Three new isoflavones from the Pueraria montana var. lobata (Willd.) and their bioactivities

异黄酮素 烟草花叶病毒 黄酮类 葛根 IC50型 传统医学 多酚 化学 花叶病毒 立体化学 阳性对照 大豆苷 体外 异黄酮 洛巴塔 萃取(化学) 染料木素 类黄酮 生物化学 生物 病毒 色谱法 植物病毒 抗氧化剂 医学 病理 替代医学 病毒学
作者
Cui Tinghui,Tang Shiyun,Chunbo Liu,Zhenjie Li,Qin Zhu,You Junheng,Si Xiaoxi,Zhang Fengmei,Pei He,Zhihua Liu,Ming-Ming Miao,Guang Yu Yang,Shen Qinpeng,Lihong Jiang
出处
期刊:Natural Product Research [Taylor & Francis]
卷期号:32 (23): 2817-2824 被引量:13
标识
DOI:10.1080/14786419.2017.1385008
摘要

Three new isoflavones, 7-acetyl-4',6-dimethoxy-isoflavone (1), 7-acetyl-4'-hydroxy-6-methoxy-isoflavone (2) and 7-acetyl-6,8-dimethoxy-4'-hydroxy-isoflavone (3), together with five known flavones (4-8), were isolated from the Pueraria montana var. lobata (Willd.). Their structures were elucidated by spectroscopic methods, including extensive 1D- and 2D NMR techniques. Compounds 1-8 were evaluated for their anti-tobacco mosaic virus (anti-TMV) activities. The results showed that compounds 1 and 2 exhibited high anti-TMV activities with inhibition rates of 36.8 and 33.6%, respectively. The inhibition rates are higher than that of positive control. The other compounds also showed potential anti-TMV activities with inhibition rates in the range of 21.8~28.4%, respectively. The cytotoxicities of compounds 1-3 against five human tumour cell lines (NB4, A549, SHSY5Y, PC3 and MCF7) were also tested. The results revealed that compounds 1-3 showed weak inhibitory activities against some tested human tumour cell lines with IC50 values in the range of 1.2-3.6 μM.

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