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Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)

The front cover picture shows a prefluorescent phosphine‐based probe reacting with nitroxyl (HNO) and S‐nitrosothiol (RSNO), nitrogen oxide‐derived biological signals. Both species react with the prefluorescent probe, but only the product from the HNO reaction can complete a further chemical ligatio...

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Detalles Bibliográficos
Autores principales: Miao, Zhengrui, King, S. Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906477/
http://dx.doi.org/10.1002/open.201600031
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author Miao, Zhengrui
King, S. Bruce
author_facet Miao, Zhengrui
King, S. Bruce
author_sort Miao, Zhengrui
collection PubMed
description The front cover picture shows a prefluorescent phosphine‐based probe reacting with nitroxyl (HNO) and S‐nitrosothiol (RSNO), nitrogen oxide‐derived biological signals. Both species react with the prefluorescent probe, but only the product from the HNO reaction can complete a further chemical ligation pathway that results in fluorescence, indicating the presence of HNO. The product of the probe with RSNO does not complete this ligation and does not generate a fluorescent species. These phosphine‐based probes thus demonstrate a selectivity for HNO over RSNO based on their chemical reactivity and can be used in biological systems to differentiate these species. More information can be found in the Communication by S. Bruce King and Z. Miao on page 110 in Issue 2, 2016 (DOI: 10.1002/open.201500200).[Image: see text]
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spelling pubmed-49064772016-06-15 Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016) Miao, Zhengrui King, S. Bruce ChemistryOpen Cover Pictures The front cover picture shows a prefluorescent phosphine‐based probe reacting with nitroxyl (HNO) and S‐nitrosothiol (RSNO), nitrogen oxide‐derived biological signals. Both species react with the prefluorescent probe, but only the product from the HNO reaction can complete a further chemical ligation pathway that results in fluorescence, indicating the presence of HNO. The product of the probe with RSNO does not complete this ligation and does not generate a fluorescent species. These phosphine‐based probes thus demonstrate a selectivity for HNO over RSNO based on their chemical reactivity and can be used in biological systems to differentiate these species. More information can be found in the Communication by S. Bruce King and Z. Miao on page 110 in Issue 2, 2016 (DOI: 10.1002/open.201500200).[Image: see text] John Wiley and Sons Inc. 2016-04-13 /pmc/articles/PMC4906477/ http://dx.doi.org/10.1002/open.201600031 Text en © 2016 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
spellingShingle Cover Pictures
Miao, Zhengrui
King, S. Bruce
Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title_full Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title_fullStr Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title_full_unstemmed Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title_short Cover Picture: Comparison of Reductive Ligation‐Based Detection Strategies for Nitroxyl (HNO) and S‐Nitrosothiols (ChemistryOpen 2/2016)
title_sort cover picture: comparison of reductive ligation‐based detection strategies for nitroxyl (hno) and s‐nitrosothiols (chemistryopen 2/2016)
topic Cover Pictures
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906477/
http://dx.doi.org/10.1002/open.201600031
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