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新型吡唑大黄素衍生物的合成、DNA结合及细胞毒性

Synthesis, DNA binding and cytotoxicity of new pyrazole emodin derivatives.

作者信息

Tan J-H, Zhang Q-X, Huang Z-S, Chen Y, Wang X-D, Gu L-Q, Wu J Y

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510080, China.

出版信息

Eur J Med Chem. 2006 Sep;41(9):1041-7. doi: 10.1016/j.ejmech.2006.04.006. Epub 2006 May 22.

Abstract

A series of new anthrapyrazoles were derived from emodin by attaching various cationic alkyl amino side chains onto a pyrazole ring which had been incorporated into the anthraquinone chromophore. Compared with emodin, the derivatives had significantly higher DNA binding affinity based on interaction with calf thymus DNA, and much more potent cytotoxicity against different tumor cells. The derivatives with a mono-cationic alkyl side chain exhibited the highest DNA binding affinity and cytotoxicity.

摘要

通过将各种阳离子烷基氨基侧链连接到已并入蒽醌发色团的吡唑环上,从大黄素衍生出一系列新的蒽并吡唑。与大黄素相比,基于与小牛胸腺DNA的相互作用,这些衍生物具有显著更高的DNA结合亲和力,并且对不同肿瘤细胞具有更强的细胞毒性。具有单阳离子烷基侧链的衍生物表现出最高的DNA结合亲和力和细胞毒性。

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