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Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents
Cancer threatens human health and life. Therefore, it is particularly important to develop safe and effective antitumor drugs. Microtubules, the main component of cytoskeleton, play an important role in maintaining cell morphology, mitosis, and signal transduction, which are one of important targets...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014799/ https://www.ncbi.nlm.nih.gov/pubmed/36936533 http://dx.doi.org/10.3389/fchem.2023.1096666 |
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author | Wang, Chao Shi, Lingyu Yang, Shanbo Chang, Jing Liu, Wenjing Zeng, Jun Meng, Jingsen Zhang, Renshuai Xing, Dongming |
author_facet | Wang, Chao Shi, Lingyu Yang, Shanbo Chang, Jing Liu, Wenjing Zeng, Jun Meng, Jingsen Zhang, Renshuai Xing, Dongming |
author_sort | Wang, Chao |
collection | PubMed |
description | Cancer threatens human health and life. Therefore, it is particularly important to develop safe and effective antitumor drugs. Microtubules, the main component of cytoskeleton, play an important role in maintaining cell morphology, mitosis, and signal transduction, which are one of important targets of antitumor drug research and development. Colchicine binding site inhibitors have dual effects of inhibiting proliferation and destroying blood vessels. In recent years, a series of inhibitors targeting this target have been studied and some progress has been made. XRP44X has a novel structure and overcomes some disadvantages of traditional inhibitors. It is also a multifunctional molecule that regulates not only the function of tubulin but also a variety of biological pathways. Therefore, the structure, synthesis, structure-activity relationship, and biological activity of XRP44X analogues reported in recent years were summarized in this paper, to provide a useful reference for the rational design of efficient colchicine binding site inhibitors. |
format | Online Article Text |
id | pubmed-10014799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100147992023-03-16 Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents Wang, Chao Shi, Lingyu Yang, Shanbo Chang, Jing Liu, Wenjing Zeng, Jun Meng, Jingsen Zhang, Renshuai Xing, Dongming Front Chem Chemistry Cancer threatens human health and life. Therefore, it is particularly important to develop safe and effective antitumor drugs. Microtubules, the main component of cytoskeleton, play an important role in maintaining cell morphology, mitosis, and signal transduction, which are one of important targets of antitumor drug research and development. Colchicine binding site inhibitors have dual effects of inhibiting proliferation and destroying blood vessels. In recent years, a series of inhibitors targeting this target have been studied and some progress has been made. XRP44X has a novel structure and overcomes some disadvantages of traditional inhibitors. It is also a multifunctional molecule that regulates not only the function of tubulin but also a variety of biological pathways. Therefore, the structure, synthesis, structure-activity relationship, and biological activity of XRP44X analogues reported in recent years were summarized in this paper, to provide a useful reference for the rational design of efficient colchicine binding site inhibitors. Frontiers Media S.A. 2023-03-01 /pmc/articles/PMC10014799/ /pubmed/36936533 http://dx.doi.org/10.3389/fchem.2023.1096666 Text en Copyright © 2023 Wang, Shi, Yang, Chang, Liu, Zeng, Meng, Zhang and Xing. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Wang, Chao Shi, Lingyu Yang, Shanbo Chang, Jing Liu, Wenjing Zeng, Jun Meng, Jingsen Zhang, Renshuai Xing, Dongming Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title | Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title_full | Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title_fullStr | Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title_full_unstemmed | Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title_short | Research progress on antitumor activity of XRP44X and analogues as microtubule targeting agents |
title_sort | research progress on antitumor activity of xrp44x and analogues as microtubule targeting agents |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014799/ https://www.ncbi.nlm.nih.gov/pubmed/36936533 http://dx.doi.org/10.3389/fchem.2023.1096666 |
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