Hybrid Antibiotics Based on Azithromycin and Glycopeptides: Synthesis and Antibacterial Activity.

Q4 Medicine
Antibiotiki i Khimioterapiya Pub Date : 2016-01-01
S S Printsevskaya, A M Korolev, E B Isakova, E P Mirchink, A N Tevyashova
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引用次数: 0

Abstract

A series of hybrid antibiotics on the basis of azithromycin and glycopeptides with the glycopeptide molecule attached via the aminoalkylcarbamoyl spacer to 11-position of the macrolide was synthesized. All the synthesized compounds demonstrated equal or superior to azithromycin and vancomycin antibacterial activity against 7 tested strains of grampositive bacteria. The new hybrid antibiotics were more active than azithromycin or vancomycin against S.pneumoniae ATCC 49619. Some of the compounds were active against E.faecium and E.faecalis strains resistant to vancomycin.

阿奇霉素与糖肽类混合抗生素的合成及抗菌活性研究。
以阿奇霉素和糖肽为基础合成了一系列杂化抗生素,糖肽分子通过氨基烷基氨甲酰间隔基团连接到大环内酯的11位。所有化合物对7株革兰氏阳性菌的抑菌活性均优于或等于阿奇霉素和万古霉素。新型杂交抗生素对肺炎链球菌ATCC 49619的活性高于阿奇霉素和万古霉素。部分化合物对耐万古霉素的粪肠杆菌和粪肠杆菌有活性。
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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来源期刊
Antibiotiki i Khimioterapiya
Antibiotiki i Khimioterapiya Medicine-Infectious Diseases
CiteScore
0.80
自引率
0.00%
发文量
46
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