Mirvish S S, Wallcave L, Eagen M, Shubik P
Science. 1972 Jul 7;177(4043):65-8. doi: 10.1126/science.177.4043.65.
The formation of carcinogenic N-nitroso compounds by the chemical reaction between nitrous acid and oxytetracycline, morpholine, piperazine, N-methylaniline, methylurea, and (in some experiments) dimethylamine was blocked by ascorbic acid. The extent of blocking depended on the compound nitrosated and on the experimental conditions. Urea and ammonium sulfamate were less effective as blocking agents. The possibility of in vivo formation of carcinogenic N-nitroso compounds from drugs could be lessened by the combination of such drugs with the ascorbic acid.
亚硝酸与土霉素、吗啉、哌嗪、N-甲基苯胺、甲基脲以及(在某些实验中)二甲胺之间发生化学反应生成致癌性N-亚硝基化合物的过程被抗坏血酸阻断。阻断程度取决于被亚硝化的化合物以及实验条件。尿素和氨基磺酸铵作为阻断剂的效果较差。此类药物与抗坏血酸联合使用可降低体内由药物形成致癌性N-亚硝基化合物的可能性。