Biological Evaluation of Pyrrolo [3, 2-d] pyrimidine Derivatives as Antibacterial Agents against Pathogenic Bacteria

Maryam Kouhkan, Ramin Javahershenas, J. Khalafy
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Abstract

Background: Pyrimidine molecules' biological and chemotherapeutic importance in the medicinal world has been overlooked in many reports. We have previously synthesized new series of pyrrolo [3,2-d]pyrimidine derivatives (4a-4f) and here, we evaluate the antibacterial activity of these derivatives against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and Salmonella bacteria. Materials and Methods: The agar well diffusion and agar dilution methods were used for determining inhibition zone diameter and minimum inhibitory concentration during preliminary evaluation of antimicrobial activity against gram-positive and gram-negative bacteria. Statistical analysis using Microsoft Excel 2010 was based on three independent experiments and the results were expressed as mean. Results: Some of the synthesized compounds exhibited antibacterial activity against the tested bacteria. Conclusion: Our findings indicate the antibacterial potential of the six novel synthetic pyrrolo[3,2-d]pyrimidine compounds.
吡咯[3,2 -d]嘧啶衍生物抗菌病原菌的生物学评价
背景:嘧啶分子在医学上的生物学和化学治疗的重要性在许多报道中被忽视。我们已经合成了一系列新的吡咯[3,2-d]嘧啶衍生物(4a-4f),在这里,我们评估了这些衍生物对金黄色葡萄球菌、铜绿假单胞菌、大肠杆菌和沙门氏菌的抑菌活性。材料与方法:采用琼脂孔扩散法和琼脂稀释法测定抑菌带直径和最小抑菌浓度,初步评价其对革兰氏阳性菌和革兰氏阴性菌的抑菌活性。3次独立实验采用Microsoft Excel 2010进行统计分析,结果以均数表示。结果:部分合成的化合物对实验细菌具有抑菌活性。结论:6个新型合成吡咯[3,2-d]嘧啶类化合物具有抗菌潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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