食欲素受体
增食欲素
上瘾
焦虑
受体
医学
失眠症
药理学
心理学
嗜睡症
神经科学
神经肽
内科学
精神科
莫达非尼
作者
Christoph Boss,John Gatfield,Christine Brotschi,Bibia Heidmann,Thierry Sifferlen,Markus von Raumer,G. Schmidt,Jodi T. Williams,Alexander Treiber,Catherine Roch
出处
期刊:ChemMedChem
[Wiley]
日期:2020-09-16
卷期号:15 (23): 2286-2305
被引量:44
标识
DOI:10.1002/cmdc.202000453
摘要
Abstract Since its discovery in 1998, the orexin system has been of interest to the research community as a potential therapeutic target for the treatment of sleep/wake disorders, stress and anxiety disorders, addiction or eating disorders. It consists of two G protein‐coupled receptors, the orexin 1 and orexin 2 receptors, and two neuropeptides with agonistic effects, the orexin A and orexin B peptides. Herein we describe our efforts leading to the identification of a promising set of dual orexin receptor antagonists (DORAs) which subsequently went through physiology‐based pharmacokinetic and pharmacodynamic modelling> [1] and finally led to the selection of daridorexant, currently in phase 3 clinical trials for the treatment of insomnia disorders.
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