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Bioorganic & Medicinal Chemistry Letters|May 1, 2012
Identification of aryl dihydrouracil derivatives as palm initiation site inhibitors of HCV NS5B polymeraseYaya Liu, Ben Hock Lim, Wen W Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|March 5, 2005
Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of N-1-heteroalkyl-4-hydroxyquinolon-3-yl-benzothiadiazinesJohn K Pratt, Pamela Donner, Keith F McDaniel, et al.
Bioorganic & Medicinal Chemistry Letters|May 7, 2013
Discovery of pyrido[2,3-d]pyrimidine-based inhibitors of HCV NS5ADavid A DeGoey, David A Betebenner, David J Grampovnik, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2006
Inhibitors of HCV NS5B polymerase: synthesis and structure-activity relationships of N-alkyl-4-hydroxyquinolon-3-yl-benzothiadiazine sulfamidesA Chris Krueger, Darold L Madigan, Wen W Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|February 21, 2012
Novel hepatitis C virus replicon inhibitors: synthesis and structure-activity relationships of fused pyrimidine derivativesA Chris Krueger, Darold L Madigan, David W Beno, et al.
Biochemistry|January 22, 2003
Influenza neuraminidase inhibitors: structure-based design of a novel inhibitor seriesVincent Stoll, Kent D Stewart, Clarence J Maring, et al.
Bioorganic & Medicinal Chemistry Letters|February 15, 2011
Hepatitis C NS5B polymerase inhibitors: functional equivalents for the benzothiadiazine moietyDouglas K Hutchinson, Charles A Flentge, Pamela L Donner, et al.
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