Abstract:
A series of novel pyrano2, 3-dtrizaole compounds were synthesized and their
α-glucosidase inhibitory activities were evaluated by
in vitro enzyme assay. The experimental data demonstrated that compound
10f showed up to 10-fold higher inhibition (IC
50 74.0 ± 1.3 μmol·L
−1) than acarbose. The molecular docking revealed that compound
10f could bind to
α-glucosidase
via the hydrophobic,
π-π stacking, and hydrogen bonding interactions. The results may benefit further structural modifications to find new and potent
α-glucosidase inhibitors.