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GPR55配体发现的进展

Advances Towards The Discovery of GPR55 Ligands.

作者信息

Morales Paula, Jagerovic Nadine

机构信息

Instituto de Química Médica, Consejo Superior de Investigaciones Científicas, Calle Juan de la Cierva, 3, Madrid E-28230, Spain.

出版信息

Curr Med Chem. 2016;23(20):2087-100. doi: 10.2174/0929867323666160425113836.

Abstract

The G-protein-coupled receptor 55 (GPR55) was identified in 1999. It was proposed as a novel member of the endocannabinoid system due to the fact that some endogenous, plant-derived and synthetic cannabinoid ligands act on GPR55. However, the complexity of the cellular downstream signaling pathways related to GPR55 activation delayed the discovery of selective GPR55 ligands. It was only a few years ago that the high throughput screening of libraries of pharmaceutical companies and governmental organizations allowed to identify selective GPR55 agonists and antagonists. Since then, several GPR55 modulator scaffolds have been reported. The relevance of GPR55 has been explored in diverse physiological and pathological processes revealing its role in inflammation, neuropathic pain, bone physiology, diabetes and cancer. Considering GPR55 as a new promising therapeutic target, there is a clear need for new selective and potent GPR55 modulators. This review will address a current structural update of GPR55 ligands.

摘要

G蛋白偶联受体55(GPR55)于1999年被发现。由于一些内源性、植物源性和合成大麻素配体作用于GPR55,它被提议作为内源性大麻素系统的一个新成员。然而,与GPR55激活相关的细胞下游信号通路的复杂性延迟了选择性GPR55配体的发现。直到几年前,制药公司和政府组织的文库高通量筛选才得以鉴定出选择性GPR55激动剂和拮抗剂。从那时起,已经报道了几种GPR55调节剂支架。GPR55在多种生理和病理过程中的相关性已被探索,揭示了其在炎症、神经性疼痛、骨骼生理、糖尿病和癌症中的作用。考虑到GPR55是一个新的有前景的治疗靶点,显然需要新的选择性和强效GPR55调节剂。本综述将阐述GPR55配体的当前结构更新情况。

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