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Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media
[Image: see text] We report the self-assembly of a hydrophilic 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) derivative into a discrete and thermally stable hexadecameric supramolecule in aqueous media. We demonstrate that this hexadecamer is isostructural to the one formed by a related lipophilic deri...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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American Chemical Society
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646872/ https://www.ncbi.nlm.nih.gov/pubmed/18642917 http://dx.doi.org/10.1021/ja8039019 |
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author | García-Arriaga, Marilyn Hobley, Gerard Rivera, José M. |
author_facet | García-Arriaga, Marilyn Hobley, Gerard Rivera, José M. |
author_sort | García-Arriaga, Marilyn |
collection | PubMed |
description | [Image: see text] We report the self-assembly of a hydrophilic 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) derivative into a discrete and thermally stable hexadecameric supramolecule in aqueous media. We demonstrate that this hexadecamer is isostructural to the one formed by a related lipophilic derivative in organic media. This mAG moiety represents a rare example of a small-molecule recognition motif that is capable of assembling isostructurally and with high fidelity in both organic and aqueous media. |
format | Text |
id | pubmed-2646872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-26468722009-03-20 Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media García-Arriaga, Marilyn Hobley, Gerard Rivera, José M. J Am Chem Soc [Image: see text] We report the self-assembly of a hydrophilic 8-(m-acetylphenyl)-2′-deoxyguanosine (mAG) derivative into a discrete and thermally stable hexadecameric supramolecule in aqueous media. We demonstrate that this hexadecamer is isostructural to the one formed by a related lipophilic derivative in organic media. This mAG moiety represents a rare example of a small-molecule recognition motif that is capable of assembling isostructurally and with high fidelity in both organic and aqueous media. American Chemical Society 2008-07-22 2008-08-13 /pmc/articles/PMC2646872/ /pubmed/18642917 http://dx.doi.org/10.1021/ja8039019 Text en Copyright © 2008 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. 40.75 |
spellingShingle | García-Arriaga, Marilyn Hobley, Gerard Rivera, José M. Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title | Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title_full | Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title_fullStr | Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title_full_unstemmed | Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title_short | Isostructural Self-Assembly of 2′-Deoxyguanosine Derivatives in Aqueous and Organic Media |
title_sort | isostructural self-assembly of 2′-deoxyguanosine derivatives in aqueous and organic media |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646872/ https://www.ncbi.nlm.nih.gov/pubmed/18642917 http://dx.doi.org/10.1021/ja8039019 |
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