## Abstract Six new triterpene glycosides, repensosides A–F (**1**–**6**, resp.), were isolated from the roots of __Gypsophila repens__ L. Their structures, established by extensive 1D‐ and 2D‐NMR spectroscopic experiments as well as MS analyses, were found to be based on gypsogenic acid (or gypsog
A Major Triterpenoid Saponin from Gypsophila oldhamiana
✍ Scribed by Hong Bai; Ying Zhong; Yan-Ying Xie; Yuan-Shu Wang; Lu Liu; Ling Zhou; Ju Wang; Yan-Ling Mu; Chun-Xu Zuo
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 80 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1612-1872
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A new saponin, gypoldoside A (1), was isolated from the roots of Gypsophila oldhamiana. On the basis of in‐depth NMR‐spectroscopic and mass‐spectrometric analysis, in combination with chemical evidence, its structure was established as 3‐O‐{β‐D‐galactopyranosyl‐(1→2)‐[β‐D‐xylopyranosyl‐(1→3)]‐β‐D‐glucuronopyranosyl}quillaic acid 28‐[α‐L‐arabinopyranosyl‐(1→2)‐α‐L‐arabinopyranosyl‐(1→3)‐β‐D‐xylopyranosyl‐(1→4)‐α‐L‐rhamnopyranosyl‐(1→2)‐β‐D‐fucopyranosyl] ester. Compound 1 was found to be highly active against three different human cancer cell lines, with IC~50~ values in the low micromolar range.
📜 SIMILAR VOLUMES
## Abstract A pair of new oleanane‐type nortriterpene saponin epimers, neogypsoside A (**1**) and B (**2)** (__Fig. 1__) with neogypsogenin A (**3**) and neogypsogenin B (**4**) as the two new aglycons, as well as the two known triterpene saponins **5** and **6** __(Fig. 1__), were isolated from th
## Abstract The seven new triterpenoid saponins **1**–**7** were isolated from the roots of __Gypsophila paniculata__ L. Their structures were established by 1D‐ and 2D‐NMR techniques, HR‐MS, and acid hydrolysis. The isolated compounds include 3,28‐__O__‐bidesmosides with or without a 4‐methoxycinn
A novel triterpenoid saponin was isolated from Gypsophilu cupilluris (Forssk.) and its structure and conformational behaviour were investigated by one-and two-dimensional 'H and 13C NMR spectroscopy.