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Biologically Oriented Hybrids of Indole and Hydantoin Derivatives
Indoles and hydantoins are important heterocycles scaffolds which present in numerous bioactive compounds which possess various biological activities. Moreover, they are essential building blocks in organic synthesis, particularly for the preparation of important hybrid molecules. The series of hybr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866919/ https://www.ncbi.nlm.nih.gov/pubmed/36677661 http://dx.doi.org/10.3390/molecules28020602 |
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author | Kochetkov, Konstantin A. Gorunova, Olga N. Bystrova, Natalia A. |
author_facet | Kochetkov, Konstantin A. Gorunova, Olga N. Bystrova, Natalia A. |
author_sort | Kochetkov, Konstantin A. |
collection | PubMed |
description | Indoles and hydantoins are important heterocycles scaffolds which present in numerous bioactive compounds which possess various biological activities. Moreover, they are essential building blocks in organic synthesis, particularly for the preparation of important hybrid molecules. The series of hybrid compounds containing indoles and imidazolidin-2-one moiety with direct C–C bond were synthesized using an amidoalkylation one-pot reaction. All compounds were investigated as a growth regulator for germination, growth and development of wheat seeds (Triticum aestivum L). Their effect on drought resistance at very low concentrations (4 × 10(−5) M) was evaluated. The study highlighted identified the leading compounds, 3a and 3e, with higher growth-regulating activity than the indole-auxin analogues. |
format | Online Article Text |
id | pubmed-9866919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98669192023-01-22 Biologically Oriented Hybrids of Indole and Hydantoin Derivatives Kochetkov, Konstantin A. Gorunova, Olga N. Bystrova, Natalia A. Molecules Communication Indoles and hydantoins are important heterocycles scaffolds which present in numerous bioactive compounds which possess various biological activities. Moreover, they are essential building blocks in organic synthesis, particularly for the preparation of important hybrid molecules. The series of hybrid compounds containing indoles and imidazolidin-2-one moiety with direct C–C bond were synthesized using an amidoalkylation one-pot reaction. All compounds were investigated as a growth regulator for germination, growth and development of wheat seeds (Triticum aestivum L). Their effect on drought resistance at very low concentrations (4 × 10(−5) M) was evaluated. The study highlighted identified the leading compounds, 3a and 3e, with higher growth-regulating activity than the indole-auxin analogues. MDPI 2023-01-06 /pmc/articles/PMC9866919/ /pubmed/36677661 http://dx.doi.org/10.3390/molecules28020602 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Kochetkov, Konstantin A. Gorunova, Olga N. Bystrova, Natalia A. Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title | Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title_full | Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title_fullStr | Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title_full_unstemmed | Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title_short | Biologically Oriented Hybrids of Indole and Hydantoin Derivatives |
title_sort | biologically oriented hybrids of indole and hydantoin derivatives |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9866919/ https://www.ncbi.nlm.nih.gov/pubmed/36677661 http://dx.doi.org/10.3390/molecules28020602 |
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