Department of Pharmaceutical Sciences, UNT System College of Pharmacy, University of North Texas Health Science Center, Fort Worth, TX, USA.
Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX, USA.
Expert Opin Ther Pat. 2021 Aug;31(8):687-708. doi: 10.1080/13543776.2021.1903431. Epub 2021 Mar 31.
Group II metabotropic glutamate (mGlu) receptors have emerged as an attractive potential target for the development of novel CNS therapeutics in areas such as Alzheimer's disease (AD), anxiety, cognitive disorders, depression, and others. Several small molecules that act as negative allosteric modulators (NAMs) on these receptors have demonstrated efficacy and/or target engagement in animal models, and one molecule (decoglurant) has been advanced into clinical trials.
This review summarizes patent applications published between January 2015 and November 2020. It is divided into three sections: (1) small molecule nonselective mGlu NAMs, (2) small molecule selective mGlu NAMs, and (3) small molecule selective mGlu NAMs.
Much progress has been made in the discovery of novel small molecule mGlu NAMs. Still, chemical diversity remains somewhat limited and room for expansion remains. Progress with mGlu NAMs has been more limited; however, some promising molecules have been disclosed. The process of elucidating the precise role of each receptor in the diseases associated with group II receptors has begun. Continued studies in animals with selective NAMs for both receptors will be critical in the coming years to inform researchers on the right compound profile and patient population for clinical development.
II 型代谢型谷氨酸(mGlu)受体已成为开发新型中枢神经系统治疗药物的有吸引力的潜在靶点,这些治疗药物可用于治疗阿尔茨海默病(AD)、焦虑症、认知障碍、抑郁症等多种疾病。几种作为这些受体负变构调节剂(NAM)的小分子已在动物模型中显示出疗效和/或靶标结合,其中一种分子(decoglurant)已进入临床试验阶段。
本综述总结了 2015 年 1 月至 2020 年 11 月期间公布的专利申请。它分为三个部分:(1)小分子非选择性 mGlu NAMs,(2)小分子选择性 mGlu NAMs,(3)小分子选择性 mGlu NAMs。
在发现新型小分子 mGlu NAMs 方面已经取得了很大进展。然而,化学多样性仍然有些有限,仍有扩展的空间。mGlu NAMs 的进展较为有限;然而,已经披露了一些有前途的分子。阐明每个受体在与 II 型受体相关疾病中的精确作用的过程已经开始。在未来几年中,对两种受体的选择性 NAMs 进行动物研究将至关重要,这将为研究人员提供有关正确化合物特征和临床开发患者群体的信息。