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首页> 外文期刊>Bioorganic and medicinal chemistry >Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities.
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Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities.

机译:类黄酮作为流感病毒神经氨酸酶抑制剂的构效关系及其体外抗病毒活性。

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摘要

Flavonoids are polyphenolic compounds that widely exist in plant kingdom, and the structure-activity relationship (SAR) of 25 flavonoids was studied on neuraminidase (NA) activity of influenza virus. Three typical influenza virus strains A/PR/8/34 (H1N1), A/Jinan/15/90 (H3N2), and B/Jiangshu/10/2003 were used as the source of NAs, the average of IC(50)s of these compounds on these NAs was used in the SAR analysis. The order of potency for NA inhibition was as follows: aurones>flavon(ol)es>isoflavones>flavanon(ol)es and flavan(ol)es. The SAR analysis of flavonoids on influenza virus NAs revealed that for good inhibitory effect, the 4'-OH, 7-OH, C4O, and C2C3 functionalities were essential, and the presence of a glycosylation group greatly reduced NA inhibition. The in vitro anti-viral activities of eight flavonoids were evaluated using a cytopathic effect (CPE) reduction method, the assay results confirmed the SAR as influenza virus neuraminidase inhibitors. The findings of this study provide important information for the exploitation and utilization of flavonoids as NA inhibitors for influenza treatment.
机译:黄酮类化合物是植物界中广泛存在的多酚类化合物,研究了25种黄酮类化合物与流感病毒的神经氨酸酶(NA)活性之间的构效关系(SAR)。三种典型的流感病毒株A / PR / 8/34(H1N1),A / Jinan / 15/90(H3N2)和B / Jiangshu / 10/2003被用作NA的来源,IC的平均值(50)这些化合物在这些NA上的一个或多个用于SAR分析。 NA抑制的效力顺序如下:金酮>黄酮(ol)es>异黄酮>黄酮(ol)es和黄烷(ol)es。黄酮类化合物对流感病毒NAs的SAR分析表明,为获得良好的抑制作用,4'-OH,7-OH,C4O和C2C3功能至关重要,糖基化基团的存在大大降低了NA的抑制作用。使用细胞病变作用(CPE)降低方法评估了八个类黄酮的体外抗病毒活性,测定结果证实了SAR是流感病毒神经氨酸酶抑制剂。这项研究的发现为黄酮类作为NA流感抑制剂的开发和利用提供了重要的信息。

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