首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis and antibacterial activity of 3-O-carbamoyl derivatives of 6,11-di-O-methylerythromycin A: a novel class of acylides.
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Synthesis and antibacterial activity of 3-O-carbamoyl derivatives of 6,11-di-O-methylerythromycin A: a novel class of acylides.

机译:6,11-二-O-甲基红霉素A的3-O-氨基甲酰基衍生物的合成及其抗菌活性:一类新的酰化物。

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摘要

A novel series of acylides, 3-O-carbamoyl derivatives of 6,11-di-O-methylerythromycin A, were synthesized and evaluated for their antibacterial activity. These compounds have significant antibacterial activity against gram-positive pathogens, including erythromycin-resistant but methicillin-susceptible Staphylococcus aureus, erythromycin-resistant and methicillin-resistant S. aureus, erythromycin-resistant Streptococcus pneumoniae, and gram-negative pathogens, such as Haemophilus influenzae. Among the derivatives tested, compounds 4p, 4r, 4w, 4x and 4z were found to have potent activity against most susceptible and resistant bacteria. Compound 4p exhibited excellent antibacterial activity in comparison to the others.
机译:合成了一系列新的酰化物,即6,11-二-O-甲基红霉素A的3-O-氨基甲酰基衍生物,并对其抗菌活性进行了评估。这些化合物对革兰氏阳性病原体具有显着的抗菌活性,这些病原体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肺炎链球菌和革兰氏阴性病原体,例如嗜血杆菌。在测试的衍生物中,发现化合物4p,4r,4w,4x和4z对大多数易感和耐药细菌具有有效的活性。与其他化合物相比,化合物4p具有出色的抗菌活性。

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