N9-Substituted N(6)-[(3-methylbut-2-en-1-yl)amino]purine derivatives and their biological activity in selected cytokinin bioassays
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F11%3A10224990" target="_blank" >RIV/61989592:15310/11:10224990 - isvavai.cz</a>
Alternative codes found
RIV/61389030:_____/11:00368655
Result on the web
<a href="http://dx.doi.org/10.1016/j.bmc.2011.09.052" target="_blank" >http://dx.doi.org/10.1016/j.bmc.2011.09.052</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.bmc.2011.09.052" target="_blank" >10.1016/j.bmc.2011.09.052</a>
Alternative languages
Result language
angličtina
Original language name
N9-Substituted N(6)-[(3-methylbut-2-en-1-yl)amino]purine derivatives and their biological activity in selected cytokinin bioassays
Original language description
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 moietyof iP and cytokinin activity of the prepared compounds. The prepared derivatives were characterized by C, H, N elemental analyses, thin layer chromatography, high performance liquid chromatography, melting point determinations, CI+ mass spectral measurement, and by NMR spectroscopy. Biological activity of prepared compounds was assessed in three in vitro cytokinin bioassays (tobacco callus, wheat leaf senescence, and Amaranthus bioassay).
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Bioorganic & Medicinal Chemistry
ISSN
0968-0896
e-ISSN
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Volume of the periodical
19
Issue of the periodical within the volume
23
Country of publishing house
GB - UNITED KINGDOM
Number of pages
13
Pages from-to
7244-7251
UT code for WoS article
000296752300031
EID of the result in the Scopus database
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