Hemminki K
Carcinogenesis. 1983;4(7):901-4. doi: 10.1093/carcin/4.7.901.
Propane sultone was reacted with guanosine and DNA at pH 6--7.5, and te reaction products were purified by Sephadex chromatography and h.p.l.c. The products were characterized by u.v. spectra, loss of tritium from the C-8 position and dissociation properties. The main product was shown to be an N-7-alkyl guanosine, accounting for greater than 90% of the total product. Similar evidence suggested that two of the minor adducts were N-1 and O6 alkyl derivatives, accounting for approximately 1.6 and 0.5% of the total adduct, respectively. N-7 and N-1 alkyl guanine were also detected in DNA reacted with propane sultone.
在pH 6 - 7.5条件下,使丙烷磺酸内酯与鸟苷及DNA发生反应,反应产物通过葡聚糖凝胶色谱法和高效液相色谱法进行纯化。通过紫外光谱、C - 8位氚的损失以及解离特性对产物进行表征。结果表明主要产物是N - 7 - 烷基鸟苷,占总产物的90%以上。类似证据表明两种次要加合物是N - 1和O6烷基衍生物,分别约占总加合物的1.6%和0.5%。在与丙烷磺酸内酯反应的DNA中也检测到了N - 7和N - 1烷基鸟嘌呤。