| Literature DB >> 27560285 |
Gang Li1, Yi Huan1, Baokun Yuan1, Jin Wang1, Qian Jiang1, Ziyun Lin1, Zhufang Shen2, Haihong Huang3.
Abstract
A series of xanthine derivatives as potent dual ligands targeting DPP-IV and GPR119 was discovered through an approach of the merged pharmacophores of GPR119 agonists and DPP-IV inhibitor linagliptin. Systematic optimization of general structure 5 led to the identification of compound 20i with selective DPP-IV inhibition, good GPR119 agonism activity and favorable metabolic stability. Docking study was performed to elucidate the potent DPP-IV inhibition of 20i. Compound 20i may serve as a tool compound for further design of anti-diabetic drugs targeting both DPP-IV and GPR119.Entities:
Keywords: DPP-IV; Dual ligands; GPR119; Merged pharmacophores; Xanthine derivatives
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Year: 2016 PMID: 27560285 DOI: 10.1016/j.ejmech.2016.08.023
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514