Kanamienamide, an enamide with an enol ether, was isolated from the marine cyanobacterium Moorea bouillonii. The gross structure was established by spectroscopic analyses, and the relative stereochemistry was elucidated on the basis of the analyses of NOESY correlations and H-H coupling constants. The absolute configuration was determined on the basis of the chiral HPLC analysis of the N-Me-Leu derived from kanamienamide. This is the first report of a natural product that possesses an N-Me-enamide adjacent to an enol ether. Kanamienamide showed growth-inhibitory activity toward HeLa cells with an IC value of 2.5 μM and induced apoptosis-like cell death.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.6b02364 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!