RRC ID 70461
著者 Sugawara K, Watarai H, Ise Y, Yokose H, Morii Y, Yamawaki N, Okada S, Matsunaga S.
タイトル Structure Elucidation of Calyxoside B, a Bipolar Sphingolipid from a Marine Sponge Cladocroce sp. through the Use of Beckmann Rearrangement.
ジャーナル Mar Drugs
Abstract Marine sponges are an excellent source of biologically active secondary metabolites. We focus on deep-sea sponges for our discovery study. A marine sponge Cladocroce sp. exhibited cytotoxic activity in the bioactivity screening. From this sponge a previously unreported cytotoxic glycosphingolipid, calyxoside B, was isolated and the structure of this compound was elucidated by analyses of MS and NMR spectra and chemical derivatization. We converted the ketone in the middle of a long aliphatic chain into an oxime to which was applied Beckmann rearrangement to afford two positional isomers of amides. The products were subjected to acidic hydrolysis followed by LC-MS analysis, permitting us to assign unequivocally the position of the ketone. Calyxoside B shows cytotoxicity against HeLa cells with an IC50 value of 31 µM and also weakly stimulated the production of cytokines in mice.
巻・号 19(6)
公開日 2021-5-21
DOI 10.3390/md19060287
PII md19060287
PMID 34063932
PMC PMC8224005
MeSH Amides / chemistry Animals Cytokines / metabolism Cytotoxins / chemistry* Cytotoxins / isolation & purification Cytotoxins / pharmacology Glycosphingolipids / chemistry* Glycosphingolipids / isolation & purification Glycosphingolipids / pharmacology HeLa Cells Humans Mice, Inbred C57BL Mice, Knockout Molecular Structure Porifera / chemistry* Stereoisomerism
IF 4.073
リソース情報
ヒト・動物細胞 HeLa(RCB0007)