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Discovery of (R)-6-Cyclopentyl-6-(2-(2,6-diethylpyridin-4-yl)ethyl)-3-((5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methyl)-4-hydroxy-5,6-dihydropyran-2-one (PF-00868554) as a Potent and Orally Available Hepatitis C Virus Polymerase Inhibitor

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hep.22357openalex-snapshot
R1626 plus peginterferon Alfa‐2a provides potent suppression of hepatitis C virus RNA and significant antiviral synergy in combination with ribavirin†
inferredcites →https://doi.org/10.1016/j.bmcl.2006.06.065openalex-snapshot
Identification and structure-based optimization of novel dihydropyrones as potent HCV RNA polymerase inhibitors
inferredcites →https://doi.org/10.1016/s0168-8278(08)60068-9openalex-snapshot
66 POTENT ANTIVIRAL ACTIVITY OF THE HCV NUCLEOSIDE POLYMERASE INHIBITOR R7128 WITH PEG-IFN AND RIBAVIRIN: INTERIM RESULTS OF R7128 500MG BID FOR 28 DAYS
inferredcites →https://doi.org/10.1016/s0168-8278(08)60590-5openalex-snapshot
588 IN VITRO ANTIVIRAL ACTIVITY AND PHARMACOLOGY OF IDX184, A NOVEL AND POTENT INHIBITOR OF HCV REPLICATION
inferredcites →https://doi.org/10.1021/jm0704447openalex-snapshot
Allosteric Inhibitors of Hepatitis C Polymerase: Discovery of Potent and Orally Bioavailable Carbon-Linked Dihydropyrones
inferredcites →https://doi.org/10.1038/nrd2411openalex-snapshot
The way forward in HCV treatment — finding the right path
inferredcites →https://doi.org/10.1097/00004836-200003000-00005openalex-snapshot
Hepatitis C
inferredcites →https://doi.org/10.1124/pr.58.3.6openalex-snapshot
Pharmacogenetics, Drug-Metabolizing Enzymes, and Clinical Practice
inferredcites →https://doi.org/10.1128/aac.00834-07openalex-snapshot
In Vitro Resistance Study of AG-021541, a Novel Nonnucleoside Inhibitor of the Hepatitis C Virus RNA-Dependent RNA Polymerase
inferredcites →https://doi.org/10.1128/aac.01008-06openalex-snapshot
Development of a Novel Dicistronic Reporter-Selectable Hepatitis C Virus Replicon Suitable for High-Throughput Inhibitor Screening
inferredcites →https://doi.org/10.1128/jvi.77.13.7575-7581.2003openalex-snapshot
Crystallographic Identification of a Noncompetitive Inhibitor Binding Site on the Hepatitis C Virus NS5B RNA Polymerase Enzyme
inferredcites →https://doi.org/10.1556/oh.2008.28bopenalex-snapshot
The 43rd Annual Meeting of the European Association for the Study of the Liver (EASL), Milan, Italy, April 23–27, 2008
inferredcites →https://doi.org/10.2174/187152606776056698openalex-snapshot
Nucleoside Analog Inhibitors of Hepatitis C Virus Replication

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Design, Synthesis and Anticancer Activity of New Quinolines, Quinazolines and 1,2,4-Triazoles with Pyrido[2,3-d] Pyrimidines
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Pharmacology and Mechanisms of Action of Antiviral Drugs: Polymerase Inhibitors
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Recent Advances in the Field of Naturally Occurring 5,6‐Dihydropyran‐2‐ones
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Quadri‐Synergetic Effect for Highly Effective Carbon Dioxide Fixation and Its Application to Indoloquinolinone
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Novel 4‐Thiazolidinones as Non‐Nucleoside Inhibitors of Hepatitis C Virus NS5B RNA‐Dependent RNA Polymerase
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Optimization of Thienopyrrole‐Based Finger‐Loop Inhibitors of the Hepatitis C Virus NS5B Polymerase
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Synthesis and antimicrobial activity of new 1,2,4‐triazole, 1,3,4‐oxadiazole, 1,3,4‐thiadiazole, thiopyrane, thiazolidinone, and azepine derivatives
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Synthesis of new pyrazoles, oxadiazoles, triazoles, pyrrolotriazines, and pyrrolotriazepines as potential cytotoxic agents
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Structure-Activity Relationships in the Development of Allosteric Hepatitis C Virus RNA-Dependent RNA Polymerase Inhibitors: Ten Years of Research
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Thumb inhibitor binding eliminates functionally important dynamics in the hepatitis C virus RNA polymerase
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Tactics to Avoid Inhibition of Cytochrome P450s
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Evolution of HCV NS5B Non-nucleoside Inhibitors
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Hepatitis C Virus-Specific Directly Acting Antiviral Drugs
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Syntheses and in vitro biological screening of 1-aryl-10H-[1,2,4]triazolo[3′,4′:3,4][1,2,4]triazino[5,6-b]indoles
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Erratum to: Syntheses and in vitro biological screening of 1-aryl-10H-[1,2,4]triazolo[3′,4′:3,4][1,2,4]triazino[5,6-b]indoles
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Biological activities of [1,2,4]triazolo[1,5-a]pyrimidines and analogs
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Synthesis, docking, and biological evaluation of thiazolidinone derivatives against hepatitis C virus genotype 4a
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Direct-Acting Antiviral Agents for the Treatment of Hepatitis C Virus Infection
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Design and Development of HCV NS5B Polymerase Inhibitors
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Computational and Artificial Intelligence Techniques for Drug Discovery and Administration
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RNA-dependent RNA polymerase inhibitors: Current progress and potential for COVID-19 treatment
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Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry
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Allosteric and dynamic control of RNA-dependent RNA polymerase function and fidelity
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Discovery of substituted N-phenylbenzenesulphonamides as a novel class of non-nucleoside hepatitis C virus polymerase inhibitors
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Resolution of the interaction mechanisms and characteristics of non-nucleoside inhibitors of hepatitis C virus polymerase
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Computational study on the drug resistance mechanism of HCV NS5B RNA-dependent RNA polymerase mutants V494I, V494A, M426A, and M423T to Filibuvir
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Broad-spectrum non-nucleoside inhibitors for caliciviruses
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The design, synthesis and biological evaluations of C-6 or C-7 substituted 2-hydroxyisoquinoline-1,3-diones as inhibitors of hepatitis C virus
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Pyridobenzothiazole derivatives as new chemotype targeting the HCV NS5B polymerase
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C-6 aryl substituted 4-quinolone-3-carboxylic acids as inhibitors of hepatitis C virus
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Inhibitors for the hepatitis C virus RNA polymerase explored by SAR with advanced machine learning methods
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Design and synthesis of l- and d-phenylalanine derived rhodanines with novel C5-arylidenes as inhibitors of HCV NS5B polymerase
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The discovery and structure–activity relationships of pyrano[3,4-b]indole based inhibitors of hepatitis C virus NS5B polymerase
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The discovery and structure–activity relationships of pyrano[3,4-b]indole-based inhibitors of hepatitis C virus NS5B polymerase
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Design and synthesis of lactam–thiophene carboxylic acids as potent hepatitis C virus polymerase inhibitors
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The role of resistance in HCV treatment
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Application of 1,2,4-triazolo[1,5 -a ]pyrimidines for the design of coordination compounds with interesting structures and new biological properties
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Computational study on the drug resistance mechanism of hepatitis C virus NS5B RNA-dependent RNA polymerase mutants to BMS-791325 by molecular dynamics simulation and binding free energy calculations
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Quantum molecular modeling of hepatitis C virus inhibition through non-structural protein 5B polymerase receptor binding of C5-arylidene rhodanines
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2-Heteroarylimino-5-arylidene-4-thiazolidinones as a new class of non-nucleoside inhibitors of HCV NS5B polymerase
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1,2,4-Triazolo[1,5-a]pyrimidines in drug design
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Insight into non-nucleoside triazole-based systems as viral polymerases inhibitors
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Synthesis, anticancer activity and molecular docking of new quinolines, quinazolines and 1,2,4-triazoles with pyrido[2,3-d] pyrimidines
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Determination and control of TEMPO, a potentially genotoxic free radical reagent used in the synthesis of filibuvir
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Discovery of novel Hepatitis C virus inhibitor targeting multiple allosteric sites of NS5B polymerase
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An overview of the most used synthetic pathways of 1,2,4-triazolo[1,5-a]pyrimidines
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7-(Substituted amino)-5-methylthioazolo[1,5-a]pyrimidines: Synthesis, cytotoxic properties in vitro and molecular docking
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Computational predictions suggest that structural similarity in viral polymerases may lead to comparable allosteric binding sites
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Dual Allosteric Inhibitors Jointly Modulate Protein Structure and Dynamics in the Hepatitis C Virus Polymerase
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Discovery of Novel Thiophene-Based, Thumb Pocket 2 Allosteric Inhibitors of the Hepatitis C NS5B Polymerase with Improved Potency and Physicochemical Profiles
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A New Fluorogenic Small-Molecule Labeling Tool for Surface Diffusion Analysis and Advanced Fluorescence Imaging of β-Site Amyloid Precursor Protein-Cleaving Enzyme 1 Based on Silicone Rhodamine: SiR-BACE1
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Benzimidazoazapurines: Design, Synthesis, and Photophysical Study
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Iridium-Catalyzed Asymmetric Allylic Substitution Reaction of 4-Hydroxypyran-2-one
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Pfizer Global Virtual Library (PGVL): A Chemistry Design Tool Powered by Experimentally Validated Parallel Synthesis Information
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Quinoxalin-2(1H)-One Derivatives As Inhibitors Against Hepatitis C Virus
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Structure–Activity Relationship (SAR) Development and Discovery of Potent Indole-Based Inhibitors of the Hepatitis C Virus (HCV) NS5B Polymerase
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A Novel Class of Highly Potent Irreversible Hepatitis C Virus NS5B Polymerase Inhibitors
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Nucleoside, Nucleotide, and Non-Nucleoside Inhibitors of Hepatitis C Virus NS5B RNA-Dependent RNA-Polymerase
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Discovery of the First Thumb Pocket 1 NS5B Polymerase Inhibitor (BILB 1941) with Demonstrated Antiviral Activity in Patients Chronically Infected with Genotype 1 Hepatitis C Virus (HCV)
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Structure-Based Discovery of Pyrazolobenzothiazine Derivatives As Inhibitors of Hepatitis C Virus Replication
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The Versatile Nature of the 6-Aminoquinolone Scaffold: Identification of Submicromolar Hepatitis C Virus NS5B Inhibitors
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Discovery of GS-9669, a Thumb Site II Non-Nucleoside Inhibitor of NS5B for the Treatment of Genotype 1 Chronic Hepatitis C Infection
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Identification and Biological Evaluation of a Series of 1H-Benzo[de]isoquinoline-1,3(2H)-diones as Hepatitis C Virus NS5B Polymerase Inhibitors
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Synthesis and Anti-HCV Activity of 4-Hydroxyamino α-Pyranone Carboxamide Analogues
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Synthesis of Filibuvir. Part I. Diastereoselective Preparation of a β-Hydroxy Alkynyl Oxazolidinone and Conversion to a 6,6-Disubstituted 2 H -Pyranone
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Synthesis of Filibuvir. Part III. Development of a Process for the Reductive Coupling of an Aldehyde and a β-Keto-lactone
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Understanding the drug resistance mechanism of hepatitis C virus NS5B to PF-00868554 due to mutations of the 423 site: a computational study
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Total synthesis and stereochemical assignment of cryptolatifolione
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Heteronuclear d–d and d–f Ru( ii )/M complexes [M = Gd( iii ), Yb( iii ), Nd( iii ), Zn( ii ) or Mn( ii )] of ligands combining phenanthroline and aminocarboxylate binding sites: combined relaxivity, cell imaging and photophysical studies
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Recent advances in the discovery of potent RNA-dependent RNA-polymerase (RdRp) inhibitors targeting viruses
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Synthesis of a 5,6-Dihydropyran-2-one Derivative with Dual Anti-Cell-Migration and Anticancer Activity
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Hydrogen/Deuterium Exchange Kinetics Demonstrate Long Range Allosteric Effects of Thumb Site 2 Inhibitors of Hepatitis C Viral RNA-dependent RNA Polymerase
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NMR reveals the intrinsically disordered domain 2 of NS5A protein as an allosteric regulator of the hepatitis C virus RNA polymerase NS5B
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Probing the “fingers” domain binding pocket of Hepatitis C virus NS5B RdRp and D559G resistance mutation via molecular docking, molecular dynamics simulation and binding free energy calculations
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Insights into structural dynamics of allosteric binding sites in HCV RNA-dependent RNA polymerase
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HCV drug discovery aimed at viral eradication
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Antiviral Candidates for Treating Hepatitis E Virus Infection
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Preclinical Characterization of PF-00868554, a Potent Nonnucleoside Inhibitor of the Hepatitis C Virus RNA-Dependent RNA Polymerase
inferred← citeshttps://doi.org/10.1128/aac.02052-12openalex-snapshot
Preclinical Characterization of GS-9669, a Thumb Site II Inhibitor of the Hepatitis C Virus NS5B Polymerase
inferred← citeshttps://doi.org/10.1128/aac.03052-14openalex-snapshot
Genotypic and Phenotypic Analyses of Hepatitis C Virus Variants Observed in Clinical Studies of VX-222, a Nonnucleoside NS5B Polymerase Inhibitor
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Cross-Genotypic Examination of Hepatitis C Virus Polymerase Inhibitors Reveals a Novel Mechanism of Action for Thumb Binders
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Biochemical Study of the Comparative Inhibition of Hepatitis C Virus RNA Polymerase by VX-222 and Filibuvir
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Multiple virtual screening approaches for finding new Hepatitis c virus RNA-dependent RNA polymerase inhibitors: Structure-based screens and molecular dynamics for the pursue of new poly pharmacological inhibitors
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Etodolac Thiosemicarbazides:A novel class of hepatitis C virus NS5B polymerase inhibitors
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Microwave assisted synthesis of some novel Flurbiprofen hydrazide hydrazones as anti-HCV NS5B and anticancer agents
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Structural and Regulatory Elements of HCV NS5B Polymerase – β-Loop and C-Terminal Tail – Are Required for Activity of Allosteric Thumb Site II Inhibitors
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Hepatitis C virus virology and new treatment targets
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New developments in small molecular compounds for anti-hepatitis C virus (HCV) therapy
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Advancements in the Synthesis of Triazolopyrimidines
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Triazolopyrimidine Nuclei: Privileged Scaffolds for Developing Antiviral Agents with a Proper Pharmacokinetic Profile
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Triazolopyrimidine Derivatives: An Updated Review on Recent Advances in Synthesis, Biological Activities and Drug Delivery Aspects
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Synthesis and Antimicrobial Activity of Novel 1, 2, 4-Triazolopyrimidofuroquinazolinones from Natural Furochromones (Visnagenone and Khellinone)
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Anti-cancer and anti-hepatitis C virus NS5B polymerase activity of etodolac 1,2,4-triazoles
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Synthesis and Characterization of Celecoxib Derivatives as Possible Anti-Inflammatory, Analgesic, Antioxidant, Anticancer and Anti-HCV Agents
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Targeting the RdRp of Emerging RNA Viruses: The Structure-Based Drug Design Challenge
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Broad-Spectrum Host-Based Antivirals Targeting the Interferon and Lipogenesis Pathways as Potential Treatment Options for the Pandemic Coronavirus Disease 2019 (COVID-19)
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Antiviral Therapy for Hepatitis C Virus: Beyond the Standard of Care
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Inhibitors of the Hepatitis C Virus Polymerase; Mode of Action and Resistance
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Biophysical Mode-of-Action and Selectivity Analysis of Allosteric Inhibitors of Hepatitis C Virus (HCV) Polymerase
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Procyanidin B1 Purified from Cinnamomi Cortex Suppresses Hepatitis C Virus Replication
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Design and synthesis of antivirals benzimidazoles and quinoxalines
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Non-Nucleoside Inhibitors of Hepatitis C Virus Polymerase: Current Progress and Future Challenges
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Allosteric Inhibition of the Hepatitis C Virus NS5B Polymerase: In Silico Strategies for Drug Discovery and Development
inferred← citeshttps://doi.org/10.70675/6b806816ze3ddz4d4ezbb14z09f168aeafc8openalex-snapshot
Investigation of the hepatitis C virus RNA polymerase NS5B in solution by nuclear magnetic resonance and its interaction with intrinsically disordered domain 2 of the NS5A protein
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