In Vitro Antiviral Profile of Ruzasvir, a Potent and Pangenotype Inhibitor of Hepatitis C Virus NS5A

Author:

Asante-Appiah Ernest1,Liu Rong1,Curry Stephanie1,McMonagle Patricia1,Agrawal Sony2,Carr Donna2,Rokosz Laura2,Lahser Frederick1ORCID,Bystol Karin1,Chase Robert1,Black Stuart1,Ferrari Eric1,Ingravallo Paul1,Tong Ling3,Yu Wensheng3,Kozlowski Joseph3

Affiliation:

1. Department of Infectious Diseases, Merck & Co., Inc., Kenilworth, New Jersey, USA

2. Department of In Vitro Pharmacology, Merck & Co., Inc., Kenilworth, New Jersey, USA

3. Department of Medicinal Chemistry, Merck & Co., Inc., Kenilworth, New Jersey, USA

Abstract

Inhibition of NS5A has emerged as an attractive strategy to intervene in hepatitis C virus (HCV) replication. Ruzasvir (formerly MK-8408) was developed as a novel NS5A inhibitor to improve upon the potency and barrier to resistance of early compounds.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Tandem construction of biological relevant aliphatic 5-membered N-heterocycles;European Journal of Medicinal Chemistry;2022-05

2. HCV Replicon Systems: Workhorses of Drug Discovery and Resistance;Frontiers in Cellular and Infection Microbiology;2020-06-30

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