Trends in GPCR drug discovery: new agents, targets and indications

G蛋白偶联受体 药物发现 药品 医学 计算生物学 药理学 生物信息学 数据科学 受体 计算机科学 生物 内科学
作者
Alexander S. Hauser,Misty M. Attwood,Mathias Rask‐Andersen,Helgi B. Schiöth,David E. Gloriam
出处
期刊:Nature Reviews Drug Discovery [Nature Portfolio]
卷期号:16 (12): 829-842 被引量:2693
标识
DOI:10.1038/nrd.2017.178
摘要

G protein-coupled receptors (GPCRs) are the most intensively studied class of drug targets. This article presents a pioneering analysis of all GPCR-targeted drugs and agents that are currently in clinical trials, and discusses the trends across molecule types, drug targets and therapeutic indications. G protein-coupled receptors (GPCRs) are the most intensively studied drug targets, mostly due to their substantial involvement in human pathophysiology and their pharmacological tractability. Here, we report an up-to-date analysis of all GPCR drugs and agents in clinical trials, which reveals current trends across molecule types, drug targets and therapeutic indications, including showing that 475 drugs (~34% of all drugs approved by the US Food and Drug Administration (FDA)) act at 108 unique GPCRs. Approximately 321 agents are currently in clinical trials, of which ~20% target 66 potentially novel GPCR targets without an approved drug, and the number of biological drugs, allosteric modulators and biased agonists has increased. The major disease indications for GPCR modulators show a shift towards diabetes, obesity and Alzheimer disease, although several central nervous system disorders are also highly represented. The 224 (56%) non-olfactory GPCRs that have not yet been explored in clinical trials have broad untapped therapeutic potential, particularly in genetic and immune system disorders. Finally, we provide an interactive online resource to analyse and infer trends in GPCR drug discovery.
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