Number of the records: 1  

Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonate using NMR spectroscopy

  1. 1.
    0310038 - ÚOCHB 2009 RIV CZ eng C - Conference Paper (international conference)
    Dračínský, Martin - Krečmerová, Marcela - Holý, Antonín
    Study of chemical stability of antivirally active 5-azacytosine acyclic nucleoside phosphonate using NMR spectroscopy.
    [Studium chemické stability antivirově aktivních 5-azacytosin acyklických nukleosidfosfonátů pomocí NMR spektroskopie.]
    Chemistry of Nucleic Acid Components. Praha: Institute of Organic Chemistry and Biochemistry ASCR, 2008 - (Hocek, M.), s. 338-340. Collection Symposium Series, 10. ISBN 978-80-86241-29-6.
    [Symposium on Chemistry of Nucleic Acid Components /14./. Český Krumlov (CZ), 08.06.2008-13.06.2008]
    R&D Projects: GA MŠMT 1M0508; GA AV ČR 1QS400550501
    Institutional research plan: CEZ:AV0Z40550506
    Keywords : 5-azacytosine * decomposition * acyclic nucleoside phosphonates
    Subject RIV: CC - Organic Chemistry

    Hydrolytic decomposition of four 5-azacytosine acyclic nucleoside phosphonates was studied. Products of the decomposition are carbamoylguanidine derivatives. Stability and decomposition products of HPMP-5-azaC (a 5-azacytosine derivative with strong antiviral activity) differ from the other derivatives.

    Byly studovány hydrolytické rozklady čtyř 5-azacytosin acyklických nukleosidfosfonátů. Produktem rozkladu jsou karbamoylguanidinové deriváty. Stabilita a rozkladné produkty HPMP-5-azaC (5-azacytosinový derivát s vysokou protivirovou aktivitou) se odlišují od ostatních derivátů.
    Permanent Link: http://hdl.handle.net/11104/0162021
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.