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Heterometallic BODIPY-Based Molecular Squares Obtained by Self-Assembly: Synthesis and Biological Activities
[Image: see text] Metal-based multinuclear supramolecules with different functionalities designed by self-assembly represent a growing area of research due to their versatile applications, particularly as anticancer agents. Four novel boron dipyrromethene (BODIPY)-based octacationic heterometallic m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705193/ https://www.ncbi.nlm.nih.gov/pubmed/31460447 http://dx.doi.org/10.1021/acsomega.9b01328 |
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author | Gupta, Gajendra You, Yeji Hadiputra, Rizky Jung, Jaehoon Kang, Dong-Ku Lee, Chang Yeon |
author_facet | Gupta, Gajendra You, Yeji Hadiputra, Rizky Jung, Jaehoon Kang, Dong-Ku Lee, Chang Yeon |
author_sort | Gupta, Gajendra |
collection | PubMed |
description | [Image: see text] Metal-based multinuclear supramolecules with different functionalities designed by self-assembly represent a growing area of research due to their versatile applications, particularly as anticancer agents. Four novel boron dipyrromethene (BODIPY)-based octacationic heterometallic molecular squares, 3–6 were synthesized by self-assembly via reaction of dipyridyl BODIPY ligands with suitable 90° palladium and platinum acceptors. The formation of the as-synthesized molecular squares was confirmed by multinuclear NMR spectroscopy, elemental analysis, high resolution electrospray mass spectrometry, UV–vis spectroscopy, and fluorescence spectroscopy. The square molecular structures of 4 and 6 were further rationalized theoretically using the PM7 semi-empirical method. The activities of the supramolecules against cancer cells were tested using cell lines of various malignant and nonmalignant origins. Complexes 3–6 showed high cytotoxicity toward cancer cells but 7.0 to 15.2 times lower cytotoxic effects were observed against nonmalignant human kidney epithelial cells (HEK-293). Particularly, complexes 3–6 provided 2.1–6.0 times lower IC(50) values as compared to cisplatin in HCT116 cells. Interestingly, BDP ligand-containing complexes (3 and 4) induced cytotoxicity through apoptosis, whereas BDPCC-based complexes (5 and 6) induced cell death by necrosis. This study presents a novel series of iron-based heteroatomic palladium and platinum complexes that exhibit substantial potential as drug candidates for anticancer therapy. |
format | Online Article Text |
id | pubmed-6705193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67051932019-08-27 Heterometallic BODIPY-Based Molecular Squares Obtained by Self-Assembly: Synthesis and Biological Activities Gupta, Gajendra You, Yeji Hadiputra, Rizky Jung, Jaehoon Kang, Dong-Ku Lee, Chang Yeon ACS Omega [Image: see text] Metal-based multinuclear supramolecules with different functionalities designed by self-assembly represent a growing area of research due to their versatile applications, particularly as anticancer agents. Four novel boron dipyrromethene (BODIPY)-based octacationic heterometallic molecular squares, 3–6 were synthesized by self-assembly via reaction of dipyridyl BODIPY ligands with suitable 90° palladium and platinum acceptors. The formation of the as-synthesized molecular squares was confirmed by multinuclear NMR spectroscopy, elemental analysis, high resolution electrospray mass spectrometry, UV–vis spectroscopy, and fluorescence spectroscopy. The square molecular structures of 4 and 6 were further rationalized theoretically using the PM7 semi-empirical method. The activities of the supramolecules against cancer cells were tested using cell lines of various malignant and nonmalignant origins. Complexes 3–6 showed high cytotoxicity toward cancer cells but 7.0 to 15.2 times lower cytotoxic effects were observed against nonmalignant human kidney epithelial cells (HEK-293). Particularly, complexes 3–6 provided 2.1–6.0 times lower IC(50) values as compared to cisplatin in HCT116 cells. Interestingly, BDP ligand-containing complexes (3 and 4) induced cytotoxicity through apoptosis, whereas BDPCC-based complexes (5 and 6) induced cell death by necrosis. This study presents a novel series of iron-based heteroatomic palladium and platinum complexes that exhibit substantial potential as drug candidates for anticancer therapy. American Chemical Society 2019-08-01 /pmc/articles/PMC6705193/ /pubmed/31460447 http://dx.doi.org/10.1021/acsomega.9b01328 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Gupta, Gajendra You, Yeji Hadiputra, Rizky Jung, Jaehoon Kang, Dong-Ku Lee, Chang Yeon Heterometallic BODIPY-Based Molecular Squares Obtained by Self-Assembly: Synthesis and Biological Activities |
title | Heterometallic BODIPY-Based Molecular Squares Obtained
by Self-Assembly: Synthesis and Biological Activities |
title_full | Heterometallic BODIPY-Based Molecular Squares Obtained
by Self-Assembly: Synthesis and Biological Activities |
title_fullStr | Heterometallic BODIPY-Based Molecular Squares Obtained
by Self-Assembly: Synthesis and Biological Activities |
title_full_unstemmed | Heterometallic BODIPY-Based Molecular Squares Obtained
by Self-Assembly: Synthesis and Biological Activities |
title_short | Heterometallic BODIPY-Based Molecular Squares Obtained
by Self-Assembly: Synthesis and Biological Activities |
title_sort | heterometallic bodipy-based molecular squares obtained
by self-assembly: synthesis and biological activities |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6705193/ https://www.ncbi.nlm.nih.gov/pubmed/31460447 http://dx.doi.org/10.1021/acsomega.9b01328 |
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