Mutagenicity of nitrobenzyl derivatives: potential bioreductive anticancer agents

T.R. Juneja, Anju Bala, Punit Kumar, R.L. Gupta
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引用次数: 7

Abstract

Ortho-meta-and para-nitrobenzyl bromides alcohols ethers and esters were synthesized and tested for their mutagenicity toward Salmonella typhimurium TA100, TA100NR (nitroreductase deficient) and TA98 in absence of S9 mix and in TA100 with S9 mix. Compounds of the ortho-and meta-series were non mutagenic with and without S9 mix. Except for the alcohol and ether, the compounds of the para-series were mutagenic in TA100 with activity sequence propionate > butyrate > benzoate > acetate > bromide and this specific activity was reduced considerably by S9 mix. The Ames Salmonella test system does not seem to be an appropriate model to evaluate mutagenicity of o-nitrobenzyls. However, further work is in progress to test all the compounds for mutagenicity in mammalian system

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硝基苯衍生物的致突变性:潜在的生物还原抗癌剂
合成了邻间硝基苄基溴醚和对硝基苄基溴醚和酯类,并对鼠伤寒沙门菌TA100、TA100NR(缺乏硝基还原酶)和TA98进行了诱变性试验。邻系和元系化合物在有无S9混合物的情况下均无致突变性。除醇类和醚类化合物外,该系列化合物对TA100具有诱变作用,活性序列为丙酸酯>丁酸盐比;苯甲酸酯比;醋酸比;溴化物和S9混合物大大降低了这一比活性。Ames沙门氏菌检测系统似乎不是评价邻硝基苯致突变性的合适模型。然而,进一步的工作正在进行中,以测试所有化合物的致突变性在哺乳动物系统
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