G蛋白偶联受体
敌手
受体
药理学
免疫系统
药物发现
小分子
发病机制
受体拮抗剂
医学
化学
生物
免疫学
生物信息学
内科学
生物化学
作者
Michiko Murakoshi,Harumi Kuwabara,Masaru Nagasaki,Yu Mei Xiong,Jeff D. Reagan,Hiroaki Maeda,Futoshi Nara
标识
DOI:10.1080/10799893.2016.1247861
摘要
GPR142 is a G-protein-coupled receptor (GPCR), whose most potent and efficacious ligand has been reported as being the natural amino acid l-tryptophan. GPR142 is highly expressed in pancreatic β-cells and immune cells, suggesting the receptor may play a role in the pathogenesis and development of diabetes or inflammatory diseases. In a previous report, we developed GPR142 agonists as insulin secretagogues. In this report, we show the discovery of a selective, potent small-molecule GPR142 antagonist, CLP-3094, and its pharmacological characteristics. These data support targeting this receptor for the treatment of chronic inflammatory diseases.
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