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
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- disease
- methyl
- cycloalkyl
- syndrome
- 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
Links
- 0 CC(C)[n]1c2cc(Br)cc(C(NCc3c(C)cc(*)nc3OC)=O)c2c(C)c1 Chemical compound CC(C)[n]1c2cc(Br)cc(C(NCc3c(C)cc(*)nc3OC)=O)c2c(C)c1 0.000 description 2
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)
| Country | Link |
|---|---|
| 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) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013075084A1 (en) | 2011-11-18 | 2013-05-23 | Constellation Pharmaceuticals | Modulators of methyl modifying enzymes, compositions and uses thereof |
| CA2862289C (en) | 2012-02-10 | 2019-11-26 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| AU2013361079B2 (en) * | 2012-12-21 | 2018-07-26 | Epizyme, Inc. | 1,4-pyridone bicyclic heteroaryl compounds |
| WO2014151142A1 (en) | 2013-03-15 | 2014-09-25 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| US9045477B2 (en) | 2013-03-15 | 2015-06-02 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
| WO2015023915A1 (en) | 2013-08-15 | 2015-02-19 | 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 |
| WO2015120372A2 (en) * | 2014-02-10 | 2015-08-13 | University Of Rochester | Compositions and methods to inhibit ezh2 for the treatment of cardiovascular diseases |
| CN106255693A (zh) * | 2014-03-07 | 2016-12-21 | 葛兰素史密斯克莱知识产权（第2 号）有限公司 | Zeste增强子同源物2的抑制剂 |
| SMT202000123T1 (it) | 2014-03-17 | 2020-05-08 | Daiichi Sankyo Co Ltd | Derivati 1,3-benzodiossolici come inibitori di ezh1 e/o di ezh2 |
| CN107148419A (zh) * | 2014-10-28 | 2017-09-08 | 葛兰素史密斯克莱知识产权（第2 号）有限公司 | Zeste增强子同源物2抑制剂 |
| 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 |
| TW201636344A (zh) | 2014-12-05 | 2016-10-16 | 美國禮來大藥廠 | Ｅｚｈ２抑制劑 |
| JP2018522045A (ja) * | 2015-08-03 | 2018-08-09 | コンステレーション・ファーマシューティカルズ・インコーポレイテッドＣｏｎｓｔｅｌｌａｔｉｏｎ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ，Ｉｎｃ． | Ｅｚｈ２阻害剤および制御性ｔ細胞機能の調節 |
| 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 |
| US10676479B2 (en) * | 2016-06-20 | 2020-06-09 | Novartis Ag | Imidazolepyridine compounds and uses thereof |
| AU2017323112B2 (en) * | 2016-09-07 | 2020-11-26 | Haihe Biopharma Co., Ltd. | Pyrido five-element aromatic ring compound, preparation method therefor and use thereof |
| EP3529242A1 (en) | 2016-10-19 | 2019-08-28 | 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 |
| 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 |
| CN109761960B (zh) * | 2019-02-25 | 2021-08-31 | 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 |
| US11535621B2 (en) * | 2019-07-31 | 2022-12-27 | 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 |
| MX2022007936A (es) | 2019-12-25 | 2022-10-27 | Nippon Shinyaku Co Ltd | Agente profilactico y/o terapeutico para la prostatitis cronica/sindrome de dolor pelvico cronico. |
| TW202241418A (zh) | 2021-01-29 | 2022-11-01 | 美商律幫治療股份有限公司 | 作為cd38之抑制劑的喹啉及氮雜喹啉 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2584713B1 (fr) | 1985-07-11 | 1988-09-09 | Roussel Uclaf | Nouveaux derives de l'indole carboxamide, leurs sels, procede et intermediaires de preparation, application a titre de medicaments et compositions les renfermant |
| DE10022925A1 (de) | 2000-05-11 | 2001-11-15 | Basf Ag | Substituierte Indole als PARP-Inhibitoren |
| EP1633740B1 (en) | 2003-06-19 | 2011-11-09 | GlaxoSmithKline LLC | 5-(acylamino)indazole derivatives as kinase inhibitors |
| US20050059682A1 (en) | 2003-09-12 | 2005-03-17 | Supergen, Inc., A Delaware Corporation | Compositions and methods for treatment of cancer |
| AU2005229522A1 (en) * | 2004-03-11 | 2005-10-13 | Actelion Pharmaceuticals Ltd. | Indol-1-yl-acetic acid derivatives |
| WO2007053114A1 (en) * | 2005-10-31 | 2007-05-10 | S*Bio Pte Ltd | Method of predicting a response to hdac inhibitors |
| WO2008109534A1 (en) * | 2007-03-02 | 2008-09-12 | Mdrna, Inc. | Nucleic acid compounds for inhibiting ezh2 gene expression and uses thereof |
| WO2009006577A2 (en) * | 2007-07-03 | 2009-01-08 | The Regents Of The University Of Michigan | Compositions and methods for inhibiting ezh2 |
| WO2009048958A2 (en) | 2007-10-08 | 2009-04-16 | The Board Of Regents Of The University Of Texas System | Methods and compositions involving chitosan nanoparticles |
| AR070398A1 (es) | 2008-02-22 | 2010-03-31 | Gruenenthal Chemie | Derivados sustituidos de indol |
| CN104557914A (zh) | 2008-09-26 | 2015-04-29 | 新加坡科技研究局 | 3-脱氮瓶菌素衍生物 |
| US9107942B2 (en) * | 2008-10-31 | 2015-08-18 | University Of Rochester | Methods of diagnosing and treating fibrosis |
| US8642602B2 (en) * | 2009-02-04 | 2014-02-04 | University Of Georgia Research Foundation, Inc. | Method of inhibiting fibrogenesis and treating fibrotic disease |
| ES2528269T3 (es) | 2010-05-07 | 2015-02-06 | Glaxosmithkline Llc | Azaindazoles |
| WO2011140325A1 (en) | 2010-05-07 | 2011-11-10 | Glaxosmithkline Llc | Indazoles |
| US8536179B2 (en) * | 2010-05-07 | 2013-09-17 | Glaxosmithkline Llc | Indoles |
| EP3323820B1 (en) * | 2011-02-28 | 2023-05-10 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
-
2012
- 2012-11-02 CA CA2854447A patent/CA2854447A1/en not_active Abandoned
- 2012-11-02 CN CN201280066115.XA patent/CN104039956A/zh active Pending
- 2012-11-02 ES ES12845460.0T patent/ES2600161T3/es active Active
- 2012-11-02 KR KR1020147014677A patent/KR20140095073A/ko not_active Withdrawn
- 2012-11-02 WO PCT/US2012/063235 patent/WO2013067296A1/en not_active Ceased
- 2012-11-02 US US14/355,964 patent/US9242962B2/en not_active Expired - Fee Related
- 2012-11-02 AU AU2012332297A patent/AU2012332297B2/en not_active Ceased
- 2012-11-02 RU RU2014122546A patent/RU2621148C2/ru not_active IP Right Cessation
- 2012-11-02 BR BR112014010803A patent/BR112014010803A2/pt not_active IP Right Cessation
- 2012-11-02 EP EP12845460.0A patent/EP2773754B1/en active Active
- 2012-11-02 JP JP2014540115A patent/JP6005753B2/ja not_active Expired - Fee Related
-
2015
- 2015-11-30 US US14/953,546 patent/US9446041B2/en not_active Expired - Fee Related
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