| Literature DB >> 28656523 |
Jinying Chen1, Zitai Sang2, Lu Li3, Linhong He2, Liang Ma2.
Abstract
A series of fused-pyrimidine derivatives were prepared and evaluated for their agonistic activities against human GPR119. Compound 9i showed high potent agonistic activity against HEK293T cells over-expressing human GPR119 and improved glucose tolerance in dose-dependent manner, as well as promoted insulin secretion. In a DIO mice model, 9i also ameliorated the obese-related symptoms by decreasing the body weights without markedly changing food intake, normalized some serum biomarkers, such as ALT, AST, ALP, GLU, CHOL, HDL, and LDL, and exerted therapeutic activity on fat deposition in liver tissue. We consider 9i to have utility as a GPR119 agonists for the treatment of type 2 diabetes mellitus and obese-related symptoms.Entities:
Keywords: CAMP; GPR119 agonists; OGTT; Obesity; Type II diabetes
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Year: 2017 PMID: 28656523 DOI: 10.1007/s11030-017-9755-6
Source DB: PubMed Journal: Mol Divers ISSN: 1381-1991 Impact factor: 2.943