Abstract
A series of novel benzimidazole-based 1,3,4-oxadiazole-1,2,3-triazole conjugates has been synthesized and evaluated for GSK-3 beta inhibitory activity in vitro. Compounds 7q, 7b, 7e and 7n exhibited significant inhibition with sub-micromolar IC50 values (0.15, 0.27, 0.32 and 0.39 mu M respectively) and were examined further for antidepressant activity by forced swim test (FST) and tail suspension test (TST) models in Wistar rats. In both TST and FST models, all the test compounds were found to significantly reduce the immobility time period (displaying antidepressant-like activity) in comparison to a normal saline treated control group. Compound 7q was found to be the most active. Molecular docking studies of the active compounds 7q, 7b, 7e and 7n were also performed against GSK-3 beta to gain an understanding of their binding interactions.