Maciejewska Dorota, Szpakowska Iwona, Wolska Irena, Niemyjska Maria, Mascini Marco, Maj-Zurawska Magdalena
Department of Organic Chemistry, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02 097 Warsaw, Poland.
Bioelectrochemistry. 2006 Sep;69(1):1-9. doi: 10.1016/j.bioelechem.2005.09.003. Epub 2005 Nov 22.
Facile and practical electrochemical DNA bioassay, X-ray diffraction analysis, synthesis and 1H and 13C NMR data of the 5,5'-disubstituted-3,3'-methanediyl-bis-indoles are reported. On the basis of electrochemical measurements we have hypothesized that the analyzed bis-indoles have an effect on human tumor cells due to DNA binding at adenine-thymidine deoxynucleotides rich region in a concentration/substituent dependent manner. Interesting N-H...pi and hydrogen-bonding intermolecular interactions were observed which may differentiate their biological features. The 5,5'-dimethoxy-3,3'-methanediyl-bis-indole (2) was found to reduce considerably the growth of cancer cell lines HOP-92 (lung), A498 (renal) and MDA-MB-231/1TCC (breast). The results indicate that title compounds could be interesting as potential antitumoral chemotherapeutics.
报道了5,5'-二取代-3,3'-亚甲基双吲哚的简便实用的电化学DNA生物测定、X射线衍射分析、合成以及1H和13C NMR数据。基于电化学测量,我们推测所分析的双吲哚由于以浓度/取代基依赖的方式与富含腺嘌呤-胸腺嘧啶脱氧核苷酸的区域结合DNA,从而对人肿瘤细胞产生影响。观察到有趣的N-H...π和氢键分子间相互作用,这可能会区分它们的生物学特性。发现5,5'-二甲氧基-3,3'-亚甲基双吲哚(2)能显著降低癌细胞系HOP-92(肺癌)、A498(肾癌)和MDA-MB-231/1TCC(乳腺癌)的生长。结果表明,标题化合物作为潜在的抗肿瘤化疗药物可能具有吸引力。