## Abstract The marine sponge __Agelas clathrodes__ was analyzed for glyβcosphingolipids, and four cerebrosides (1aβ4a) were isolated, each as a mixture of homologs. The structure of the new glycosphingolipid 1a was elucidated by extensive NMR studies of its peracetate and by chemical analysis. The
Glycolipids from sponges, III. Glycosyl ceramides from the marine spongeAgelas conifera
β Scribed by Costantino, Valeria ;Fattorusso, Ernesto ;Mangoni, Alfonso
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 454 KB
- Volume
- 1995
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The glycosphingolipid (GSL) composition of the marine sponge Agelas conifera was investigated. In addition to three GSLs previous isolated from Agelas clathrodes (2aβ4a), the novel Ξ±βglycosylceramide 1a was isolated as a major component of the GSL mixture, and its structure was elucidated by extensive NMR studies and by chemical analysis.
π SIMILAR VOLUMES
## Abstract A specimen of the marine sponge __Agelas longissima__ was analyzed for glycosphingolipids. Three cerebrosides 1aβ3a were isolated, each as a mixture of homologs. The structure of the new glycosphingolipid 1a was elucidated by extensive NMR studies of its peracetate derivative and chemic
## Abstract A new 4βsulfated ceramide, ircisulfamide (=__N__β[(1__S__\*,2__S__\*,3__R__\*)β2βhydroxyβ1β(hydroxymethyl)β3β(sulfooxy)heptadecyl]hexadecanamide; **1**), and a new glycosphingolipid, ircicerebroside (=(2__R__\*)β__N__β{(1__S__\*,2__R__\*,3__E__,7__E__)β1β[(__Ξ²__βDβglucopyranosyloxy)meth