Back to Search
Start Over
Design, synthesis and biological evaluation of triazole, sulfonamide and sulfonyl urea derivatives of N-acylhomoserine lactone as quorum sensing inhibitors.
- Source :
-
Journal of Molecular Structure . Jan2024:Part 1, Vol. 1295, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- • A novel series of triazole, sulfonamide and sulfonyl urea derivatives of N -acylhomoserine lactones (HSL) have been prepared. • These novel molecules were screened against Chromobacterium violaceum ATCC 12472 for their quorum sensing inhibitory (QSI) activity. • Among them, compounds 6, 7 and 14 showed comparable antibacterial activities with reference to penicillin and streptomycin as 37.5 µg/mL, while compounds 7, 13 and 17 exhibited promising QSI activity. Triazole, sulfonamide and sulfonyl urea derivatives of N -acylhomoserine lactones (AHLs) have been prepared from homoserine lactone hydrobromide which in turn is derived from l -methionine. The molecules were screened against Chromobacterium violaceum ATCC 12472 for their quorum sensing inhibitory (QSI) activity. Among them, compounds 6, 7 and 14 were exhibited comparable antibacterial activities with reference to penicillin and streptomycin as 37.5 µg/mL, while compounds 7, 13 and 17 exhibited promising QSI activity. These compounds represent a synthetically accessible class of AHL analogs could find utility to improve their potency. [Display omitted] [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00222860
- Volume :
- 1295
- Database :
- Academic Search Index
- Journal :
- Journal of Molecular Structure
- Publication Type :
- Academic Journal
- Accession number :
- 173118134
- Full Text :
- https://doi.org/10.1016/j.molstruc.2023.136547