Novel 5-alkenylthiothiazolidinone scaffold discovery as Multi-Chitinases inhibitors to arrest the molting of Asian corn borer

Abstract

Chitinases are crucial enzymes in insect growth and development processes and have thus become potential targets for the control of insect pests. Rhodanine (5-alkenylthiothiazolidinone) is an important fragment with various biological activities in agriculture. Therefore, 24 novel 5-alkenylthiothiazolidinone derivatives were designed and synthesized by introducing a hydrophobic hydrocarbon chain and a benzylformamide group on the basis of the conserved binding cavity of three chitinases, OfChtI, OfChtII and OfChi-h. These 5-alkenylthiothiazolidinone analogs were found for the first time to have inhibitory effects on OfChtII, except for their ability to inhibit the other two known chitinases, OfChtI and OfChi-h. The inhibitory activities of the target compounds against OfChtI and OfChi-h ranged from 40 % to 95 % at a concentration of 100 μM. In particular, some compounds were also found to have an inhibitory rate of 50 % against OfChtII. Among them, the Ki values of the most potent compound 5e-9 were 5.82, 27.5 and 6.77 μM against OfChtI, OfChtII and OfChi-h, respectively. The inhibition mechanism studies revealed that both π stacking interactions and hydrophobic interactions were vital for the binding of Compound 5e-9 with the three chitinases. A lethal and sublethal bioassay study revealed that Compound 5e-9 could affect the growth and development of Asian corn borers. This work suggested that 5-alkenylthiothiazolidinone could be a novel inhibitor scaffold against multichitinase for the development of insect growth regulators.