Design, Synthesis, Molecular Docking, and Antibacterial Evaluation of Some Novel Flouroquinolone Derivatives as Potent Antibacterial Agent

<div>H-bond interactions between target protein 2XCT and studied compounds. Binding interaction of docked compound (<b>8g</b>) with topoisomerase II DNA gyrase enzymes.</div>

The Scientific World Journal

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Figure 2

Figure 2: Design, Synthesis, Molecular Docking, and Antibacterial Evaluation of Some Novel Flouroquinolone Derivatives as Potent Antibacterial Agent 