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pubmed-article:17848089pubmed:abstractTextGuided by the brine shrimp lethality assay, eight new cerebrosides (1-8) have been isolated from an extract of the marine sponge Haliclona (Reniera) sp. A novel feature of these cerebrosides was the presence of unprecedented amide-linked long-chain fatty acid moieties. The planar structures of the cerebrosides (1-8) were established by 1D and 2D NMR spectroscopic techniques, mass spectrometric analyses, and chemical degradation methods. The isolated compounds did not display cytotoxicity to a panel of five human solid tumor cell lines.lld:pubmed
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pubmed-article:17848089pubmed:articleTitleRenierosides, cerebrosides from a marine sponge Haliclona (Reniera) sp.lld:pubmed
pubmed-article:17848089pubmed:affiliationCollege of Pharmacy, Pusan National University, Busan 609-735, Korea.lld:pubmed
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