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Carboranes as unique pharmacophores in antitumor medicinal chemistry
Carborane is a carbon-boron molecular cluster that can be viewed as a 3D analog of benzene. It features special physical and chemical properties, and thus has the potential to serve as a new type of pharmacophore for drug design and discovery. Based on the relative positions of two cage carbons, ico...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807988/ https://www.ncbi.nlm.nih.gov/pubmed/35141397 http://dx.doi.org/10.1016/j.omto.2022.01.005 |
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author | Chen, Yu Du, Fukuan Tang, Liyao Xu, Jinrun Zhao, Yueshui Wu, Xu Li, Mingxing Shen, Jing Wen, Qinglian Cho, Chi Hin Xiao, Zhangang |
author_facet | Chen, Yu Du, Fukuan Tang, Liyao Xu, Jinrun Zhao, Yueshui Wu, Xu Li, Mingxing Shen, Jing Wen, Qinglian Cho, Chi Hin Xiao, Zhangang |
author_sort | Chen, Yu |
collection | PubMed |
description | Carborane is a carbon-boron molecular cluster that can be viewed as a 3D analog of benzene. It features special physical and chemical properties, and thus has the potential to serve as a new type of pharmacophore for drug design and discovery. Based on the relative positions of two cage carbons, icosahedral closo-carboranes can be classified into three isomers, ortho-carborane (o-carborane, 1,2-C(2)B(10)H(12)), meta-carborane (m-carborane, 1,7-C(2)B(10)H(12)), and para-carborane (p-carborane, 1,12-C(2)B(10)H(12)), and all of them can be deboronated to generate their nido- forms. Cage compound carborane and its derivatives have been demonstrated as useful chemical entities in antitumor medicinal chemistry. The applications of carboranes and their derivatives in the field of antitumor research mainly include boron neutron capture therapy (BNCT), as BNCT/photodynamic therapy dual sensitizers, and as anticancer ligands. This review summarizes the research progress on carboranes achieved up to October 2021, with particular emphasis on signaling transduction pathways, chemical structures, and mechanistic considerations of using carboranes. |
format | Online Article Text |
id | pubmed-8807988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-88079882022-02-08 Carboranes as unique pharmacophores in antitumor medicinal chemistry Chen, Yu Du, Fukuan Tang, Liyao Xu, Jinrun Zhao, Yueshui Wu, Xu Li, Mingxing Shen, Jing Wen, Qinglian Cho, Chi Hin Xiao, Zhangang Mol Ther Oncolytics Review Carborane is a carbon-boron molecular cluster that can be viewed as a 3D analog of benzene. It features special physical and chemical properties, and thus has the potential to serve as a new type of pharmacophore for drug design and discovery. Based on the relative positions of two cage carbons, icosahedral closo-carboranes can be classified into three isomers, ortho-carborane (o-carborane, 1,2-C(2)B(10)H(12)), meta-carborane (m-carborane, 1,7-C(2)B(10)H(12)), and para-carborane (p-carborane, 1,12-C(2)B(10)H(12)), and all of them can be deboronated to generate their nido- forms. Cage compound carborane and its derivatives have been demonstrated as useful chemical entities in antitumor medicinal chemistry. The applications of carboranes and their derivatives in the field of antitumor research mainly include boron neutron capture therapy (BNCT), as BNCT/photodynamic therapy dual sensitizers, and as anticancer ligands. This review summarizes the research progress on carboranes achieved up to October 2021, with particular emphasis on signaling transduction pathways, chemical structures, and mechanistic considerations of using carboranes. American Society of Gene & Cell Therapy 2022-01-10 /pmc/articles/PMC8807988/ /pubmed/35141397 http://dx.doi.org/10.1016/j.omto.2022.01.005 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chen, Yu Du, Fukuan Tang, Liyao Xu, Jinrun Zhao, Yueshui Wu, Xu Li, Mingxing Shen, Jing Wen, Qinglian Cho, Chi Hin Xiao, Zhangang Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title | Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title_full | Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title_fullStr | Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title_full_unstemmed | Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title_short | Carboranes as unique pharmacophores in antitumor medicinal chemistry |
title_sort | carboranes as unique pharmacophores in antitumor medicinal chemistry |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807988/ https://www.ncbi.nlm.nih.gov/pubmed/35141397 http://dx.doi.org/10.1016/j.omto.2022.01.005 |
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