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• W4321498722 abstract "Abstract The effectiveness of treating bacterial infections is seriously threatened by the emergence of bacterial resistance to chemical treatment. Growth of microbes in biofilm is one of the main causes of resistance to antimicrobial drugs. Quorum sensing (QS) inhibition, which targets the QS signalling system by obstructing cell‐cell communication, was developed as an alternative treatment by creating innovative anti‐biofilm drugs. Therefore, the goal of this study is to develop novel antimicrobial drugs that are effective against Pseudomonas aeruginosa by inhibiting QS and acting as anti‐biofilm agents. In this study, N ‐(2‐ and 3‐pyridinyl)benzamide derivatives were selected to design and syntheses. Antibiofilm activity was revealed by all the synthesized compounds and the biofilm was visibly impaired, and the OD 595nm readings of solubilized biofilm cells presented a momentous difference between the treated and untreated biofilms. The best anti‐QS zone was observed for compound 5d and found to be 4.96 mm. Through in silico research, the physicochemical characteristics and binding manner of these produced compounds were examined. For the purpose of understanding the stability of the protein and ligand complex, molecular dynamic simulation was also carried out. The overall findings showed that N ‐(2‐ and 3‐pyridinyl)benzamide derivatives could be the key to creating effective newer anti‐quorum sensing drugs that are effective against different bacteria." @default.
• W4321498722 created "2023-02-23" @default.
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• W4321498722 date "2023-02-21" @default.
• W4321498722 modified "2023-10-16" @default.
• W4321498722 title "Synthesis, Biological Evaluation and <i>in Silico</i> Study of <i>N</i>‐(2‐ and 3‐Pyridinyl)benzamide Derivatives as Quorum Sensing Inhibitors against <i>Pseudomonas aeruginosa</i>" @default.
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• W4321498722 doi "https://doi.org/10.1002/cbdv.202201191" @default.
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• W4321498722 hasPublicationYear "2023" @default.
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