首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, biological evaluation and 2D-QSAR analysis of benzoxazoles as antimicrobial agents.
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Synthesis, biological evaluation and 2D-QSAR analysis of benzoxazoles as antimicrobial agents.

机译:苯并恶唑类抗菌剂的合成,生物学评估和2D-QSAR分析。

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摘要

A new series of 5(or 6)-nitro/amino-2-(substituted phenyl/benzyl)benzoxazole derivatives were synthesized and evaluated for antibacterial and antifungal activities against Staphylococcus aureus, Bacillus subtilis, Klebsiella pneumoniae, Pseudomonas aeruginosa, Escherichia coli, Candida albicans and their drug-resistant isolate. Microbiological results indicated that the synthesized compounds possessed a broad spectrum of activity against the tested microorganisms at MIC values between > 400 and 12.5 microg/ml. The results against B. subtilis, P. aeruginosa, drug-resistant B. subtilis, drug-resistant E. coli, and C. albicans isolate for these kinds of structures are quite encouraging. The 2D-QSAR analysis of a set of newly and previously synthesized benzoxazoles tested for growth inhibitory activity against B. subtilis ATCC 6633 was performed by using the multivariable regression analysis. The activity contributions for substituent effects of these compounds were determined from the correlation equationfor predictions of the lead optimization.
机译:合成了一系列新的5(或6)-硝基/氨基-2-(取代的苯基/苄基)苯并恶唑衍生物,并评估了其对金黄色葡萄球菌,枯草芽孢杆菌,肺炎克雷伯菌,铜绿假单胞菌,大肠杆菌,念珠菌的抗菌和抗真菌活性。白色念珠菌及其耐药分离株。微生物学结果表明,所合成的化合物在MIC值> 400至12.5 microg / ml时,具有针对被测微生物的广谱活性。针对这些结构针对枯草芽孢杆菌,铜绿假单胞菌,耐药枯草芽孢杆菌,耐药大肠杆菌和白色念珠菌分离株的结果令人鼓舞。使用多变量回归分析对一组新的和先前合成的苯并恶唑进行了2D-QSAR分析,测试了其对枯草芽孢杆菌ATCC 6633的生长抑制活性。这些化合物对取代基效应的活性贡献是通过相关方程确定的,以预测铅的最优化。

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