变构调节
神经科学
Sigma-1受体
受体
变构调节剂
化学
信号转导
功能选择性
药物发现
药理学
心理学
计算生物学
G蛋白偶联受体
兴奋剂
医学
生物
生物化学
作者
Na Ye,Wangzhi Qin,Sheng Tian,Qingfeng Xu,Eric A. Wold,Jia Zhou,Xuechu Zhen
标识
DOI:10.1021/acs.jmedchem.0c01192
摘要
The sigma-1 (σ1) 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 σ1 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 σ1 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 σ1 receptors, including their history, function, reported crystal structures, and roles in neurological diseases, as well as a useful collation of new chemical entities as σ1 selective orthosteric ligands or allosteric modulators.
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