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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...

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Autores principales: Wang, Chao, Shi, Lingyu, Yang, Shanbo, Chang, Jing, Liu, Wenjing, Zeng, Jun, Meng, Jingsen, Zhang, Renshuai, Xing, Dongming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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.
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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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