JP2013519680A5 - - Google Patents
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- Publication number
- JP2013519680A5 JP2013519680A5 JP2012552997A JP2012552997A JP2013519680A5 JP 2013519680 A5 JP2013519680 A5 JP 2013519680A5 JP 2012552997 A JP2012552997 A JP 2012552997A JP 2012552997 A JP2012552997 A JP 2012552997A JP 2013519680 A5 JP2013519680 A5 JP 2013519680A5
- Authority
- JP
- Japan
- Prior art keywords
- hydroxy
- chromen
- trifluoromethyl
- group
- oxo
- 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
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- -1 N, N-dimethylamino Chemical group 0.000 claims 30
- 150000003839 salts Chemical class 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 9
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 150000003536 tetrazoles Chemical class 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- IKNZBNHVVQIRTO-UHFFFAOYSA-N 2h-tetrazole-5-carboxylic acid Chemical compound OC(=O)C=1N=NNN=1 IKNZBNHVVQIRTO-UHFFFAOYSA-N 0.000 claims 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 2
- 201000003883 Cystic fibrosis Diseases 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- ZVTQYRVARPYRRE-UHFFFAOYSA-N oxadiazol-4-one Chemical compound O=C1CON=N1 ZVTQYRVARPYRRE-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 claims 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- AQYIDERAMPMQQN-UHFFFAOYSA-N 2-(difluoromethyl)-7-hydroxy-3-[4-(2h-tetrazol-5-yl)phenyl]chromen-4-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)F)=C2C(C=C1)=CC=C1C1=NN=NN1 AQYIDERAMPMQQN-UHFFFAOYSA-N 0.000 claims 1
- DSPLFQVWRBCFBY-UHFFFAOYSA-N 3-[2-chloro-4-(2h-tetrazol-5-yl)phenyl]-7-hydroxy-2-(trifluoromethyl)chromen-4-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C(=C1)Cl)=CC=C1C1=NN=NN1 DSPLFQVWRBCFBY-UHFFFAOYSA-N 0.000 claims 1
- SROZAXRHCDMWDN-UHFFFAOYSA-N 3-[3-chloro-4-(2h-tetrazol-5-yl)phenyl]-7-hydroxy-2-(trifluoromethyl)chromen-4-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C=C1Cl)=CC=C1C1=NN=NN1 SROZAXRHCDMWDN-UHFFFAOYSA-N 0.000 claims 1
- JTJFNTFGSXGQCE-UHFFFAOYSA-N 3-[3-chloro-4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]phenyl]-2h-1,2,4-oxadiazol-5-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C(=C1)Cl)=CC=C1C1=NOC(=O)N1 JTJFNTFGSXGQCE-UHFFFAOYSA-N 0.000 claims 1
- SEOPFLCETNIRME-UHFFFAOYSA-N 3-[3-fluoro-4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]phenyl]-2h-1,2,4-oxadiazol-5-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C(=C1)F)=CC=C1C1=NOC(=O)N1 SEOPFLCETNIRME-UHFFFAOYSA-N 0.000 claims 1
- RRVFSAKXCOIFRP-UHFFFAOYSA-N 3-[4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]phenyl]-2h-1,2,4-oxadiazol-5-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C=C1)=CC=C1C1=NOC(=O)N1 RRVFSAKXCOIFRP-UHFFFAOYSA-N 0.000 claims 1
- HNHMUAMHKJROPF-UHFFFAOYSA-N 3-[4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]phenyl]-2h-1,2,4-thiadiazol-5-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C=C1)=CC=C1C1=NSC(=O)N1 HNHMUAMHKJROPF-UHFFFAOYSA-N 0.000 claims 1
- FUHSYKWZNQTLKC-UHFFFAOYSA-N 3-fluoro-4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]benzoic acid Chemical compound FC1=CC(C(=O)O)=CC=C1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O FUHSYKWZNQTLKC-UHFFFAOYSA-N 0.000 claims 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- DYTYZNFCPKSNSW-UHFFFAOYSA-N 4-(7-hydroxy-2-methyl-4-oxothiochromen-3-yl)benzoic acid Chemical compound CC=1SC2=CC(O)=CC=C2C(=O)C=1C1=CC=C(C(O)=O)C=C1 DYTYZNFCPKSNSW-UHFFFAOYSA-N 0.000 claims 1
- BOJHURJUTNFAKS-UHFFFAOYSA-N 4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]-3-methylbenzoic acid Chemical compound CC1=CC(C(O)=O)=CC=C1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O BOJHURJUTNFAKS-UHFFFAOYSA-N 0.000 claims 1
- QUFCZPQVMSDJLQ-UHFFFAOYSA-N 4-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]-n-methylsulfonylbenzamide Chemical compound C1=CC(C(=O)NS(=O)(=O)C)=CC=C1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O QUFCZPQVMSDJLQ-UHFFFAOYSA-N 0.000 claims 1
- LXKDWHZAQSLWQP-UHFFFAOYSA-N 4-[8-fluoro-7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=C(C(F)(F)F)OC2=C(F)C(O)=CC=C2C1=O LXKDWHZAQSLWQP-UHFFFAOYSA-N 0.000 claims 1
- HPCCACKAELJHMO-UHFFFAOYSA-N 4-[[3-(4-carboxyphenyl)-7-hydroxy-4-oxothiochromen-2-yl]methyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CC1=C(C=2C=CC(=CC=2)C(O)=O)C(=O)C2=CC=C(O)C=C2S1 HPCCACKAELJHMO-UHFFFAOYSA-N 0.000 claims 1
- QHJHGEIEGPHPHU-UHFFFAOYSA-N 5-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O QHJHGEIEGPHPHU-UHFFFAOYSA-N 0.000 claims 1
- NTGQSLDMFCZSEC-UHFFFAOYSA-N 5-[7-hydroxy-4-oxo-2-(trifluoromethyl)chromen-3-yl]thiophene-3-carboxylic acid Chemical compound OC(=O)C1=CSC(C=2C(C3=CC=C(O)C=C3OC=2C(F)(F)F)=O)=C1 NTGQSLDMFCZSEC-UHFFFAOYSA-N 0.000 claims 1
- IYLSFMCJATULBG-UHFFFAOYSA-N 7-hydroxy-2-methyl-3-[4-(2h-tetrazol-5-yl)phenyl]chromen-4-one Chemical compound CC=1OC2=CC(O)=CC=C2C(=O)C=1C(C=C1)=CC=C1C1=NN=NN1 IYLSFMCJATULBG-UHFFFAOYSA-N 0.000 claims 1
- ZXBGKUANALHIOU-UHFFFAOYSA-N 7-hydroxy-2-methyl-3-[4-(2h-tetrazol-5-yl)phenyl]thiochromen-4-one Chemical compound CC=1SC2=CC(O)=CC=C2C(=O)C=1C(C=C1)=CC=C1C1=NN=NN1 ZXBGKUANALHIOU-UHFFFAOYSA-N 0.000 claims 1
- FGJSNLPJDMQOJH-UHFFFAOYSA-N 7-hydroxy-3-[4-(2h-tetrazol-5-yl)phenyl]-2-(trifluoromethyl)chromen-4-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC(C(F)(F)F)=C2C(C=C1)=CC=C1C1=NN=NN1 FGJSNLPJDMQOJH-UHFFFAOYSA-N 0.000 claims 1
- JSURXDDJUXDRSW-UHFFFAOYSA-N 7-hydroxy-3-[4-(2h-tetrazol-5-yl)phenyl]chromen-4-one Chemical compound C=1C(O)=CC=C(C2=O)C=1OC=C2C(C=C1)=CC=C1C1=NN=NN1 JSURXDDJUXDRSW-UHFFFAOYSA-N 0.000 claims 1
- VNVIRBPUPMNXGH-KYZUINATSA-N C1([C@H]2CC[C@@H](CC2)C2=C(OC=3C(C2=O)=CC=C(C=3)O)C(F)(F)F)=NN=NN1 Chemical compound C1([C@H]2CC[C@@H](CC2)C2=C(OC=3C(C2=O)=CC=C(C=3)O)C(F)(F)F)=NN=NN1 VNVIRBPUPMNXGH-KYZUINATSA-N 0.000 claims 1
- VPJXLPFRLZWPRZ-KYZUINATSA-N C1C[C@@H](C(=O)O)CC[C@@H]1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O Chemical compound C1C[C@@H](C(=O)O)CC[C@@H]1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O VPJXLPFRLZWPRZ-KYZUINATSA-N 0.000 claims 1
- VPJXLPFRLZWPRZ-DTORHVGOSA-N C1C[C@@H](C(=O)O)CC[C@H]1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O Chemical compound C1C[C@@H](C(=O)O)CC[C@H]1C1=C(C(F)(F)F)OC2=CC(O)=CC=C2C1=O VPJXLPFRLZWPRZ-DTORHVGOSA-N 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- QSSJZLPUHJDYKF-UHFFFAOYSA-N Cc(cc1)ccc1C(OC)=O Chemical compound Cc(cc1)ccc1C(OC)=O QSSJZLPUHJDYKF-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US30395210P | 2010-02-12 | 2010-02-12 | |
| US61/303,952 | 2010-02-12 | ||
| PCT/US2011/024353 WO2011100433A1 (en) | 2010-02-12 | 2011-02-10 | Novel s-nitrosoglutathione reductase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015190968A Division JP2016040285A (ja) | 2010-02-12 | 2015-09-29 | 新規のｓ−ニトロソグルタチオンレダクターゼ阻害剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013519680A JP2013519680A (ja) | 2013-05-30 |
| JP2013519680A5 true JP2013519680A5 (cg-RX-API-DMAC7.html) | 2014-03-20 |
| JP5878484B2 JP5878484B2 (ja) | 2016-03-08 |
Family
ID=44368117
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012552997A Expired - Fee Related JP5878484B2 (ja) | 2010-02-12 | 2011-02-10 | 新規のｓ−ニトロソグルタチオンレダクターゼ阻害剤 |
| JP2015190968A Pending JP2016040285A (ja) | 2010-02-12 | 2015-09-29 | 新規のｓ−ニトロソグルタチオンレダクターゼ阻害剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015190968A Pending JP2016040285A (ja) | 2010-02-12 | 2015-09-29 | 新規のｓ−ニトロソグルタチオンレダクターゼ阻害剤 |
Country Status (20)
Families Citing this family (27)
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| WO2011099978A1 (en) * | 2010-02-12 | 2011-08-18 | N30 Pharmaceuticals, Llc | Chromone inhibitors of s-nitrosoglutathione reductase |
| US8759548B2 (en) * | 2010-02-12 | 2014-06-24 | N30 Pharmaceuticals, Inc. | S-nitrosoglutathione reductase inhibitors |
| KR101886459B1 (ko) | 2010-10-08 | 2018-08-07 | 니발리스 테라퓨틱스, 인코포레이티드 | S-나이트로소글루타티온 리덕타제 억제제로서의 신규한 치환된 퀴놀린 화합물 |
| CA2821412A1 (en) | 2010-12-16 | 2012-06-21 | N30 Pharmaceuticals, Inc. | Novel substituted bicyclic aromatic compounds as s-nitrosoglutathione reductase inhibitors |
| WO2012170371A1 (en) * | 2011-06-10 | 2012-12-13 | N30 Pharmaceuticals, Llc | Compounds as s-nitrosoglutathione reductase inhibitors |
| ES2586213T3 (es) | 2011-10-31 | 2016-10-13 | Xenon Pharmaceuticals Inc. | Compuestos de bencenosulfonamida y su uso como agentes terapéuticos |
| CN104093716B (zh) | 2011-10-31 | 2017-06-23 | 克赛农制药股份有限公司 | 联芳醚磺酰胺化合物及其作为治疗剂的用途 |
| HK1209100A1 (en) * | 2012-05-22 | 2016-03-24 | 基因泰克有限公司 | N-substituted benzamides and their use in the treatment of pain |
| KR101663436B1 (ko) | 2012-07-06 | 2016-10-06 | 제넨테크, 인크. | N-치환된 벤즈아미드 및 이의 사용 방법 |
| KR20150131233A (ko) | 2013-03-14 | 2015-11-24 | 제넨테크, 인크. | 치환된 트리아졸로피리딘 및 이의 사용 방법 |
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| CN105793238B (zh) | 2013-11-27 | 2019-12-24 | 基因泰克公司 | 经取代的苯甲酰胺及其使用方法 |
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| EP3436432B1 (en) | 2016-03-30 | 2021-01-27 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| BR112019007763A2 (pt) | 2016-10-17 | 2019-07-02 | Genentech Inc | composto de fórmula, composição farmacêutica, métodos para tratar uma doença ou condição, para tratar dores, para diminuir o fluxo de íons e para tratar prurido, uso de um composto e invenção |
| CN110546148A (zh) | 2017-03-24 | 2019-12-06 | 基因泰克公司 | 作为钠通道抑制剂的4-哌啶-n-(嘧啶-4-基)色满-7-磺酰胺衍生物 |
| WO2018177993A1 (de) | 2017-03-31 | 2018-10-04 | Bayer Cropscience Aktiengesellschaft | Pyrazole zur bekämpfung von arthropoden |
| AR114263A1 (es) | 2018-02-26 | 2020-08-12 | Genentech Inc | Compuestos terapéuticos y métodos para utilizarlos |
| CN111936494A (zh) | 2018-03-30 | 2020-11-13 | 豪夫迈·罗氏有限公司 | 作为钠通道抑制剂的取代的氢-吡啶并-吖嗪 |
| TW202003490A (zh) | 2018-05-22 | 2020-01-16 | 瑞士商赫孚孟拉羅股份公司 | 治療性化合物及其使用方法 |
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| US8759548B2 (en) * | 2010-02-12 | 2014-06-24 | N30 Pharmaceuticals, Inc. | S-nitrosoglutathione reductase inhibitors |
| WO2011099978A1 (en) | 2010-02-12 | 2011-08-18 | N30 Pharmaceuticals, Llc | Chromone inhibitors of s-nitrosoglutathione reductase |
| WO2012170371A1 (en) * | 2011-06-10 | 2012-12-13 | N30 Pharmaceuticals, Llc | Compounds as s-nitrosoglutathione reductase inhibitors |
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2012
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