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Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors

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    0345730 - ÚOCHB 2011 RIV GB eng J - Journal Article
    Šála, Michal - De Palma, A. M. - Hřebabecký, Hubert - Nencka, Radim - Dračínský, Martin - Leyssen, P. - Neyts, J. - Holý, Antonín
    Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors.
    Bioorganic & Medicinal Chemistry. Roč. 18, č. 12 (2010), s. 4374-4384. ISSN 0968-0896. E-ISSN 1464-3391
    R&D Projects: GA MŠMT 1M0508
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : 6-chloropurine * coxsackievirus B3 * bicyclo[2.2.1]heptane
    Subject RIV: CC - Organic Chemistry
    Impact factor: 2.978, year: 2010

    Novel class of coxsackievirus inhibitors derived from a bicyclo[2.2.1]heptane was synthetised and target compounds were tested for antiviral activity against coxsackievirus B3. Most analogues showed activity in the low micromolar range with minimal cytotoxicity.
    Permanent Link: http://hdl.handle.net/11104/0186933

     
     
Number of the records: 1  

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