Design, synthesis and
larvicidal
activity of novel imidazo[2,1‐
b
][1,3,4]thiadiazole carboxamides against
Anopheles arabiensis
Indasi J Gopikumar, Michelyne Haroun, Komala Pandurangan, Arnab Dutta, Deepak Chopra, Raquel M Gleiser, Christophe Tratrat, Subramanya Hegde, Sreeharsha Nagaraja, Mahesh Attimarad, Anroop B Nair, Mohamed A Morsy, Katharigatta N Venugopala, Pran Kishore Deb Abstract
BACKGROUND
Widespread resistance among malaria vectors to conventional insecticides, coupled with the limited availability of insecticides with novel mechanisms of action, necessitates the discovery of new chemical scaffolds for vector control. Anopheles arabiensis is an important malaria vector in sub‐Saharan Africa and poses additional control challenges due to its behavioral adaptability and rising insecticide resistance. This study aimed to design, synthesize, characterize, and evaluate novel 6‐(4‐substituted phenyl)imidazo[2,1‐ b ][1,3,4]thiadiazole‐2‐carboxamide derivatives ( 6a–6i ) as potential larvicidal agents.
RESULTS
Novel derivatives were synthesized and evaluated against third‐instar
A. arabiensis
larvae. At 4 μg/
CONCLUSION
The findings identify imidazo[2,1‐ b ][1,3,4]thiadiazole as a promising scaffold for developing new larvicidal chemotypes. Compound 6e represents the most promising lead and provides a basis for further optimization and validation of this scaffold for innovative malaria‐vector control strategies. © 2026 Society of Chemical Industry.