KR102042290B1 - 글루타미나제의 헤테로사이클릭 억제제 - Google Patents
글루타미나제의 헤테로사이클릭 억제제 Download PDFInfo
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- KR102042290B1 KR102042290B1 KR1020147016922A KR20147016922A KR102042290B1 KR 102042290 B1 KR102042290 B1 KR 102042290B1 KR 1020147016922 A KR1020147016922 A KR 1020147016922A KR 20147016922 A KR20147016922 A KR 20147016922A KR 102042290 B1 KR102042290 B1 KR 102042290B1
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- VMZCDNSFRSVYKQ-UHFFFAOYSA-N O=C(Cc1ccccc1)Cl Chemical compound O=C(Cc1ccccc1)Cl VMZCDNSFRSVYKQ-UHFFFAOYSA-N 0.000 description 3
- IVTDVOFOSZGNFV-UHFFFAOYSA-N Nc1ccc(CCCCc2nnc(NC(Cc3ccccc3)=O)[s]2)nn1 Chemical compound Nc1ccc(CCCCc2nnc(NC(Cc3ccccc3)=O)[s]2)nn1 IVTDVOFOSZGNFV-UHFFFAOYSA-N 0.000 description 2
- RMJGJCXFHIYRLC-UHFFFAOYSA-N C#Cc1ccc(NC(Cc2ccccc2)=O)nn1 Chemical compound C#Cc1ccc(NC(Cc2ccccc2)=O)nn1 RMJGJCXFHIYRLC-UHFFFAOYSA-N 0.000 description 1
- KOFXIKUIZPRLPW-UHFFFAOYSA-N CC(C)(C)OC(NCc1cccc(CC(Nc2nnc(CCCCc3nnc(NC(Cc4ccccc4)=O)[s]3)cc2)=O)c1)=O Chemical compound CC(C)(C)OC(NCc1cccc(CC(Nc2nnc(CCCCc3nnc(NC(Cc4ccccc4)=O)[s]3)cc2)=O)c1)=O KOFXIKUIZPRLPW-UHFFFAOYSA-N 0.000 description 1
- RZKMTAUGYVLQJA-UHFFFAOYSA-N CC(C)(C)OC([n]1cnc(CC(Nc2nnc(CCCCc3ccc(NC(Cc4cccc(OC(F)(F)F)c4)=O)nn3)[s]2)=O)c1)=O Chemical compound CC(C)(C)OC([n]1cnc(CC(Nc2nnc(CCCCc3ccc(NC(Cc4cccc(OC(F)(F)F)c4)=O)nn3)[s]2)=O)c1)=O RZKMTAUGYVLQJA-UHFFFAOYSA-N 0.000 description 1
- NMLKWNFTAYLVGP-UHFFFAOYSA-N CC(C)(C)OC([n]1nc(C)c(CC(Nc2nnc(CCCCc3ccc(NC(Cc4cc(OC(F)(F)F)ccc4)=O)nn3)[s]2)=O)c1C)=O Chemical compound CC(C)(C)OC([n]1nc(C)c(CC(Nc2nnc(CCCCc3ccc(NC(Cc4cc(OC(F)(F)F)ccc4)=O)nn3)[s]2)=O)c1C)=O NMLKWNFTAYLVGP-UHFFFAOYSA-N 0.000 description 1
- BJFLOFQOVMXKCV-UHFFFAOYSA-N CC(N1Cc2c(CC(Nc3nnc(CCCCc4ccc(NC(Cc5ccccc5)=O)nn4)[s]3)=O)cccc2C1)=O Chemical compound CC(N1Cc2c(CC(Nc3nnc(CCCCc4ccc(NC(Cc5ccccc5)=O)nn4)[s]3)=O)cccc2C1)=O BJFLOFQOVMXKCV-UHFFFAOYSA-N 0.000 description 1
- HBMUOJKLBFYROU-UHFFFAOYSA-N CC(OCC(Nc1nnc(CCSCCc2nnc(NC(COC(C)=O)=O)[s]2)[s]1)=O)=O Chemical compound CC(OCC(Nc1nnc(CCSCCc2nnc(NC(COC(C)=O)=O)[s]2)[s]1)=O)=O HBMUOJKLBFYROU-UHFFFAOYSA-N 0.000 description 1
- OLJCRCQTPILEMB-VSGBNLITSA-N CC[C@](C(Nc1nnc(CCCCc2nnc(NC([C@@](CC)(c3ccccc3)O)=O)[s]2)[s]1)=O)(c1ccccc1)O Chemical compound CC[C@](C(Nc1nnc(CCCCc2nnc(NC([C@@](CC)(c3ccccc3)O)=O)[s]2)[s]1)=O)(c1ccccc1)O OLJCRCQTPILEMB-VSGBNLITSA-N 0.000 description 1
- GJLYBUCQNVZWDJ-UHFFFAOYSA-N COc1cc(CC(Nc2nnc(CCCCc(cc3)nnc3NC(Cc3ccccc3)=O)[s]2)=O)cc(OC)c1 Chemical compound COc1cc(CC(Nc2nnc(CCCCc(cc3)nnc3NC(Cc3ccccc3)=O)[s]2)=O)cc(OC)c1 GJLYBUCQNVZWDJ-UHFFFAOYSA-N 0.000 description 1
- WQKCSRVDFWJXTL-UHFFFAOYSA-N Cc1n[o]c(Cc2cc(CC(Nc3ccc(CCCCc4nnc(NC(Cc5ccccc5)=O)[s]4)nn3)=O)ccc2)n1 Chemical compound Cc1n[o]c(Cc2cc(CC(Nc3ccc(CCCCc4nnc(NC(Cc5ccccc5)=O)[s]4)nn3)=O)ccc2)n1 WQKCSRVDFWJXTL-UHFFFAOYSA-N 0.000 description 1
- QTDJPUBMMYYHTJ-UHFFFAOYSA-N Cc1n[o]c(Cc2cccc(CC(O)=O)c2)n1 Chemical compound Cc1n[o]c(Cc2cccc(CC(O)=O)c2)n1 QTDJPUBMMYYHTJ-UHFFFAOYSA-N 0.000 description 1
- LCYWEIAHUKFLOL-UHFFFAOYSA-N N#CCCCCc1ccc(NC(Cc2ccccc2)=O)nn1 Chemical compound N#CCCCCc1ccc(NC(Cc2ccccc2)=O)nn1 LCYWEIAHUKFLOL-UHFFFAOYSA-N 0.000 description 1
- DTXVKPOKPFWSFF-UHFFFAOYSA-N Nc(nn1)ccc1Cl Chemical compound Nc(nn1)ccc1Cl DTXVKPOKPFWSFF-UHFFFAOYSA-N 0.000 description 1
- HZHBGIJCHVVVFY-UHFFFAOYSA-N Nc1nnc(CCCCc2ccc(NC(Cc3ccccc3)=O)nn2)[s]1 Chemical compound Nc1nnc(CCCCc2ccc(NC(Cc3ccccc3)=O)nn2)[s]1 HZHBGIJCHVVVFY-UHFFFAOYSA-N 0.000 description 1
- MIMHLMWXWNPRHF-UHFFFAOYSA-N Nc1nnc(CCCCc2nnc(N)[o]2)[o]1 Chemical compound Nc1nnc(CCCCc2nnc(N)[o]2)[o]1 MIMHLMWXWNPRHF-UHFFFAOYSA-N 0.000 description 1
- FXLSMCSUYSZCFA-UHFFFAOYSA-N Nc1nnc(CCCCc2nnc(N)[s]2)[s]1 Chemical compound Nc1nnc(CCCCc2nnc(N)[s]2)[s]1 FXLSMCSUYSZCFA-UHFFFAOYSA-N 0.000 description 1
- WNIPOWMSXRXGMP-UHFFFAOYSA-N Nc1nnc(CCCc2nnc(N)[s]2)[s]1 Chemical compound Nc1nnc(CCCc2nnc(N)[s]2)[s]1 WNIPOWMSXRXGMP-UHFFFAOYSA-N 0.000 description 1
- ZJVZJCAPXRNFML-UHFFFAOYSA-N O=C(C(c1ccccc1)N1CCNCC1)Nc1nnc(CCSCCc2nnc(NC(C(c3ccccc3)N3CCNCC3)=O)[s]2)[s]1 Chemical compound O=C(C(c1ccccc1)N1CCNCC1)Nc1nnc(CCSCCc2nnc(NC(C(c3ccccc3)N3CCNCC3)=O)[s]2)[s]1 ZJVZJCAPXRNFML-UHFFFAOYSA-N 0.000 description 1
- FBMFFBGPUNBCNP-UHFFFAOYSA-N O=C(Cc(cccc1F)c1F)Nc1nnc(CCCCc2ccc(NC(Cc3cc(OC(F)(F)F)ccc3)=O)nn2)[s]1 Chemical compound O=C(Cc(cccc1F)c1F)Nc1nnc(CCCCc2ccc(NC(Cc3cc(OC(F)(F)F)ccc3)=O)nn2)[s]1 FBMFFBGPUNBCNP-UHFFFAOYSA-N 0.000 description 1
- HHLUIUZVGQITDO-UHFFFAOYSA-N O=C(Cc1cc(F)cc(F)c1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)(F)F)ccc2)=O)[s]1 Chemical compound O=C(Cc1cc(F)cc(F)c1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)(F)F)ccc2)=O)[s]1 HHLUIUZVGQITDO-UHFFFAOYSA-N 0.000 description 1
- OOQPQPACUZLVEV-UHFFFAOYSA-N O=C(Cc1cc(OCC(F)(F)F)ccc1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)(F)F)ccc2)=O)[s]1 Chemical compound O=C(Cc1cc(OCC(F)(F)F)ccc1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)(F)F)ccc2)=O)[s]1 OOQPQPACUZLVEV-UHFFFAOYSA-N 0.000 description 1
- YTYFGUNQXSXKAS-UHFFFAOYSA-N O=C(Cc1cccc(CNC(c2ccccc2)=O)c1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2ccccc2)=O)[s]1 Chemical compound O=C(Cc1cccc(CNC(c2ccccc2)=O)c1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2ccccc2)=O)[s]1 YTYFGUNQXSXKAS-UHFFFAOYSA-N 0.000 description 1
- NOPXWABNQUETOC-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc(nn1)ccc1Cl Chemical compound O=C(Cc1ccccc1)Nc(nn1)ccc1Cl NOPXWABNQUETOC-UHFFFAOYSA-N 0.000 description 1
- GWWPGZKUMAWWLH-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc(nn1)ccc1I Chemical compound O=C(Cc1ccccc1)Nc(nn1)ccc1I GWWPGZKUMAWWLH-UHFFFAOYSA-N 0.000 description 1
- KRTRGYMEOYWRKI-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)F)ccc2)=O)[s]1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCCc(cc2)nnc2NC(Cc2cc(OC(F)F)ccc2)=O)[s]1 KRTRGYMEOYWRKI-UHFFFAOYSA-N 0.000 description 1
- KXHJPVXZTRTJMB-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCCc2ccc(NC(NCc3ccccc3)=O)nn2)[s]1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCCc2ccc(NC(NCc3ccccc3)=O)nn2)[s]1 KXHJPVXZTRTJMB-UHFFFAOYSA-N 0.000 description 1
- AIIZCODOYXZUAY-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(C(c3cccc(Cl)c3)OC(CCN3CCOCC3)=O)=O)[s]2)cc1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(C(c3cccc(Cl)c3)OC(CCN3CCOCC3)=O)=O)[s]2)cc1 AIIZCODOYXZUAY-UHFFFAOYSA-N 0.000 description 1
- DZTLTBFMHGSANB-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(Cc3ccccc3)=O)[o]2)[o]1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(Cc3ccccc3)=O)[o]2)[o]1 DZTLTBFMHGSANB-UHFFFAOYSA-N 0.000 description 1
- AMZWCCRFPBPFAY-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(Cc3ccccc3)=O)[s]2)[s]1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCCc2nnc(NC(Cc3ccccc3)=O)[s]2)[s]1 AMZWCCRFPBPFAY-UHFFFAOYSA-N 0.000 description 1
- COSPOTYTNSRZGK-UHFFFAOYSA-N O=C(Cc1ccccc1)Nc1nnc(CCCc2nnc(NC(Cc3ccccc3)=O)[s]2)[s]1 Chemical compound O=C(Cc1ccccc1)Nc1nnc(CCCc2nnc(NC(Cc3ccccc3)=O)[s]2)[s]1 COSPOTYTNSRZGK-UHFFFAOYSA-N 0.000 description 1
- SCUVTVHPGZQTCC-UHFFFAOYSA-N OCC(C(Nc1nnc(CCCCc2nnc(NC(C(CO)c3ccccc3)=O)[s]2)[s]1)=O)c1ccccc1 Chemical compound OCC(C(Nc1nnc(CCCCc2nnc(NC(C(CO)c3ccccc3)=O)[s]2)[s]1)=O)c1ccccc1 SCUVTVHPGZQTCC-UHFFFAOYSA-N 0.000 description 1
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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| US61/665,370 | 2012-06-28 | ||
| US201261727195P | 2012-11-16 | 2012-11-16 | |
| US61/727,195 | 2012-11-16 | ||
| PCT/US2012/065816 WO2013078123A1 (en) | 2011-11-21 | 2012-11-19 | Heterocyclic inhibitors of glutaminase |
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| KR20150000866A KR20150000866A (ko) | 2015-01-05 |
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Cited By (1)
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| KR20150085053A (ko) * | 2012-11-16 | 2015-07-22 | 칼리테라 바이오사이언시즈 인코포레이티드 | 헤테로사이클릭 글루타미나아제 억제제 |
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| WO2015061432A1 (en) * | 2013-10-25 | 2015-04-30 | Calithera Biosciences, Inc. | Treatment of viral infections with inhibitors of glutaminase |
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| CN103880777B (zh) * | 2014-03-06 | 2015-12-30 | 陕西科技大学 | 一种制备双噻二唑二胺的方法 |
| US20150258082A1 (en) * | 2014-03-14 | 2015-09-17 | Francesco Parlati | Combination therapy with glutaminase inhibitors |
| BR112016021620A2 (pt) * | 2014-03-21 | 2018-07-10 | Agios Pharmaceuticals Inc | compostos e seus métodos de uso |
| CR20160497A (es) * | 2014-04-30 | 2016-12-20 | Pfizer | Derivados de diheterociclo enlazado a cicloalquilo |
| GB201409624D0 (en) * | 2014-05-30 | 2014-07-16 | Astrazeneca Ab | 1,3,4-thiadiazole compounds and their use in treating cancer |
| SG11201610333VA (en) * | 2014-06-13 | 2017-01-27 | Calithera Biosciences Inc | Combination therapy with glutaminase inhibitors |
| AU2015283850B2 (en) | 2014-07-03 | 2020-06-04 | Board Of Regents, University Of Texas System | GLS1 inhibitors for treating disease |
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| WO2016054388A1 (en) | 2014-10-03 | 2016-04-07 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | Glutaminase inhibitors |
| BR112017020780A2 (pt) * | 2015-03-30 | 2018-06-26 | Calithera Biosciences Inc | métodos de administração de inibidores de glutaminase |
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| ES2794868T3 (es) * | 2015-06-30 | 2020-11-19 | Univ Texas | Inhibidores de GLS1 para el tratamiento de enfermedades |
| EP3359150A4 (en) * | 2015-10-05 | 2019-11-06 | Calithera Biosciences, Inc. | COMBINATION THERAPY WITH GLUTAMINASE INHIBITORS AND IMMUNO-ONCOLOGICAL AGENTS |
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| TW201730188A (zh) * | 2015-11-30 | 2017-09-01 | 阿斯特捷利康公司 | 1,3,4-噻二唑化合物及其在治療癌症中之用途 |
| TW201731511A (zh) * | 2015-11-30 | 2017-09-16 | 阿斯特捷利康公司 | 1,3,4-噻二唑化合物及其在治療癌症中之用途 |
| TW201733587A (zh) * | 2015-11-30 | 2017-10-01 | 阿斯特捷利康公司 | 1,3,4-噻二唑化合物及其在治療癌症中之用途 |
| JP6976248B2 (ja) | 2015-12-22 | 2021-12-08 | ボード オブ リージェンツ、ザ ユニバーシテイ オブ テキサス システム | (r)−1−(4−(6−(2−(4−(3,3−ジフルオロシクロブトキシ)−6−メチルピリジン−2−イル)アセトアミド)ピリダジン−3−イル)−2−フルオロブチル)−n−メチル−1h−1,2,3−トリアゾール−4−カルボキサミドの塩形態および多形体 |
| KR20190040302A (ko) | 2016-08-25 | 2019-04-17 | 칼리테라 바이오사이언시즈, 인코포레이티드 | 글루타미나제 억제제와의 병용 요법 |
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| EP3576726A1 (en) | 2017-02-06 | 2019-12-11 | Massachusetts Institute Of Technology | Methods and products related to glutaminase inhibitors |
| CN107137401A (zh) * | 2017-03-28 | 2017-09-08 | 刘纪君 | 一种治疗产后抑郁症的药物组合物 |
| CN106860460B (zh) * | 2017-03-29 | 2019-04-23 | 上海市第一人民医院 | 谷氨酰胺酶抑制剂cb-839在制备治疗雌激素敏感型子宫内膜癌的药物中的应用 |
| EP3640250B1 (en) | 2017-06-13 | 2021-12-15 | Medshine Discovery Inc. | Compound as gls1 inhibitor |
| RU2020112558A (ru) | 2017-10-18 | 2021-11-18 | Боард Оф Регентс, Зе Юниверсити Оф Тексас Систем | Терапия на основе ингибитора глутаминазы |
| WO2020078350A1 (zh) * | 2018-10-16 | 2020-04-23 | 南京明德新药研发有限公司 | 噻二唑衍生物及其作为gls1抑制剂的应用 |
| CN110746416A (zh) * | 2019-09-05 | 2020-02-04 | 中国药科大学 | 含有三氮唑结构的谷氨酰胺酶gls1抑制剂或其可药用的盐、其制备方法及用途 |
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| CN116023375A (zh) * | 2021-10-25 | 2023-04-28 | 成都苑东生物制药股份有限公司 | 一种杂环类衍生物、其制备方法及用途 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20150085053A (ko) * | 2012-11-16 | 2015-07-22 | 칼리테라 바이오사이언시즈 인코포레이티드 | 헤테로사이클릭 글루타미나아제 억제제 |
| KR102220175B1 (ko) * | 2012-11-16 | 2021-02-24 | 칼리테라 바이오사이언시즈, 인코포레이티드 | 헤테로사이클릭 글루타미나아제 억제제 |
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