Abstract
Three new cytotoxic glycolipids, erylusamine TA (8), erylusine (9) and erylusidine (10) have been isolated from a Red Sea sponge tentatively identified as Erylus cf. lendenfeldi. The structure of the three compounds was determined by interpretation of 2D NMR and FABMS data as trisaccharides of long-chain oxodihydroxyfatty acid amides formed with N,N-dimethyl-1,5- pentanediamine to yield 8 with ω-N,N-dimethylaminobutyl-N-methyl-1,3 - propanediamine to yield 9 and with 4-(aminobutyl) guanidine to yield 10 (R3=COCH2CH(CH3)2).
Original language | English |
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Pages (from-to) | 7921-7928 |
Number of pages | 8 |
Journal | Tetrahedron |
Volume | 52 |
Issue number | 23 |
DOIs | |
State | Published - 3 Jun 1996 |