Vrábel Milan, Pohl Radek, Votruba Ivan, Sajadi Mohsen, Kovalenko Sergey A, Ernsting Nikolaus P, Hocek Michal
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Gilead & IOCB Research Center, Flemingovo nam. 2, CZ-16610, Prague 6, Czech Republic.
Org Biomol Chem. 2008 Aug 21;6(16):2852-60. doi: 10.1039/b805632c. Epub 2008 Jun 16.
The synthesis of the title 7-deazaadenine 2'-deoxyribonucleosides bearing bipyridine, phenanthroline or terpyridine ligands linked to position 7 via an acetylene or phenylene spacer is reported based on aqueous cross-coupling reactions of unprotected 7-iodo-7-deaza-2'-deoxyadenosine with ligand-functionalized acetylenes or boronic acids. The aqueous cross-coupling with acetylene or boronate building blocks containing the Ru(bpy)(3)-type of complex gave the corresponding Ru-containing nucleosides. Photophysical and electrochemical properties were studied and the most efficient type of complex was selected for future luminescent and redox labelling of DNA. The title nucleosides also showed some cytostatic and anti-HCV activities.
基于未保护的7-碘-7-脱氮-2'-脱氧腺苷与配体功能化乙炔或硼酸的水相交叉偶联反应,报道了通过乙炔或亚苯基间隔基与7位相连的含联吡啶、菲咯啉或三联吡啶配体的标题7-脱氮腺嘌呤2'-脱氧核糖核苷的合成。与含Ru(bpy)(3)型配合物的乙炔或硼酸酯结构单元的水相交叉偶联得到了相应的含钌核苷。研究了光物理和电化学性质,并选择了最有效的配合物类型用于未来DNA的发光和氧化还原标记。标题核苷还表现出一些细胞生长抑制和抗丙型肝炎病毒活性。