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[靶向G蛋白偶联受体:变构方法]

[G-protein-coupled receptors targeting: the allosteric approach].

作者信息

Sebag Julien A, Pantel Jacques

机构信息

Department of Molecular Physiology and Biophysics, Vanderbilt School of Medicine, Nashville, TN, USA.

出版信息

Med Sci (Paris). 2012 Oct;28(10):845-51. doi: 10.1051/medsci/20122810012. Epub 2012 Oct 12.

Abstract

G-protein-coupled receptors (GPCR) are a major family of drug targets. Essentially all drugs targeting these receptors on the market compete with the endogenous ligand (agonists or antagonists) for binding the receptor. Recently, non-competitive compounds binding to distinct sites from the cognate ligand were documented in various classes of these receptors. These compounds, called allosteric modulators, generally endowed of a better selectivity are able to modulate specifically the endogenous signaling of the receptor. To better understand the promising potential of this class of GPCRs targeting compounds, this review highlights the properties of allosteric modulators, the strategies used to identify them and the challenges associated with the development of these compounds.

摘要

G蛋白偶联受体(GPCR)是主要的药物靶点家族。基本上,市场上所有针对这些受体的药物都与内源性配体(激动剂或拮抗剂)竞争结合受体。最近,在这类受体的不同类别中发现了与同源配体结合位点不同的非竞争性化合物。这些化合物被称为变构调节剂,通常具有更好的选择性,能够特异性调节受体的内源性信号传导。为了更好地理解这类靶向GPCR化合物的潜在前景,本综述重点介绍了变构调节剂的特性、识别它们所采用的策略以及与这些化合物开发相关的挑战。

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