Biochemical mechanism of hepatitis C virus inhibition by the broad-spectrum antiviral arbidol - Wikidata - awgldk - TriplyDB

Biochemical mechanism of hepatitis C virus inhibition by the broad-spectrum antiviral arbidol

Biochemical mechanism of hepatitis C virus inhibition by the broad-spectrum antiviral arbidol

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Low pH-dependent Hepatitis C Virus Membrane Fusion Depends on E2 Integrity, Target Lipid Composition, and Density of Virus Particles The Synthetic Antiviral Drug Arbidol Inhibits Globally Prevalent Pathogenic Viruses Mechanism of inhibition of enveloped virus membrane fusion by the antiviral drug arbidol Emerging antiviral strategies to interfere with influenza virus entry.Differential in vitro effects of intravenous versus oral formulations of silibinin on the HCV life cycle and inflammation.Microwave-assisted synthesis of small molecules targeting the infectious diseases tuberculosis, HIV/AIDS, malaria and hepatitis C.Hepatitis C virus experimental model systems and antiviral drug research.The delivery of arbidol by salt engineering: synthesis, physicochemical properties and pharmacokinetics.Development of novel entry inhibitors targeting emerging viruses.Pharmacokinetics, metabolism, and excretion of the antiviral drug arbidol in humans.Antiviral strategies against influenza virus: towards new therapeutic approaches.A Potent, Broad-Spectrum Antiviral Agent that Targets Viral Membranes.Multiple effects of silymarin on the hepatitis C virus lifecycle.5-(Perylen-3-yl)ethynyl-arabino-uridine (aUY11), an arabino-based rigid amphipathic fusion inhibitor, targets virion envelope lipids to inhibit fusion of influenza virus, hepatitis C virus, and other enveloped viruses The Location of the Protonated and Unprotonated Forms of Arbidol in the Membrane: A Molecular Dynamics Study.Glucuronidation of the broad-spectrum antiviral drug arbidol by UGT isoforms.Arbidol (Umifenovir): A Broad-Spectrum Antiviral Drug That Inhibits Medically Important Arthropod-Borne Flaviviruses.The Antiviral Drug Arbidol Inhibits Zika Virus.Blocking HCV entry as potential antiviral therapy

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Biochemical mechanism of hepatitis C virus inhibition by the broad-spectrum antiviral arbidol

http://www.wikidata.org/entity/Q24653452

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2007 nî lūn-bûn

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2007 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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Biochemical mechanism of hepat ...... oad-spectrum antiviral arbidol

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Eve-Isabelle Pécheur

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Fanny Alcaras

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Jennifer Molle

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Michael Roberts

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Stephen J Polyak

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Yury S Boriskin

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P2860

Arbidol: a broad-spectrum antiviral that inhibits acute and chronic HCV infection

Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes

Time- and Temperature-Dependent Activation of Hepatitis C Virus for Low-pH-Triggered Entry

Functional analysis of hepatitis C virus envelope proteins, using a cell-cell fusion assay.

Production of infectious genotype 1a hepatitis C virus (Hutchinson strain) in cultured human hepatoma cells

Construction and characterization of infectious intragenotypic and intergenotypic hepatitis C virus chimeras

Replication of subgenomic hepatitis C virus RNAs in a hepatoma cell line

Cell entry of hepatitis C virus requires a set of co-receptors that include the CD81 tetraspanin and the SR-B1 scavenger receptor

Sensitivity of various influenza virus strains to arbidol. Influence of arbidol combination with different antiviral drugs on reproduction of influenza virus A

Mechanism of action of interferon and ribavirin in treatment of hepatitis C

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10.1021/BI700181J

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François-Loïc Cosset

Dimitri Lavillette

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2007-05-22T00:00:00Z

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