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2000
Volume 17, Issue 12
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

Platensimycin, an active metabolite of Streptomyces platensis, was initially discovered by a combination of RNA interferin induced gene-silencing and library screening to microbial extracts. Platensimycin selectively inhibits β- ketoacyl-acyl carrier protein (ACP) synthase II (FabF) that is recognized as an effective broad-spectrum antibiotic against drug-resistant microorganism strains. Its novel scaffold and extraordinary antibacterial activity have drawn great attentions in recent years. So far, a number of synthetic strategies have been explored for the total synthesis of platensimycin. Moreover, many analogues have been investigated in terms of structure-activity relationships (SAR). This review provides a detailed overview of updated studies on platensimycin, focusing on various total and formal synthetic strategies, development of analogues, and the structure-activity relationships.

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/content/journals/cmc/10.2174/092986710790827852
2010-04-01
2025-05-09
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/content/journals/cmc/10.2174/092986710790827852
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  • Article Type:
    Research Article
Keyword(s): analogues; antibiotic; discovery; FabF; platencin; Platensimycin; SAR; total synthetic strategies
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