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Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases
The cell division cycle 25 phosphatases (CDC25A, B, and C; E.C. 3.1.3.48) are key regulator of the cell cycle in human cells. Their aberrant expression has been associated with the insurgence and development of various types of cancer, and with a poor clinical prognosis. Therefore, CDC25 phosphatase...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010111/ https://www.ncbi.nlm.nih.gov/pubmed/27774816 http://dx.doi.org/10.1080/14756366.2016.1238364 |
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author | Evain-Bana, Emilie Schiavo, Lucie Bour, Christophe Lanfranchi, Don Antoine Berardozzi, Simone Ghirga, Francesca Bagrel, Denyse Botta, Bruno Hanquet, Gilles Mori, Mattia |
author_facet | Evain-Bana, Emilie Schiavo, Lucie Bour, Christophe Lanfranchi, Don Antoine Berardozzi, Simone Ghirga, Francesca Bagrel, Denyse Botta, Bruno Hanquet, Gilles Mori, Mattia |
author_sort | Evain-Bana, Emilie |
collection | PubMed |
description | The cell division cycle 25 phosphatases (CDC25A, B, and C; E.C. 3.1.3.48) are key regulator of the cell cycle in human cells. Their aberrant expression has been associated with the insurgence and development of various types of cancer, and with a poor clinical prognosis. Therefore, CDC25 phosphatases are a valuable target for the development of small molecule inhibitors of therapeutic relevance. Here, we used an integrated strategy mixing organic chemistry with biological investigation and molecular modeling to study novel quinonoid derivatives as CDC25 inhibitors. The most promising molecules proved to inhibit CDC25 isoforms at single digit micromolar concentration, becoming valuable tools in chemical biology investigations and profitable leads for further optimization. [Image: see text] |
format | Online Article Text |
id | pubmed-6010111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60101112018-07-11 Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases Evain-Bana, Emilie Schiavo, Lucie Bour, Christophe Lanfranchi, Don Antoine Berardozzi, Simone Ghirga, Francesca Bagrel, Denyse Botta, Bruno Hanquet, Gilles Mori, Mattia J Enzyme Inhib Med Chem Original Article The cell division cycle 25 phosphatases (CDC25A, B, and C; E.C. 3.1.3.48) are key regulator of the cell cycle in human cells. Their aberrant expression has been associated with the insurgence and development of various types of cancer, and with a poor clinical prognosis. Therefore, CDC25 phosphatases are a valuable target for the development of small molecule inhibitors of therapeutic relevance. Here, we used an integrated strategy mixing organic chemistry with biological investigation and molecular modeling to study novel quinonoid derivatives as CDC25 inhibitors. The most promising molecules proved to inhibit CDC25 isoforms at single digit micromolar concentration, becoming valuable tools in chemical biology investigations and profitable leads for further optimization. [Image: see text] Taylor & Francis 2016-10-23 /pmc/articles/PMC6010111/ /pubmed/27774816 http://dx.doi.org/10.1080/14756366.2016.1238364 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/Licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/Licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Evain-Bana, Emilie Schiavo, Lucie Bour, Christophe Lanfranchi, Don Antoine Berardozzi, Simone Ghirga, Francesca Bagrel, Denyse Botta, Bruno Hanquet, Gilles Mori, Mattia Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title | Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title_full | Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title_fullStr | Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title_full_unstemmed | Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title_short | Synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of CDC25 phosphatases |
title_sort | synthesis, biological evaluation and molecular modeling studies on novel quinonoid inhibitors of cdc25 phosphatases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010111/ https://www.ncbi.nlm.nih.gov/pubmed/27774816 http://dx.doi.org/10.1080/14756366.2016.1238364 |
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