Influenza A virus (IAV) infection is a major public health threat leading to significant morbidity and mortality. The emergence of drug-resistant virus strains highlights the urgent need to develop novel antiviral drugs with alternative modes of action. Pentagalloylglucose (PGG), a naturally occurring polyphenolic compound, possesses a broad spectrum of biological activities. In this study, we found that PGG has anti-influenza-virus activity, and investigated its possible mechanism(s) of action in vitro. Both pre-incubation of virus prior to infection and post-exposure of infected cells with PGG significantly inhibited virus yields. Influenza-virus-induced hemagglutination of chicken red blood cells was inhibited by PGG treatment, suggestin...
Abstract Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione deriv...
We identified new inhibitors of influenza virus hemagglutinin(HA)–mediated fusion, having a similar ...
Various influenza virus entry inhibitors are being developed as therapeutic antiviral agents in ongo...
Influenza A virus (IAV) infection is a major public health threat leading to significant morbidity a...
Hemagglutinin (HA) is essential for Influenza A virus infection, but its diversity of subtypes prese...
A set of polyphenol compounds was synthesized and assayed for their ability in inhibiting influenza ...
International audienceA set of polyphenol compounds was synthesized and assayed for their ability in...
Objectives: Drugs that target host cell processes can be employed to complement drugs that specifica...
Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione derivative, af...
Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione derivative, af...
Objectives: Drugs that target host cell processes can be employed to complement drugs that specifica...
Paper Poster Session 3 - P32 Recent advances in molecular diagnosis and epidemiology of viral respir...
Hemagglutinin (HA) of the influenza virus plays a crucial role in the early stage of the viral life ...
Abstract Background Neuraminidase (NA) inhibitors used for influenza therapy are believed to prevent...
Isoquercitrin (IQC) is a component abundantly present in many plants and is known to have an anti-vi...
Abstract Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione deriv...
We identified new inhibitors of influenza virus hemagglutinin(HA)–mediated fusion, having a similar ...
Various influenza virus entry inhibitors are being developed as therapeutic antiviral agents in ongo...
Influenza A virus (IAV) infection is a major public health threat leading to significant morbidity a...
Hemagglutinin (HA) is essential for Influenza A virus infection, but its diversity of subtypes prese...
A set of polyphenol compounds was synthesized and assayed for their ability in inhibiting influenza ...
International audienceA set of polyphenol compounds was synthesized and assayed for their ability in...
Objectives: Drugs that target host cell processes can be employed to complement drugs that specifica...
Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione derivative, af...
Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione derivative, af...
Objectives: Drugs that target host cell processes can be employed to complement drugs that specifica...
Paper Poster Session 3 - P32 Recent advances in molecular diagnosis and epidemiology of viral respir...
Hemagglutinin (HA) of the influenza virus plays a crucial role in the early stage of the viral life ...
Abstract Background Neuraminidase (NA) inhibitors used for influenza therapy are believed to prevent...
Isoquercitrin (IQC) is a component abundantly present in many plants and is known to have an anti-vi...
Abstract Aim: The aim of this study was to determine whether GSH-C4, a hydrophobic glutathione deriv...
We identified new inhibitors of influenza virus hemagglutinin(HA)–mediated fusion, having a similar ...
Various influenza virus entry inhibitors are being developed as therapeutic antiviral agents in ongo...