首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antibacterial evaluation of novel 8-fluoro Norfloxacin derivatives as potential probes for methicillin and vancomycin-resistant Staphylococcus aureus.
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Synthesis and antibacterial evaluation of novel 8-fluoro Norfloxacin derivatives as potential probes for methicillin and vancomycin-resistant Staphylococcus aureus.

机译:新型8-氟诺氟沙星衍生物的合成和抗菌评估,作为耐甲氧西林和耐万古霉素的金黄色葡萄球菌的潜在探针。

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摘要

A series of novel 8-fluoro Norfloxacin derivatives and the hybrids of its piperazinyl derivatives incorporated with 1,3,5-triazine and pyrimidine were synthesized. All the above compounds were evaluated for their antibacterial activity against Klebsiella pneumoniae, methicillin-resistant Staphylococcus aureus and methicillin & vancomycin-resistant S. aureus. Among all, compounds having Morpholine, N-methyl/phenyl/benzyl/pyrimidinyl piperazines and n-butylamine substitution at C-7 position, have shown increased potency in comparison to norfloxacin and ciprofloxacin.
机译:合成了一系列新型的8-氟诺氟沙星衍生物及其哌嗪基衍生物与1,3,5-三嗪和嘧啶的杂化物。评价上述所有化合物对肺炎克雷伯菌,耐甲氧西林的金黄色葡萄球菌和耐甲氧西林和万古霉素的金黄色葡萄球菌的抗菌活性。在所有化合物中,与诺氟沙星和环丙沙星相比,在C-7位具有吗啉,N-甲基/苯基/苄基/嘧啶基哌嗪和正丁胺取代的化合物显示出更高的效价。

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