Acanthifoliosides, minor steroidal saponins from the Caribbean sponge Pandaros acanthifolium

Erik L. Regalado, Carlos Jiménez-Romero, Gregory Genta-Jouve, Deniz Tasdemir, Philippe Amade, Clara Nogueiras, Olivier P. Thomas

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

25 Citations (Scopus)

Abstract

Seven novel steroid glycosides, acanthifoliosides A-F (1-6), and the methyl ester of 6 (7), were isolated from the marine sponge Pandaros acanthifolium as minor components. Acanthifoliosides are characterized by a rare C-15 and C-16 oxidized D ring, which was previously found in saponins produced by starfishes. Very uncommon is the presence of additional sugar residues at C-15 or C-16. Their structures were determined on the basis of extensive spectroscopic analyses, including two-dimensional NMR and HRESIMS data. The absolute configurations of the aglycones were assigned by comparison between experimental and TDDFT calculated CD spectra of 1, whereas the absolute configurations of the monosaccharide units were determined by chiral GC analyses of the acid methanolysates. Some of the acanthifoliosides exhibit moderate antiprotozoal activity but to a lesser extent than the most potent pandarosides.

Original languageEnglish
Pages (from-to)1011-1018
Number of pages8
JournalTetrahedron
Volume67
Issue number5
DOIs
Publication statusPublished - 4 Feb 2011
Externally publishedYes

Keywords

  • Circular dichroism
  • Marine sponge
  • NMR
  • Pandaros
  • Steroidal saponin

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