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In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011
SR9009 and SR9011 are attractive as performance-enhancing substances due to their REV-ERB agonist effects and thus circadian rhythm modulation activity. Although no pharmaceutical preparations are available yet, illicit use of SR9009 and SR9011 for doping purposes can be anticipated, especially sinc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085709/ https://www.ncbi.nlm.nih.gov/pubmed/27706103 http://dx.doi.org/10.3390/ijms17101676 |
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author | Geldof, Lore Deventer, Koen Roels, Kris Tudela, Eva Van Eenoo, Peter |
author_facet | Geldof, Lore Deventer, Koen Roels, Kris Tudela, Eva Van Eenoo, Peter |
author_sort | Geldof, Lore |
collection | PubMed |
description | SR9009 and SR9011 are attractive as performance-enhancing substances due to their REV-ERB agonist effects and thus circadian rhythm modulation activity. Although no pharmaceutical preparations are available yet, illicit use of SR9009 and SR9011 for doping purposes can be anticipated, especially since SR9009 is marketed in illicit products. Therefore, the aim was to identify potential diagnostic metabolites via in vitro metabolic studies to ensure effective (doping) control. The presence of SR9009 could be demonstrated in a black market product purchased over the Internet. Via human liver microsomal metabolic assays, eight metabolites were detected for SR9009 and fourteen metabolites for SR9011 by liquid chromatography–high resolution mass spectrometry (LC–HRMS). Structure elucidation was performed for all metabolites by LC–HRMS product ion scans in both positive and negative ionization mode. Retrospective data analysis was applied to 1511 doping control samples previously analyzed by a full-scan LC–HRMS screening method to verify the presence of SR9009, SR9011 and their metabolites. So far, the presence of neither the parent compound nor the metabolites could be detected in routine urine samples. However, to further discourage use of these potentially harmful compounds, incorporation of SR9009 and SR9011 into screening methods is highly recommended. |
format | Online Article Text |
id | pubmed-5085709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50857092016-11-01 In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 Geldof, Lore Deventer, Koen Roels, Kris Tudela, Eva Van Eenoo, Peter Int J Mol Sci Article SR9009 and SR9011 are attractive as performance-enhancing substances due to their REV-ERB agonist effects and thus circadian rhythm modulation activity. Although no pharmaceutical preparations are available yet, illicit use of SR9009 and SR9011 for doping purposes can be anticipated, especially since SR9009 is marketed in illicit products. Therefore, the aim was to identify potential diagnostic metabolites via in vitro metabolic studies to ensure effective (doping) control. The presence of SR9009 could be demonstrated in a black market product purchased over the Internet. Via human liver microsomal metabolic assays, eight metabolites were detected for SR9009 and fourteen metabolites for SR9011 by liquid chromatography–high resolution mass spectrometry (LC–HRMS). Structure elucidation was performed for all metabolites by LC–HRMS product ion scans in both positive and negative ionization mode. Retrospective data analysis was applied to 1511 doping control samples previously analyzed by a full-scan LC–HRMS screening method to verify the presence of SR9009, SR9011 and their metabolites. So far, the presence of neither the parent compound nor the metabolites could be detected in routine urine samples. However, to further discourage use of these potentially harmful compounds, incorporation of SR9009 and SR9011 into screening methods is highly recommended. MDPI 2016-10-03 /pmc/articles/PMC5085709/ /pubmed/27706103 http://dx.doi.org/10.3390/ijms17101676 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Geldof, Lore Deventer, Koen Roels, Kris Tudela, Eva Van Eenoo, Peter In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title | In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title_full | In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title_fullStr | In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title_full_unstemmed | In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title_short | In Vitro Metabolic Studies of REV-ERB Agonists SR9009 and SR9011 |
title_sort | in vitro metabolic studies of rev-erb agonists sr9009 and sr9011 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085709/ https://www.ncbi.nlm.nih.gov/pubmed/27706103 http://dx.doi.org/10.3390/ijms17101676 |
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