Cytotoxic Iridoid Glycosides from the Aerial Parts of Paederia foetida

IF 0.9 4区 化学 Q4 CHEMISTRY, MEDICINAL
Jiang Hu, Guihua Yu, Fengming Xu, Tao Lv, Qiang Li, Feng Gao
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引用次数: 0

Abstract

Two previously undescribed iridoid glycosides, 6′-O-trans-caffeoyl-(4S,6R)-3,4-dihydro-3α- methylthioasperulosid (1) and 6′-O-trans-feruloyl-(4S,6R)-3,4-dihydro-2′-O-3α-paederosid (2), were isolated from the 90% EtOH extract of the aerial part of Paederia foetida L. The structures of the new compounds were elucidated by spectral methods such as 1D and 2D (1H–1H COSY, HMQC, and HMBC) NMR spectroscopy, HR-ESI-MS, as well as ECD data. The isolated compounds were tested in vitro for cytotoxic activity against five tumor cell lines. These results revealed that 2 exhibited some cytotoxicities against all the tested tumor cell lines with IC50 value less than 20.0 μM and provided a scientific basis for further processing and utilization of P. foetida.

黄连地上部的细胞毒性环烯醚萜苷
从叶青90% EtOH提取液中分离到6′- o-反式-咖啡基-(4S,6R)-3,4-二氢-3α-甲基硫代asperulosid(1)和6′- o-反式-阿魏酰-(4S,6R)-3,4-二氢-2′- o-3α- paederosid(2)两个先前未被描述的环烯醚萜苷类化合物,并通过1D和2D (1H-1H COSY, HMQC, HMBC) NMR波谱、HR-ESI-MS以及ECD数据等光谱方法对其结构进行了鉴定。分离得到的化合物在体外对5种肿瘤细胞系进行了细胞毒活性测试。结果表明,2对所有肿瘤细胞系均表现出一定的细胞毒性,IC50值均小于20.0 μM,为豆腐竹的进一步加工利用提供了科学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemistry of Natural Compounds
Chemistry of Natural Compounds 化学-有机化学
CiteScore
1.40
自引率
25.00%
发文量
265
审稿时长
7.8 months
期刊介绍: Chemistry of Natural Compounds publishes reviews and general articles about the structure of different classes of natural compounds, the chemical characteristics of botanical families, genus, and species, to establish the comparative laws and connection between physiological activity and the structure of substances.
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