The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
Novel Glycopeptide Antibiotics: N-Alkylated Derivatives Active Against Vancomycin-Resistant Enterococci
MICHAEL J. RODRIGUEZNANCY J. SNYDERMARK J. ZWEIFELSTEPHEN C. WILKIEDOUGLAS R. STACKROBIN D.G. COOPERTHALIA I. NICASDEBORAH L. MULLENTHOMAS F. BUTLERRICHARD C. THOMPSON
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1998 Volume 51 Issue 6 Pages 560-569

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Abstract

LY264826 (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 subtle 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 against vancomycin-resistant enterococci (MIC's < 1.0 μg/ml) as well as activity against staphylococci and streptococci as good or better than vancomycin.

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© Japan Antibiotics Research Association
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