Jha Amitabh, Mukherjee Chandrani, Rolle Alfred J, De Clercq Erik, Balzarini Jan, Stables James P
Department of Chemistry, Acadia University, Wolfville, NS, Canada B4P 2R6.
Bioorg Med Chem Lett. 2007 Aug 15;17(16):4545-50. doi: 10.1016/j.bmcl.2007.05.094. Epub 2007 Jun 7.
A series of nine 1-(4-((E)-3-arylacryloyl)phenyl)-1H-pyrrole-2,5-diones 3a-i (4'-aminochalcone-based maleimides) was synthesized as candidate cytotoxic agents. The efficacy of these potential cytotoxics were evaluated against three representative cell lines and more than half of the drug candidates proved to exhibit significant cytostatic activity in vitro. QSAR studies using statistical analyses on several physicochemical parameters and IC50 values resulted in a few very important correlations which will aid in later the amplification of the project. Representative test compounds were well tolerated by mice in in vivo survival and toxicity studies.
合成了一系列九个1-(4-((E)-3-芳基丙烯酰基)phenyl)-1H-吡咯-2,5-二酮3a-i(基于4'-氨基查尔酮的马来酰亚胺)作为候选细胞毒性剂。针对三种代表性细胞系评估了这些潜在细胞毒性剂的功效,超过一半的候选药物在体外表现出显著的细胞生长抑制活性。使用统计分析对几个物理化学参数和IC50值进行的定量构效关系(QSAR)研究得出了一些非常重要的相关性,这将有助于该项目后续的拓展。在体内生存和毒性研究中,代表性测试化合物在小鼠体内耐受性良好。