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槲皮素及相关化合物的诱变活性。

Mutagenic activity of quercetin and related compounds.

作者信息

Bjeldanes L F, Chang G W

出版信息

Science. 1977 Aug 5;197(4303):577-8. doi: 10.1126/science.327550.

Abstract

The mutagenic activities of several flavonoids and flavonoid metabolites were examined by means of Salmonella typhimurium mutants that reveal base-pair substitution and frameshift mutagens. Of the compounds tested (naringin, rutin, neohesperetin, hesperetin, dihydroquercetin, quercetin, quercetin pentaacetate, permethylquercetin, m-hydroxyphenylacetic acid, and m,p-dihydroxyphenylacetic acid), only quercetin was mutagenic without microsomal activation. With activation, however, the mutagenic activity of quercetin was increased significantly and that of quercetin pentaacetate was revealed. The health implications of these findings and aspects of flavonoid structural requirements for mutagenic activity are discussed.

摘要

利用能显示碱基对置换和移码诱变剂的鼠伤寒沙门氏菌突变体,检测了几种黄酮类化合物及其代谢产物的诱变活性。在所测试的化合物(柚皮苷、芦丁、新橙皮苷、橙皮苷、二氢槲皮素、槲皮素、槲皮素五乙酸酯、全甲基槲皮素、间羟基苯乙酸和间、对二羟基苯乙酸)中,只有槲皮素在没有微粒体激活的情况下具有诱变作用。然而,经过激活后,槲皮素的诱变活性显著增加,并且还显示出槲皮素五乙酸酯的诱变活性。讨论了这些发现对健康的影响以及黄酮类化合物诱变活性的结构要求方面。

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