Amić Dragan, Davidović-Amić Dusanka, Beslo Drago, Rastija Vesna, Lucić Bono, Trinajstić Nenad
Faculty of Agriculture, The Josip Juraj Strossmayer University, P.O. Box 719, HR-31107 Osijek, Croatia.
Curr Med Chem. 2007;14(7):827-45. doi: 10.2174/092986707780090954.
Flavonoids are a group of naturally occurring phytochemicals abundantly present in fruits, vegetables, and beverages such as wine and tea. In the past two decades, flavonoids have gained enormous interest because of their beneficial health effects such as anti-inflammatory, cardio-protective and anticancer activities. These findings have contributed to the dramatic increase in the consumption and use of dietary supplements containing high concentrations of plant flavonoids. The pharmacological effect of flavonoids is mainly due to their antioxidant activity and their inhibition of certain enzymes. In spite of abundant data, structural requirements and mechanisms underlying these effects have not been fully understood. This review presents the current knowledge about structure-activity relationships (SARs) and quantitative structure-activity relationships (QSARs) of the antioxidant activity of flavonoids. SAR and QSAR can provide useful tools for revealing the nature of flavonoid antioxidant action. They may also help in the design of new and efficient flavonoids, which could be used as potential therapeutic agents.
黄酮类化合物是一类天然存在的植物化学物质,大量存在于水果、蔬菜以及葡萄酒和茶等饮品中。在过去二十年里,黄酮类化合物因其抗炎、心脏保护和抗癌等有益健康的作用而备受关注。这些研究结果导致含有高浓度植物黄酮类化合物的膳食补充剂的消费和使用大幅增加。黄酮类化合物的药理作用主要归因于其抗氧化活性及其对某些酶的抑制作用。尽管有大量数据,但这些作用背后的结构要求和机制尚未完全明确。本综述介绍了目前关于黄酮类化合物抗氧化活性的构效关系(SARs)和定量构效关系(QSARs)的知识。SAR和QSAR可为揭示黄酮类化合物抗氧化作用的本质提供有用工具。它们还可能有助于设计新型高效的黄酮类化合物,这些化合物可作为潜在的治疗药物。