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N9-Substituted N(6)-[(3-methylbut-2-en-1-yl)amino]purine derivatives and their biological activity in selected cytokinin bioassays

  1. 1.
    SYSNO ASEP0368655
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleN9-Substituted N(6)-[(3-methylbut-2-en-1-yl)amino]purine derivatives and their biological activity in selected cytokinin bioassays
    Author(s) Mik, V. (CZ)
    Szüčová, Lucie (UEB-Q) RID, ORCID
    Spíchal, Lukáš (UEB-Q) RID, ORCID
    Plíhal, O. (CZ)
    Nisler, Jaroslav (UEB-Q) RID, ORCID
    Zahajská, L. (CZ)
    Doležal, Karel (UEB-Q) RID, ORCID
    Strnad, Miroslav (UEB-Q) RID, ORCID
    Number of authors8
    Source TitleBioorganic & Medicinal Chemistry. - : Elsevier - ISSN 0968-0896
    Roč. 19, č. 23 (2011), s. 7244-7251
    Number of pages8 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsN6-[(3-Methylbut-2-en-1-yl)amino]purine ; Isopentenyladenine derivatives ; N9-Substituted derivatives ; Cytokinins ; Cytokinin receptors
    Subject RIVEF - Botanics
    R&D ProjectsED0007/01/01 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GA522/09/1576 GA ČR - Czech Science Foundation (CSF)
    UT WOS000296752300031
    DOI10.1016/j.bmc.2011.09.052
    AnnotationRational design is one of the latest ways how to evaluate particular activity of signal molecules, for example cytokinin derivatives. A series of N(6)-[(3-methylbut-2-en-1-yl)amino]purine (iP) derivatives specifically substituted at the N9 atom of purine moiety by tetrahydropyran-2-yl, ethoxyethyl, and C2-C4 alkyl chains terminated by various functional groups were prepared. The reason for this rational design was to reveal the relationship between specific substitution at the N9 atom of purine moiety of iP and cytokinin activity of the prepared compounds. The synthesis was carried out either via 6-chloro-9-substituted intermediates prepared originally from 6-chloropurine, or by a direct alkylation of N9 atom of N(6)-[(3-methylbut-2-en-1-yl)amino]purine.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2012
Number of the records: 1  

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