Marine Drugs · 2013 · 56 citations · 18 references
Life SciencesBiochemistryBotanyMarine BiodiversityNatural Product BiosynthesisPhylogeneticsMarine Natural Product BiosynthesisTerpenoid BiosynthesisBioactive Compounds From Marine SpongesMarine Sponge MetabolitesMarine Sponge Natural Product BiosynthesisMarine TerpenoidsSaponin BiosynthesisSponge PhylogenySponge SystematicsSponges-derived Metabolites
The chemical investigation of the recently described Mediterranean Homoscleromorpha sponge Oscarella balibaloi revealed an original family of five closely related glucosylated sesterterpenes 1-4, named balibalosides. Their structure elucidation was mainly inferred from NMR and HRMS data analyses. Balibalosides differ by the pattern of acetyl substitutions on the three sugar residues linked to the same aglycone sesterterpenoid core. From a biosynthetic perspective, these compounds may represent intermediates in the pathways leading to more complex sesterterpenes frequently found in Dictyoceratida, a sponge Order belonging to Demospongiae, a clade which is phylogenetically distinct from the Homoscleromorpha. While steroid and triterpenoid saponins were already well known from marine sponges, balibalosides are the first examples of glycosilated sesterterpenes.
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Arjan A. van de Loosdrecht, R.H.J. Beelen, GJ Ossenkoppele et al. · Journal of Immunological Methods · 1994 · 802 citations · Full text
Medicine, Hematology, Oncology +7
Studies on succinate-tetrazolium reductase systems
T. F. Slater, B. C. Sawyer, Ursula Sträuli · Biochimica et Biophysica Acta · 1963 · 768 citations