Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1366965 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
A novel class of inhibitors of the hepatitis C virus [substituted 2-(2-fluorophenyl)-5H-imidazo[4,5-c]pyridines] is described. Introduction of a fluorine in position 2 of the 2-phenyl substituent of the lead anti-pestivirus compound 1 (5-[(4-bromophenyl)methyl]-2-phenyl-5H-imidazo[4,5-c]pyridine) resulted in an analogue with selective activity against HCV in the subgenomic replicon system.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Gerhard Puerstinger, Jan Paeshuyse, Erik De Clercq, Johan Neyts,