CN111683936A - 多取代苯环化合物、制备方法及其用途 - Google Patents
多取代苯环化合物、制备方法及其用途 Download PDFInfo
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- CN111683936A CN111683936A CN201980011701.6A CN201980011701A CN111683936A CN 111683936 A CN111683936 A CN 111683936A CN 201980011701 A CN201980011701 A CN 201980011701A CN 111683936 A CN111683936 A CN 111683936A
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- Prior art keywords
- alkyl
- methyl
- radical
- amino
- ethyl
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- -1 Polysubstituted benzene ring compound Chemical class 0.000 title claims description 695
- 238000002360 preparation method Methods 0.000 title claims description 142
- 150000001875 compounds Chemical class 0.000 claims abstract description 319
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 24
- 201000010099 disease Diseases 0.000 claims abstract description 20
- 230000001404 mediated effect Effects 0.000 claims abstract description 12
- 150000003254 radicals Chemical class 0.000 claims description 291
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 138
- 229910052736 halogen Inorganic materials 0.000 claims description 111
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 98
- 150000002367 halogens Chemical class 0.000 claims description 71
- 125000000623 heterocyclic group Chemical group 0.000 claims description 66
- 125000000217 alkyl group Chemical group 0.000 claims description 45
- 125000003118 aryl group Chemical group 0.000 claims description 41
- 206010028980 Neoplasm Diseases 0.000 claims description 40
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 37
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 36
- 150000003839 salts Chemical class 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 33
- 125000003386 piperidinyl group Chemical group 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 29
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 24
- 125000002757 morpholinyl group Chemical group 0.000 claims description 18
- 125000004193 piperazinyl group Chemical group 0.000 claims description 18
- 125000001188 haloalkyl group Chemical group 0.000 claims description 17
- MJYFVDNMTKLGTH-UHFFFAOYSA-N 4-bromo-6-(3,4-dichlorophenyl)sulfanyl-1-[[4-(dimethylcarbamoyl)phenyl]methyl]indole-2-carboxylic acid Chemical compound BrC1=C2C=C(N(C2=CC(=C1)SC1=CC(=C(C=C1)Cl)Cl)CC1=CC=C(C=C1)C(N(C)C)=O)C(=O)O MJYFVDNMTKLGTH-UHFFFAOYSA-N 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
- 239000008194 pharmaceutical composition Substances 0.000 claims description 16
- 201000011510 cancer Diseases 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 14
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 14
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 13
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 13
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 13
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000003554 tetrahydropyrrolyl group Chemical group 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- NXZIGGBPLGAPTI-UHFFFAOYSA-N tert-butyl 6-oxa-3-azabicyclo[3.1.0]hexane-3-carboxylate Chemical group C1N(C(=O)OC(C)(C)C)CC2OC21 NXZIGGBPLGAPTI-UHFFFAOYSA-N 0.000 claims description 9
- KPHHWQMMJDEWGR-QABDSSMZSA-N FC1(CCC(CC1)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@H](O[C@H](C1)C)C)C)CC)F Chemical compound FC1(CCC(CC1)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@H](O[C@H](C1)C)C)C)CC)F KPHHWQMMJDEWGR-QABDSSMZSA-N 0.000 claims description 8
- GGLNDNKXJRVPGE-HNUBOUNVSA-N FC1(CCC(CC1)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2OC)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@@H](O[C@@H](C1)C)C)C)CC)F Chemical compound FC1(CCC(CC1)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2OC)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@@H](O[C@@H](C1)C)C)C)CC)F GGLNDNKXJRVPGE-HNUBOUNVSA-N 0.000 claims description 8
- DJQIJCOCCMTCLC-UHFFFAOYSA-N 5-cyclobutyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CCC1)C=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC DJQIJCOCCMTCLC-UHFFFAOYSA-N 0.000 claims description 7
- YBFJGHGZCBTDEJ-UHFFFAOYSA-N 5-cyclobutyloxy-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CCC1)OC=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC YBFJGHGZCBTDEJ-UHFFFAOYSA-N 0.000 claims description 7
- GHKASUUFSFNMHA-UHFFFAOYSA-N 5-cyclopropyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CC1)C=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC GHKASUUFSFNMHA-UHFFFAOYSA-N 0.000 claims description 7
- AWEGTPPFDJUPRI-UHFFFAOYSA-N 8-oxabicyclo[3.2.1]octane Chemical compound C1CCC2CCC1O2 AWEGTPPFDJUPRI-UHFFFAOYSA-N 0.000 claims description 7
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- GKDFNQMXWUFBPO-UHFFFAOYSA-N N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-5-[2-(hydroxymethyl)cyclopropyl]-2-methylbenzamide Chemical compound CC1=C(C(NC(=C1)C)=O)CNC(C1=C(C(=CC(=C1)C1C(C1)CO)N(C1CCOCC1)CC)C)=O GKDFNQMXWUFBPO-UHFFFAOYSA-N 0.000 claims description 7
- BFAKENXZKHGIGE-UHFFFAOYSA-N bis(2,3,5,6-tetrafluoro-4-iodophenyl)diazene Chemical compound FC1=C(C(=C(C(=C1F)I)F)F)N=NC1=C(C(=C(C(=C1F)F)I)F)F BFAKENXZKHGIGE-UHFFFAOYSA-N 0.000 claims description 7
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
- WKGZCRKQBIQQOF-UHFFFAOYSA-N 5-(3,3-difluorocyclobutyl)oxy-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound FC1(CC(C1)OC=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC)F WKGZCRKQBIQQOF-UHFFFAOYSA-N 0.000 claims description 6
- KTQLUWCDIBNFCP-UHFFFAOYSA-N 5-(3,3-dimethylcyclobutyl)oxy-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound CC1=C(C(NC(=C1)C)=O)CNC(C1=C(C(=CC(=C1)OC1CC(C1)(C)C)N(C1CCOCC1)CC)C)=O KTQLUWCDIBNFCP-UHFFFAOYSA-N 0.000 claims description 6
- ILRROJGFPCBBLQ-UHFFFAOYSA-N 5-[2-[(4,4-difluoropiperidin-1-yl)methyl]cyclopropyl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound FC1(CCN(CC1)CC1C(C1)C=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC)F ILRROJGFPCBBLQ-UHFFFAOYSA-N 0.000 claims description 6
- IBQQOPZMHUCQEV-XHHUQBGOSA-N 5-[2-[[(2R,6S)-2,6-dimethylmorpholin-4-yl]methyl]cyclopropyl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound CC1=C(C(NC(=C1)C)=O)CNC(C1=C(C(=CC(=C1)C1C(C1)CN1C[C@H](O[C@H](C1)C)C)N(C1CCOCC1)CC)C)=O IBQQOPZMHUCQEV-XHHUQBGOSA-N 0.000 claims description 6
- JZGMCTDJHWGURD-UHFFFAOYSA-N 5-cyclobutylsulfanyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CCC1)SC=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC JZGMCTDJHWGURD-UHFFFAOYSA-N 0.000 claims description 6
- YDVPGAWMJNAPHR-UHFFFAOYSA-N 5-cyclobutylsulfinyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CCC1)S(=O)C=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC YDVPGAWMJNAPHR-UHFFFAOYSA-N 0.000 claims description 6
- RNALJCVYRYTPLA-UHFFFAOYSA-N 5-cyclobutylsulfonyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-[ethyl(oxan-4-yl)amino]-2-methylbenzamide Chemical compound C1(CCC1)S(=O)(=O)C=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC RNALJCVYRYTPLA-UHFFFAOYSA-N 0.000 claims description 6
- OWARKIAQVZAPSP-MCZWQBSQSA-N C(C)(=O)N1CCN(CC1)[C@@H]1C[C@H](C1)OC=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC Chemical compound C(C)(=O)N1CCN(CC1)[C@@H]1C[C@H](C1)OC=1C=C(C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=1)C)N(C1CCOCC1)CC OWARKIAQVZAPSP-MCZWQBSQSA-N 0.000 claims description 6
- KRFMFTSFVRPWNA-IRMJDAGDSA-N C12CC(CC(CC1)O2)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@H](O[C@H](C1)C)C)C)CC Chemical compound C12CC(CC(CC1)O2)N(C=1C(=C(C(=O)NCC=2C(NC(=CC=2C)C)=O)C=C(C=1)O[C@@H]1C[C@H](C1)N1C[C@H](O[C@H](C1)C)C)C)CC KRFMFTSFVRPWNA-IRMJDAGDSA-N 0.000 claims description 6
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Classifications
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
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- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/82—Amides; Imides in position 3
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
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- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
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Abstract
本发明提供了一种式(I)所示的新型EZH2抑制剂化合物以及使用该抑制剂化合物预防或治疗EZH2介导的疾病的用途。
Description
PCT国内申请,说明书已公开。
Claims (26)
- PCT国内申请,权利要求书已公开。
Priority Applications (1)
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CN202110916254.8A CN113480525B (zh) | 2018-07-27 | 2019-07-26 | 多取代苯环化合物、制备方法及其用途 |
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CN2018097635 | 2018-07-27 | ||
CNPCT/CN2018/097635 | 2018-07-27 | ||
PCT/CN2019/098019 WO2020020374A1 (zh) | 2018-07-27 | 2019-07-26 | 多取代苯环化合物、制备方法及其用途 |
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CN201980011701.6A Active CN111683936B (zh) | 2018-07-27 | 2019-07-26 | 多取代苯环化合物、制备方法及其用途 |
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KR (1) | KR20210040077A (zh) |
CN (2) | CN113480525B (zh) |
AU (1) | AU2019312416B2 (zh) |
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WO2021249305A1 (zh) * | 2020-06-08 | 2021-12-16 | 南京明德新药研发有限公司 | 联苯类化合物 |
CN116348459A (zh) * | 2020-10-13 | 2023-06-27 | 苏州信诺维医药科技股份有限公司 | 多取代苯环化合物马来酸盐的晶型、其制备方法及其应用 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013173441A2 (en) * | 2012-05-16 | 2013-11-21 | Glaxosmithkline Llc | Enhancer of zeste homolog 2 inhibitors |
WO2014049488A1 (en) * | 2012-09-28 | 2014-04-03 | Pfizer Inc. | Benzamide and heterobenzamide compounds |
CN104080769A (zh) * | 2011-04-13 | 2014-10-01 | Epizyme股份有限公司 | 芳基或杂芳基取代苯化合物 |
CN108314677A (zh) * | 2017-01-17 | 2018-07-24 | 中国科学院合肥物质科学研究院 | 一种新型的ezh2抑制剂及其用途 |
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---|---|---|---|---|
CA2751563A1 (en) | 2009-02-04 | 2010-08-12 | Jelena Mann | Methods of inhibiting fibrogenesis and treating fibrotic disease |
JP5864546B2 (ja) * | 2010-05-07 | 2016-02-17 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC | インダゾール |
PT2566327T (pt) | 2010-05-07 | 2017-05-26 | Glaxosmithkline Llc | Indoles |
WO2012051492A2 (en) | 2010-10-14 | 2012-04-19 | University Of Georgia Research Foundation, Inc. | Compounds and methods for inhibiting hiv latency |
EP2681216B1 (en) * | 2011-02-28 | 2017-09-27 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
TWI598336B (zh) * | 2011-04-13 | 2017-09-11 | 雅酶股份有限公司 | 經取代之苯化合物 |
US9206128B2 (en) * | 2011-11-18 | 2015-12-08 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
RU2704445C2 (ru) * | 2012-03-12 | 2019-10-28 | Эпизайм, Инк. | Ингибиторы ezh2 человека и способы их применения |
JP2016520645A (ja) * | 2013-06-06 | 2016-07-14 | グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー2、リミテッドGlaxosmithkline Intellectual Property No.2 Limited | Zesteホモログ2エンハンサー阻害剤 |
MY192603A (en) * | 2014-03-17 | 2022-08-29 | Daiichi Sankyo Co Ltd | 1,3-benzodioxole derivative |
WO2015200650A1 (en) * | 2014-06-25 | 2015-12-30 | Epizyme, Inc. | Substituted benzene and 6,5-fused bicyclic heteroaryl compounds |
WO2017025493A1 (en) * | 2015-08-12 | 2017-02-16 | Bayer Pharma Aktiengesellschaft | Quinoline ezh2 inhibitors |
CN107573336B (zh) * | 2016-07-05 | 2021-01-19 | 四川大学 | 苯并杂环-甲酰胺-吡啶酮衍生物及其制备方法和用途 |
-
2019
- 2019-07-26 KR KR1020217005272A patent/KR20210040077A/ko not_active Application Discontinuation
- 2019-07-26 WO PCT/CN2019/098019 patent/WO2020020374A1/zh unknown
- 2019-07-26 EP EP19840459.2A patent/EP3831822A4/en active Pending
- 2019-07-26 CN CN202110916254.8A patent/CN113480525B/zh active Active
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104080769A (zh) * | 2011-04-13 | 2014-10-01 | Epizyme股份有限公司 | 芳基或杂芳基取代苯化合物 |
WO2013173441A2 (en) * | 2012-05-16 | 2013-11-21 | Glaxosmithkline Llc | Enhancer of zeste homolog 2 inhibitors |
WO2014049488A1 (en) * | 2012-09-28 | 2014-04-03 | Pfizer Inc. | Benzamide and heterobenzamide compounds |
CN108314677A (zh) * | 2017-01-17 | 2018-07-24 | 中国科学院合肥物质科学研究院 | 一种新型的ezh2抑制剂及其用途 |
Non-Patent Citations (1)
Title |
---|
KEVIN W. KUNTZ ET AL.: "The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat", 《J. MED. CHEM.》 * |
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US20210308141A1 (en) | 2021-10-07 |
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AU2019312416A1 (en) | 2021-02-11 |
CN113480525B (zh) | 2024-02-27 |
EP3831822A1 (en) | 2021-06-09 |
JP2021531307A (ja) | 2021-11-18 |
CN113480525A (zh) | 2021-10-08 |
CA3106589A1 (en) | 2020-01-30 |
EP3831822A4 (en) | 2022-03-23 |
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