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黄酮类天然化合物抗病毒活性的结构基础

Structural basis for antiviral activity of flavonoids-naturally occurring compounds.

作者信息

Wleklik M, Luczak M, Panasiak W, Kobus M, Lammer-Zarawska E

机构信息

Department of Virology Institute of Biostructure Medical Academy of Warsaw, Poland.

出版信息

Acta Virol. 1988 Nov;32(6):522-5.

PMID:2906224
Abstract

The effect of different substituents of quercetin and luteolin on the ability to inhibit the herpes simplex virus (HSV-1) replication in RK-13 cells was studied. It seems that parent compounds with free hydroxyl groups at C-5, C-7, C-3', C-4' and additionally at C-3 have the highest activity. Substitution of those groups caused decrease of or completely abolished the antiviral activity of the tested compounds.

摘要

研究了槲皮素和木犀草素不同取代基对其抑制单纯疱疹病毒1型(HSV - 1)在RK - 13细胞中复制能力的影响。似乎在C - 5、C - 7、C - 3'、C - 4'以及另外在C - 3处带有游离羟基的母体化合物具有最高活性。这些基团的取代导致测试化合物的抗病毒活性降低或完全丧失。

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Structural basis for antiviral activity of flavonoids-naturally occurring compounds.黄酮类天然化合物抗病毒活性的结构基础
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