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使用 OX 受体拮抗活性治疗和预防各种治疗病症(WO2012081692)。

Treatment and prevention of various therapeutic conditions using OX receptor antagonistic activity (WO2012081692).

机构信息

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

出版信息

Expert Opin Ther Pat. 2013 Feb;23(2):273-7. doi: 10.1517/13543776.2013.749240. Epub 2013 Jan 3.

Abstract

Application WO2012081692 from Taisho Pharmaceutical Co. Ltd. claims pyrazole-based antagonists of the orexin-1 and orexin-2 receptors. Utility in a number of therapeutic areas is claimed, including the treatment of sleep disorders; the most likely use of the claimed compounds. Data from in vitro functional assays are presented, with the claimed compounds typically being dual orexin receptor antagonists (DORAs) or having moderate selectivity for orexin-1. Structurally, the claimed compounds represent a variation on established DORA SAR themes and translate features of clinical compounds into a pyrazole-based scaffold. Example 52, the most potent molecule in the application, has similar molecular weight and lipophilicity to suvorexant, the most advanced DORA, with broadly comparable potency in functional assays.

摘要

来自大正制药株式会社的 WO2012081692 申请声称是食欲素-1 和食欲素-2 受体的吡唑类拮抗剂。该申请声称这些化合物在许多治疗领域具有用途,包括治疗睡眠障碍;这是所声称的化合物最有可能的用途。申请中提供了来自体外功能测定的数据,所声称的化合物通常是双重食欲素受体拮抗剂(DORAs),或者对食欲素-1 具有中等选择性。从结构上看,所声称的化合物代表了已确立的 DORA SAR 主题的变化,并将临床化合物的特征转化为基于吡唑的支架。申请中的最有效分子 52 号示例,其分子量和脂溶性与最先进的 DORA 苏沃雷生相似,在功能测定中具有大致相当的效力。

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