Journal of Medicinal Chemistry · 2008 · 142 citations · 8 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryMolecular PharmacologySignal TransductionG Protein-coupled Receptor SignalingGastrointestinal PharmacologyIncretin-based TherapiesLigand BindingReceptor PharmacologyAgonist ActivityCamp SignalingIn Vivo StudiesIncretin BiologyIncretin HormonesIncretin PhysiologyIncretin SignalingOrphan G Protein-coupled Receptors
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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Jin Fu, Silvana Gaetani, Fariba Oveisi et al. · Nature · 2003 · 1.1K citations · Full text
Zhi‐Liang Chu, Christopher J. Carroll, Jean Alfonso et al. · Endocrinology · 2008 · 380 citations