Wang C Y, Muraoka K, Bryan G T
Cancer Res. 1975 Dec;35(12):3611-7.
Thirty-two heterocyclic compounds, including 24 nitroheterocycles, 7 aminoheterocycles and derivatives, and 1 thiophene lacking a nitro group, were tested for mutagenic activity in Salmonella typhimurium TA 98 and TA 100. All the nitroheterocycles (11 new), including nitrofurans, nitrothiophenes, nitropyrroles, and 1 nitroimidazole, were mutagenic in TA 100; 13 were also mutagenic in TA 98. 5-Nitro-2-furoic acid, a noncarcinogen, was mutagenic in TA 100. Seven carcinogenic nitroheterocycles were mutagenic in both strains. Seven aminoheterocycles (4 new), aminothiophenes and aminothiazole derivatives, and 1 thiophene without a nitro group were not mutagenic. Both TA 98 and TA 100 were uvrB and lacked the ability of excision repair of DNA. Among the 24 mutagenic nitroheterocycles, only 13 compounds exhibited bacterial killing effects, suggesting that more than 1 mechanism may be involved in the interaction of nitroheterocycles with bacterial DNA.
对32种杂环化合物进行了鼠伤寒沙门氏菌TA 98和TA 100的致突变活性测试,其中包括24种硝基杂环化合物、7种氨基杂环化合物及其衍生物,以及1种不含硝基的噻吩。所有硝基杂环化合物(11种为新化合物),包括硝基呋喃、硝基噻吩、硝基吡咯和1种硝基咪唑,在TA 100中具有致突变性;13种在TA 98中也具有致突变性。非致癌物5-硝基-2-呋喃甲酸在TA 100中具有致突变性。7种致癌硝基杂环化合物在两种菌株中均具有致突变性。7种氨基杂环化合物(4种为新化合物)、氨基噻吩和氨基噻唑衍生物,以及1种不含硝基的噻吩没有致突变性。TA 98和TA 100均为uvrB,缺乏DNA切除修复能力。在24种具有致突变性的硝基杂环化合物中,只有13种化合物表现出细菌杀伤作用,这表明硝基杂环化合物与细菌DNA的相互作用可能涉及多种机制。