Abstract
Three new acetylated triterpene saponins 1-3 were isolated from the roots of Carpolobia alba and C. lutea. Their structures were established mainly by 2D NMR techniques as 3-O-β-D-glucopyranosyl-presenegenin-28-O-β-D-galactopyranosyl- (1→4)-[β-D-xylopyranosyl-(1→3)]-β-D-xylopyranosyl- (1→4)-α-L-rhamnopyranosyl-(1→2)-(3,4-di-O-acetyl)-β -D-fucopyranosyl ester, 3-O-β-D-glucopyranosylpresenegenin-28-O-β-D-galactopyranosyl- (1→4)-[α-L-arabinopyranosyl-(1→3)]-β-D-xylopyranosyl- (1→4)-α-L-rhamnopyranosyl-(1→2)-(3,4-di-O-acetyl)-β -D-fucopyranosyl ester, and 3-O-β-D-glucopyranosylpresenegenin-28-O-β-D-xylopyranosyl- (1→4)-[β-D-apiofuranosyl-(1→3)]-α-L-rhamnopyranosyl- (1→2)-(3,4-di-O-acetyl)-β-D-fucopyranosyl ester, respectively.
Original language | English |
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Pages (from-to) | 553-557 |
Number of pages | 5 |
Journal | Journal of Natural Products |
Volume | 65 |
Issue number | 4 |
DOIs | |
Publication status | Published - May 11 2002 |
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Molecular Medicine
- Pharmacology
- Pharmaceutical Science
- Drug Discovery
- Complementary and alternative medicine
- Organic Chemistry