Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377771 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
The SAR development is described for a series of N-acyl pyrrolidine inhibitors of the Hepatitis C virus RNA-dependent RNA polymerase, NS5B, from tractable Δ21 enzyme inhibitors to an example with antiviral activity in a cellular assay (HCV replicon).
Graphical abstractOptimisation of a series of N-acyl pyrrolidine inhibitors of the Hepatitis C Virus RNA-dependent RNA polymerase, NS5B, from tractable enzyme inhibitors to an example with antiviral activity in a cellular assay (HCV replicon).Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
George Burton, Thomas W. Ku, Thomas J. Carr, Terry Kiesow, Robert T. Sarisky, Juili Lin-Goerke, Glenn A. Hofmann, Martin J. Slater, David Haigh, Dashyant Dhanak, Victor K. Johnson, Nigel R. Parry, Pia Thommes,