Formation of S-[2-(N7-guanyl)ethyl] adducts by the postulated S-(2-chloroethyl)cysteinyl and S-(2-chloroethyl)glutathionyl conjugates of 1,2-dichloroethane.
Formation of S-[2-(N7-guanyl)ethyl] adducts by the postulated S-(2-chloroethyl)cysteinyl and S-(2-chloroethyl)glutathionyl conjugates of 1,2-dichloroethane.
复制标题
通过假定的 1,2-二氯乙烷的 S-(2-氯乙基)半胱氨酰和 S-(2-氯乙基)谷胱甘肽缀合物形成 S-[2-(N7-鸟苷基)乙基]加合物。
DOI:
10.1021/bi00381a035
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发表时间:
1987
期刊:
影响因子:
2.9
通讯作者:
Reed,DJ
中科院分区:
文献类型:
--
作者:
Foureman,GL;Reed,DJ
Materials and MethodsAll chemicals used were of the highest grade available from commercial sources. The synthesis of both S-(2-chloroethyl) glutathione (CEG) and S-(2-chloroethyl)-L-cysteine (CEC) was as reported in Reed and Foureman (1986) and in Schasteen and Reed (1983). The CEG was 90% pure as determined by high-performance liquid chromatography (HPLC), the main contaminant being the hydrolysis product; CEC was> 95% pure by the same criteria. Bulk preparation of the deoxyguanosine adducts for chem-ical analysis was accomplished by adding, as the dry powder, 227 µ of either CEC (42 mg) or CEG (85 mg) to 4 mL