发明申请
US20100204242A1 Piperazine Derivative Having Affinity for the Histamine H3 Receptor
失效
哌嗪衍生物具有组胺H3受体的亲和力
- 专利标题: Piperazine Derivative Having Affinity for the Histamine H3 Receptor
- 专利标题(中): 哌嗪衍生物具有组胺H3受体的亲和力
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申请号: US12676158申请日: 2008-09-04
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公开(公告)号: US20100204242A1公开(公告)日: 2010-08-12
- 发明人: Desmond John Best , Sing Yeung Mak , Barry Sidney Orlek , Geracimos Rassias , Pamela Joan Theobald
- 申请人: Desmond John Best , Sing Yeung Mak , Barry Sidney Orlek , Geracimos Rassias , Pamela Joan Theobald
- 专利权人: Glaxo Group Limited
- 当前专利权人: Glaxo Group Limited
- 优先权: GB0717336.2 20070906; GB0814987.4 20080815
- 国际申请: PCT/EP08/61664 WO 20080904
- 主分类号: A61K31/496
- IPC分类号: A61K31/496 ; C07D405/12 ; A61P25/00 ; A61P25/28
摘要:
The present invention relates to 1-(1-methylethyl)-4-{[4-(tetrahydro-2H-pyran-4-yloxy)phenyl]carbonyl}piperazine or a pharmaceutically acceptable salt thereof, in particular the hydrochloride salt thereof and crystalline forms of the hydrochloride salt; to processes for the preparation of the compound or its salt; to compositions containing it; and to its use in the treatment or prophylaxis of neurological or psychiatric diseases, such as cognitive impairment, fatigue or a sleep disorder, for example in a mammal such as a human.The compound or a salt thereof has affinity for and is an antagonist and/or inverse agonist of the histamine H3 receptor.
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