| Literature DB >> 18698756 |
Graeme Semple1, Beatriz Fioravanti, Guillherme Pereira, Imelda Calderon, Jane Uy, Karoline Choi, Yifeng Xiong, Albert Ren, Michael Morgan, Vibha Dave, William Thomsen, David J Unett, Charles Xing, Stuart Bossie, Chris 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.Entities:
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Year: 2008 PMID: 18698756 DOI: 10.1021/jm8006867
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446