CN104039956A - 治疗方法 - Google Patents
治疗方法 Download PDFInfo
- Publication number
- CN104039956A CN104039956A CN201280066115.XA CN201280066115A CN104039956A CN 104039956 A CN104039956 A CN 104039956A CN 201280066115 A CN201280066115 A CN 201280066115A CN 104039956 A CN104039956 A CN 104039956A
- Authority
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- China
- Prior art keywords
- methyl
- alkyl
- oxo
- pyridyl
- indole
- 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.)
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- 0 Cc1cc(C(NCC2=C(*)C(*)=C(*)NC2=O)=O)c(c(*)c(**)[n]2*)c2c1* Chemical compound Cc1cc(C(NCC2=C(*)C(*)=C(*)NC2=O)=O)c(c(*)c(**)[n]2*)c2c1* 0.000 description 12
- DUMXCFWBHDYNBI-UHFFFAOYSA-N Bc1cc(C(OC)=O)c(c(C)c[n]2C(C)C)c2c1 Chemical compound Bc1cc(C(OC)=O)c(c(C)c[n]2C(C)C)c2c1 DUMXCFWBHDYNBI-UHFFFAOYSA-N 0.000 description 1
- AQVRRAMZUAVKEP-JYOAFUTRSA-N C/C=N\C(C=C(C)NC1=O)=C1C#N Chemical compound C/C=N\C(C=C(C)NC1=O)=C1C#N AQVRRAMZUAVKEP-JYOAFUTRSA-N 0.000 description 1
- JRBSKJJARAQBJU-UHFFFAOYSA-N CC(C)C(c1c(c(C)c[n]2C(C)C)c2cc(C#N)c1)=O Chemical compound CC(C)C(c1c(c(C)c[n]2C(C)C)c2cc(C#N)c1)=O JRBSKJJARAQBJU-UHFFFAOYSA-N 0.000 description 1
- DAWLUKQZPRPNLR-UHFFFAOYSA-N CC(C)C1=CC=C(C)c(c(C(OC)=O)cc(Br)c2)c2N1 Chemical compound CC(C)C1=CC=C(C)c(c(C(OC)=O)cc(Br)c2)c2N1 DAWLUKQZPRPNLR-UHFFFAOYSA-N 0.000 description 1
- PAGZBMNNZRULIR-UHFFFAOYSA-N CC(C)[n](cc1)c(C2)c1C(C(O)=O)=CC2SC Chemical compound CC(C)[n](cc1)c(C2)c1C(C(O)=O)=CC2SC PAGZBMNNZRULIR-UHFFFAOYSA-N 0.000 description 1
- RNPGMZHLGOIQIL-UHFFFAOYSA-N CC(C)[n]1c2cc(-c3cc(C=O)c(CC=C)cc3)cc(C(OC)=O)c2c(C)c1 Chemical compound CC(C)[n]1c2cc(-c3cc(C=O)c(CC=C)cc3)cc(C(OC)=O)c2c(C)c1 RNPGMZHLGOIQIL-UHFFFAOYSA-N 0.000 description 1
- JQFZJLFAPQUEEP-UHFFFAOYSA-N CC(C)[n]1c2cc(C(F)(F)F)cc([Br]=C)c2cc1 Chemical compound CC(C)[n]1c2cc(C(F)(F)F)cc([Br]=C)c2cc1 JQFZJLFAPQUEEP-UHFFFAOYSA-N 0.000 description 1
- TXSKYAVMLOWWLN-UHFFFAOYSA-N CC(C)[n]1c2cc(CCNC(OC(C)(C)C)=O)cc(C(O)=O)c2c(C)c1 Chemical compound CC(C)[n]1c2cc(CCNC(OC(C)(C)C)=O)cc(C(O)=O)c2c(C)c1 TXSKYAVMLOWWLN-UHFFFAOYSA-N 0.000 description 1
- AEANTDNERWAHPN-UHFFFAOYSA-N CC(N1)=CC(COC)=C(CN)C1=O Chemical compound CC(N1)=CC(COC)=C(CN)C1=O AEANTDNERWAHPN-UHFFFAOYSA-N 0.000 description 1
- KYKNBCQOWFDDBF-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2cc(OCCN3CCN(C)CC3)cc3c2cc[n]3C(C)C)=O)C1O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2cc(OCCN3CCN(C)CC3)cc3c2cc[n]3C(C)C)=O)C1O KYKNBCQOWFDDBF-UHFFFAOYSA-N 0.000 description 1
- KPFSQBKJYHWFME-UHFFFAOYSA-N COC(c1c(cc[nH]2)c2cc(Br)c1)=O Chemical compound COC(c1c(cc[nH]2)c2cc(Br)c1)=O KPFSQBKJYHWFME-UHFFFAOYSA-N 0.000 description 1
- NJURFVIRNYOQKU-UHFFFAOYSA-N COC(c1c(cc[n]2C3CCC3)c2cc(Br)c1)=O Chemical compound COC(c1c(cc[n]2C3CCC3)c2cc(Br)c1)=O NJURFVIRNYOQKU-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- C07D401/12—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 linked by a chain containing hetero atoms as chain links
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- C12N9/10—Transferases (2.)
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
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- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Diabetes (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Molecular Biology (AREA)
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- Urology & Nephrology (AREA)
- Endocrinology (AREA)
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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 (1)
| Publication Number | Publication Date |
|---|---|
| CN104039956A true CN104039956A (zh) | 2014-09-10 |
Family
ID=48192800
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201280066115.XA Pending CN104039956A (zh) | 2011-11-04 | 2012-11-02 | 治疗方法 |
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) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105541801A (zh) * | 2016-01-18 | 2016-05-04 | 常州大学 | Ezh2甲基转移酶抑制剂gsk126的合成方法 |
| CN108136011A (zh) * | 2015-08-03 | 2018-06-08 | 星座制药公司 | Ezh2抑制剂和调节性t细胞功能的调制 |
| 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 |
| CN109761960A (zh) * | 2019-02-25 | 2019-05-17 | 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 |
| CN113444086A (zh) * | 2014-11-06 | 2021-09-28 | 达纳-法伯癌症研究所股份有限公司 | Ezh2抑制剂及其用途 |
| CN113784963A (zh) * | 2019-05-20 | 2021-12-10 | 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 |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
| 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 |
| CN110191879A (zh) * | 2017-01-25 | 2019-08-30 | 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 |
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| CN109761960A (zh) * | 2019-02-25 | 2019-05-17 | 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 |
| 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 |
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| CN113784963B (zh) * | 2019-05-20 | 2024-02-27 | 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 |
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| US9446041B2 (en) | 2016-09-20 |
| US20140256739A1 (en) | 2014-09-11 |
| EP2773754A1 (en) | 2014-09-10 |
| AU2012332297B2 (en) | 2016-01-07 |
| KR20140095073A (ko) | 2014-07-31 |
| CA2854447A1 (en) | 2013-05-10 |
| RU2014122546A (ru) | 2015-12-20 |
| AU2012332297A1 (en) | 2014-05-22 |
| RU2621148C2 (ru) | 2017-05-31 |
| BR112014010803A2 (pt) | 2017-04-25 |
| JP2015501784A (ja) | 2015-01-19 |
| ES2600161T3 (es) | 2017-02-07 |
| US20160074394A1 (en) | 2016-03-17 |
| EP2773754A4 (en) | 2015-06-10 |
| EP2773754B1 (en) | 2016-08-03 |
| WO2013067296A1 (en) | 2013-05-10 |
| JP6005753B2 (ja) | 2016-10-12 |
| US9242962B2 (en) | 2016-01-26 |
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