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新型抗肿瘤药物与DNA的嵌入结合:二吡啶并[4,3-b][3,4-f]吲哚

Intercalative binding to DNA of new antitumoral agents: dipyrido [4,3-b] [3,4-f] indoles.

作者信息

Tourbez-Perrin M, Pochon F, Ducrocq C, Rivalle C, Bisagni E

出版信息

Bull Cancer. 1980;67(1):9-13.

PMID:7362892
Abstract

The study of new intercalating DNA agents has led to the synthesis of dipyrido [4,3-b] [3,4-f] indole derivatives. These compounds bind preferentially to helical DNA and their affinity constants range from 10(6) to 10(7) M-1. The most active derivative against L1210 mouse leukemia produces viscosity changes in sheared fragments of linear DNA and in circular PM2 DNA on binding, indicating an intercalation process. The unwinding angle is estimated to be 18(0). This active derivative binds preferentially to A-T base pairs.

摘要

新型嵌入DNA试剂的研究已促成了二吡啶并[4,3 - b][3,4 - f]吲哚衍生物的合成。这些化合物优先与螺旋DNA结合,其亲和常数范围为10(6)至10(7) M-1。对L1210小鼠白血病最具活性的衍生物在结合时会使线性DNA的剪切片段和环状PM2 DNA产生粘度变化,表明存在嵌入过程。解旋角估计为18(0)。这种活性衍生物优先与A - T碱基对结合。

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