Discovery of Dual Orexin Receptor Antagonists (DORAs) for the Treatment of Insomnia

被引:2
|
作者
Coleman, Paul J. [1 ]
Cox, Christopher D. [1 ]
Roecker, Anthony J. [1 ]
机构
[1] Merck Res Labs, Dept Med Chem, West Point, PA 19486 USA
关键词
Brain penetration; diazepane; g-protein coupled receptor; insomnia; neuropeptide; orexin; sleep; SLEEP; NARCOLEPSY; RATS; NEURONS; HYPOCRETIN-1; PEPTIDES; POTENT; MICE; NEUROPEPTIDES; BIOACTIVATION;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Orexins are excitatory neuropeptides that have a critical role in maintaining wakefulness. Orexin receptor antagonists promote sleep in animals and humans. Indeed, small molecule orexin receptor antagonists have demonstrated clinical proof-of-concept in the treatment of primary insomnia. This review describes optimization of orexin receptor antagonists across diverse structural classes with a focus on how molecules were designed to optimize potency, physicochemical properties, pharmacokinetics, brain penetration, and in vivo activity.
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页码:696 / 725
页数:30
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