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A series of new potentially multi-targeting antimicrobial naphthalimide-derived fluconazole analogs were designed and conveniently synthesized from 4-bromonaphthalic anhydride.Their structures were characterized by 1H NMR,13C NMR and HRMS spectra.Bioactivity assays revealed that some prepared compounds exhibited significantly inhibitory efficiencies towards bacteria and fungi.Remarkably,the derivative 11e could effectively inhibit the growth of Acinetobacter baumannii with MIC value of 0.013 μmol/L.