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Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain
MV. Diachkov, K. Ferrer, J. Oklestkova, L. Rarova, V. Bazgier, M. Kvasnica
Language English Country Switzerland
Document type Journal Article
Grant support
GA19-01383S
Grant Agency of the Czech Republic
CZ.02.1.01/0.0/0.0/16_019/0000827
European Regional Development Fund
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33375728
DOI
10.3390/ijms22010155
Knihovny.cz E-resources
- MeSH
- Arabidopsis drug effects growth & development MeSH
- Brassinosteroids chemical synthesis chemistry pharmacology MeSH
- Nitrogen chemistry MeSH
- Molecular Structure MeSH
- Chemistry Techniques, Synthetic * MeSH
- Plant Development drug effects MeSH
- Publication type
- Journal Article MeSH
Brassinosteroids are a class of plant hormones that regulate a broad range of physiological processes such as plant growth, development and immunity, including the suppression of biotic and abiotic stresses. In this paper, we report the synthesis of new brassinosteroid analogues with a nitrogen-containing side chain and their biological activity on Arabidopis thaliana. Based on molecular docking experiments, two groups of brassinosteroid analogues were prepared with short and long side chains in order to study the impact of side chain length on plants. The derivatives with a short side chain were prepared with amide, amine and ammonium functional groups. The derivatives with a long side chain were synthesized using amide and ammonium functional groups. A total of 25 new brassinosteroid analogues were prepared. All 25 compounds were tested in an Arabidopsis root sensitivity bioassay and cytotoxicity screening. The synthesized substances showed no significant inhibitory activity compared to natural 24-epibrassinolide. In contrast, in low concentration, several compounds (8a, 8b, 8e, 16e, 22a and 22e) showed interesting growth-promoting activity. The cytotoxicity assay showed no toxicity of the prepared compounds on cancer and normal cell lines.
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