Abstract
We describe the research that led to the discovery of compound 40 (ruzasvir, MK-8408), a pan-genotypic HCV nonstructural protein 5A (NS5A) inhibitor with a "flat" GT1 mutant profile. This NS5A inhibitor contains a unique tetracyclic indole core while maintaining the imidazole-proline-valine Moc motifs of our previous NS5A inhibitors. Compound 40 is currently in early clinical trials and is under evaluation as part of an all-oral DAA regimen for the treatment of chronic HCV infection.
MeSH terms
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Animals
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Antiviral Agents / chemistry*
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Antiviral Agents / pharmacokinetics
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Antiviral Agents / pharmacology*
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Cell Line
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Dogs
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Haplorhini
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Hepacivirus / drug effects*
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Hepacivirus / genetics
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Heterocyclic Compounds, 4 or More Rings / chemistry*
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Heterocyclic Compounds, 4 or More Rings / pharmacokinetics
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Heterocyclic Compounds, 4 or More Rings / pharmacology*
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Humans
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Polymorphism, Genetic*
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Pyrrolidines / chemistry*
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Pyrrolidines / pharmacokinetics
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Pyrrolidines / pharmacology*
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Rats
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Structure-Activity Relationship
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Thiazoles / chemistry*
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Thiazoles / pharmacokinetics
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Thiazoles / pharmacology*
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Viral Nonstructural Proteins / antagonists & inhibitors*
Substances
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Antiviral Agents
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Heterocyclic Compounds, 4 or More Rings
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Pyrrolidines
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Thiazoles
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Viral Nonstructural Proteins
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NS-5 protein, hepatitis C virus
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ruzasvir