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Synthesis of Some 1,5-Benzodiazepine Derivatives as a New Class of Antimicrobial Agents

机译:某些1,5-苯二氮卓类衍生物的合成作为一类新型的抗菌剂

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摘要

A series of ceric ammonium nitrate promoted 1,5-benzodiazapine derivatives(A-K)were synthesised and characterized by IR,~1H/~(13)C NMR,mass and elemental analysis.The in vitro antibacterial and antifungal activities of the compounds were evaluated by paper disc diffusion method.The minimum inhibitory concentration(MIC)of the compounds was also determined by agar streak dilution method.Compound E was found to exhibit the most potent in vitro antimicrobial activity with MIC of 1.2,1.2,1.3,1.2,3.2 and >100 mu g mL~(-1)against B.subtilis,P.vulgaris,K.pneumoniae,P.aeruginosa,Candida albicans.
机译:通过IR,〜1H /〜(13)C NMR,质谱和元素分析等方法合成了一系列硝酸铈铵促进的1,5-苯二氮杂卓衍生物(AK),并对其体外抗菌活性进行了评价。通过纸片扩散法测定化合物的最小抑菌浓度(MIC)。琼脂条纹稀释法测定化合物E的体外抑菌活性。MIC为1.2、1.2、1.3、1.2、3.2和> 100μg mL〜(-1)的抗枯草芽孢杆菌,寻常型假单胞菌,肺炎克雷伯菌,铜绿假单胞菌和白色念珠菌。

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