Nix C E, Brewen B, Lijinsky W, Epler J L
Mutat Res. 1980 Nov;73(1):93-100. doi: 10.1016/0027-5107(80)90138-4.
The mutagenic activity of 7 nitrosopiperazines, 2 nitropyrrolidines, and 3 nitrosomorpholines was examined in the X-linked recessive-lethal assay of Drosophila melanogaster. Mutagenicity is also reported for a series of cyclic nitrosamines that differ in structure only in the number of carbon atoms in the ring. Of the 18 compounds tested, 6 (nitrosopiperazine; 2,3,5,6-tetramethyldinitrosopiperazine; nitrosoproline; 2,5-dimethylnitrosopyrrolidine; nitrosothiomorpholine; and nitrosooctamethyleneimine) were nonmutagenic. As we reported earlier in investigations with the nitrosopiperidines, substitutions with methyl groups at all of the alpha-carbon atoms reduce or eliminate the mutagenic activity of dinitrosopiperazine and nitrosopyrrolidine.
在果蝇的X连锁隐性致死试验中检测了7种亚硝基哌嗪、2种硝基吡咯烷和3种亚硝基吗啉的致突变活性。还报告了一系列仅在环中碳原子数量上结构不同的环状亚硝胺的致突变性。在测试的18种化合物中,6种(亚硝基哌嗪;2,3,5,6-四甲基二亚硝基哌嗪;亚硝基脯氨酸;2,5-二甲基亚硝基吡咯烷;亚硝基硫代吗啉;和亚硝基八亚甲基亚胺)无致突变性。正如我们之前在对亚硝基哌啶的研究中所报告的,在所有α-碳原子上用甲基取代会降低或消除二亚硝基哌嗪和亚硝基吡咯烷的致突变活性。