Design, synthesis, and exploration of antibacterial activity of 6H-1,2-oxazin-6-ones.

ABSTRACT: This study reports the in silico design of 30 6H-1,2-oxazin-6-ones against DHFR and PTC antimicrobial targets. Docking compounds 1, 3, 4, 6, and 8 with both enzymes was favorable, outperforming Trimethoprim with DHFR. Therefore, 12 6H-1,2-oxazin-6-ones, including the most promising compounds, were synthesized through an aminolysis reaction of β-cyanoketones with hydroxylamine hydrochloride, obtaining moderate to high yields (55-88%). Subsequently, antibacterial studies were conducted against five bacteria: four Gram-positive MRSA (ATCC 43300 and three clinical isolates) and one Gram-negative (E. coli ATCC 25922). Compounds 1, 2, 3, 4, 6, and 8 inhibited bacterial growth with MIC values ranging from 3.125 to 200 μg mL^-1. Compound 1 showed better activi

SUBMITTER: Alcantar-Zavala E 

PROVIDER: S-EPMC11285021 | biostudies-literature | 2024 Jul

REPOSITORIES: biostudies-literature