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食欲素受体拮抗剂:历史回顾与未来机遇

Orexin Receptor Antagonists: Historical Perspectives and Future Opportunities.

作者信息

Andrews Stephen P, Aves Sarah J, Christopher John A, Nonoo Rebecca

机构信息

Heptares Therapeutics Ltd, BioPark, Broadwater Road, Welwyn Garden City, AL7 3AX, UK.

出版信息

Curr Top Med Chem. 2016;16(29):3438-3469. doi: 10.2174/1568026616666150929111607.

Abstract

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.

摘要

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。

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