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4-(1,1-Dioxo-1,4-dihydro-1lambda6-benzo[1,4]thiazin-3-yl)-5-hydroxy-2H-pyridazin-3-ones as potent inhibitors of HCV NS5B polymerase.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2008 Aug 15; Vol. 18 (16), pp. 4628-32. Date of Electronic Publication: 2008 Jul 10. - Publication Year :
- 2008
-
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).
- Subjects :
- Caco-2 Cells
Crystallography, X-Ray methods
Drug Design
Hepacivirus drug effects
Humans
Inhibitory Concentration 50
Models, Chemical
Molecular Conformation
Pyridazines chemistry
Structure-Activity Relationship
Thiazines chemistry
Thiazines pharmacology
Time Factors
Chemistry, Pharmaceutical methods
Hepacivirus enzymology
Microsomes, Liver enzymology
Pyridazines chemical synthesis
Pyridazines pharmacology
Thiazines chemical synthesis
Viral Nonstructural Proteins antagonists & inhibitors
Viral Nonstructural Proteins chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 18
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 18662878
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.07.014