365A4 (en) 2016-04-22 2019-10-16 Dana-Farber Cancer Institute, Inc. EZH2 INHIBITORS AND USES THEREOF
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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
JP2021531340A (ja) 2018-07-09 2021-11-18 フォンダシヨン、アジール、デ、アブグルスFondation Asile Des Aveugles 眼障害を治療するためのprc2サブユニットの阻害
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
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WO2013067296A1 (en) 2013-05-10
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US20140256739A1 (en) 2014-09-11
CN104039956A (zh) 2014-09-10
CA2854447A1 (en) 2013-05-10
US9446041B2 (en) 2016-09-20
AU2012332297A1 (en) 2014-05-22
AU2012332297B2 (en) 2016-01-07
BR112014010803A2 (pt) 2017-04-25
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