Lindsley Craig W, Emmitte Kyle A
Vanderbilt University, Medical Research Building IV, Nashville, TN 37232, USA.
Curr Opin Drug Discov Devel. 2009 Jul;12(4):446-57.
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.
代谢型谷氨酸受体5(mGluR5)的负变构调节剂(NAMs)作为中枢神经系统多种疾病的潜在治疗方法,在制药行业引起了极大关注。特征明确的小分子mGluR5 NAMs已在多种疾病的临床前模型中显示出疗效,近年来也有此类NAMs临床疗效的报道。在过去两年中,新小分子的发现与开发以及已知化合物的临床评估都取得了重大进展。临床前药物发现工作的最新进展采用了多种策略来发现新的化学骨架,包括对已知化合物进行结构修饰、基于已知化合物合理设计新的化学骨架以及开发针对结构不同的新骨架的筛选方法。mGluR5 NAMs在临床应用方面的进展也带来了近期的重要成果,包括概念验证研究的完成。