Curvall M, Florin I, Jansson T
Toxicology. 1982;23(1):1-10. doi: 10.1016/0300-483x(82)90036-1.
A series of indole derivatives and some analogues were tested for mutagenic activity using a histidine-requiring mutant of Salmonella typhimurium (TA 98). Quantitative tests were performed with and without addition of a liver fraction (S-9) from rats induced with Aroclor 1254. Three compounds, 2,3-dimethylindole, 2,3,5-trimethylindole and 2,3,6-trimethylindole, showed a mutagenic effect which was not increased on metabolic activation. The influence on the mutagenic activity of the number and positions of the substituents attached to the indole skeleton is discussed.
使用鼠伤寒沙门氏菌(TA 98)的组氨酸需求突变体,对一系列吲哚衍生物及其一些类似物进行了致突变活性测试。在添加和不添加用多氯联苯混合物Aroclor 1254诱导的大鼠肝脏组分(S - 9)的情况下进行了定量测试。三种化合物,2,3 - 二甲基吲哚、2,3,5 - 三甲基吲哚和2,3,6 - 三甲基吲哚,表现出致突变作用,且代谢活化后该作用未增强。讨论了吲哚骨架上取代基的数量和位置对致突变活性的影响。