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一种1-硝基-9-氨基吖啶衍生物(抗肿瘤药物“利达克林”(硝吖啶)的类似物)中DNA交联的嵌入模型。

Intercalation model for DNA-cross linking in a 1-nitro-9-aminoacridine derivative, an analog of the antitumor agent "ledakrin" (nitracrine).

作者信息

Stallings W C, Glusker J P, Carrell H L, Bogucka-Ledóchowska M, Ledóchowski A, Stezowski J J

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111.

出版信息

J Biomol Struct Dyn. 1984 Dec;2(3):511-24. doi: 10.1080/07391102.1984.10507588.

Abstract

Ledakrin (nitracrine), C-283, is a 1-nitro-9-aminoacridine derivative that is used in Poland as an antitumor agent. In order to investigate the basis of the activity of this compound the structure of another analog, [9-(3-dimethyl-1-methylpropylimino)-1-nitro-9,10-dihydroacridin e], C-829, that has similar activity, was determined by X-ray crystallographic techniques and was compared with that of ledakrin, already reported in the literature. In both molecules the proximity of the 1-nitro to the substituted 9-aminoacridine group causes extensive distortions. These compounds are believed to act, after metabolic "activation", by cross-linking DNA. Such cross-linking does not occur in the absence of the 1-nitro group or if the nitro group is moved to the 2-, 3- or 4-position. Computer-assisted model-building has been used to test possible intercalative models. It has shown that functional groups on C-829 or C-283 are, when the acridine portion of the molecule is intercalated as in a proflavine dinucleoside phosphate complex, in positions suitable for DNA cross-linking by activated 1-nitro-9-aminoacridine derivatives.

摘要

利达克林(硝吖啶),C - 283,是一种1 - 硝基 - 9 - 氨基吖啶衍生物,在波兰用作抗肿瘤药物。为了研究该化合物活性的基础,通过X射线晶体学技术确定了另一种具有相似活性的类似物[9 - (3 - 二甲基 - 1 - 甲基丙基亚氨基)- 1 - 硝基 - 9,10 - 二氢吖啶],C - 829的结构,并将其与文献中已报道的利达克林的结构进行了比较。在这两种分子中,1 - 硝基与取代的9 - 氨基吖啶基团的接近导致了广泛的扭曲。据信这些化合物在代谢“活化”后通过交联DNA起作用。在没有1 - 硝基基团或硝基移至2 -、3 - 或4 - 位时不会发生这种交联。计算机辅助模型构建已用于测试可能的嵌入模型。结果表明,当分子的吖啶部分像在原黄素二核苷磷酸复合物中那样嵌入时,C - 829或C - 283上的官能团处于适合被活化的1 - 硝基 - 9 - 氨基吖啶衍生物进行DNA交联的位置。

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