Inhibition of feline (FIPV) and human (SARS) coronavirus by semisynthetic derivatives of glycopeptide antibiotics

被引:53
作者
Balzarini, Jan
Keyaerts, Els
Vijgen, Leen
Egberink, Herman
De Clercq, Erik
Van Ranst, Marc
Printsevskaya, Svetlana S.
Olsufyeva, Eugenia N.
Solovieva, Svetlana E.
Preobrazhenskaya, Maria N.
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
[2] Univ Utrecht, Inst Virol, Fac Vet Med, Utrecht, Netherlands
[3] Russian Acad Med Sci, Gause Inst New Antibiot, Moscow, Russia
关键词
coronaviruses; FIPV; SARS; glycopeptide antibiotics; vancomycin; teicoplanin; eremomycin;
D O I
10.1016/j.antiviral.2006.03.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Various semisynthetic derivatives of glycopeptide antibiotics including vancomycin, eremomycin, teicoplanin, ristocetin A and DA-40926 have been evaluated for their inhibitory activity against feline infectious peritonitis virus (FIPV) and human (SARS-CoV, Frankfurt-1 strain) coronavirus in cell culture in comparison with their activity against human immunodeficiency virus (HIV). Several glycopeptide derivatives modified with hydrophobic substituents showed selective antiviral activity. For the most active compounds, the 50% effective concentrations (EC50) were in the lower micromolar range. In general, removal of the carbohydrate parts of the molecules did not affect the antiviral activity of the compounds. Some compounds showed inhibitory activity against both, whereas other compounds proved inhibitory to either, FIPV or SARS-CoV There was no close correlation between the EC50 values of the glycopeptide derivatives for FIPV or SARS-CoV (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:20 / 33
页数:14
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