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Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain
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-cont...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795425/ https://www.ncbi.nlm.nih.gov/pubmed/33375728 http://dx.doi.org/10.3390/ijms22010155 |
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author | Diachkov, Mikhail V. Ferrer, Karoll Oklestkova, Jana Rarova, Lucie Bazgier, Vaclav Kvasnica, Miroslav |
author_facet | Diachkov, Mikhail V. Ferrer, Karoll Oklestkova, Jana Rarova, Lucie Bazgier, Vaclav Kvasnica, Miroslav |
author_sort | Diachkov, Mikhail V. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7795425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77954252021-01-10 Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain Diachkov, Mikhail V. Ferrer, Karoll Oklestkova, Jana Rarova, Lucie Bazgier, Vaclav Kvasnica, Miroslav Int J Mol Sci Article 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. MDPI 2020-12-25 /pmc/articles/PMC7795425/ /pubmed/33375728 http://dx.doi.org/10.3390/ijms22010155 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Diachkov, Mikhail V. Ferrer, Karoll Oklestkova, Jana Rarova, Lucie Bazgier, Vaclav Kvasnica, Miroslav Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title | Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title_full | Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title_fullStr | Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title_full_unstemmed | Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title_short | Synthesis and Biological Activity of Brassinosteroid Analogues with a Nitrogen-Containing Side Chain |
title_sort | synthesis and biological activity of brassinosteroid analogues with a nitrogen-containing side chain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795425/ https://www.ncbi.nlm.nih.gov/pubmed/33375728 http://dx.doi.org/10.3390/ijms22010155 |
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