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Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review
It is over 50 years since the discovery of microtubules, and they have become one of the most important drug targets for anti-cancer therapies. Microtubules are predominantly composed of the protein tubulin, which contains a number of different binding sites for small-molecule drugs. There is contin...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168938/ https://www.ncbi.nlm.nih.gov/pubmed/31947889 http://dx.doi.org/10.3390/ph13010008 |
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author | McLoughlin, Eavan C. O’Boyle, Niamh M. |
author_facet | McLoughlin, Eavan C. O’Boyle, Niamh M. |
author_sort | McLoughlin, Eavan C. |
collection | PubMed |
description | It is over 50 years since the discovery of microtubules, and they have become one of the most important drug targets for anti-cancer therapies. Microtubules are predominantly composed of the protein tubulin, which contains a number of different binding sites for small-molecule drugs. There is continued interest in drug development for compounds targeting the colchicine-binding site of tubulin, termed colchicine-binding site inhibitors (CBSIs). This review highlights CBSIs discovered through diverse sources: from natural compounds, rational design, serendipitously and via high-throughput screening. We provide an update on CBSIs reported in the past three years and discuss the clinical status of CBSIs. It is likely that efforts will continue to develop CBSIs for a diverse set of cancers, and this review provides a timely update on recent developments. |
format | Online Article Text |
id | pubmed-7168938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71689382020-04-20 Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review McLoughlin, Eavan C. O’Boyle, Niamh M. Pharmaceuticals (Basel) Review It is over 50 years since the discovery of microtubules, and they have become one of the most important drug targets for anti-cancer therapies. Microtubules are predominantly composed of the protein tubulin, which contains a number of different binding sites for small-molecule drugs. There is continued interest in drug development for compounds targeting the colchicine-binding site of tubulin, termed colchicine-binding site inhibitors (CBSIs). This review highlights CBSIs discovered through diverse sources: from natural compounds, rational design, serendipitously and via high-throughput screening. We provide an update on CBSIs reported in the past three years and discuss the clinical status of CBSIs. It is likely that efforts will continue to develop CBSIs for a diverse set of cancers, and this review provides a timely update on recent developments. MDPI 2020-01-03 /pmc/articles/PMC7168938/ /pubmed/31947889 http://dx.doi.org/10.3390/ph13010008 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review McLoughlin, Eavan C. O’Boyle, Niamh M. Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title | Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title_full | Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title_fullStr | Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title_full_unstemmed | Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title_short | Colchicine-Binding Site Inhibitors from Chemistry to Clinic: A Review |
title_sort | colchicine-binding site inhibitors from chemistry to clinic: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168938/ https://www.ncbi.nlm.nih.gov/pubmed/31947889 http://dx.doi.org/10.3390/ph13010008 |
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