[n-甲基-n-亚硝基苄胺对大鼠的毒性和致癌性的变化通过在氮附近的c原子甲基取代(作者译)]。

F Schweinsberg, M Kouros, K Manncke, K Rieth
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引用次数: 0

摘要

在n -亚硝基-n -甲基苄胺(NMBA)的氮附近的c原子上用甲基取代导致LD显著降低50:n -亚硝基-n -甲基苄胺:18 mg/kg (Druckrey等,1967)n -亚硝基-n -甲基-(1-苯基)-乙胺(I): 600 mg/kg n -亚硝基-n -甲基-2-(2-苯基)-丙胺(II): 2100 mg/kg n -亚硝基-n -乙基-苄胺(III):在NMBA (NMPEA I)部分的亚甲基上取代甲基也降低了致癌活性,但在所有动物中产生食道癌和咽喉癌;在选择的条件下,两个h原子被甲基(NMPPA, II)取代导致肿瘤不发生,因为激活步骤没有质子可用。NMBA (NEBA, III)的n -甲基被n -乙基交换后,其致癌性没有变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Change of toxicity and carcinogenicity of n-methyl-n-nitrosobenzylamine in rats by methylsubstitution at the c-atoms adjacent to nitrogen (author's transl)].

Substitution with a methyl group at the C-atoms adjacent to nitrogen of N-nitroso-N-methylbenzylamine (NMBA) results in a considerable reduction LD 50: N-nitroso-N-methylbenzylamine : 18 mg/kg (Druckrey et al., 1967) N-nitroso-N-methyl-(1-phenyl)-ethylamine (I) : 600 mg/kg N-nitroso-N-methyl-2-(2-phenyl)-propylamine (II) : 2100 mg/kg N-nitroso-N-ethyl-benzylamine (III) : 250 mg/kg Substitution with a methyl group at the methylene of the moiety of NMBA (NMPEA I) reduces also the carcinogenic activity, but it produces in all animals carcinomas of the oesophagus and the pharynx; the replacement of both H-atoms by methyl groups (NMPPA, II) causes under the condition chosen no development of tumors, because for the activation step no proton is available. The exchange of N-methyl by N-ethyl of NMBA (NEBA, III) however produces no change in the carcinogenicity.

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