Academic Journal
Diamide-based sulfonamide derivatives as new urease inhibitors: Synthesis, biological evaluation, and computational studies.
| Title: | Diamide-based sulfonamide derivatives as new urease inhibitors: Synthesis, biological evaluation, and computational studies. |
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| Authors: | Mohammadi Oshnari A; Chemistry and Chemical Engineering Research Center of Iran (CCERCI), P.O. Box 14335-186, Tehran, Iran., Mohammadi AA; Chemistry and Chemical Engineering Research Center of Iran (CCERCI), P.O. Box 14335-186, Tehran, Iran. Electronic address: aliamohammadi@yahoo.com., Ahmad I; Division of Computer-Aided Drug Design, Department of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, India; Department of Pharmaceutical Chemistry, Prof. Ravindra Nikam College of Pharmacy, Gondur, Dhule, 424002, Maharashtra, India., Ekhtiari Z; Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran., Tahmasebi E; Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran., Mohammadi-Khanaposhtani M; Pharmaceutical Sciences Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran., Amanlou M; Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran., Mahdavi M; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran. |
| Source: | Bioorganic chemistry [Bioorg Chem] 2026 Sep 15; Vol. 180, pp. 110240. Date of Electronic Publication: 2026 Jul 10. |
| Publication Type: | Journal Article |
| Language: | English |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 1303703 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1090-2120 (Electronic) Linking ISSN: 00452068 NLM ISO Abbreviation: Bioorg Chem Subsets: MEDLINE |
| Imprint Name(s): | Publication: Amsterdam : Elsevier Original Publication: New York, London, Academic Press. |
| MeSH Terms: | Urease*/antagonists & inhibitors , Urease*/metabolism , Sulfonamides*/chemistry , Sulfonamides*/pharmacology , Sulfonamides*/chemical synthesis , Enzyme Inhibitors*/chemical synthesis , Enzyme Inhibitors*/pharmacology , Enzyme Inhibitors*/chemistry, Structure-Activity Relationship ; Molecular Docking Simulation ; Molecular Structure ; Molecular Dynamics Simulation ; Dose-Response Relationship, Drug |
| Abstract: | Sulfonamide is a well-recognized bioactive functional group in medicinal chemistry that has gained significant attention owing to its broad application potential in this field. In this work, a new series of diamide-based sulfonamide derivatives, compounds 10a-g and 11a-e, was specifically designed as urease inhibitors and synthesized via the reaction of azlactone derivatives with 4-aminobenzenesulfonamide. The structures of the synthesized compounds were confirmed using 1H and 13C NMR spectroscopy, FT-IR spectroscopy, CHN elemental analysis, and LC-MS. Interestingly, all synthesized derivatives displayed outstanding urease inhibitory activity, with IC (Copyright © 2026. Published by Elsevier Inc.) |
| Competing Interests: | Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. |
| Contributed Indexing: | Keywords: Alum; Azlactone; Diamide; Sulfonamide; Urease |
| Substance Nomenclature: | EC 3.5.1.5 (Urease) 0 (Sulfonamides) 0 (Enzyme Inhibitors) |
| Entry Date(s): | Date Created: 20260714 Date Completed: 20260725 Latest Revision: 20260725 |
| Update Code: | 20260725 |
| DOI: | 10.1016/j.bioorg.2026.110240 |
| PMID: | 42447748 |
| Database: | MEDLINE |
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