| Literature DB >> 29388431 |
Andrew D Steele1, Guillaume Ernouf1, Young Eun Lee2, William M Wuest1.
Abstract
The baulamycins were identified as in vitro siderophore biosynthesis inhibitors. Diverted total synthesis was used to construct the natural products and eight strategic analogues, three of which had improved inhibitory activity. Biological testing then revealed that membrane damage is the predominant mode of action in Staphylococcus aureus cells.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29388431 PMCID: PMC5869691 DOI: 10.1021/acs.orglett.8b00054
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005