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非嵌入性DNA结合抗肿瘤化合物。

Nonintercalative DNA-binding antitumour compounds.

作者信息

Baguley B C

出版信息

Mol Cell Biochem. 1982 Apr 2;43(3):167-81. doi: 10.1007/BF00223008.

Abstract

A family of compounds which appear to bind reversibly to double stranded DNA without intercalation between DNA base pairs has been defined. Methods are described by which this non-intercalative binding can be characterised using ultraviolet spectrometry, fluorimetry with ethidium as a probe, viscometry and other hydrodynamic techniques, circular dichroism and nuclear magnetic resonance spectrometry. Antibiotics which fall into this family include the antibiotics distamycin A, netropsin, mithramycin, chromomycin and olivomycin. Synthetic antitumour agents include diarylamidines such as berenil, phthalanilides, aromatic bisguanylhydrazones and bisquaternary ammonium heterocycles. A survey has been made of the general requirements of this family of compounds for DNA binding and biological activity. Binding of drugs to the minor groove of the DNA double helix appears to be the most likely mechanism for the antitumour action of these compounds.

摘要

已经定义了一类化合物,这类化合物似乎能与双链DNA可逆结合,且不会插入DNA碱基对之间。文中描述了一些方法,通过这些方法可以利用紫外光谱法、以溴化乙锭为探针的荧光法、粘度测定法和其他流体动力学技术、圆二色性和核磁共振光谱法来表征这种非插入性结合。属于这一类的抗生素包括抗生素偏端霉素A、纺锤菌素、光神霉素、色霉素和橄榄霉素。合成抗肿瘤剂包括二芳基脒,如贝尼尔、酞酰苯胺、芳香双胍腙和双季铵杂环。已经对这类化合物与DNA结合和生物活性的一般要求进行了调查。药物与DNA双螺旋小沟的结合似乎是这些化合物抗肿瘤作用最可能的机制。

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