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Discovery of Ruzasvir (MK-8408): A Potent, Pan-Genotype HCV NS5A Inhibitor with Optimized Activity against Common Resistance-Associated Polymorphisms.

Ling TongWensheng YuLei ChenOleg SelyutinMichael P DwyerAnilkumar G NairRobert MazzolaJae-Hun KimDeyou ShaJingjun YinRebecca T RuckIan W DaviesBin HuBin ZhongJinglai HaoTao JiShuai ZanRong LiuSony AgrawalEllen XiaStephanie CurryPatricia McMonagleKarin BystolFrederick LahserDonna CarrLaura RokoszPaul IngravalloShiying ChenKung-I FengMark CartwrightErnest Asante-AppiahJoseph A Kozlowski
Published in: Journal of medicinal chemistry (2016)
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.
Keyphrases
  • hepatitis c virus
  • dengue virus
  • clinical trial
  • small molecule
  • human immunodeficiency virus
  • zika virus
  • randomized controlled trial
  • combination therapy
  • anti inflammatory
  • replacement therapy
  • wild type