内大麻素系统
大麻素受体
药物发现
大麻素受体拮抗剂
大麻素
大麻素受体激动剂
合成大麻素
G蛋白偶联受体
药理学
利莫那班
神经科学
化学
生物
受体
信号转导
生物信息学
细胞生物学
生物化学
兴奋剂
作者
Paula Morales,Nadine Jagerovic
标识
DOI:10.2174/0929867323666160425113836
摘要
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. Keywords: Agonist, Antagonist, Cannabinoid, Endocannabinoid, GPCR, GPR55, Structure.
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