GPCR药物发现:新的药物、靶点和适应症

Javier Sánchez Lorente, Aleksandr V. Sokolov, Gavin Ferguson, Helgi B. Schiöth, Alexander S. Hauser, David E. Gloriam
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引用次数: 0

摘要

G蛋白偶联受体(gpcr)是最大的药物靶标家族之一,反映了它们参与许多病理生理过程。在这篇综述中,我们分析了GPCR超家族的药物发现趋势,包括已经获得监管部门批准或正在进行临床试验的化合物、靶点和适应症。我们发现有516种靶向gpcr的获批药物,占获批药物总数的36%。这些药物作用于121个GPCR靶点,占所有非感觉GPCR靶点的三分之一。此外,337种靶向133种gpcr的药物,包括30种新靶点,正在临床试验中进行研究。值得注意的是,这些药物中有165种已被批准用于其他适应症的药物,新型药物越来越多地成为变构调节剂和生物制剂。值得注意的是,针对GPCR的糖尿病和肥胖药物在2023年的销售额接近300亿美元,并且GPCR调节剂在代谢疾病、肿瘤和免疫学领域的临床试验数量正在强劲增长。最后,我们强调了尚未开发的靶标疾病关联和信号通路偏倚的潜力。总之,这篇综述为GPCR已用药和潜在可用药提供了最新的参考,为未来GPCR药物的发现和开发提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

GPCR drug discovery: new agents, targets and indications

GPCR drug discovery: new agents, targets and indications

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.

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