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阿斯特里醌与脱氧核糖核酸的体外相互作用。

Interaction of asterriquinone with deoxyribonucleic acid in vitro.

作者信息

Shimizu S, Koshimura S

机构信息

Faculty of Pharmaceutical Sciences, Kanazawa University, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1990 Sep;38(9):2617-9. doi: 10.1248/cpb.38.2617.

Abstract

The interaction of asterriquinone (ARQ), a novel antitumor agent isolated from Aspergillus fungi, with deoxyribonucleic acid (DNA), has been studied. The binding of ARQ in vitro with DNA (calf thymus) was ascertained by its behavior in gel filtration using a Sephadex G-25 column at pH 5.4. Some ARQ analogs having no, or less, antitumor activity did not exhibit any evidence of interaction with DNA under the same condition. From the results obtained in this work, the pKa value of ARQs seemed to be critical between 6 and 7 for their binding to DNA and for exhibition of antitumor activity. Also, ARQ showed serious membrane deformations and an inhibitory effect on the membranous adenosine triphosphatase of Ehrlich carcinoma cells.

摘要

对从曲霉菌中分离出的新型抗肿瘤药物紫衫醌(ARQ)与脱氧核糖核酸(DNA)的相互作用进行了研究。通过在pH 5.4条件下使用葡聚糖G - 25柱进行凝胶过滤实验,确定了ARQ在体外与DNA(小牛胸腺DNA)的结合情况。一些没有或只有较弱抗肿瘤活性的ARQ类似物在相同条件下未表现出与DNA相互作用的迹象。根据这项工作获得的结果,ARQ的pKa值在6至7之间对于其与DNA的结合以及抗肿瘤活性的发挥似乎至关重要。此外,ARQ还导致了严重的膜变形,并对艾氏癌细胞的膜腺苷三磷酸酶产生抑制作用。

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