Structural Assignment of Poecillastrins B and C, Macrolide Lactams from the Deep-Water Caribbean Sponge<i>Poecillastra</i>Species

Kentaro Takada, Byoung Wook Choi, Mohammad A Rashid, William R. Gamble, John H. Cardellina, Que N. Van, John R. Lloyd, James B. McMahon, Kirk R. Gustafson

Journal of Natural Products · 2006 · 25 citations · 10 references

Concepts

Abstract

Two new chondropsin-type macrolide lactams, poecillastrins B (1) and C (2), were isolated from aqueous extracts of the marine sponge Poecillastra sp. These trace metabolites were isolated in low yield (400-600 microg), and their structures were determined primarily by analysis of NMR data acquired using a cyrogenically cooled probe. High-quality 1D and 2D NMR data sets allowed complete assignment of the spectroscopic data and defined the new structures as 35-membered ring analogues of poecillastrin A (3). Compounds 1 and 2 showed potent cytotoxic activity against a human melanoma tumor cell line (LOX) with an IC50 value of less than 1 microg/mL.

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