Literature DB >> 29388431

Diverted Total Synthesis of the Baulamycins and Analogues Reveals an Alternate Mechanism of Action.

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.

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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


  18 in total

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