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A facile one pot synthesis of novel pyrimidine derivatives of 1,5-benzodiazepines via domino reaction and their antibacterial evaluation

机译:通过多米诺反应和抗菌评估,容易罐合成1,5-苯并二氮杂卓的新嘧啶衍生物及其抗菌评估

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摘要

A new series of pyrimidine (8, 14, 18 and 23) embellished analogues of 1,5-benzodiazepines were synthesized by the one-pot domino approach using the catalyst DABCO (1,4-diazabicyclo [2.2.2]octane). For each compound synthesized, anti-microbial efficacy was determined using broth microdilution assay and half maximal inhibitory concentration (IC50). Furthermore, FESEM (Field emission scanning electron microscope) studies were also carried out to observe the effect of the structure of test compounds on the morphology of both Gram-positive (S. aureus) and Gram-negative (E. coli) cell walls. The leakage of nucleotides and their integral components from compromised bacterial cells was assessed by plotting the optical density (OD) with respect to time of exposure at 320 nm. Anti-bacterial studies revealed that compound 23 was most active against targeted bacterial species. Results of the antibacterial study indicated that all the test compounds possess significant antibacterial potential against targeted bacterial strains. Amongst all, in the FE-SEM study, compound 23 caused marked alteration in bacterial cell morphology and resulted in maximum leakage of cell nucleotides in bacterial strains as compared to controls. Further efforts are required to establish their efficacy as antibacterial agents in clinical management.
机译:通过使用催化剂Dabco(1,4-二氮杂双环[2.2.2]辛烷值)通过单壶Domino方法合成1,5-苯二氮藻的新一系列嘧啶(8,14,18和23)缀饰的类似物。对于合成的每种化合物,使用肉汤微量脱离测定和半最大抑制浓度(IC 50)测定抗微生物功效。此外,还进行了FeSEM(现场发射扫描电子显微镜)研究,以观察试验化合物结构对革兰阳性(S.UUREUS)和革兰氏阴性(大肠杆菌)细胞壁的形态的影响。通过在320nm处的暴露时间绘制光密度(OD)来评估核苷酸泄漏及其来自受损细菌细胞的整体组分。抗细菌研究表明,化合物23对靶向细菌物种最活跃。抗菌研究的结果表明,所有测试化合物都具有针对靶向细菌菌株的显着抗菌潜力。其中,在Fe-SEM研究中,化合物23导致细菌细胞形态的显着改变,并与对照相比,细菌菌株中的细胞核苷酸中的最大泄漏。进一步的努力需要在临床管理中确定它们作为抗菌剂的疗效。

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