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Thiol Reactive Probes and Chemosensors
Thiols are important molecules in the environment and in biological processes. Cysteine (Cys), homocysteine (Hcy), glutathione (GSH) and hydrogen sulfide (H(2)S) play critical roles in a variety of physiological and pathological processes. The selective detection of thiols using reaction-based probe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522992/ https://www.ncbi.nlm.nih.gov/pubmed/23202239 http://dx.doi.org/10.3390/s121115907 |
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author | Peng, Hanjing Chen, Weixuan Cheng, Yunfeng Hakuna, Lovemore Strongin, Robert Wang, Binghe |
author_facet | Peng, Hanjing Chen, Weixuan Cheng, Yunfeng Hakuna, Lovemore Strongin, Robert Wang, Binghe |
author_sort | Peng, Hanjing |
collection | PubMed |
description | Thiols are important molecules in the environment and in biological processes. Cysteine (Cys), homocysteine (Hcy), glutathione (GSH) and hydrogen sulfide (H(2)S) play critical roles in a variety of physiological and pathological processes. The selective detection of thiols using reaction-based probes and sensors is very important in basic research and in disease diagnosis. This review focuses on the design of fluorescent and colorimetric probes and sensors for thiol detection. Thiol detection methods include probes and labeling agents based on nucleophilic addition and substitution, Michael addition, disulfide bond or Se-N bond cleavage, metal-sulfur interactions and more. Probes for H(2)S are based on nucleophilic cyclization, reduction and metal sulfide formation. Thiol probe and chemosensor design strategies and mechanism of action are discussed in this review. |
format | Online Article Text |
id | pubmed-3522992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-35229922013-01-09 Thiol Reactive Probes and Chemosensors Peng, Hanjing Chen, Weixuan Cheng, Yunfeng Hakuna, Lovemore Strongin, Robert Wang, Binghe Sensors (Basel) Review Thiols are important molecules in the environment and in biological processes. Cysteine (Cys), homocysteine (Hcy), glutathione (GSH) and hydrogen sulfide (H(2)S) play critical roles in a variety of physiological and pathological processes. The selective detection of thiols using reaction-based probes and sensors is very important in basic research and in disease diagnosis. This review focuses on the design of fluorescent and colorimetric probes and sensors for thiol detection. Thiol detection methods include probes and labeling agents based on nucleophilic addition and substitution, Michael addition, disulfide bond or Se-N bond cleavage, metal-sulfur interactions and more. Probes for H(2)S are based on nucleophilic cyclization, reduction and metal sulfide formation. Thiol probe and chemosensor design strategies and mechanism of action are discussed in this review. Molecular Diversity Preservation International (MDPI) 2012-11-19 /pmc/articles/PMC3522992/ /pubmed/23202239 http://dx.doi.org/10.3390/s121115907 Text en © 2012 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Peng, Hanjing Chen, Weixuan Cheng, Yunfeng Hakuna, Lovemore Strongin, Robert Wang, Binghe Thiol Reactive Probes and Chemosensors |
title | Thiol Reactive Probes and Chemosensors |
title_full | Thiol Reactive Probes and Chemosensors |
title_fullStr | Thiol Reactive Probes and Chemosensors |
title_full_unstemmed | Thiol Reactive Probes and Chemosensors |
title_short | Thiol Reactive Probes and Chemosensors |
title_sort | thiol reactive probes and chemosensors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3522992/ https://www.ncbi.nlm.nih.gov/pubmed/23202239 http://dx.doi.org/10.3390/s121115907 |
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