Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug (PSI-7977) for the treatment of hepatitis C virus.
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Recent Advances in Antiviral Therapy for Chronic Hepatitis CDaclatasvir-sofosbuvir combination therapy with or without ribavirin for hepatitis C virus infection: from the clinical trials to real lifeSofosbuvir, a Significant Paradigm Change in HCV TreatmentImpact of new treatment options for hepatitis C virus infection in liver transplantationInhibitors of the Hepatitis C Virus Polymerase; Mode of Action and ResistanceNew era for management of chronic hepatitis C virus using direct antiviral agents: A reviewSofosbuvir, a NS5B polymerase inhibitor in the treatment of hepatitis C: a review of its clinical potentialSynthesis of nucleoside phosphate and phosphonate prodrugsChutes and ladders in hepatitis C nucleoside drug developmentProdrugs of phosphonates and phosphates: crossing the membrane barrierChanging the face of hepatitis C management - the design and development of sofosbuvirSpatiotemporal analysis of hepatitis C virus infectionViral replication. Structural basis for RNA replication by the hepatitis C virus polymeraseThe FDA-approved drug sofosbuvir inhibits Zika virus infectionClinical Laboratory Testing in the Era of Directly Acting Antiviral Therapies for Hepatitis CSensitivity of mitochondrial transcription and resistance of RNA polymerase II dependent nuclear transcription to antiviral ribonucleosidesBroad-spectrum agents for flaviviral infections: dengue, Zika and beyondFuture of liver disease in the era of direct acting antivirals for the treatment of hepatitis CBiophysical Mode-of-Action and Selectivity Analysis of Allosteric Inhibitors of Hepatitis C Virus (HCV) Polymerase.Real-World Efficacy of Daclatasvir and Sofosbuvir, With and Without Ribavirin, in HIV/HCV Coinfected Patients With Advanced Liver Disease in a French Early Access Cohort.Preclinical characterization of BMS-791325, an allosteric inhibitor of hepatitis C Virus NS5B polymerase.Efficiency of incorporation and chain termination determines the inhibition potency of 2'-modified nucleotide analogs against hepatitis C virus polymeraseA liquid chromatography-tandem mass spectrometry method for the quantitative determination of diastereomers of a phosphoramidate nucleotide prodrug (PSI-7851) in human plasma.A cutting-edge view on the current state of antiviral drug development.Direct-acting antiviral agents for hepatitis C virus infection.Repurposing of the antihistamine chlorcyclizine and related compounds for treatment of hepatitis C virus infection.Substrates and Inhibitors of SAMHD1.Inhibition of hepatitis C virus replicon RNA synthesis by PSI-352938, a cyclic phosphate prodrug of β-D-2'-deoxy-2'-α-fluoro-2'-β-C-methylguanosine.Activity and the metabolic activation pathway of the potent and selective hepatitis C virus pronucleotide inhibitor PSI-353661.Design, synthesis and biological evaluation of phosphorodiamidate prodrugs of antiviral and anticancer nucleosides.Novel and sensitive UPLC-MS/MS method for quantification of sofosbuvir in human plasma: application to a bioequivalence study.Thiophene-expanded guanosine analogues of Gemcitabine.Re-re-treatment of hepatitis C virus: Eight patients who relapsed twice after direct-acting-antiviral drugsA multifunctional catalyst that stereoselectively assembles prodrugs.Highly efficient full-length hepatitis C virus genotype 1 (strain TN) infectious culture system.Global epidemiology of hepatocellular carcinoma: an emphasis on demographic and regional variability.Preclinical characterization of GS-9669, a thumb site II inhibitor of the hepatitis C virus NS5B polymeraseDiscovery, Optimization, and Characterization of Novel Chlorcyclizine Derivatives for the Treatment of Hepatitis C Virus Infection.Pharmacokinetics, safety, and tolerability of GS-9851, a nucleotide analog polymerase inhibitor for hepatitis C virus, following single ascending doses in healthy subjects.Pharmacokinetics, pharmacodynamics, and tolerability of GS-9851, a nucleotide analog polymerase inhibitor, following multiple ascending doses in patients with chronic hepatitis C infection.
P2860
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P2860
Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug (PSI-7977) for the treatment of hepatitis C virus.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@ast
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@en
Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug
@nl
type
label
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@ast
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@en
Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug
@nl
prefLabel
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@ast
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@en
Discovery of a β-d-2'-deoxy-2'-α-fluoro-2'-β-C-methyluridine nucleotide prodrug
@nl
P2093
P356
P1476
Discovery of a β-d-2'-deoxy-2' ...... reatment of hepatitis C virus.
@en
P2093
Angela M Lam
Bruce S Ross
Christine Espiritu
Congrong Niu
Dhanapalan Nagarathnam
Donghui Bao
Hai-Ren Zhang
Holly M Micolochick Steuer
Meg Keilman
P304
P356
10.1021/JM100863X
P407
P577
2010-10-01T00:00:00Z