| Literature DB >> 30277650 |
Guillaume Ernouf1, Ingrid K Wilt1, Sara Zahim1, William M Wuest1,2.
Abstract
Epoxy isonitrile containing natural products often possess specific and potent antibacterial activity against Gram-positive pathogens. This scaffold, however, is extremely labile under acidic and basic conditions, undergoing a Payne rearrangement to produce a stable epoxy ketone metabolite and releasing hydrogen cyanide. We synthesized and performed biological assays with epoxy ketone containing metabolites and identified that the epoxy isonitrile moiety is pertinent for biological activity. Serendipitously, we discovered an α,β-unsaturated epoxy ketone analogue that exhibited moderate activity against Staphylococcus aureus.Entities:
Keywords: Staphylococcus aureus; antibiotics; bioorganic chemistry; epoxy isonitrile; natural products
Mesh:
Substances:
Year: 2018 PMID: 30277650 PMCID: PMC6462814 DOI: 10.1002/cbic.201800550
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164