Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 4, Sumneytown Pike, West Point, PA 19486, USA.
Curr Top Med Chem. 2011;11(6):696-725. doi: 10.2174/1568026611109060696.
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.
食欲素是一种兴奋性神经肽,在维持清醒状态方面起着关键作用。食欲素受体拮抗剂在动物和人类中促进睡眠。事实上,小分子食欲素受体拮抗剂已经在原发性失眠的治疗中证明了临床概念的验证。本文综述了不同结构类别中食欲素受体拮抗剂的优化,重点介绍了如何设计分子以优化效力、物理化学性质、药代动力学、脑穿透和体内活性。