Design and synthesis of novel polycycles based on the 3H-pyrrolo/6,7-dihydropyrido[1,2-a]indole scaffold as templates for pharmaceutical development
作者:Marco Derudas、Nicolino Pala、Vanna Sanna、Roberto Dallocchio、Alessandro Dessì、Anna Maria Roggio、Mario Sechi
DOI:10.1002/jhet.710
日期:2011.9
In the course of our work aimed at developing novel heterocycles of pharmaceutical interest, we designed and synthesized several polycyclic templates as potential substrates to be used in drug design. We obtained a set of condensed ring systems as versatile structural platforms to generate potential DNA‐interactive agents and/or reversible inhibitors of enzymes such as topoisomerases, poly(ADP‐ribose)
在我们旨在开发新的药用杂环的工作过程中,我们设计并合成了几种多环模板,作为可用于药物设计的潜在底物。我们获得了一套稠环系统作为通用的结构平台,以生成潜在的DNA相互作用剂和/或可逆酶抑制剂,例如拓扑异构酶,聚(ADP-核糖)聚合酶-1(PARP-1),端粒酶,以及特别是细胞周期蛋白依赖性激酶。在此,我们报告了这些杂芳族体系的设计,合成,结构研究和初步的DNA结合亲和力。J.杂环化学。(2011)。