可药性
G蛋白偶联受体
神经科学
受体
药物发现
生物
孤儿受体
医学
生物信息学
药理学
遗传学
基因
转录因子
作者
Andrew A. Bolinger,Andrew Frazier,Jun‐Ho La,John Allen,Jia Zhou
标识
DOI:10.1021/acschemneuro.3c00479
摘要
G protein-coupled receptors (GPCRs) are successful druggable targets, making up around 35% of all FDA-approved medications. However, a large number of receptors remain orphaned, with no known endogenous ligand, representing a challenging but untapped area to discover new therapeutic targets. Among orphan GPCRs (oGPCRs) of interest, G protein-coupled receptor 37 (GPR37) is highly expressed in the central nervous system (CNS), particularly in the spinal cord and oligodendrocytes. While its cellular signaling mechanisms and endogenous receptor ligands remain elusive, GPR37 has been implicated in several important neurological conditions, including Parkinson's disease (PD), inflammation, pain, autism, and brain tumors. GPR37 structure, signaling, emerging physiology, and pharmacology are reviewed while integrating a discussion on potential therapeutic indications and opportunities.
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