Quercetin/oleic acid-based G-protein-coupled receptor 40 ligands as new insulin secretion modulators

Future Med Chem. 2017 Oct;9(16):1873-1885. doi: 10.4155/fmc-2017-0113. Epub 2017 Oct 24.

Abstract

Aim: Management of Type 2 diabetes mellitus by diet is achievable at the early stage of the disease; patients usually underestimate this approach and an appropriate drug therapy is required.

Results: Starting from quercetin and oleic acid, that have effect on insulin secretion, a small set of hybrid molecules was synthesized. Insulin secretion was evaluated in both in vitro and ex vivo models. AV1 was able to enhance insulin secretion dose dependently, behaving as a conceivable agonist of G-protein-coupled receptor 40.

Conclusion: AV1 represents an interesting tool that interacts with G-protein-coupled receptor 40. Further studies will be carried out to evaluate the exact binding mode, and also to enlarge the library of these antidiabetic agents. [Formula: see text].

Keywords: GPR40 molecular docking; antidiabetic drugs; insulin secretion; quercetin/oleic acid-based hybrid molecules.

MeSH terms

  • Animals
  • Benzopyrans / chemical synthesis*
  • Benzopyrans / chemistry
  • Benzopyrans / pharmacology
  • Cell Line
  • Computer Simulation
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Humans
  • Hypoglycemic Agents / chemical synthesis*
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / pharmacology
  • Insulin / pharmacology*
  • Ligands
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Oleic Acid / chemistry*
  • Pancreas / drug effects
  • Quercetin / chemistry*
  • Receptors, G-Protein-Coupled / metabolism*

Substances

  • Benzopyrans
  • Hypoglycemic Agents
  • Insulin
  • Ligands
  • Receptors, G-Protein-Coupled
  • Oleic Acid
  • Quercetin