CN109937041A - 一种ezh2抑制剂与btk抑制剂联合在制备治疗肿瘤的药物中的用途 - Google Patents
一种ezh2抑制剂与btk抑制剂联合在制备治疗肿瘤的药物中的用途 Download PDFInfo
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
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- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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Abstract
本发明涉及一种EZH2抑制剂与BTK抑制剂联合在制备治疗肿瘤的药物中的用途。
Description
PCT国内申请,说明书已公开。
Claims (15)
- PCT国内申请,权利要求书已公开。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710350614 | 2017-05-18 | ||
CN2017103506146 | 2017-05-18 | ||
PCT/CN2018/087246 WO2018210296A1 (zh) | 2017-05-18 | 2018-05-17 | 一种ezh2抑制剂与btk抑制剂联合在制备治疗肿瘤的药物中的用途 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109937041A true CN109937041A (zh) | 2019-06-25 |
CN109937041B CN109937041B (zh) | 2022-04-12 |
Family
ID=64273344
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201880004347.XA Active CN109937041B (zh) | 2017-05-18 | 2018-05-17 | 一种ezh2抑制剂与btk抑制剂联合在制备治疗肿瘤的药物中的用途 |
Country Status (13)
Country | Link |
---|---|
US (1) | US11065239B2 (zh) |
EP (1) | EP3626239A4 (zh) |
JP (1) | JP7125952B2 (zh) |
KR (1) | KR102635949B1 (zh) |
CN (1) | CN109937041B (zh) |
AU (1) | AU2018269262B2 (zh) |
BR (1) | BR112019023632A2 (zh) |
CA (1) | CA3058241A1 (zh) |
MX (1) | MX2019012938A (zh) |
MY (1) | MY201580A (zh) |
RU (1) | RU2762893C2 (zh) |
TW (1) | TWI810185B (zh) |
WO (1) | WO2018210296A1 (zh) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10626116B2 (en) * | 2016-01-05 | 2020-04-21 | Jiangsu Hengrui Medicine Co., Ltd. | Crystalline form of BTK kinase inhibitor and preparation method thereof |
EP3890782A2 (en) * | 2018-12-03 | 2021-10-13 | Stichting Het Nederlands Kanker Instituut- Antoni van Leeuwenhoek Ziekenhuis | Ezh2- fgfr inhibition in cancer |
CN111499642A (zh) * | 2019-01-31 | 2020-08-07 | 江苏恒瑞医药股份有限公司 | 吡咯并[2,3-d]哒嗪-7-酮类衍生物的可药用盐、晶型及其制备方法 |
CN110372562B (zh) | 2019-07-09 | 2021-04-06 | 上海再启生物技术有限公司 | 一种btk激酶抑制剂关键中间体的晶型及其制备方法 |
WO2021063332A1 (zh) * | 2019-09-30 | 2021-04-08 | 江苏恒瑞医药股份有限公司 | 一种ezh2抑制剂与cdk4/6抑制剂联合在制备治疗肿瘤药物中的用途 |
WO2023244918A1 (en) | 2022-06-13 | 2023-12-21 | Treeline Biosciences, Inc. | Quinolone bcl6 bifunctional degraders |
WO2023244917A1 (en) | 2022-06-13 | 2023-12-21 | Treeline Biosciences, Inc. | 1,8-naphthyridin-2-one heterobifunctional bcl6 degraders |
Citations (7)
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WO2013067300A1 (en) * | 2011-11-04 | 2013-05-10 | Glaxosmithkline Intellectual Property (No. 2) Limited | Method of treatment |
CN103987842A (zh) * | 2011-09-30 | 2014-08-13 | 葛兰素史密斯克莱有限责任公司 | 治疗癌症的方法 |
US20150065483A1 (en) * | 2011-02-28 | 2015-03-05 | Epizyme, Inc. | Substituted 6,5-Fused Bicyclic Heteroaryl Compounds |
WO2015146159A1 (en) * | 2014-03-25 | 2015-10-01 | Ono Pharmaceutical Co., Ltd. | Prophylactic agent and/or therapeutic agent for diffuse large b-cell lymphoma |
WO2016007185A1 (en) * | 2014-07-07 | 2016-01-14 | Eternity Bioscience Inc. | Aminopyridazinone compounds as protein kinase inhibitors |
CN105263496A (zh) * | 2013-04-08 | 2016-01-20 | 药品循环有限责任公司 | 依鲁替尼联合疗法 |
CN105263497A (zh) * | 2013-04-08 | 2016-01-20 | 拜耳制药股份公司 | 取代的2,3-二氢咪唑并[1,2-c]喹唑啉治疗淋巴瘤的用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA111305C2 (uk) | 2012-12-21 | 2016-04-11 | Пфайзер Інк. | Конденсовані лактами арилу та гетероарилу |
US20160303135A1 (en) * | 2013-12-06 | 2016-10-20 | Epizyme, Inc. | Combination therapy for treating cancer |
WO2016014859A1 (en) * | 2014-07-25 | 2016-01-28 | Pharmacyclics Llc | Bet inhibitor and bruton's tyrosine kinase inhibitor combinations |
KR20180081587A (ko) * | 2015-11-19 | 2018-07-16 | 지앙수 헨그루이 메디슨 컴퍼니 리미티드 | 벤조푸란 유도체, 이의 제조 방법 및 의학에서의 이의 용도 |
-
2018
- 2018-05-17 EP EP18802340.2A patent/EP3626239A4/en active Pending
- 2018-05-17 CN CN201880004347.XA patent/CN109937041B/zh active Active
- 2018-05-17 RU RU2019138222A patent/RU2762893C2/ru active
- 2018-05-17 KR KR1020197035448A patent/KR102635949B1/ko active IP Right Grant
- 2018-05-17 MY MYPI2019006504A patent/MY201580A/en unknown
- 2018-05-17 TW TW107116782A patent/TWI810185B/zh active
- 2018-05-17 MX MX2019012938A patent/MX2019012938A/es unknown
- 2018-05-17 AU AU2018269262A patent/AU2018269262B2/en active Active
- 2018-05-17 BR BR112019023632-5A patent/BR112019023632A2/pt unknown
- 2018-05-17 US US16/611,969 patent/US11065239B2/en active Active
- 2018-05-17 JP JP2019561276A patent/JP7125952B2/ja active Active
- 2018-05-17 CA CA3058241A patent/CA3058241A1/en active Pending
- 2018-05-17 WO PCT/CN2018/087246 patent/WO2018210296A1/zh active Application Filing
Patent Citations (7)
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US20150065483A1 (en) * | 2011-02-28 | 2015-03-05 | Epizyme, Inc. | Substituted 6,5-Fused Bicyclic Heteroaryl Compounds |
CN103987842A (zh) * | 2011-09-30 | 2014-08-13 | 葛兰素史密斯克莱有限责任公司 | 治疗癌症的方法 |
WO2013067300A1 (en) * | 2011-11-04 | 2013-05-10 | Glaxosmithkline Intellectual Property (No. 2) Limited | Method of treatment |
CN105263496A (zh) * | 2013-04-08 | 2016-01-20 | 药品循环有限责任公司 | 依鲁替尼联合疗法 |
CN105263497A (zh) * | 2013-04-08 | 2016-01-20 | 拜耳制药股份公司 | 取代的2,3-二氢咪唑并[1,2-c]喹唑啉治疗淋巴瘤的用途 |
WO2015146159A1 (en) * | 2014-03-25 | 2015-10-01 | Ono Pharmaceutical Co., Ltd. | Prophylactic agent and/or therapeutic agent for diffuse large b-cell lymphoma |
WO2016007185A1 (en) * | 2014-07-07 | 2016-01-14 | Eternity Bioscience Inc. | Aminopyridazinone compounds as protein kinase inhibitors |
Non-Patent Citations (1)
Title |
---|
UITDEHAAG, JOOST C. M等: "Cell Panel Profiling Reveals Conserved Therapeutic Clusters and Differentiates the Mechanism of Action of Different PI3K/mTOR, Aurora Kinase and EZH2 Inhibitors", 《MOLECULAR CANCER THERAPEUTICS》 * |
Also Published As
Publication number | Publication date |
---|---|
AU2018269262B2 (en) | 2021-12-02 |
MY201580A (en) | 2024-03-02 |
US20210030736A1 (en) | 2021-02-04 |
TWI810185B (zh) | 2023-08-01 |
CN109937041B (zh) | 2022-04-12 |
KR102635949B1 (ko) | 2024-02-14 |
JP7125952B2 (ja) | 2022-08-25 |
TW201900171A (zh) | 2019-01-01 |
RU2019138222A (ru) | 2021-06-18 |
EP3626239A1 (en) | 2020-03-25 |
JP2020519588A (ja) | 2020-07-02 |
AU2018269262A1 (en) | 2019-10-31 |
US11065239B2 (en) | 2021-07-20 |
BR112019023632A2 (pt) | 2020-08-18 |
CA3058241A1 (en) | 2018-11-22 |
EP3626239A4 (en) | 2021-03-10 |
RU2019138222A3 (zh) | 2021-07-30 |
MX2019012938A (es) | 2019-12-16 |
RU2762893C2 (ru) | 2021-12-23 |
KR20200007851A (ko) | 2020-01-22 |
WO2018210296A1 (zh) | 2018-11-22 |
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