mGluR5负变构调节剂的研究进展。

Craig W Lindsley, Kyle A Emmitte
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引用次数: 0

摘要

代谢性谷氨酸受体亚型5 (mGluR5)的负变构调节剂(NAMs)作为多种中枢神经系统疾病的潜在治疗方法引起了制药行业的极大兴趣。表征良好的小分子mGluR5 NAMs已在几种疾病的临床前模型中显示出疗效,近年来已报道了此类NAMs临床疗效的例子。在过去的两年中,无论是新小分子的发现和开发,还是已知化合物的临床评价,都取得了重大进展。临床前药物发现工作的最新进展是使用多种策略来发现新的化学支架,包括已知化合物的结构修饰,基于已知化合物的新化学支架的合理设计,以及开发新的,结构独特的支架的筛选方法。mGluR5 NAMs在临床环境中的进展也导致了最近的重要进展,包括完成了概念验证研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent progress in the discovery and development of negative allosteric modulators of mGluR5.

Negative allosteric modulators (NAMs) of metabotropic glutamate receptor subtype 5 (mGluR5) have attracted significant interest in the pharmaceutical industry as potential therapies for a variety of diseases of the CNS. Well-characterized small-molecule mGluR5 NAMs have demonstrated efficacy in several preclinical models of disease, and examples of the clinical efficacy of such NAMs have been reported in recent years. Advances, both in the discovery and development of new small molecules and in the clinical evaluation of known compounds, have been significant in the past 2 years. Recent progress in preclinical drug discovery efforts has used multiple strategies for the discovery of new chemical scaffolds, including the structural modification of known compounds, the rational design of new chemical scaffolds based on known compounds, and the development of screening approaches for new, structurally distinct scaffolds. Progress in the clinical setting with mGluR5 NAMs has also resulted in important recent advances, including the completion of proof-of-concept studies.

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