## Abstract For Abstract see ChemInform Abstract in Full Text.
Novel sesquiterpenes and a lactone from the Jamaican sponge Myrmekioderma styx
โ Scribed by Jiangnan Peng; Scott G. Franzblau; Fangqiu Zhang; Mark T. Hamann
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 116 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Two novel sesquiterpenes, styxone A (1) and styxone B (2), and a novel lactone, styxlactone (3), were isolated from the Jamaican sponge Myrmekioderma styx. Their structures were elucidated by detailed 1 H, 13 C and 2D NMR data and the absolute stereochemistry of styxone A and B was determined by CD spectra. Styxone A represents a novel sesquiterpene skeleton. (S)-(+)-Curcuphenol ( 4), (S)-(+)-curcudiol (5), and abolene (6) were also isolated. An activity enhancement by cyanthiwigin B (7) to curcuphenol was observed in the antimicrobial assays when the two compounds were administered together.
๐ SIMILAR VOLUMES
Together with the previously described cacospongionolide B (1) and cacospongionolide F (2) a new C2 1 terpene (3). related to cacospongionoiide B has been isolated from the sponge Fusciospongia cuvernosu, collected in the Aegean Sea. The structure and relative stereochemistry of the new compound, we