Oleanolic Acid Glycosides from Scabiosa caucasica and Scabiosa ochroleuca : Structural Analysis and Cytotoxicity
In the field of research on medicinal plants from the Armenian flora, the phytochemical study of two L. species, M. Bieb. and L. (Caprifoliaceae), has led to the isolation of five previously undescribed oleanolic acid glycosides from an aqueous-ethanolic extract of the roots: 3- -α-L-rhamnopyranosyl...
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Veröffentlicht in: | Molecules (Basel, Switzerland) Switzerland), 2023-05, Vol.28 (11), p.4329 |
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Sprache: | eng |
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Zusammenfassung: | In the field of research on medicinal plants from the Armenian flora, the phytochemical study of two
L. species,
M. Bieb. and
L. (Caprifoliaceae), has led to the isolation of five previously undescribed oleanolic acid glycosides from an aqueous-ethanolic extract of the roots: 3-
-α-L-rhamnopyranosyl-(1→3)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-
-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-
-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-
-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-
-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid, 3-
-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-
-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-
-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-
-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester. Their full structural elucidation required extensive 1D and 2D NMR experiments, as well as mass spectrometry analysis. For the biological activity of the bidesmosidic saponins and the monodesmosidic saponin, their cytotoxicity on a mouse colon cancer cell line (MC-38) was evaluated. |
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ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules28114329 |