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Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid
A series of novel potential DNA bis-intercalators were designed and synthesized, in which two glucuronic acids were linked by ethylenediamine, and the glucuronic acid was coupled with various chromophores, including quinoline, acridine, indole and purine, at the C-1 position. The preliminary binding...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759939/ https://www.ncbi.nlm.nih.gov/pubmed/23955268 http://dx.doi.org/10.3390/ijms140816851 |
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author | Zhao, Jiuyang Li, Wei Ma, Rui Chen, Shaopeng Ren, Sumei Jiang, Tao |
author_facet | Zhao, Jiuyang Li, Wei Ma, Rui Chen, Shaopeng Ren, Sumei Jiang, Tao |
author_sort | Zhao, Jiuyang |
collection | PubMed |
description | A series of novel potential DNA bis-intercalators were designed and synthesized, in which two glucuronic acids were linked by ethylenediamine, and the glucuronic acid was coupled with various chromophores, including quinoline, acridine, indole and purine, at the C-1 position. The preliminary binding properties of these compounds to calf thymus DNA (CT-DNA) have been investigated by UV-absorption and fluorescence spectroscopy. The results indicated that all the target compounds can interact with CT-DNA, and the acridine derivative, 3b, showed the highest key selection vector (KSV) value, which suggested that compound 3b binds most strongly to CT-DNA. |
format | Online Article Text |
id | pubmed-3759939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-37599392013-09-03 Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid Zhao, Jiuyang Li, Wei Ma, Rui Chen, Shaopeng Ren, Sumei Jiang, Tao Int J Mol Sci Article A series of novel potential DNA bis-intercalators were designed and synthesized, in which two glucuronic acids were linked by ethylenediamine, and the glucuronic acid was coupled with various chromophores, including quinoline, acridine, indole and purine, at the C-1 position. The preliminary binding properties of these compounds to calf thymus DNA (CT-DNA) have been investigated by UV-absorption and fluorescence spectroscopy. The results indicated that all the target compounds can interact with CT-DNA, and the acridine derivative, 3b, showed the highest key selection vector (KSV) value, which suggested that compound 3b binds most strongly to CT-DNA. MDPI 2013-08-15 /pmc/articles/PMC3759939/ /pubmed/23955268 http://dx.doi.org/10.3390/ijms140816851 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Zhao, Jiuyang Li, Wei Ma, Rui Chen, Shaopeng Ren, Sumei Jiang, Tao Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title | Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title_full | Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title_fullStr | Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title_full_unstemmed | Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title_short | Design, Synthesis and DNA Interaction Study of New Potential DNA Bis-Intercalators Based on Glucuronic Acid |
title_sort | design, synthesis and dna interaction study of new potential dna bis-intercalators based on glucuronic acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759939/ https://www.ncbi.nlm.nih.gov/pubmed/23955268 http://dx.doi.org/10.3390/ijms140816851 |
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