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- W2030601110 endingPage "1155" @default.
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- W2030601110 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 beta - 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." @default.
- W2030601110 created "2016-06-24" @default.
- W2030601110 creator A5024776655 @default.
- W2030601110 creator A5045350828 @default.
- W2030601110 date "2010-04-01" @default.
- W2030601110 modified "2023-10-12" @default.
- W2030601110 title "Recent Advances on Platensimycin: A Potential Antimicrobial Agent" @default.
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- W2030601110 doi "https://doi.org/10.2174/092986710790827852" @default.
- W2030601110 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20158476" @default.
- W2030601110 hasPublicationYear "2010" @default.
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