Andrews Stephen P, Aves Sarah J, Christopher John A, Nonoo Rebecca
Heptares Therapeutics Ltd, BioPark, Broadwater Road, Welwyn Garden City, AL7 3AX, UK.
Curr Top Med Chem. 2016;16(29):3438-3469. doi: 10.2174/1568026616666150929111607.
The orexin receptors OX1 and OX2 play important roles in the regulation of sleep-wake cycles, feeding, reward and energy homeostasis. Since these G protein-coupled receptors were deorphanised in 1998, more than 200 patents containing orexin receptor antagonists have been filed and, in 2014, suvorexant (Belsomra®) became the first of these compounds to receive approval from the FDA. Suvorexant is a dual orexin receptor antagonist (DORA) which is available for the treatment of insomnia. This review provides a historical perspective on the discovery and development of DORAs as well as selective OX1 receptor antagonists (1-SORAs) and selective OX2 receptor antagonists (2-SORAs). 2-SORAs are under clinical evaluation for their ability to modulate sleep, and 1-SORAs have shown promise for the treatment of addiction in pre-clinical animal models. Detailed medicinal chemistry case studies are presented and future opportunities for orexin receptor antagonists are considered.
食欲素受体OX1和OX2在调节睡眠-觉醒周期、进食、奖赏和能量平衡方面发挥着重要作用。自1998年这些G蛋白偶联受体被鉴定以来,已提交了200多项包含食欲素受体拮抗剂的专利申请,并且在2014年,苏沃雷生(Belsomra®)成为这些化合物中首个获得美国食品药品监督管理局批准的药物。苏沃雷生是一种双食欲素受体拮抗剂(DORA),可用于治疗失眠。本综述提供了关于DORA以及选择性OX1受体拮抗剂(1-SORA)和选择性OX2受体拮抗剂(2-SORA)发现与开发的历史视角。2-SORA因其调节睡眠的能力正在进行临床评估,而1-SORA在临床前动物模型中已显示出治疗成瘾的潜力。文中呈现了详细的药物化学案例研究,并探讨了食欲素受体拮抗剂未来的发展机遇。