发明申请
US20050165072A1 Aryl-link-aryl substituted thiazolidine-dione and oxazolidine-dione as sodium channel blockers
失效
芳基 - 芳基取代的噻唑烷二酮和恶唑烷二酮作为钠通道阻断剂
- 专利标题: Aryl-link-aryl substituted thiazolidine-dione and oxazolidine-dione as sodium channel blockers
- 专利标题(中): 芳基 - 芳基取代的噻唑烷二酮和恶唑烷二酮作为钠通道阻断剂
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申请号: US10512924申请日: 2003-04-25
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公开(公告)号: US20050165072A1公开(公告)日: 2005-07-28
- 发明人: Michelle Ayer , Prasun Chakravarty , Peter Meinke , William Parsons , Sriram Tyagarajan
- 申请人: Michelle Ayer , Prasun Chakravarty , Peter Meinke , William Parsons , Sriram Tyagarajan
- 国际申请: PCT/US03/12910 WO 20030425
- 主分类号: A61K31/421
- IPC分类号: A61K31/421 ; A61K31/422 ; A61K31/426 ; A61K31/427 ; C07D263/44 ; C07D277/20 ; C07D277/34 ; C07D417/06 ; C07D417/10 ; C07D417/12 ; C07D417/14
摘要:
Aryl-link-aryl thiazolidine-dione and aryl-link-aryl oxazolidine-dione compounds are sodium channel blockers; pharmaceutical compositions that include an effective amount of the aryl-link-aryl thiazolidine-dione and aryl-link-aryl oxazolidine-dione compounds and a pharmaceutically acceptable carrier, and a method of treatment of acute pain, chronic pain, visceral pain, inflammatory pain, or neuropathic pain, as well as initable bowel syndrome, Cnohns disease, epilepsy, partial and generalized tonic seizures, multiple sclerosis, bipolar depression, and tachy-arrhythmias by the administration of an effective amount of aryl-link-aryl thiazolidine-dione and aryl-link-aryl oxazolidine-dione compounds are described.
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