## Abstract High‐speed counter‐current chromatography (HSCCC) was applied to the preparative isolation and purification of peonidin 3‐__O__‐(6‐__O__‐(__E__)‐caffeoyl‐2‐__O__‐β‐D‐glucopyranosyl‐β‐D‐glucopyranoside)‐5‐__O__‐β‐D‐glucoside (**1**), cyanidin 3‐__O__‐(6‐__O__‐__p__‐coumaroyl)‐β‐D‐glucopy
Preparative isolation and purification of three flavonoid glycosides from Taraxacum mongolicum by high-speed counter-current chromatography
✍ Scribed by Shuyun Shi; Yuping Zhang; Yu Zhao; Kelong Huang
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 845 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1615-9306
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A preparative high‐speed counter‐current chromatography (HSCCC) was successively applied to purify three flavonoid glycosides from the aerial part of Taraxacum mongolicum, a traditional Chinese medicine. Subsequent UV, MS, and NMR analyses have led to the characterization of three flavonoid glycosides including two new compounds isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐L‐arabinopyranoside and isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐D‐glucopyranoside, and a known compound, isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐D‐xyloypyranoside, which were first isolated from T. mongolicum. The two‐phase solvent system composed of ethyl acetate/n‐butanol/water (2:1:3, v/v/v) was performed in HSCCC. Consequently, a total of 25.7 mg isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐L‐arabinopyranoside, 19.1 mg isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐D‐glucopyranoside, and 10.6 mg isoetin‐7‐O‐β‐D‐glucopyranosyl‐2′‐O‐α‐D‐xyloypyranoside were obtained with purity of 98.7, 98.3, and 99.1%, respectively, as determined by HPLC from 500 mg enriched extract after cleaning‐up by polyamide resin.
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