Dedicated to Prof. I(. Hiller on the occasion of his 65th birthday (8.XII. 95) Three new saponins 1-3 were isolated from Herniaria glubra by means of prep. HPLC and TLC. The structures were established mainly by a combination of 2D-NMR techniques (COSY, TOCSY, ROESY, HMQC, and HMBC) as 0 -a -L-rhamn
New Triterpene Saponins from Acanthophyllum pachystegium
✍ Scribed by Mohamed Haddad; Tomofumi Miyamoto; Mohammad Ramezani; Marie-Aleth Lacaille-Dubois
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- German
- Weight
- 105 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
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 FAB‐MS. The new compounds were characterized as 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‐[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).
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