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食欲素受体拮抗剂:药物化学与治疗潜力

Orexin receptor antagonists: medicinal chemistry and therapeutic potential.

作者信息

Roecker Anthony J, Coleman Paul J

机构信息

Department of Medicinal Chemistry Merck Research Laboratories, P.O. Box 4, Sumneytown Pike, West Point, PA 19486, USA.

出版信息

Curr Top Med Chem. 2008;8(11):977-87. doi: 10.2174/156802608784936746.

Abstract

Actelion Pharmaceuticals achieved clinical proof-of-concept for the treatment of insomnia in 2007 with the release of Phase II data on Almorexant, a potent dual (OX1R/OX2R) orexin receptor antagonist. GlaxoSmithKline also released clinical efficacy data on an orexin receptor antagonist in 2007 for the treatment of insomnia. With these exciting findings, the search for orexin (or hypocretin) receptor antagonists for the treatment of sleep and neurological disorders has recently increased in intensity in the pharmaceutical industry. This review will focus on the medicinal chemistry of orexin antagonists and the potential therapeutic value of this therapy for the treatment of insomnia. Receptor subtype selectivity will also be described to highlight the tools currently available to delineate receptor-specific pharmacology.

摘要

2007年,Actelion制药公司发布了关于强效双重(OX1R/OX2R)食欲素受体拮抗剂阿莫雷生的II期数据,从而实现了治疗失眠的临床概念验证。葛兰素史克公司在2007年也发布了一种食欲素受体拮抗剂治疗失眠的临床疗效数据。鉴于这些令人振奋的发现,制药行业最近对用于治疗睡眠和神经紊乱的食欲素(或下丘脑分泌素)受体拮抗剂的研究力度加大。本综述将聚焦于食欲素拮抗剂的药物化学以及该疗法治疗失眠的潜在治疗价值。还将描述受体亚型选择性,以突出目前用于描述受体特异性药理学的工具。

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