Synthesis and Evaluation Biological Activity of Six Oxapentacyclo Derivatives on Gram Negative and Gram Postive Bacteria

Figueroa‐Valverde Lauro, D. Francisco, Rosas-Nexticapa Marcela, López-Ramos, Mária, Alvarez-Ramirez Magdalena, M. Virginia, Lopez Gutierrez, Tomáš
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引用次数: 0

Abstract

There are drugs such as cephalosporin, penicillins, aminoglycosides, quinolones for the treatment of infectious diseases; however, some of these drugs can produce bacterial resistance. This research aimed to synthesize six oxapentacyclo derivatives to evaluate their biological activity against some Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae using the minimum inhibitory concentration method. The results showed that the methods used in this study produce a good yield of each product. Furthermore, the chemical structure of compounds 2 to 7 was determined using 1H and 13C NMR spectroscopic techniques. Other data showed that only compounds 3 and 5 decreased the growth bacterial of Garam-negative and Gram-positive bacteria; these data suggest that compounds 3 and 5 could be considered good antibacterial agents against infectious diseases produced by Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae.
六种氧五环衍生物的合成及对革兰氏阴性和阳性细菌的生物活性评价
有治疗传染病的药物,如头孢菌素、青霉素类、氨基糖苷类、喹诺酮类;然而,其中一些药物会产生细菌耐药性。本研究旨在合成6种oxapentacyclo衍生物,采用最小抑制浓度法评价其对金黄色葡萄球菌、大肠杆菌、肺炎克雷伯菌和肺炎链球菌的生物活性。结果表明,本研究中采用的方法对每种产品的收率都很好。此外,化合物2 ~ 7的化学结构用1H和13C核磁共振技术确定。其他数据显示,只有化合物3和5能抑制garam阴性菌和革兰氏阳性菌的生长;这些数据表明,化合物3和5可以被认为是抗金黄色葡萄球菌、大肠杆菌、肺炎克雷伯菌和肺炎链球菌所产生的传染病的良好抗菌剂。
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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CiteScore
2.40
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0.00%
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