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A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside
Ptaquiloside (Pta) is a potent carcinogen present in bracken fern and in soil matrices, that can potentially leach to the aquatic environment. More recently its presence in the milk of different farm animals has been reported. Pterosin B (Ptb) and bromopterosin (BrPt) represent the most convenient a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268148/ https://www.ncbi.nlm.nih.gov/pubmed/22592085 http://dx.doi.org/10.3390/molecules17055795 |
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author | Attya, Mohamed Nardi, Monica Tagarelli, Antonio Sindona, Giovanni |
author_facet | Attya, Mohamed Nardi, Monica Tagarelli, Antonio Sindona, Giovanni |
author_sort | Attya, Mohamed |
collection | PubMed |
description | Ptaquiloside (Pta) is a potent carcinogen present in bracken fern and in soil matrices, that can potentially leach to the aquatic environment. More recently its presence in the milk of different farm animals has been reported. Pterosin B (Ptb) and bromopterosin (BrPt) represent the most convenient analogues in the detection of ptaquiloside by mass spectrometry. Pterosin sesquiterpenes are also involved in many patented biomedical protocols. In this work we introduce a new and convenient approach to the synthesis in three steps and more than 80% yield of d(4)-pterosin B (d(4)-Ptb) and d(4)-bromopterosin (d(4)-BrPt), useful as internal standards in the quantification of ptaquiloside. |
format | Online Article Text |
id | pubmed-6268148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62681482018-12-20 A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside Attya, Mohamed Nardi, Monica Tagarelli, Antonio Sindona, Giovanni Molecules Article Ptaquiloside (Pta) is a potent carcinogen present in bracken fern and in soil matrices, that can potentially leach to the aquatic environment. More recently its presence in the milk of different farm animals has been reported. Pterosin B (Ptb) and bromopterosin (BrPt) represent the most convenient analogues in the detection of ptaquiloside by mass spectrometry. Pterosin sesquiterpenes are also involved in many patented biomedical protocols. In this work we introduce a new and convenient approach to the synthesis in three steps and more than 80% yield of d(4)-pterosin B (d(4)-Ptb) and d(4)-bromopterosin (d(4)-BrPt), useful as internal standards in the quantification of ptaquiloside. MDPI 2012-05-16 /pmc/articles/PMC6268148/ /pubmed/22592085 http://dx.doi.org/10.3390/molecules17055795 Text en © 2012 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 Attya, Mohamed Nardi, Monica Tagarelli, Antonio Sindona, Giovanni A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title | A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title_full | A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title_fullStr | A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title_full_unstemmed | A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title_short | A New Facile Synthesis of D(4)-Pterosin B and D(4)-Bromopterosin, Deuterated Analogues of Ptaquiloside |
title_sort | new facile synthesis of d(4)-pterosin b and d(4)-bromopterosin, deuterated analogues of ptaquiloside |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268148/ https://www.ncbi.nlm.nih.gov/pubmed/22592085 http://dx.doi.org/10.3390/molecules17055795 |
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