Inhibition of influenza A virus replication by rifampicin and selenocystamine.
M Hamzehei, N Ledinko
Index: J. Med. Virol. 6(2) , 169-74, (1980)
Full Text: HTML
Abstract
The effects of selenocystamine, an inhibitor of influenza virus RNA-dependent RNA polymerase in vitro activity, in the antibiotic rifampicin were studied on influenza A/PR/8/34 (HON1) infection in embryonated eggs. Both drugs completely inhibited hemagglutinating and infective virus yields when added at relatively early times postinfection. Maximal inhibition was produced by apparently noncytotoxic concentrations of 50 microgram of selenocystamine, or of 400 microgram of rifampicin, per egg.
Related Compounds
Related Articles:
Pulse radiolysis studies on reactions of hydroxyl radicals with selenocystine derivatives.
2008-04-10
[J. Phys. Chem. B 112(14) , 4441-6, (2008)]
Oxidation of glutathione and superoxide generation by inorganic and organic selenium compounds.
2008-09-01
[Biofactors 31(1) , 55-66, (2007)]
Separation of organoselenium compounds and their electrochemical detection.
2004-07-01
[Anal. Bioanal. Chem 379(5-6) , 770-6, (2004)]
2009-11-01
[Exp. Eye Res. 89(5) , 728-34, (2009)]
Cytolysis of human erythrocytes by a covalent antibody-selenium immunoconjugate.
1995-12-01
[Free Radic. Biol. Med. 19(6) , 713-24, (1995)]