CoMFA of flavonoids with antimutagenic activity against 2-amino-3-methylimidazo(4,5-f)quinoline (IQ)

C. Navajas, A. Poso, J. Gynther
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引用次数: 1

Abstract

SUMMARY The flavonoids are one of the largest groups of secondary metabo lites in plants and they are a very important part in the human nutrition. Dietary inhibitors of mutagenesis and carcinogenesis are of particular interest because they may be useful for human cancer prevention and several flavonoids have been demonstrated to have an antimutagenic effect on various mutagens or carcinogens. Using biological data for the inhibition of the mutagenic activity of IQ (2-amino-3-methylimidazo[4,5-f]quinoline) by different flavonoids, we have made a three-dimensional analysis (CoMFA) to develop a model for the structure‐ activity relationships of these compounds. Our results support the mode of action proposed earlier for the binding with the cytochrome P450 and bring a new additional possibility of interaction with the enzyme.
对2-氨基-3-甲基咪唑(4,5-f)喹啉(IQ)具有抗诱变活性的黄酮类化合物的CoMFA
黄酮类化合物是植物中最大的一类次生代谢生物,是人体营养的重要组成部分。饮食中的诱变和致癌抑制剂特别令人感兴趣,因为它们可能对人类癌症预防有用,并且几种类黄酮已被证明对各种诱变剂或致癌物具有抗诱变作用。利用不同黄酮类化合物抑制IQ(2-氨基-3-甲基咪唑[4,5-f]喹啉)致突变活性的生物学数据,我们进行了三维分析(CoMFA),建立了这些化合物的结构-活性关系模型。我们的结果支持先前提出的与细胞色素P450结合的作用模式,并带来了与酶相互作用的新可能性。
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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