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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
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SYSNO ASEP 0368655 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title N9-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, ORCIDNumber of authors 8 Source Title Bioorganic & Medicinal Chemistry. - : Elsevier - ISSN 0968-0896
Roč. 19, č. 23 (2011), s. 7244-7251Number of pages 8 s. Language eng - English Country GB - United Kingdom Keywords N6-[(3-Methylbut-2-en-1-yl)amino]purine ; Isopentenyladenine derivatives ; N9-Substituted derivatives ; Cytokinins ; Cytokinin receptors Subject RIV EF - Botanics R&D Projects ED0007/01/01 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GA522/09/1576 GA ČR - Czech Science Foundation (CSF) UT WOS 000296752300031 DOI 10.1016/j.bmc.2011.09.052 Annotation Rational 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. Workplace Institute of Experimental Botany Contact David Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469 Year of Publishing 2012
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