Okano T, Horie T, Iwaizumi M, Motohashi N
Gan. 1978 Feb;69(1):109-14.
Formation of a free radical from carcinogenic and noncarcinogenic benz[c]acridine derivatives in the presence of proteins was examined. When aqueous mixture of benz[c]acridine and protein was stirred for a long period, shielded from light, benz[c]acridines were converted into free radicals. Albumin had the greatest effect in accelerating the free radical formation, and the effect was smaller in globulin, histone, and deoxyribonuclease. The g-value of the free radicals thus obtained was 2.005. Intensity of the electron spin resonance (ESR) signals of the free radical from carcinogenic derivatives was higher than those of the free radical from noncarcinogenic derivatives. There was a corresponding correlation among the ESR signal intensity of the free radical formed from the mixed system of benz[c]acridine and protein, charge of the K-region or ring nitrogen of the compound, and carcinogenicity of benz[c]acridines.
研究了在蛋白质存在的情况下,致癌和非致癌苯并[c]吖啶衍生物形成自由基的情况。当苯并[c]吖啶与蛋白质的水性混合物在避光条件下长时间搅拌时,苯并[c]吖啶会转化为自由基。白蛋白在加速自由基形成方面的作用最大,而球蛋白、组蛋白和脱氧核糖核酸酶的作用较小。由此获得的自由基的g值为2.005。致癌衍生物产生的自由基的电子自旋共振(ESR)信号强度高于非致癌衍生物产生的自由基的信号强度。苯并[c]吖啶与蛋白质混合体系形成的自由基的ESR信号强度、化合物K区域或环氮的电荷以及苯并[c]吖啶的致癌性之间存在相应的相关性。