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Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity
A series of new Knoevenagel adducts, bearing two indolinone systems, has been synthesized and evaluated on 60 human cancer cell lines according to protocols available at the National Cancer Institute (Bethesda, MD, USA). Some derivatives proved to be potent antiproliferative agents, showing GI(50) v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537952/ https://www.ncbi.nlm.nih.gov/pubmed/34684858 http://dx.doi.org/10.3390/molecules26206277 |
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author | Morigi, Rita Catanzaro, Elena Locatelli, Alessandra Calcabrini, Cinzia Pellicioni, Valentina Leoni, Alberto Fimognari, Carmela |
author_facet | Morigi, Rita Catanzaro, Elena Locatelli, Alessandra Calcabrini, Cinzia Pellicioni, Valentina Leoni, Alberto Fimognari, Carmela |
author_sort | Morigi, Rita |
collection | PubMed |
description | A series of new Knoevenagel adducts, bearing two indolinone systems, has been synthesized and evaluated on 60 human cancer cell lines according to protocols available at the National Cancer Institute (Bethesda, MD, USA). Some derivatives proved to be potent antiproliferative agents, showing GI(50) values in the submicromolar range. Compound 5b emerged as the most active and was further studied in Jurkat cells in order to determine the effects on cell-cycle phases and the kind of cell death induced. Finally, oxidative stress and DNA damage induced by compound 5b were also analyzed. |
format | Online Article Text |
id | pubmed-8537952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85379522021-10-24 Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity Morigi, Rita Catanzaro, Elena Locatelli, Alessandra Calcabrini, Cinzia Pellicioni, Valentina Leoni, Alberto Fimognari, Carmela Molecules Article A series of new Knoevenagel adducts, bearing two indolinone systems, has been synthesized and evaluated on 60 human cancer cell lines according to protocols available at the National Cancer Institute (Bethesda, MD, USA). Some derivatives proved to be potent antiproliferative agents, showing GI(50) values in the submicromolar range. Compound 5b emerged as the most active and was further studied in Jurkat cells in order to determine the effects on cell-cycle phases and the kind of cell death induced. Finally, oxidative stress and DNA damage induced by compound 5b were also analyzed. MDPI 2021-10-16 /pmc/articles/PMC8537952/ /pubmed/34684858 http://dx.doi.org/10.3390/molecules26206277 Text en © 2021 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 Morigi, Rita Catanzaro, Elena Locatelli, Alessandra Calcabrini, Cinzia Pellicioni, Valentina Leoni, Alberto Fimognari, Carmela Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title | Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title_full | Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title_fullStr | Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title_full_unstemmed | Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title_short | Synthesis and Biological Evaluation of New Bis-Indolinone Derivatives Endowed with Cytotoxic Activity |
title_sort | synthesis and biological evaluation of new bis-indolinone derivatives endowed with cytotoxic activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8537952/ https://www.ncbi.nlm.nih.gov/pubmed/34684858 http://dx.doi.org/10.3390/molecules26206277 |
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