Abstract
AbstractDaptomycin is a calcium-dependent cyclic lipodepsipeptide antibiotic that is used in the clinic for treating serious infections caused by Gram-positive bacteria. In this account, I present a summary of the research that has been conducted in my group on daptomycin’s total chemical synthesis, its structure–activity relationships, and its mechanism of action, since we began our studies a decade ago.1 Introduction2 Solid-Phase Synthesis of Daptomycin by an On-Resin Cyclization3 α-Azido Acids and Alternative Routes to Daptomycin by On-Resin Cyclization4 Synthesis of Daptomycin by an Off-Resin Cyclization5 SAR Studies on Daptomycin6 Oligomerization of Daptomycin on Membranes7 The Chiral Target of Daptomycin8 SAR Studies on Phosphatidylglycerol9 Conclusions
Funder
Natural Sciences and Engineering Research Council of Canada
Canadian Institutes of Health Research
Cited by
3 articles.
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