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亚硝化西咪替丁的致突变性。

Mutagenicity of nitrosated cimetidines.

作者信息

Ichinotsubo D, MacKinnon E A, Liu C, Rice S, Mower H F

出版信息

Carcinogenesis. 1981;2(4):261-4. doi: 10.1093/carcin/2.4.261.

Abstract

Dinitrosocimetidine and mononitrosocimetidine were tested in a series of short term assay systems. Both compounds were mutagenic in the absence of rat liver microsomes. The dinitrosocimetidine produced higher mutagenic or clastogenic effects at concentrations that were 50 to 500 times lower than the concentrations at which the mononitrosocimetidine produces its maximum effects. The most sensitive short term assay system was the Chinese hamster ovary cell culture system. Dinitrosocimetidine caused sister chromatid exchanges at a concentration of 10(-8) M and chromosome aberrations at 10(-7) M in this system. Dinitrosocimetidine had moderate activity in the bacterial short term assay systems. In the Ames test, strain TA 100 was the most sensitive. The compound was of lower activity in the E. coli WP-2 and the E. coli rec- systems.

摘要

在一系列短期检测系统中对二亚硝基西咪替丁和单亚硝基西咪替丁进行了测试。两种化合物在无大鼠肝微粒体的情况下均具有致突变性。二亚硝基西咪替丁在比单亚硝基西咪替丁产生最大效应时的浓度低50至500倍的浓度下产生更高的致突变或致断裂效应。最敏感的短期检测系统是中国仓鼠卵巢细胞培养系统。在该系统中,二亚硝基西咪替丁在浓度为10^(-8) M时引起姐妹染色单体交换,在10^(-7) M时引起染色体畸变。二亚硝基西咪替丁在细菌短期检测系统中具有中等活性。在艾姆斯试验中,TA 100菌株最为敏感。该化合物在大肠杆菌WP - 2和大肠杆菌rec - 系统中的活性较低。

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