Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu 215123, China.
Chemical Biology Program, Department of Pharmacology and Toxicology, and Center for Addiction Research, University of Texas Medical Branch, Galveston, Texas 77555, United States.
J Med Chem. 2020 Dec 24;63(24):15187-15217. doi: 10.1021/acs.jmedchem.0c01192. Epub 2020 Oct 28.
The sigma-1 (σ) receptor, an enigmatic protein originally classified as an opioid receptor subtype, is now understood to possess unique structural and functional features of its own and play critical roles to widely impact signaling transduction by interacting with receptors, ion channels, lipids, and kinases. The σ receptor is implicated in modulating learning, memory, emotion, sensory systems, neuronal development, and cognition and accordingly is now an actively pursued drug target for various neurological and neuropsychiatric disorders. Evaluation of the five selective σ receptor drug candidates (pridopidine, ANAVEX2-73, SA4503, S1RA, and T-817MA) that have entered clinical trials has shown that reaching clinical approval remains an evasive and important goal. This review provides up-to-date information on the selective targeting of σ receptors, including their history, function, reported crystal structures, and roles in neurological diseases, as well as a useful collation of new chemical entities as σ selective orthosteric ligands or allosteric modulators.
西格玛-1(σ)受体,一种最初被归类为阿片受体亚型的神秘蛋白,现在被认为具有独特的结构和功能特征,通过与受体、离子通道、脂质和激酶相互作用,广泛影响信号转导。σ 受体参与调节学习、记忆、情绪、感觉系统、神经元发育和认知,因此现在是各种神经和神经精神疾病的积极药物靶点。对已进入临床试验的五种选择性 σ 受体药物候选物(普里多吡啶、ANAVEX2-73、SA4503、S1RA 和 T-817MA)的评估表明,达到临床批准仍然是一个难以捉摸且重要的目标。本综述提供了有关 σ 受体选择性靶向的最新信息,包括其历史、功能、报告的晶体结构以及在神经疾病中的作用,以及作为 σ 选择性正位配体或变构调节剂的新化学实体的有用分类。