PubAg

Main content area

Antiplatelet aggregation triterpene saponins from the leaves of Ilex kudingcha

Author:
Yang, Bao, Yang, Tao, Tan, Qinglong, Zhu, Jinping, Zhou, Lian, Xiong, Tianqin, Zhao, Zhongxiang, Jin, Jing
Source:
Phytochemistry letters 2015 v.13 pp. 302-307
ISSN:
1874-3900
Subject:
Ilex kaushue, acid hydrolysis, adenosine diphosphate, inhibitory concentration 50, leaves, methanol, nuclear magnetic resonance spectroscopy, platelet aggregation, triterpenoid saponins
Abstract:
Two new ursane-type triterpene saponins, 3-O-β-d-glucopyranosyl(1→3)-[α-l-rhamnopyranosyl(1→2)]-α-l-arabinopyranosylurs-12,19(29)-dien-28-oic acid 28-O-α-l-rhamnopyranosyl(1→2)-β-d-glucopyranosyl ester (1) and 3-O-β-d-glucopyranosyl(1→3)-[α-l-rhamnopyranosyl(1→2)]-α-l-arabinopyranosyl-19α,20α-dihydroxyurs-12-en-28-oic acid 28-O-α-l-rhamnopyranosyl(1→2)-β-d-glucopyranosyl ester (2), along with thirteen known triterpene saponins were isolated from the n-BuOH part of the MeOH extraction of the leaves of Ilex kudingcha C.J. Tseng (also called “Ku-Ding-Cha”). The structures of new compounds were elucidated on the basis of detailed spectroscopic analysis, including HR-ESI-TOF-MS, 1D and 2D-NMR experiments, and by acid hydrolysis. All the compounds were screened for antiplatelet aggregation activity in vitro, and compounds 1, 2, 3, 7, 12 and 15 showed significant inhibition of platelet aggregation induced by ADP (5μM) with IC50 values of 14.7±3.7, 11.3±2.5, 17.4±4.6, 20.5±3.1, 8.1±1.5 and 18.9±4.2μM, respectively.
Agid:
5443104