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Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids
Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hyb...
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/PMC9860848/ https://www.ncbi.nlm.nih.gov/pubmed/36677683 http://dx.doi.org/10.3390/molecules28020626 |
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author | Németh-Rieder, Alexandra Keglevich, Péter Hunyadi, Attila Latif, Ahmed Dhahir Zupkó, István Hazai, László |
author_facet | Németh-Rieder, Alexandra Keglevich, Péter Hunyadi, Attila Latif, Ahmed Dhahir Zupkó, István Hazai, László |
author_sort | Németh-Rieder, Alexandra |
collection | PubMed |
description | Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hybrids were investigated on 60 cell lines of 9 common cancer types (NCI60) in vitro as antitumor agents. Some of them proved to have a significant antiproliferative effect. |
format | Online Article Text |
id | pubmed-9860848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98608482023-01-22 Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids Németh-Rieder, Alexandra Keglevich, Péter Hunyadi, Attila Latif, Ahmed Dhahir Zupkó, István Hazai, László Molecules Article Hybrid compounds of flavones, namely chrysin and kaempferol, and substituted 1,2,3-triazole derivatives, were synthesized by click reaction of the intermediate O-propargyl derivatives. 4-Fluoro- and 4-nitrobenzyl-1,2,3-triazole-containing hybrid molecules were prepared. The mono- and bis-coupled hybrids were investigated on 60 cell lines of 9 common cancer types (NCI60) in vitro as antitumor agents. Some of them proved to have a significant antiproliferative effect. MDPI 2023-01-07 /pmc/articles/PMC9860848/ /pubmed/36677683 http://dx.doi.org/10.3390/molecules28020626 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 | Article Németh-Rieder, Alexandra Keglevich, Péter Hunyadi, Attila Latif, Ahmed Dhahir Zupkó, István Hazai, László Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title | Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title_full | Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title_fullStr | Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title_full_unstemmed | Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title_short | Synthesis and In Vitro Anticancer Evaluation of Flavone—1,2,3-Triazole Hybrids |
title_sort | synthesis and in vitro anticancer evaluation of flavone—1,2,3-triazole hybrids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860848/ https://www.ncbi.nlm.nih.gov/pubmed/36677683 http://dx.doi.org/10.3390/molecules28020626 |
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