Synthesis and structure-activity relationships of novel anti-hepatitis C agents: N3,5′-cyclo-4-(β-D-ribofuranosyl)-vic-triazolo[4, 5-b]pyridin-5-one derivatives
The prevalence of hepatitis C virus infection in the United states, 1988 through 1994
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Combination therapy with interferon-alpha and ribavirin for hepatitis C: Practical treatment issues
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3,5′-Cyclo-4-(β-D-ribofuranosyl)-vic- triazolo[4,5-b]-pyridin-5-one, a novel compound with potential anti-hepatitis C virus activity
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2,5′-anhydrouridine and 2,5′-anhydro-5-fluorouridine. One-step conversion of uridine and 5′fluorouridine into their corresponding 2,5′-anhydronucleosides
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Synthesis, structural and conformational assignments, and conversions of pyridine and triazopyridine nucleosides
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Dynamics of subgenomic hepatitis C virus replicon RNA levels in Huh-7 cells after exposure to nucleoside antimetabolites
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Ribonucleoside analogue that blocks replication of bovine viral diarrhea and hepatitis C virus in culture
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Activity of 3′-azido-3′-deoxythymidine nucleotide dimers in primary lymphocytes infected with human immunodeficiency virus type 1
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