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1-硝基-9-氨基吖啶衍生物与DNA的复合物

Complexes of derivatives of 1-nitro-9-aminoacridine with DNA.

作者信息

Filipski J, Marczyński B, Chorazy M

出版信息

Acta Biochim Pol. 1975;22(2):119-29.

PMID:239508
Abstract

Substituted 1-nitro-9-aminoacridine derivatives were shown to inhibit RNA and to a lesser extent protein synthesis in cultured human cells. Complex formation between the compounds studied and DNA were considered to be responsible for their cytostatic action. Two types of complexes differing in their binding forces were found. The biological activity of the studied compounds seems not to be dependent on the existence of a positive charge on the acridine ring.

摘要

取代的1-硝基-9-氨基吖啶衍生物在培养的人类细胞中显示出抑制RNA的作用,对蛋白质合成的抑制作用较小。所研究的化合物与DNA之间形成的复合物被认为是其细胞生长抑制作用的原因。发现了两种结合力不同的复合物类型。所研究化合物的生物活性似乎不依赖于吖啶环上正电荷的存在。

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