新型交联剂的设计与合成。

Shuhei Kusano, Keiichi Hattori, Shuhei Imoto, Fumi Nagatsugi
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引用次数: 1

摘要

在此之前,我们利用含有2-氨基-6-乙烯嘌呤衍生物的寡脱氧核苷酸(ODN)与DNA靶位点的胞嘧啶碱基进行了高效和选择性的交联反应(1)。基于这些结果,我们设计了新型交联剂,该交联剂是具有两个氢键位点的嘧啶衍生物,乙烯基作为反应基团。本文报道了具有新型交联剂潜力的嘧啶衍生物的合成研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and synthesis of the novel cross-linking agent.

Previously, we have developed a highly efficient and selective cross-linking reaction to the cytosine base at the target site of DNA using the oligodeoxynucleotide (ODN) containing 2-amino-6-vinylpurine derivative (1). Based on these results, we have designed the novel cross-linking agents, which are pyrimidine derivatives having two hydrogen bond sites and vinyl group as a reactive moiety. In this paper, we wish to report the results to investigate on the synthesis of the pyrimidine derivatives having potential as novel cross-linking agents.

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