posted on 2011-04-25, 00:00authored byRhys Finlayson, A. Norrie Pearce, Michael J. Page, Marcel Kaiser, Marie-Lise Bourguet-Kondracki, Jacquie L. Harper, Victoria L. Webb, Brent R. Copp
Two new indole spermidine alkaloids, didemnidines A (1) and B (2), have been isolated from the New Zealand ascidian Didemnum sp. The structures of the metabolites, determined by analysis of 2D NMR spectra and confirmed via synthesis, embody an indole-3-glyoxylamide moiety linked to the N1 position of spermidine, the latter motif being particularly rare among marine natural products. Didemnidine B and a synthetic precursor exhibited mild in vitro growth inhibition of Plasmodium falciparum with IC50's of 15 and 8.4 μM, respectively.