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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...

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Autores principales: Morigi, Rita, Catanzaro, Elena, Locatelli, Alessandra, Calcabrini, Cinzia, Pellicioni, Valentina, Leoni, Alberto, Fimognari, Carmela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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