ArticleFrontiers in chemistry2025
A novel thiazole-sulfonamide hybrid molecule as a promising dual tubulin/carbonic anhydrase IX inhibitor with anticancer activity.
Article in Frontiers in chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Article
- Design, synthesis, and antiproliferative activity of novel thiazole-based derivatives as tubulin polymerization inhibitors targeting the colchicine binding site.RSC advances · 2026Article
- Review
- Discovery of a Novel Coumarin/Thiazole Chalcone Hybrid as a Potent Dual Inhibitor of Tubulin and Carbonic Anhydrases IX & XII with Promising Anti-Proliferative Activity.Molecules (Basel, Switzerland) · 2026Article
- Rapid Discovery of CD38 Inhibitor via DNA-Encoded Natural Product Library Screening.Molecules (Basel, Switzerland) · 2026Article
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Authors and funding
8 authors.
Funding
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Abstract
Introduction: Multitargeted anticancer agents can overcome resistance by simultaneously modulating key pathways. This study reports a novel thiazole -chalcone/sulfonamide hybrid (compound 7) designed to inhibit both tubulin polymerization and carbonic anhydrase IX (CA IX). Methods: Compound 7 was synthesized through a five-step sequence and characterized by NMR and elemental analysis. Its cytotoxicity was assessed against cancer (HT-29, A549, 786-O, MCF-7) and normal (WI-38) cell lines. Tubulin polymerization and CA isoform inhibition (I, II, IX, XII) were evaluated. Apoptosis induction was confirmed by measuring p53, Bax, Bcl-2, and caspases 3 and 9. Molecular docking, ADMET, and DFT studies supported mechanistic insights. Results and discussion: Compound 7 showed potent activity against HT-29 cells (IC
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