| Literature DB >> 33965860 |
Assem H Eldeeb1, Mahmoud F Abo-Ashour2, Andrea Angeli3, Alessandro Bonardi4, Deena S Lasheen5, Eman Z Elrazaz5, Alessio Nocentini4, Paola Gratteri6, Hatem A Abdel-Aziz7, Claudiu T Supuran8.
Abstract
New series of benzenesulfonamide and benzoic acid derivatives were designed and synthesized using tail/dual tail approach to improve potency and selectivity as carbonic anhydrase inhibitors. The synthesized compounds evaluated as CAIs against isoforms hCA I, II, IV and IX with acetazolamide (AAZ) as standard inhibitor. The benzenesulfonamide derivatives 7a-d, 8a-h, 12a-c, 13a and 15a-c showed moderate to potent inhibitory activity with selectivity toward isoform hCA II, especially, compound 13a with (Ki = 7.6 nM), while the benzoic acid analogues 12d-f, 13b and 15d-f didn't show any activity except compounds 12d,f and 15e that showed weak activity. Additionally, molecular docking was performed for compounds 7a, 8a, 8e, 12a, 13a and 15a on isoform hCA I, II to illustrate the possible interaction with the active site to justify the inhibitory activity.Entities:
Keywords: Benzenesulfonamides; Carbonic anhydrase inhibitors; Dual tail approaches; Molecular docking; Synthesis; Tail approaches
Year: 2021 PMID: 33965860 DOI: 10.1016/j.ejmech.2021.113486
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514