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Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates
This paper presents a study on a series of quaternary ammonium salt (QAS) derivatives of glucopyranosides with an elongated hydrophobic hydrocarbon chain. The new N-[6-(β-D-glucopyranosyloxy)hexyl]ammonium bromides and their O-acetyl derivatives were analyzed via (1)H and (13)C NMR spectroscopy. The...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979630/ https://www.ncbi.nlm.nih.gov/pubmed/27559394 http://dx.doi.org/10.3762/bjoc.12.138 |
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author | Dmochowska, Barbara Sikora, Karol Woziwodzka, Anna Piosik, Jacek Podgórska, Beata |
author_facet | Dmochowska, Barbara Sikora, Karol Woziwodzka, Anna Piosik, Jacek Podgórska, Beata |
author_sort | Dmochowska, Barbara |
collection | PubMed |
description | This paper presents a study on a series of quaternary ammonium salt (QAS) derivatives of glucopyranosides with an elongated hydrophobic hydrocarbon chain. The new N-[6-(β-D-glucopyranosyloxy)hexyl]ammonium bromides and their O-acetyl derivatives were analyzed via (1)H and (13)C NMR spectroscopy. The mutagenic activity of the newly synthesized QAS was investigated using two different techniques: The Vibrio harveyi luminescence assay and the Ames test. The obtained results support previous findings contesting QAS safety and indicate that QAS, specifically pyridinium derivatives, might be mutagenic. |
format | Online Article Text |
id | pubmed-4979630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-49796302016-08-24 Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates Dmochowska, Barbara Sikora, Karol Woziwodzka, Anna Piosik, Jacek Podgórska, Beata Beilstein J Org Chem Full Research Paper This paper presents a study on a series of quaternary ammonium salt (QAS) derivatives of glucopyranosides with an elongated hydrophobic hydrocarbon chain. The new N-[6-(β-D-glucopyranosyloxy)hexyl]ammonium bromides and their O-acetyl derivatives were analyzed via (1)H and (13)C NMR spectroscopy. The mutagenic activity of the newly synthesized QAS was investigated using two different techniques: The Vibrio harveyi luminescence assay and the Ames test. The obtained results support previous findings contesting QAS safety and indicate that QAS, specifically pyridinium derivatives, might be mutagenic. Beilstein-Institut 2016-07-12 /pmc/articles/PMC4979630/ /pubmed/27559394 http://dx.doi.org/10.3762/bjoc.12.138 Text en Copyright © 2016, Dmochowska et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Dmochowska, Barbara Sikora, Karol Woziwodzka, Anna Piosik, Jacek Podgórska, Beata Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title | Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title_full | Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title_fullStr | Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title_full_unstemmed | Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title_short | Mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
title_sort | mutagenic activity of quaternary ammonium salt derivatives of carbohydrates |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979630/ https://www.ncbi.nlm.nih.gov/pubmed/27559394 http://dx.doi.org/10.3762/bjoc.12.138 |
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