发明申请
US20070232636A1 Substituted Diaza-Spiro-[5.5]-Undecane Derivaties and Their Use as Neurokinin Antagonists
失效
取代的Diaza-Spiro- [5.5] - 十二烷衍生物及其作为神经激肽拮抗剂的用途
- 专利标题: Substituted Diaza-Spiro-[5.5]-Undecane Derivaties and Their Use as Neurokinin Antagonists
- 专利标题(中): 取代的Diaza-Spiro- [5.5] - 十二烷衍生物及其作为神经激肽拮抗剂的用途
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申请号: US11547889申请日: 2005-04-04
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公开(公告)号: US20070232636A1公开(公告)日: 2007-10-04
- 发明人: Frans Janssens , Bruno Schoentjes , Sophie Coupa , Alain Poncelet , Yvan Simonnet
- 申请人: Frans Janssens , Bruno Schoentjes , Sophie Coupa , Alain Poncelet , Yvan Simonnet
- 优先权: EPPCT/EP04/50457 20040406
- 国际申请: PCT/EP05/51508 WO 20050404
- 主分类号: A61K31/438
- IPC分类号: A61K31/438 ; C07D215/00
摘要:
This invention concerns substituted diaza-spiro-[5.5]-undecane derivatives having neurokinin antagonistic activity, in particular NK1 antagonistic activity, a combined NK1/NK2 antagonistic activity, a combined NK1/NK3 antagonistic activity and a combined NK1/NK2/NK3 antagonistic activity, their preparation, compositions comprising them and their use as a medicine, in particular for the treatment and/or prophylaxis of schizophrenia, emesis, anxiety and depression, irritable bowel syndrome (IBS), circadian rhythm disturbances, pre-eclampsia, nociception, pain, in particular visceral and neuropathic pain, pancreatitis, neurogenic inflammation, asthma, COPD and micturition disorders such as urinary incontinence. The compounds according to the invention can be represented by general Formula (I) and comprises also the pharmaceutically acceptable acid or base addition salts thereof, the stereochemically isomeric forms thereof, the N-oxide form thereof and prodrugs thereof, wherein all substituents are defined as in Claim 1.
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