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N -Acylsulfonamide: a valuable moiety to design new sulfa drug analogues.

Authors :
Amador R
Tahrioui A
Barreau M
Lesouhaitier O
Smietana M
Clavé G
Source :
RSC medicinal chemistry [RSC Med Chem] 2023 Jul 04; Vol. 14 (8), pp. 1567-1571. Date of Electronic Publication: 2023 Jul 04 (Print Publication: 2023).
Publication Year :
2023

Abstract

Sulfonamides are the oldest class of antibiotics, discovered more than 80 years ago. They are still used today despite the appearance of drug resistance phenomena that limit their prescription. Since the discovery and use of the first sulfa drugs, many analogues have been synthesized in order to obtain new active molecules able to circumvent bacterial resistance. Structurally similar to sulfonamide, the N -acylsulfonamide group arouses interest in the field of medicinal chemistry due to specific physico-chemical properties. We report here the synthesis and antibacterial/antibiofilm activities of 18 sulfa drug analogues with an N -acylsulfonamide moiety. These derivatives were obtained efficiently by sulfo-click reactions between readily available thioacid and sulfonyl azide synthons.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2632-8682
Volume :
14
Issue :
8
Database :
MEDLINE
Journal :
RSC medicinal chemistry
Publication Type :
Academic Journal
Accession number :
37593573
Full Text :
https://doi.org/10.1039/d3md00229b