Abstract
GPR119 is increasingly seen as an attractive target for the treatment of type II diabetes and other elements of the metabolic syndrome. During a programme aimed at developing agonists of the GPR119 receptor, we identified compounds that were potent with reduced hERG liabilities, that had good pharmacokinetic properties and that displayed excellent glucose-lowering effects in vivo. However, further profiling in a GPR119 knock-out (KO) mouse model revealed that the biological effects were not exclusively due to GPR119 agonism, highlighting the value of transgenic animals in drug discovery programs.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
-
Administration, Oral
-
Animals
-
Diabetes Mellitus, Experimental / drug therapy
-
Drug Evaluation, Preclinical
-
ERG1 Potassium Channel
-
Ether-A-Go-Go Potassium Channels / metabolism
-
Humans
-
Hypoglycemic Agents / chemistry*
-
Hypoglycemic Agents / pharmacokinetics
-
Hypoglycemic Agents / therapeutic use
-
Mice
-
Mice, Inbred C57BL
-
Mice, Knockout
-
Receptors, G-Protein-Coupled / agonists*
-
Receptors, G-Protein-Coupled / deficiency
-
Receptors, G-Protein-Coupled / genetics
-
Receptors, G-Protein-Coupled / metabolism
-
Structure-Activity Relationship
Substances
-
ERG1 Potassium Channel
-
Ether-A-Go-Go Potassium Channels
-
GPR119 protein, human
-
Gpr119 protein, mouse
-
Hypoglycemic Agents
-
KCNH2 protein, human
-
Receptors, G-Protein-Coupled