University of Pittsburgh, Center for Chemical Methodologies and Library Development, Pittsburgh, PA 15260, USA.
Bioorg Med Chem Lett. 2010 May 1;20(9):2968-73. doi: 10.1016/j.bmcl.2010.03.002. Epub 2010 Mar 6.
We describe the structure-activity relationship of the C1-group of pyrano[3,4-b]indole based inhibitors of HCV NS5B polymerase. Further exploration of the allosteric binding site led to the discovery of the significantly more potent compound 12.
我们描述了基于吡喃并[3,4-b]吲哚的 HCV NS5B 聚合酶抑制剂 C1 组的构效关系。进一步探索变构结合位点导致发现了效力显著增强的化合物 12。