Abstract
We studied the capacity amino acid derivatives of adamantane to inhibit replication of highly virulent avian influenza A/duck/Novosibirsk/56/05 (H5N1) virus in cultures of swine embryonic kidney cells. Amino acid derivatives of adamantane H-His-Rem and Ad(CH2-Ser-OMe)2 were characterized by lower toxicity than remantadine previously used in the treatment of influenza. Histidine-containing adamantane derivative (H-His-Rem) was the most effective and low-toxic inhibitor of influenza А/H5N1 virus replication and can be recommended for clinical trials to produce a preparation for the treatment and prevention of influenza.
MeSH terms
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Adamantane / analogs & derivatives
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Adamantane / chemical synthesis
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Adamantane / pharmacology*
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Animals
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Antiviral Agents / chemical synthesis
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Antiviral Agents / pharmacology*
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Cell Line
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Embryo, Mammalian
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Epithelial Cells / cytology
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Epithelial Cells / drug effects*
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Epithelial Cells / virology
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Histidine / chemistry
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Humans
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Influenza A Virus, H5N1 Subtype / drug effects*
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Influenza A Virus, H5N1 Subtype / pathogenicity*
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Influenza A Virus, H5N1 Subtype / physiology
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Kidney / cytology
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Kidney / drug effects
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Kidney / virology
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Rimantadine / pharmacology
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Serine / chemistry
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Swine
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Virulence
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Virus Replication / drug effects*
Substances
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Antiviral Agents
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Rimantadine
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Serine
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Histidine
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Adamantane