![BICYCLIC SULFONAMIDE COMPOUNDS AS SODIUM CHANNEL INHIBITORS](/abs-image/US/2016/02/18/US20160046626A1/abs.jpg.150x150.jpg)
基本信息:
- 专利标题: BICYCLIC SULFONAMIDE COMPOUNDS AS SODIUM CHANNEL INHIBITORS
- 专利标题(中):双酚磺酰胺化合物作为钠通道抑制剂
- 申请号:US14920833 申请日:2015-10-22
- 公开(公告)号:US20160046626A1 公开(公告)日:2016-02-18
- 发明人: Matthew WEISS , Alessandro BOEZIO , Christiane BOEZIO , John R. BUTLER , Margaret Yuhua CHU-MOYER , Erin F. DIMAURO , Thomas DINEEN , Russell GRACEFFA , Angel GUZMAN-PEREZ , Hongbing HUANG , Charles KREIMAN , Daniel LA , Isaac E. MARX , Benjamin Charles MILGRAM , Hanh Nho NGUYEN , Emily Anne PETERSON , Karina R. VAIDA , Brian SPARLING
- 申请人: AMGEN INC.
- 主分类号: C07D471/04
- IPC分类号: C07D471/04 ; C07D417/12 ; C07D413/14 ; C07D413/12 ; C07D401/12
摘要:
The present invention provides compounds of Formula I, and pharmaceutically acceptable salts thereof, that are inhibitors of voltage-gated sodium channels, in particular Nav1.7. The compounds are useful for the treatment of diseases associated with the activity of sodium channels such as pain disorders and itch. Also provided are pharmaceutical compositions containing compounds of the present invention.
摘要(中):
本发明提供式I化合物及其药学上可接受的盐,其是电压门控钠通道的抑制剂,特别是Nav1.7。 该化合物可用于治疗与钠通道活性相关的疾病,例如疼痛障碍和瘙痒。 还提供含有本发明化合物的药物组合物。
公开/授权文献:
- US09458152B2 Bicyclic sulfonamide compounds as sodium channel inhibitors 公开/授权日:2016-10-04
IPC结构图谱:
C | 化学;冶金 |
--C07 | 有机化学 |
----C07D | 杂环化合物 |
------C07D471/00 | 在稠环系中含有氮原子作为仅有的杂环原子、其中至少1个环是含有1个氮原子的六元环的杂环化合物,C07D451/00至C07D463/00不包括的 |
--------C07D471/02 | .在稠环系中含两个杂环 |
----------C07D471/04 | ..邻位稠环系 |