Lijinsky W, Taylor H W
J Cancer Res Clin Oncol. 1979 Jun 8;94(2):131-7. doi: 10.1007/BF00422493.
Four chlorinated derivatives of nitrosotrialkylureas were tested for carcinogenicity by oral administration by gavage to Sprague-Dawley rats. All of the compounds were very toxic, and all were carcinogenic, inducing tumors of the non-glandular stomach and of the lungs. The commonest tumors were carcinomas and papillomas of the non-glandular stomach and alveolar cell adenomas of the lungs. Nitrosochloroethyldimethylurea induced most tumors, but it was possible to administer higher doses of this compound than of the others, which were nitrosochloroethydiethylurea, nitrosomethylbis-(chloroethyl)-urea and nitrosotris-(chloroethyl)-urea. The last of these was a particularly toxic compound so that the maximum total dose given was only 0.07 millimole per rat.
通过灌胃法对斯普拉格-道利大鼠口服给予四种亚硝基三烷基脲的氯化衍生物,以测试其致癌性。所有化合物毒性都很强,且都具有致癌性,可诱发非腺胃和肺部肿瘤。最常见的肿瘤是非腺胃癌、乳头状瘤以及肺肺泡细胞腺瘤。亚硝基氯乙基二甲基脲诱发的肿瘤最多,但与其他化合物(亚硝基氯乙基二乙基脲、亚硝基甲基双(氯乙基)脲和亚硝基三(氯乙基)脲)相比,能够给予该化合物更高的剂量。其中最后一种化合物毒性特别大,因此每只大鼠给予的最大总剂量仅为0.07毫摩尔。