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Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119

机译:发现孤儿G蛋白偶联受体119的第一种有效和口服有效的激动剂

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摘要

GPR119 is a rhodopsin-like GPCR expressed in pancreatic beta-cells and incretin releasing cells in the GI tract. As with incretins, GPR119 increase,; cAMP levels in these cell types. thus making it a highly attractive potential target for the treatment of diabetes. The discovery of the first reported potent agonist of GPR119, 2-fluoro-4-methanesulfonyl-phenyl)-{6-[4-(3-isopropyl-[1,2,4]oxadiazol-5-yl)-piperidin-1-yl]-5-nitro-pyrimidin-4-yl}-amine (8g, AR231453), is described starting from an initial inverse agonist screening hit. Compound 8g showed in vivo activity in rodents and was active in an oral glucose tolerance test in mice following oral administration.
机译:GPR119是在胃肠道中的胰岛β细胞和肠降血糖素释放细胞中表达的视紫红质样GPCR。与肠降血糖素一样,GPR119增加;这些细胞类型中的cAMP水平。因此使其成为治疗糖尿病的极具吸引力的潜在目标。 GPR119的第一个有效激动剂,2-氟-4-甲磺酰基-苯基)-{6- [4-(3-异丙基-[1,2,4]恶二唑-5-基]-哌啶-1]的发现从最初的反向激动剂筛选命中开始描述-(yl)-5-硝基-嘧啶-4-基}-胺(8g,AR231453)。化合物8g在啮齿动物中显示出体内活性,并且在口服后在小鼠的口服葡萄糖耐量试验中具有活性。

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