Abstract
4-(1,1-Dioxo-1,4-dihydro-1lambda(6)-benzo[1,4]thiazin-3-yl)-5-hydroxy-2H-pyridazin-3-one analogs were discovered as a novel class of inhibitors of HCV NS5B polymerase. Structure-based design led to the identification of compound 3a that displayed potent inhibitory activities in biochemical and replicon assays (1b IC(50)<10 nM; 1b EC(50)=1.1 nM) as well as good stability toward human liver microsomes (HLM t(1/2)>60 min).
MeSH terms
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Caco-2 Cells
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Chemistry, Pharmaceutical / methods*
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Crystallography, X-Ray / methods
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Drug Design
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Hepacivirus / drug effects
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Hepacivirus / enzymology*
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Humans
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Inhibitory Concentration 50
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Microsomes, Liver / enzymology*
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Models, Chemical
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Molecular Conformation
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Pyridazines / chemical synthesis*
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Pyridazines / chemistry
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Pyridazines / pharmacology*
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Structure-Activity Relationship
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Thiazines / chemical synthesis*
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Thiazines / chemistry
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Thiazines / pharmacology
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Time Factors
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Viral Nonstructural Proteins / antagonists & inhibitors*
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Viral Nonstructural Proteins / chemistry*
Substances
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Pyridazines
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Thiazines
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Viral Nonstructural Proteins
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NS-5 protein, hepatitis C virus