Abstract
Four new triterpenoid saponins, pachystegiosides A (1), B (2), C (3), and D (4), were isolated from the roots of Acanthophyllum pachystegium K.H. Their structures were elucidated by means of a combination of homo- and heteronuclear 2D-NMR techniques (COSY, TOCSY, NOESY, HSQC, and HMBC) and by FABMS. The new compounds were characterized as 3-O-[O-β-D-galactopyranosyl-(1 → 2)-0-[β-D-xylopyranosyl-(1 → 3)β-D-glucuronopyranosyl]quillaic acid 28-[O-β-D-xylopyranosyl-(1 → 3)-O-β-D-xylopyranosyl-(1 →4)-O-α-L-rhamnopyranosyl-(1 → 2)-O-[3,4-di-O-acetyl-β D-quinovopyranosyl-(1 → 4)]-β-D-fucopyranosyl] ester (1), 3-O-[O-β-D-galactopyranosyl-(1 → 2)-O-[β-D-xylopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl]quillaic acid 28-[O-β -D-xylopyranosyl-(1 → 3)-O-β-D-xylopyranosyl-(1 → 4)-O-α-L-rhamnopyranosyl-(1 → 2)-O-[4-O-acetyl-β -D-quinovopyranosyl-(1 → 4)]-β-D-fucopyranosyl] ester (2), 3-O-[O-β-D-galactopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1 → 3)]-β-D-glucuronopyranosyl]quillaic acid 28-[O-β-D-xylopyranosyl-(1 → 4)-O-α-L-rhamnopyranosyl-(1 → 2)-O-[4-O-acetyl-β -D-quinovopyranosyl-(1 → 4)]-β-D-fucopyranosyl] ester (3), and gypsogenic acid 28-[O-β-D-glucopyranosyl-(1 → 2)-O-β -D-glucopyranosyl-(1 → 6)-O-β-D-glucopyranosyl-(1 → 3)-β-D-galactopyranosyl] ester (4).
Original language | English |
---|---|
Pages (from-to) | 73-81 |
Number of pages | 9 |
Journal | Helvetica Chimica Acta |
Volume | 87 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2004 |
All Science Journal Classification (ASJC) codes
- Drug Discovery
- Biochemistry
- Catalysis
- Inorganic Chemistry
- Physical and Theoretical Chemistry
- Organic Chemistry