Two new C21 steroidal glycosides isolated from Cynanchum komarovii

被引:0
作者
ZHAO Dan [1 ,2 ]
SU Shan-Shan [3 ]
CHEN Shao-Fei [1 ,2 ]
LU Xiao-Jie [1 ,2 ]
CHEN Gang [1 ,2 ]
WANG Yu-Bo [1 ,2 ,4 ]
SU Guang-Yue [1 ,2 ]
PEI Yue-Hu [1 ,2 ]
机构
[1] Key Laboratory of Structure-Based Drug Design & Discovery,Ministry of Education,Shenyang Pharmaceutical University
[2] School of Traditional Chinese Materia Medica,Shenyang Pharmaceutical University
[3] Testing Laboratory,Qinghai Entry Exit Inspection and Quarantine Bureau
[4] School of Pharmacy,Jinzhou Medical University
基金
中国国家自然科学基金;
关键词
Cynanchum komarovii; C21 steroidal glycosides; Cytotoxic activity;
D O I
暂无
中图分类号
R284.2 [有效成分的分离与提取];
学科分类号
1008 ;
摘要
The present study was designed to further investigate the C21steroidal glycosides in Cynanchum plants.Two new steroidal glycosides based on a 13,14:14,15-disecopregnane-type aglycone,komaroside P(1) and komaroside Q(2),together with three known compounds(3-5) were isolated from the whole herbs of Cynanchum komarovii.The aglycones of compounds 1 and 2 were two new disecopregnane.Their structures were elucidated on the basis of 1 D,2 D NMR spectroscopic data and acid hydrolysis.All the compounds(1-5) showed potent inhibitory activities against human leukemia cell lines(HL-60) with IC50 values ranging from 16.6 to 26.3 μmol·L-1,compared to the positive control 5-fluorouracil(6.4 μmol·L-1).
引用
收藏
页码:610 / 614
页数:5
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