Schering Plough Research Institute, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA.
Bioorg Med Chem Lett. 2010 Feb 15;20(4):1384-7. doi: 10.1016/j.bmcl.2010.01.007. Epub 2010 Jan 7.
Several analogs of aristolochic acids were isolated and derivatized into their lactam derivatives to study their inhibition in CDK2 assay. The study helped to derive some conclusions about the structure-activity relation around the phenanthrin moiety. Semi-synthetic aristolactam 21 showed good activity with inhibition IC50 of 35 nM in CDK2 assay. The activity of this compound was comparable to some of the most potent synthetic compounds reported in the literature.
几种马兜铃酸类似物被分离出来,并衍生为它们的内酰胺衍生物,以研究它们在 CDK2 测定中的抑制作用。这项研究有助于得出关于菲并呋喃部分周围的结构-活性关系的一些结论。半合成马兜铃内酰胺 21 在 CDK2 测定中表现出良好的活性,抑制 IC50 为 35 nM。该化合物的活性与文献中报道的一些最有效的合成化合物相当。