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PUBMED FOR HANDHELDS

Journal Abstract Search


181 related items for PubMed ID: 27639368

  • 1. Identification of an indol-based derivative as potent and selective varicella zoster virus (VZV) inhibitor.
    Musella S, di Sarno V, Ciaglia T, Sala M, Spensiero A, Scala MC, Ostacolo C, Andrei G, Balzarini J, Snoeck R, Novellino E, Campiglia P, Bertamino A, Gomez-Monterrey IM.
    Eur J Med Chem; 2016 Nov 29; 124():773-781. PubMed ID: 27639368
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  • 2. Chemotherapy of varicella-zoster virus by a novel class of highly specific anti-VZV bicyclic pyrimidine nucleosides.
    Balzarini J, McGuigan C.
    Biochim Biophys Acta; 2002 Jul 18; 1587(2-3):287-95. PubMed ID: 12084470
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  • 3. Bicyclic nucleoside inhibitors of varicella-zoster virus modified on the sugar moiety: 3' and 5' derivatives.
    Luoni GM, McGuigan C, Andrei G, Snoeck R, De Clercq E, Balzarini J.
    Antivir Chem Chemother; 2004 Nov 18; 15(6):333-41. PubMed ID: 15646647
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  • 7. Specific recognition of the bicyclic pyrimidine nucleoside analogs, a new class of highly potent and selective inhibitors of varicella-zoster virus (VZV), by the VZV-encoded thymidine kinase.
    Sienaert R, Naesens L, Brancale A, De Clercq E, McGuigan C, Balzarini J.
    Mol Pharmacol; 2002 Feb 18; 61(2):249-54. PubMed ID: 11809847
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  • 8. Influence of 6 or 8-substitution on the antiviral activity of 3-phenethylthiomethylimidazo[1,2-a]pyridine against human cytomegalovirus (HCMV) and varicella-zoster virus (VZV).
    Véron JB, Enguehard-Gueiffier C, Snoeck R, Andrei G, De Clercq E, Gueiffier A.
    Bioorg Med Chem; 2007 Nov 15; 15(22):7209-19. PubMed ID: 17869124
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  • 10. Influence of 6- or 8-substitution on the antiviral activity of 3-arylalkylthiomethylimidazo[1,2-a]pyridine against human cytomegalovirus (CMV) and varicella-zoster virus (VZV): part II.
    Véron JB, Allouchi H, Enguehard-Gueiffier C, Snoeck R, Andrei G, De Clercq E, Gueiffier A.
    Bioorg Med Chem; 2008 Nov 01; 16(21):9536-45. PubMed ID: 18835175
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  • 12. Bicyclic pyrimidine nucleoside analogues (BCNAs) as highly selective and potent inhibitors of varicella-zoster virus replication.
    Balzarini J, McGuigan C.
    J Antimicrob Chemother; 2002 Jul 01; 50(1):5-9. PubMed ID: 12096000
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  • 16. 2'-Fluorosugar analogues of the highly potent anti-varicella-zoster virus bicyclic nucleoside analogue (BCNA) Cf 1743.
    McGuigan C, Derudas M, Quintiliani M, Andrei G, Snoeck R, Henson G, Balzarini J.
    Bioorg Med Chem Lett; 2009 Nov 15; 19(22):6264-7. PubMed ID: 19833513
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  • 18. Inhibitory activity of oxyresveratrol on wild-type and drug-resistant varicella-zoster virus replication in vitro.
    Sasivimolphan P, Lipipun V, Likhitwitayawuid K, Takemoto M, Pramyothin P, Hattori M, Shiraki K.
    Antiviral Res; 2009 Oct 15; 84(1):95-7. PubMed ID: 19635502
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  • 19. Comparative activity of selected antiviral compounds against clinical isolates of varicella-zoster virus.
    Andrei G, Snoeck R, Reymen D, Liesnard C, Goubau P, Desmyter J, De Clercq E.
    Eur J Clin Microbiol Infect Dis; 1995 Apr 15; 14(4):318-29. PubMed ID: 7649195
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