Abstract
The structure of the sulfated analogue of cauloside C, a biologically active triterpenoid glycoside, was elucidated to be 3-O-[β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl]-hederagenin 23,4′,4″,6″-tetrasulfate pentasodium salt by the comparison of its13C NMR spectrum with that of cauloside C potassium salt.
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Strigina, L.I., Isakov, V.V. The structure of sulfated cauloside C. Russ J Bioorg Chem 26, 350–353 (2000). https://doi.org/10.1007/BF02759288
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DOI: https://doi.org/10.1007/BF02759288