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首页> 外文期刊>The Journal of Antibiotics: An International Journal >Synthesis and antibacterial activity of novel 4″-carbamates of 6,11-di-O-methylerythromycin A
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Synthesis and antibacterial activity of novel 4″-carbamates of 6,11-di-O-methylerythromycin A

机译:6,11-二-O-甲基红霉素A的新型4″-氨基甲酸酯的合成及抑菌活性

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摘要

A novel series of 4-carbamates of 6,11-di-O-methylerythromycin A were synthesized and evaluated. These compounds have significant antibacterial activity against Gram-positive pathogens, including erythromycin-resistant but methicillin-susceptible Staphylococcus aureus, erythromycin-resistant and methicillin-resistant Staphylococcus aureus, erythromycin-resistant Streptococcus pneumoniae and Gram-negative pathogens, such as Haemophilus influenzae To our surprise, most of the derivatives tested had potent activity against most resistant bacteria. Among these, compounds 10u, 10v, 10w and 10y were found to have potent activity against most susceptible and resistant bacteria. In particular, compound 10y exhibited excellent antibacterial activity in comparison to others.
机译:合成并评估了一系列新颖的6,11-二-O-甲基红霉素A的4-氨基甲酸酯。这些化合物对革兰氏阳性病原体具有显着的抗菌活性,包括耐红霉素但对甲氧西林敏感的金黄色葡萄球菌,耐红霉素和耐甲氧西林的金黄色葡萄球菌,耐红霉素的肺炎链球菌和革兰氏阴性嗜血杆菌病原体,例如令人惊讶的是,测试的大多数衍生物对大多数抗性细菌都具有有效的活性。在这些化合物中,发现化合物10u,10v,10w和10y具有针对大多数易感和耐药细菌的有效活性。特别地,与其他化合物相比,化合物10y表现出优异的抗菌活性。

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