Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376286 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
From chemical compound library screening using an HCV NS5B RNA-dependent RNA polymerase enzymatic assay, we identified a substituted quinoxaline hit with an IC50 of 5.5 μM. A series of substituted quinoxaline amide derivatives were synthesized based on the hit’s pharmacophore, and a good structure–activity relationship was observed. Computer modeling analysis was employed to help comprehend the SAR.
Graphical abstractA novel quinoxaline amide was found to be active against HCV NS5B RNA-dependent RNA polymerase through SAR studies.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Frank Rong, Suetying Chow, Shunqi Yan, Gary Larson, Zhi Hong, Jim Wu,