Novel benzenesulfonamide derivatives as larvicidal and antibacterial agents: insights from histopathological studies, molecular docking, and ADMET profiling.

Authors

Ahmed Abdou O Abeed, Mustafa A Fawzy, Fatma El-Zahraa A Abd El-Aziz, Heba Alsharif, Tarek H Afifi, Mohey Eldin H Shikhoun, Hanan A Ahmed, Eman S Nossier, Fawzya N M Kishk

Published in

3 Biotech. Volume 16. Issue 10. Pages 450. Epub Sep 27, 2026.

Abstract

Novel benzenesulfonamide derivatives 2-5 were synthesized via base-catalyzed Claisen-Schmidt condensation and comprehensively evaluated for dual larvicidal efficacy against Wohlfahrtia magnifica and antibacterial activity against multidrug-resistant pathogens. Evaluation against W. magnifica larvae revealed that the thienyl-pyrazole-hybridized 5 exhibited the highest larvicidal potency, driving cumulative mortality to ~92% by day 4 at a concentration of 25 mg/g. Histopathological and ultrastructural analyses confirmed that the treatments caused extensive cuticular breakdown, myofibril fragmentation, severe mitochondrial swelling, and a progressive depletion of the collagen-like extracellular matrix from ~80% down to below 15%. Acridine orange fluorescence staining corroborated treatment-dependent apoptotic nuclear condensation and fragmentation. In antibacterial screenings, the pyrrolidine-pyrazole hybrid 2 exhibited selective, dose-dependent growth inhibition against Gram-negative Klebsiella pneumoniae (inhibition zones: 15-28 mm; MIC: 10 mg/mL) and Escherichia coli (inhibition zones: 9-16 mm; MIC: 25 mg/mL), while showing no activity against Gram-positive Staphylococcus aureus. Scanning electron microscopy (SEM) verified outstanding cell envelope rupture and structural collapse in treated bacteria. In vitro enzyme assays established that compound 2 significantly inhibited E. coli DNA gyrase B (IC₅₀ = 3.188 ± 0.11 µM) and topoisomerase IV (IC₅₀ = 14.288 ± 1.25 µM). Molecular docking simulations demonstrated strong target binding poses within respective ATP-binding cavities with docking scores of -10.88 and -9.98 kcal/mol. In silico ADMET profiling indicated good oral bioavailability, a high human intestinal absorption rate of 94.87%, and a favorable drug-likeness safety window. These quantitative findings identify compound 5 as a potent larvicidal agent and compound 2 as a highly promising multi-target antibacterial lead template for managing resistant Gram-negative infections.
The online version contains supplementary material available at https://doi.org/10.1007/s13205-026-05060-y.

PMID:
42802721
Bibliographic data and abstract were imported from PubMed on 28 Sep 2026.

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