Discovery of the First Potent and Orally Efficacious Agonist of the Orphan G-Protein Coupled Receptor 119
Journal of Medicinal Chemistry2008Vol. 51(17), pp. 5172–5175
Citations Over TimeTop 10% of 2008 papers
Graeme Semple, Beatriz Fioravanti, Guilherme Rocha Pereira, Imelda Calderon, Jane Uy, Karoline Choi, Yifeng Xiong, Albert Ren, Michael Morgan, Vibha Davé, William Thomsen, David J. Unett, Charles Xing, Stuart Bossie, Christopher J. Carroll, Zhi‐Liang Chu, Andrew J. Grottick, Erin K. Hauser, James Leonard, Robert M. Jones
Abstract
GPR119 is a rhodopsin-like GPCR expressed in pancreatic beta-cells and incretin releasing cells in the GI tract. As with incretins, GPR119 increases 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.
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