| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1377200 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
Substituted N-alkyl-4-hydroxyquinolon-3-yl-benzothiadiazine sulfamides were investigated as inhibitors of genotype 1 HCV polymerase. Structure–activity relationship patterns for this class of compounds are discussed.
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Related Topics
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Chemistry
Organic Chemistry
Authors
A. Chris Krueger, Darold L. Madigan, Wen W. Jiang, Warren M. Kati, Dachun Liu, Yaya Liu, Clarence J. Maring, Sherie Masse, Keith F. McDaniel, Tim Middleton, Hongmei Mo, Akhteruzzaman Molla, Debra Montgomery, John K. Pratt, Todd W. Rockway, Rong Zhang,