## Abstract Three new acetylated flavonol glycosides, quercetin 3‐__O__‐(2,3,4‐triacetyl‐α‐rhamnopyranosyl)‐(1 → 6)‐β‐galactopyranoside, quercetin 3‐__O__‐[(2,3,4‐triacetyl‐α‐rhamnopyranosyl)‐(1 → 6)]‐3‐acetyl‐β‐galactopyranoside and quercetin 3‐__O__‐[(2,3,4‐triacetyl‐α‐rhamnopyranosyl)‐(1 → 6)]‐4
Structure elucidation of new oleanane-type glycosides from three species of Acanthophyllum
✍ Scribed by Gaoussou Timité; Anne-Claire Mitaine-Offer; Tomofumi Miyamoto; Mohammad Ramezani; Abdolhossein Rustaiyan; Jean-François Mirjolet; Olivier Duchamp; Marie-Aleth Lacaille-Dubois
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 140 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2577
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
From the roots of three species of Acanthophyllum (Caryophyllaceae), two new gypsogenic acid glycosides, 1 and 2, were isolated, 1 from A. sordidum and A. lilacinum, 2 from A. elatius and A. lilacinum, together with three known saponins, glandulosides B and C, and SAPO50. The structures of 1 and 2 were established mainly by 2D NMR techniques as 23‐O‐β‐D‐galactopyranosylgypsogenic acid‐28‐O‐β‐D‐glucopyranosyl‐(1→3)‐[β‐D‐glucopyranosyl‐(1→6)]‐β‐D‐galactopyranoside (1) and gypsogenic acid‐28‐O‐β‐D‐glucopyranosyl‐(1→3)‐[β‐D‐glucopyranosyl‐(1→6)]‐β‐D‐galactopyranoside (2). The cytotoxicity of several of these saponins was evaluated against two human colon cancer cell lines (HT‐29 and HCT 116). Copyright © 2010 John Wiley & Sons, Ltd.
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