Novel glycopeptide antibiotics:: N-alkylated derivatives active against vancomycin-resistant enterococci

被引:47
作者
Rodriguez, MJ [1 ]
Snyder, NJ [1 ]
Zweifel, MJ [1 ]
Wilkie, SC [1 ]
Stack, DR [1 ]
Cooper, RDG [1 ]
Nicas, TI [1 ]
Mullen, DL [1 ]
Butler, TF [1 ]
Thompson, RC [1 ]
机构
[1] Eli Lilly & Co, Lilly Res Labs, Infect Dis Res, Indianapolis, IN 46285 USA
关键词
D O I
10.7164/antibiotics.51.560
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
LY26426 (A82846B) is a naturally-occurring glycopeptide antibiotic, differing from vancomycin in the stereochemistry of the amino-sugar of the disaccharide function, and the presence of a third sugar attached at the benzylic position of amino acid residue 6. Despite these seemingly differences, LY264826 is approximately 10 times more active than vancomycin against the enterococci. In the pursuit of new antibiotics active against multiresistant Gram-positive organisms, an extensive side chain SAR was developed focusing on the reductive alkylation of LY264826 at the amino function of the disaccharide moiety. A new series of derivatives having varying degrees of structural diversity in the side chain (e.g. varying lengths and degrees of rigidity) was found to have potent activity staphylococci and streptococci as good or better than vancomycin.
引用
收藏
页码:560 / 569
页数:10
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