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G蛋白偶联受体药物研发:新型药物、靶点与适应症

GPCR drug discovery: new agents, targets and indications.

作者信息

Lorente Javier Sánchez, Sokolov Aleksandr V, Ferguson Gavin, Schiöth Helgi B, Hauser Alexander S, Gloriam David E

机构信息

Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Department of Surgical Sciences, Functional Pharmacology and Neuroscience, University of Uppsala, Uppsala, Sweden.

出版信息

Nat Rev Drug Discov. 2025 Mar 3. doi: 10.1038/s41573-025-01139-y.

Abstract

G protein-coupled receptors (GPCRs) form one of the largest drug target families, reflecting their involvement in numerous pathophysiological processes. In this Review, we analyse drug discovery trends for the GPCR superfamily, covering compounds, targets and indications that have reached regulatory approval or that are being investigated in clinical trials. We find that there are 516 approved drugs targeting GPCRs, making up 36% of all approved drugs. These drugs act on 121 GPCR targets, one-third of all non-sensory GPCRs. Furthermore, 337 agents targeting 133 GPCRs, including 30 novel targets, are being investigated in clinical trials. Notably, 165 of these agents are approved drugs being tested for additional indications and novel agents are increasingly allosteric modulators and biologics. Remarkably, diabetes and obesity drugs targeting GPCRs had sales of nearly US $30 billion in 2023 and the numbers of clinical trials for GPCR modulators in the metabolic diseases, oncology and immunology areas are increasing strongly. Finally, we highlight the potential of untapped target-disease associations and pathway-biased signalling. Overall, this Review provides an up-to-date reference for the drugged and potentially druggable GPCRome to inform future GPCR drug discovery and development.

摘要

G蛋白偶联受体(GPCRs)构成了最大的药物靶点家族之一,这反映出它们参与了众多病理生理过程。在本综述中,我们分析了GPCR超家族的药物发现趋势,涵盖已获得监管批准或正在临床试验中研究的化合物、靶点和适应症。我们发现,有516种已批准的药物靶向GPCRs,占所有已批准药物的36%。这些药物作用于121个GPCR靶点,占所有非感官GPCR的三分之一。此外,有337种靶向133个GPCR的药物(包括30个新靶点)正在临床试验中研究。值得注意的是,其中165种药物是正在测试其他适应症的已批准药物,新药物越来越多地是变构调节剂和生物制剂。引人注目的是,2023年靶向GPCR的糖尿病和肥胖药物销售额近300亿美元,代谢疾病、肿瘤学和免疫学领域中GPCR调节剂的临床试验数量正在强劲增长。最后,我们强调了未开发的靶点-疾病关联和途径偏向信号传导的潜力。总体而言,本综述为已用药和潜在可用药的GPCR组提供了最新参考,以为未来的GPCR药物发现和开发提供信息。

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