β-lactones as privileged structures for the active-site labeling of versatile bacterial enzyme classes

Thomas Böttcher, Stephan A. Sieber

Research output: Contribution to journalArticlepeer-review

147 Scopus citations

Abstract

(Chemical Equation Presented) A chemical proteomic strategy has been applied directly to bacterial proteomes, and b-lactones have been identified as important natural product derivatives with a high affinity to various enzyme classes (see picture). This approach may serve as a potent tool for the identification of novel antibacterial targets, the study of their function, and the definition of novel lead structures for the design of enzyme inhibitors.

Original languageEnglish
Pages (from-to)4600-4603
Number of pages4
JournalAngewandte Chemie International Edition in English
Volume47
Issue number24
DOIs
StatePublished - 2 Jun 2008
Externally publishedYes

Keywords

  • Biomimetic synthesis
  • Enzymes
  • Lactones medicinal chemistry
  • Proteomics

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