Abstract
Despite of many diverse biological activities exhibited by benzimidazole scaffold, it is rarely explored for the α-amylase inhibitory activity. For that purpose, 2-aryl benzimidazole derivatives 1–45 were synthesized and screened for in vitro α-amylase inhibitory activity. Structures of all synthetic compounds were deduced by various spectroscopic techniques. All compounds revealed inhibition potential with IC50 values of 1.48 ± 0.38–2.99 ± 0.14 μM, when compared to the standard acarbose (IC50 = 1.46 ± 0.26 μM). Limited SAR suggested that the variation in the inhibitory activities of the compounds are the result of different substitutions on aryl ring. In order to rationalize the binding interactions of most active compounds with the active site of α-amylase enzyme, in silico study was conducted.
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•2-Aryl benzimidazole derivatives 1–45 were synthesized.•Compounds were fully characterized by various spectroscopic techniques.•All compounds were evaluated for in vitro α-amylase inhibitory activity.•Limited structure-activity relationship was established.•Molecular docking was done to rationalize the binding interactions of most active compounds with the active site of enzyme.