Search Results - "PADALKO, Elisabeth"

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    Synthesis and Antiviral Activity Evaluation of Some New Aminoadamantane Derivatives. 2 by Kolocouris, Nicolas, Kolocouris, Antonios, Foscolos, George B, Fytas, George, Neyts, Johan, Padalko, Elisabeth, Balzarini, Jan, Snoeck, Robert, Andrei, Graciela, De Clercq, Erik

    Published in Journal of medicinal chemistry (16-08-1996)
    “…The synthesis of some new aminoadamantane derivatives is described. The new compounds were evaluated against a wide range of viruses [influenza A H1N1,…”
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    Journal Article
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    Synthesis and antiviral and cytostatic activities of carbocyclic nucleosides incorporating a modified cyclobutane ring. Part 1 : Guanosine analogues by FIGUEIRA, M. J, BLANCO, J. M, BALZARINI, J, DE CLERCQ, E, CAAMANO, O, FERNANDEZ, F, GARCIA-MERA, X, LOPEZ, C, ANDREI, G, SNOECK, R, PADALKO, E, NEYTS, J

    Published in Archiv der Pharmazie (Weinheim) (01-10-1999)
    “…Five new carbocyclic nucleosides were prepared by constructing a guanine (compounds 3, 5) or 8-azaguanine (compounds 4, 6, and 7) base on the amino group of…”
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    Journal Article
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    New neplanocin analogues. VIII. Synthesis and biological activity of 6'-C-ethyl, -ethenyl, and -ethynyl derivatives of neplanocin A by SHUTO, S, OBARA, T, BALZARINI, J, DE CLERCQ, E, MATSUDA, A, SAITO, Y, YAMASHITA, K, TANAKA, M, SASAKI, T, ANDREI, G, SNOECK, R, NEYTS, J, PADALKO, E

    Published in Chemical & pharmaceutical bulletin (01-07-1997)
    “…This report describes the synthesis and antiviral effects of (6'R)-6'-C-ethynyl, -ethenyl, and -ethyl derivatives of neplanocin A (7a, 8a, and 9a,…”
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    Journal Article
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    Synthesis and Antiviral and Cytostatic Activities of Carbocyclic Nucleosides Incorporating a Modified Cyclobutane Ring by Figueira, M. José, Blanco, J. Manuel, Caamaño, Olga, Fernández, Franco, García-Mera, Xerardo, López, Carmen, Andrei, Graciela, Snoeck, Robert, Padalko, Elisabeth, Neyts, Johan, Balzarini, Jan, Clercq, Erik De

    Published in Archiv der Pharmazie (Weinheim) (01-10-1999)
    “…Five new carbocyclic nucleosides were prepared by constructing a guanine (compounds 3, 5) or 8‐azaguanine (compounds 4, 6, and 7) base on the amino group of…”
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    Journal Article
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