Hunanamycin A, the first natural product with a pyrido[1,2,3-de] quinoxaline-2,3-dione core, was isolated from a marine-derived Bacillus hunanensis. Hunanamycin A is related to a degradation product of riboflavin but has undergone an N-prenylation and subsequent cyclization. The structure, including stereochemistry, was determined by NMR and MS methods. Hunanamycin A exhibits a minimum inhibitory concentration (MIC) of 12.4 μM against the bacterial pathogen Salmonella enterica.
|Original language||English (US)|
|Number of pages||4|
|State||Published - Jan 18 2013|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry