JP2017532360A5 - - Google Patents
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- Publication number
- JP2017532360A5 JP2017532360A5 JP2017522890A JP2017522890A JP2017532360A5 JP 2017532360 A5 JP2017532360 A5 JP 2017532360A5 JP 2017522890 A JP2017522890 A JP 2017522890A JP 2017522890 A JP2017522890 A JP 2017522890A JP 2017532360 A5 JP2017532360 A5 JP 2017532360A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- oxo
- dimethyl
- carboxamide
- propyl
- 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
- 150000001875 compounds Chemical class 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 15
- 239000011780 sodium chloride Substances 0.000 claims 15
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 206010038389 Renal cancer Diseases 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 201000010982 kidney cancer Diseases 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- -1 oxazolylmethyl Chemical group 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- IDUHGUNBWPHVAI-UHFFFAOYSA-N 5-[1-[4-(dimethylamino)cyclohexyl]propyl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-4-methylthiophene-3-carboxamide Chemical compound S1C=C(C(=O)NCC=2C(NC(C)=CC=2C)=O)C(C)=C1C(CC)C1CCC(N(C)C)CC1 IDUHGUNBWPHVAI-UHFFFAOYSA-N 0.000 claims 1
- OCVFHWCDYDBBRP-UHFFFAOYSA-N 5-[1-[4-(dimethylamino)piperidin-1-yl]ethyl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-4-methylthiophene-3-carboxamide Chemical compound S1C=C(C(=O)NCC=2C(NC(C)=CC=2C)=O)C(C)=C1C(C)N1CCC(N(C)C)CC1 OCVFHWCDYDBBRP-UHFFFAOYSA-N 0.000 claims 1
- LVGCTQDARMZPSW-UHFFFAOYSA-N 5-[1-[4-(dimethylamino)piperidin-1-yl]propyl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-4-methylthiophene-3-carboxamide Chemical compound S1C=C(C(=O)NCC=2C(NC(C)=CC=2C)=O)C(C)=C1C(CC)N1CCC(N(C)C)CC1 LVGCTQDARMZPSW-UHFFFAOYSA-N 0.000 claims 1
- XHROKJJCFRMCBT-UHFFFAOYSA-N 5-[[4-(dimethylamino)cyclohexyl]-ethylamino]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-4-methylthiophene-3-carboxamide Chemical compound S1C=C(C(=O)NCC=2C(NC(C)=CC=2C)=O)C(C)=C1N(CC)C1CCC(N(C)C)CC1 XHROKJJCFRMCBT-UHFFFAOYSA-N 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010005949 Bone cancer Diseases 0.000 claims 1
- 210000004556 Brain Anatomy 0.000 claims 1
- 208000003174 Brain Neoplasms Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- QWNARTFIXGUQQK-UHFFFAOYSA-N C(#N)N=C(NC)N1CCC(CC1)=C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C Chemical compound C(#N)N=C(NC)N1CCC(CC1)=C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C QWNARTFIXGUQQK-UHFFFAOYSA-N 0.000 claims 1
- FWCNVCGKQUQSRK-UHFFFAOYSA-N C(#N)N=C(NC)N1CCC(CC1)C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C Chemical compound C(#N)N=C(NC)N1CCC(CC1)C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C FWCNVCGKQUQSRK-UHFFFAOYSA-N 0.000 claims 1
- QYQMXWRRXKMXGX-UHFFFAOYSA-N CC1=C(C(NC(=C1)C)=O)CN1C(C2=C(CC1)SC(=C2C)C(CC)C1CCN(CC1)CC(C)F)=O Chemical compound CC1=C(C(NC(=C1)C)=O)CN1C(C2=C(CC1)SC(=C2C)C(CC)C1CCN(CC1)CC(C)F)=O QYQMXWRRXKMXGX-UHFFFAOYSA-N 0.000 claims 1
- ABYOCYPONVIIAR-UHFFFAOYSA-N CC1=C(C(NC(=C1)C)=O)CN1C(C2=C(CC1)SC(=C2C)C(CC)N1CCC(CC1)N(C)C)=O Chemical compound CC1=C(C(NC(=C1)C)=O)CN1C(C2=C(CC1)SC(=C2C)C(CC)N1CCC(CC1)N(C)C)=O ABYOCYPONVIIAR-UHFFFAOYSA-N 0.000 claims 1
- IUHDGIJHSJSHEB-UHFFFAOYSA-N CC1=C(C(NC(=C1)C)=O)CNC(=O)C1=CSC(=C1C)C(CC)=C1CCC(CC1)O Chemical compound CC1=C(C(NC(=C1)C)=O)CNC(=O)C1=CSC(=C1C)C(CC)=C1CCC(CC1)O IUHDGIJHSJSHEB-UHFFFAOYSA-N 0.000 claims 1
- SHUSPCBTMDNIOC-UHFFFAOYSA-N CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(CC(F)F)CC1 Chemical compound CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(CC(F)F)CC1 SHUSPCBTMDNIOC-UHFFFAOYSA-N 0.000 claims 1
- CASPUOMRDFIWFM-UHFFFAOYSA-N CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(CC1)N(C)C Chemical compound CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(CC1)N(C)C CASPUOMRDFIWFM-UHFFFAOYSA-N 0.000 claims 1
- LOYKAXLOUFUJMQ-UHFFFAOYSA-N CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(O)CC1 Chemical compound CCC(C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O)=C1CCN(O)CC1 LOYKAXLOUFUJMQ-UHFFFAOYSA-N 0.000 claims 1
- VCELFVLWXRMZGZ-UHFFFAOYSA-N CCC(C1CCN(CC(C)(C)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound CCC(C1CCN(CC(C)(C)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O VCELFVLWXRMZGZ-UHFFFAOYSA-N 0.000 claims 1
- ZGINJZVAJWSMEY-UHFFFAOYSA-N CCC(C1CCN(CC(C)(F)F)CC1)C1=C(C)C2=C(CCN(CC3=C(C)C=C(C)NC3=O)C2=O)S1 Chemical compound CCC(C1CCN(CC(C)(F)F)CC1)C1=C(C)C2=C(CCN(CC3=C(C)C=C(C)NC3=O)C2=O)S1 ZGINJZVAJWSMEY-UHFFFAOYSA-N 0.000 claims 1
- ICLKDBHKJKQWFI-UHFFFAOYSA-N CCC(C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound CCC(C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O ICLKDBHKJKQWFI-UHFFFAOYSA-N 0.000 claims 1
- ZTKJBAWUDZMEOX-IBGZPJMESA-N CC[C@@H](C1CCN(CC(C)(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound CC[C@@H](C1CCN(CC(C)(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O ZTKJBAWUDZMEOX-IBGZPJMESA-N 0.000 claims 1
- ICLKDBHKJKQWFI-GOSISDBHSA-N CC[C@H](C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound CC[C@H](C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O ICLKDBHKJKQWFI-GOSISDBHSA-N 0.000 claims 1
- JRSRYECEGGNJGA-MRXNPFEDSA-N C[C@H](C1CCN(CC(C)(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound C[C@H](C1CCN(CC(C)(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O JRSRYECEGGNJGA-MRXNPFEDSA-N 0.000 claims 1
- GTNKQQKZLOXKKJ-OAHLLOKOSA-N C[C@H](C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O Chemical compound C[C@H](C1CCN(CC(F)F)CC1)C1=C(C)C(=CS1)C(=O)NCC1=C(C)C=C(C)NC1=O GTNKQQKZLOXKKJ-OAHLLOKOSA-N 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 201000002847 Cowden syndrome Diseases 0.000 claims 1
- 206010051906 Cowden's disease Diseases 0.000 claims 1
- 102100016041 EZH2 Human genes 0.000 claims 1
- 101700041849 EZH2 Proteins 0.000 claims 1
- 206010014967 Ependymoma Diseases 0.000 claims 1
- 208000006168 Ewing Sarcoma Diseases 0.000 claims 1
- JDCNHCLKYOTREH-UHFFFAOYSA-N FC(CN1CCC(CC1)=C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C)(C)F Chemical compound FC(CN1CCC(CC1)=C(CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C)(C)F JDCNHCLKYOTREH-UHFFFAOYSA-N 0.000 claims 1
- ZTKJBAWUDZMEOX-LJQANCHMSA-N FC(CN1CCC(CC1)[C@@H](CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C)(C)F Chemical compound FC(CN1CCC(CC1)[C@@H](CC)C1=C(C(=CS1)C(=O)NCC=1C(NC(=CC=1C)C)=O)C)(C)F ZTKJBAWUDZMEOX-LJQANCHMSA-N 0.000 claims 1
- 206010017758 Gastric cancer Diseases 0.000 claims 1
- 208000007569 Giant Cell Tumors Diseases 0.000 claims 1
- 208000005017 Glioblastoma Diseases 0.000 claims 1
- 206010018338 Glioma Diseases 0.000 claims 1
- 208000005726 Inflammatory Breast Neoplasms Diseases 0.000 claims 1
- 206010021980 Inflammatory carcinoma of the breast Diseases 0.000 claims 1
- 206010024324 Leukaemias Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- 206010025650 Malignant melanoma Diseases 0.000 claims 1
- 208000000172 Medulloblastoma Diseases 0.000 claims 1
- 208000008770 Multiple Hamartoma Syndrome Diseases 0.000 claims 1
- FBXFKRLTSXFVRZ-UHFFFAOYSA-N N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-5-[ethyl-[4-[ethyl(methyl)amino]cyclohexyl]amino]-4-methylthiophene-3-carboxamide Chemical compound C1CC(N(C)CC)CCC1N(CC)C1=C(C)C(C(=O)NCC=2C(NC(C)=CC=2C)=O)=CS1 FBXFKRLTSXFVRZ-UHFFFAOYSA-N 0.000 claims 1
- 206010025310 Other lymphomas Diseases 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 208000008443 Pancreatic Carcinoma Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 206010039491 Sarcoma Diseases 0.000 claims 1
- 208000008383 Wilms Tumor Diseases 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 201000010536 head and neck cancer Diseases 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 230000001404 mediated Effects 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 201000008026 nephroblastoma Diseases 0.000 claims 1
- 201000008968 osteosarcoma Diseases 0.000 claims 1
- 201000002528 pancreatic cancer Diseases 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 claims 1
- 201000011549 stomach cancer Diseases 0.000 claims 1
- 201000010874 syndrome Diseases 0.000 claims 1
- DAUYIKBTMNZABP-UHFFFAOYSA-N thiophene-3-carboxamide Chemical compound NC(=O)C=1C=CSC=1 DAUYIKBTMNZABP-UHFFFAOYSA-N 0.000 claims 1
- 201000002510 thyroid cancer Diseases 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
- 0 **(CC1)CC*1=*(*)c1c(*)c(C(N(*)CC2=C(*)C=C(*)NC2=O)=O)c(*)[s]1 Chemical compound **(CC1)CC*1=*(*)c1c(*)c(C(N(*)CC2=C(*)C=C(*)NC2=O)=O)c(*)[s]1 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462069438P | 2014-10-28 | 2014-10-28 | |
| US62/069,438 | 2014-10-28 | ||
| US201462075596P | 2014-11-05 | 2014-11-05 | |
| US62/075,596 | 2014-11-05 | ||
| PCT/EP2015/075009 WO2016066697A1 (en) | 2014-10-28 | 2015-10-28 | Enhancer of zeste homolog 2 inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017532360A JP2017532360A (ja) | 2017-11-02 |
| JP2017532360A5 true JP2017532360A5 (US20040106767A1-20040603-C00005.png) | 2018-12-06 |
| JP6571180B2 JP6571180B2 (ja) | 2019-09-04 |
Family
ID=54360465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017522890A Expired - Fee Related JP6571180B2 (ja) | 2014-10-28 | 2015-10-28 | Ｚｅｓｔｅホモログ２エンハンサー阻害剤 |
Country Status (11)
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201708210A (zh) * | 2015-06-30 | 2017-03-01 | 葛蘭素史克智慧財產（第二）有限公司 | Ｚｅｓｔｅ同源物２增強子之抑制劑 |
| TW201718598A (zh) | 2015-08-27 | 2017-06-01 | 美國禮來大藥廠 | Ｅｚｈ２抑制劑 |
| CN109328188A (zh) * | 2016-05-05 | 2019-02-12 | 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 |
| US11311524B2 (en) | 2017-01-19 | 2022-04-26 | Daiichi Sankyo Company, Limited | Pharmaceutical composition used for treatment of HTLV-1-associated myelopathy |
| US10266542B2 (en) | 2017-03-15 | 2019-04-23 | Mirati Therapeutics, Inc. | EZH2 inhibitors |
| WO2018177993A1 (de) | 2017-03-31 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Pyrazole zur bekämpfung von arthropoden |
| CA3089639C (en) | 2018-01-31 | 2024-06-18 | Mirati Therapeutics, Inc. | Imidazo[1,2-c]pyrimidinyl compounds as prc2 inhibitors |
| EP3797108B1 (en) | 2018-05-21 | 2022-07-20 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| EP3823671B1 (en) | 2018-07-09 | 2024-02-07 | Fondation Asile Des Aveugles | Inhibition of prc2 subunits to treat eye disorders |
| CA3148444A1 (en) * | 2019-07-24 | 2021-01-28 | Constellation Pharmaceuticals, Inc. | Ezh2 inhibition therapies for the treatment of cancers |
| 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 |
| CN110950834A (zh) * | 2019-11-26 | 2020-04-03 | 济南大学 | 新型eed-ezh2相互作用小分子抑制剂的确定和评价 |
| TW202400140A (zh) | 2022-04-27 | 2024-01-01 | 日商第一三共股份有限公司 | 抗體-藥物結合物與ezh1及/或ezh2抑制劑之組合 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2012012966A (es) * | 2010-05-07 | 2013-01-22 | Glaxosmithkline Llc | Indoles. |
| TWI598336B (zh) * | 2011-04-13 | 2017-09-11 | 雅酶股份有限公司 | 經取代之苯化合物 |
| JO3438B1 (ar) * | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
| AU2012332297B2 (en) * | 2011-11-04 | 2016-01-07 | Glaxosmithkline Intellectual Property (No.2) Limited | Method of treatment |
| NZ628762A (en) * | 2012-02-10 | 2016-07-29 | Constellation Pharmaceuticals Inc | Modulators of methyl modifying enzymes, compositions and uses thereof |
| UA111305C2 (uk) * | 2012-12-21 | 2016-04-11 | Пфайзер Інк. | Конденсовані лактами арилу та гетероарилу |
| EA030196B1 (ru) * | 2013-04-30 | 2018-07-31 | Глэксосмитклайн Интеллекчуал Проперти (No.2) Лимитед | Ингибиторы энхансера zeste гомолога 2 |
| RU2016104044A (ru) * | 2013-07-10 | 2017-08-15 | Глэксосмитклайн Интеллекчуал Проперти (Nо.2) Лимитед | Ингибиторы усилителя zeste гомолога 2 |
-
2015
- 2015-10-28 CA CA2965729A patent/CA2965729A1/en not_active Abandoned
- 2015-10-28 EP EP15786958.7A patent/EP3212639A1/en not_active Withdrawn
- 2015-10-28 US US15/522,373 patent/US20170334891A1/en not_active Abandoned
- 2015-10-28 CN CN201580058856.7A patent/CN107148419A/zh active Pending
- 2015-10-28 JP JP2017522890A patent/JP6571180B2/ja not_active Expired - Fee Related
- 2015-10-28 RU RU2017118165A patent/RU2017118165A/ru not_active Application Discontinuation
- 2015-10-28 WO PCT/EP2015/075009 patent/WO2016066697A1/en active Application Filing
- 2015-10-28 AU AU2015340614A patent/AU2015340614B2/en not_active Ceased
- 2015-10-28 KR KR1020177014034A patent/KR20170068603A/ko unknown
- 2015-10-28 MA MA040848A patent/MA40848A/fr unknown
- 2015-10-28 BR BR112017008840A patent/BR112017008840A2/pt not_active Application Discontinuation
