Design, Synthesis, Antimicrobial Evaluation of Novel 2-Oxo-4-substituted Aryl-Azetidine Benzotriazole Derivatives.
Chemistry & biodiversity(2023)
摘要
A series of compounds was synthesized and characterized to explore new antimicrobial agents. These compounds were evaluated by using the agar cup plate method. The most active compound exhibited a zone of inhibition 18 & PLUSMN;0.09 mm and 19 & PLUSMN;0.09 mm against E. Coli and S. aureus, respectively. To gain insights into the intermolecular interactions, molecular docking studies were performed at the active site of the glucosamine fructose 6 phosphate synthase (GlcN 6 p) enzyme (PDB Id: 1XFF). The results of the molecular docking studies are in agreement with the pharmacological evaluation with potent compounds, exhibiting docking scores of -11.2. However, deformability, B-factor and covariance computations showed a result that the most active compound favored molecular connections with the protein. Therefore, our research is important for the development of antimicrobial agents
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关键词
benzotriazole,azetidine,microwave,molecular docking,antimicrobial activity
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