Real-World Treatment Efficacy and Safety Profile of Sofosbuvir- and Velpatasvir-Based HCV Treatment in South Korea: Multicenter Prospective Study. [PDF]
Yoon JH +8 more
europepmc +1 more source
Reinfection and Resistance Associated Substitutions Following a Minimal Monitoring Approach for Hepatitis C Virus Treatment in MINMON Trial. [PDF]
Han WM +12 more
europepmc +1 more source
Prevalence of resistance-associated substitutions (RAS) in hepatitis C virus in the Former Soviet Union countries. [PDF]
Mustafa A +6 more
europepmc +1 more source
Mechanisms and Therapeutic Strategies for HCV/HBV-Associated B-Cell Non-Hodgkin's Lymphomas: A Viewpoint. [PDF]
Carloni G, Rinaldi M.
europepmc +1 more source
Tracking the evolution of multiple in vitro HCV replicon mutants under protease inhibitor selection pressure by 454 ultra deep sequencing. [PDF]
Claes, Marijke +8 more
core
Related searches:
As a result of rapid advance medicinal chemistry, the time frame 2011–2012 has been an exciting one that has witnessed the release of the first direct acting antiviral agents (DAA). Multiple enzymatic and protein regions of the virus can serve as targets for these new drugs. One of the newest and most promising of these targets is the NS5A protein. The
Christopher O’Brien, Nicholas Agresti
openaire +1 more source
HCV NS5A replication complex inhibitors
Current Opinion in Pharmacology, 2016The development of anti-HCV drugs is one of the most successful stories of antiviral therapy. In fact, for the first time in human history we have the potential to eradicate a chronic viral infection using only orally administered direct antiviral agents (DAAs).
Min, Gao +2 more
openaire +2 more sources
Discovery of fluorobenzimidazole HCV NS5A inhibitors
Bioorganic & Medicinal Chemistry Letters, 2016Research toward a next-generation HCV NS5A inhibitor has identified fluorobenzimidazole analogs that demonstrate potent, broad-genotype in vitro activity against HCV genotypes 1-6 replicons as well as HCV NS5A variants that are orders of magnitude less susceptible to inhibition by first-generation NS5A inhibitors in comparison to wild-type replicons ...
John T, Randolph +17 more
openaire +2 more sources
The NS5A Replication Complex Inhibitors: Difference Makers?
Clinics in Liver Disease, 2011The development and approval of direct-acting antiviral agents looks set to transform the treatment of chronic hepatitis C infection. Among the agents in development are novel compounds that inhibit the function of the NS5A protein: a pleiotropic protein with a complex and essential role in viral replication.
Robert G, Gish, Nicholas A, Meanwell
openaire +2 more sources
Discovery of potent macrocyclic HCV NS5A inhibitors
Bioorganic & Medicinal Chemistry Letters, 2016HCV NS5A inhibitors have demonstrated impressive in vitro virologic profiles in HCV replicon assays and robust HCV RNA titer reduction in the clinic making them attractive components for inclusion in an all oral fixed-dose combination (FDC) regimen for the treatment of HCV infection.
Wensheng Yu +28 more
openaire +2 more sources

