Open AccessJournal Article
[Effect of a new antiviral compound 1-morpholinomethyltetrahydro-2(1H)-pyrimidinone on the interaction of influenza virus proteins with flat lipid membranes].
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TL;DR: The antiviral preparation 1-morpholinomethyltetrahydro-2(1H)-pyrimidinone (abbreviation DD-13) inhibiting reproduction of certain enveloped viruses belonging to groups of orthomyxoviruses and alphaviruses, influenza type A viruses among them, inhibited adsorption and insertion of influenza virus M protein into model bilayer lipid membranes.
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Abstract: The antiviral preparation 1-morpholinomethyltetrahydro-2(1H)-pyrimidinone (abbreviation DD-13) inhibiting reproduction of certain enveloped viruses belonging to groups of orthomyxoviruses and alphaviruses, influenza type A viruses among them, inhibited adsorption and insertion of influenza virus M protein into model bilayer lipid membranes. The preparation did not interact directly with lipid bilayers but, after pretreatment of M protein with it, inhibited M protein interaction with the membranes: adsorption and insertion into the bilayer DD-13 did not affect the interaction of influenza virus surface glycoproteins with the model lipid membranes. It is concluded that the DD-13 preparation, not interacting with the membranes directly, in native systems may modify the protein-lipid interactions at the stages of virus penetration into the cell, penetration of M protein-coated nucleocapsid into the cell nucleus through the nuclear membrane, as well as at the stage of virus particle assembly on the plasma membrane of the infected cell.
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Citations
Progress of small molecular inhibitors in the development of anti-influenza virus agents.
TL;DR: The progress of small molecular inhibitors act as antiviral agents, which include hemagglutinin (HA), RNA-dependent RNA polymerase (RdRp) inhibitors, NA inhibitors and M2 ion channel protein inhibitors etc are reviewed.
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Cycluridine: A novel antiviral effective against flaviviruses:
Angel S. Galabov,Lucia Mukova,Yuriy P Abashev,Lilia Wassilewa,Petko Tzvetkov,Vassil Minkov,Igor F Barinskiy,Charles M Rice,Sergey Ouzounov,Dorotea Sidzhakova +9 more
TL;DR: Cycluridine, an originally synthesized Mannich’s base, is highlighted as a highly effective antiviral possessing a strong inhibitory effect on bovine viral diarrhoea virus replication, leading to its magnitude of activity and selectivity placing cycluridine in the lead among all known substances with anti- bovin viral diarrhaoa virus activity.
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