Počet záznamů: 1  

Synthesis and in vitro biological evaluation of 2,6,9-trisubstituted purines targeting multiple cyclin-dependent kinases

  1. 1.
    SYSNO ASEP0395483
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSynthesis and in vitro biological evaluation of 2,6,9-trisubstituted purines targeting multiple cyclin-dependent kinases
    Tvůrce(i) Zatloukal, M. (CZ)
    Jorda, Radek (UEB-Q) ORCID, RID
    Gucký, T. (CZ)
    Řezníčková, Eva (UEB-Q) RID, ORCID
    Voller, Jiří (UEB-Q) RID, ORCID
    Pospíšil, T. (CZ)
    Malínková, V. (CZ)
    Adamcová, H. (CZ)
    Kryštof, Vladimír (UEB-Q) RID, ORCID
    Strnad, Miroslav (UEB-Q) RID, ORCID
    Zdroj.dok.European Journal of Medicinal Chemistry. - : Elsevier - ISSN 0223-5234
    Roč. 61, SI (2013), s. 61-72
    Poč.str.12 s.
    Jazyk dok.eng - angličtina
    Země vyd.FR - Francie
    Klíč. slovaCyclin-dependent kinase ; Inhibitor ; Roscovitine
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEPGAP305/12/0783 GA ČR - Grantová agentura ČR
    GA301/08/1649 GA ČR - Grantová agentura ČR
    CEZAV0Z50380511 - UEB-Q (2005-2011)
    UT WOS000316537200006
    DOI10.1016/j.ejmech.2012.06.036
    AnotaceSeveral inhibitors of cyclin-dependent kinases (CDKs), including the 2,6,9-trisubstituted purine derivative roscovitine, are currently being evaluated in clinical trials as potential anticancer drugs. Here, we describe a new series of roscovitine derivatives that show increased potency in vitro. The series was tested for cytotoxicity against six cancer cell lines and for inhibition of CDKs. For series bearing 2-(hydroxyalkylamino) moiety, cytotoxic potency strongly correlated with anti-CDK2 activity. Importantly, structural changes that increase biochemical and anticancer activities of these compounds also increase elimination half-life. The most potent compounds were investigated further to assess their ability to influence cell cycle progression, p53-regulated transcription and apoptosis. All the observed biological effects were consistent with inhibition of CDKs involved in the regulation of cell cycle and transcription.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2014
Počet záznamů: 1  

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