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在用N,N'-双(2-氯乙基)-N-亚硝基脲处理的DNA中形成交联碱基二鸟苷乙烷。

Formation of the cross-linked base, diguanylethane, in DNA treated with N,N'-bis(2-chloroethyl)-N-nitrosourea.

作者信息

Tong W P, Ludlum D B

出版信息

Cancer Res. 1981 Feb;41(2):380-2.

PMID:7448781
Abstract

A cross-linked base, diguanylethane, has been isolated and identified as a product of the reaction of N,N'-bis(2-chloroethyl)-N-nitrosourea with DNA. DNA was reacted at 37 degrees with N, N'-bis(2-chloroethyl)-N-nitrosourea in neutral aqueous solutions, isolated by precipitation with ethanol, washed, and heated briefly at 100 degrees to release a purine fraction. This fraction was separated by high-pressure liquid chromatography and found to contain both chloroethylguanine and 1,2-diguanylethane. Formation of the latter product may be related to the cytotoxicity of N,N'-bis(2-chloroethyl)-N-nitrosourea.

摘要

一种交联碱基——二鸟苷乙烷已被分离出来,并被鉴定为N,N'-双(2-氯乙基)-N-亚硝基脲与DNA反应的产物。DNA在37℃下于中性水溶液中与N,N'-双(2-氯乙基)-N-亚硝基脲反应,通过乙醇沉淀进行分离,洗涤后在100℃下短暂加热以释放嘌呤部分。该部分通过高压液相色谱法进行分离,发现同时含有氯乙基鸟嘌呤和1,2-二鸟苷乙烷。后一种产物的形成可能与N,N'-双(2-氯乙基)-N-亚硝基脲的细胞毒性有关。

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