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Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe

As a new model of chemical assay-guided natural product isolation, an effective chemodosimetric assay system was devised. Our chemical assay system features a fluorogenic chemodosimeter immobilized on a solid support, which offers advantages in identifying the desired compounds in complex natural pr...

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Detalles Bibliográficos
Autores principales: Jeon, Hongjun, Lim, Chaemin, Lee, Ji Min, Kim, Sanghee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489024/
https://www.ncbi.nlm.nih.gov/pubmed/28706669
http://dx.doi.org/10.1039/c5sc00360a
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author Jeon, Hongjun
Lim, Chaemin
Lee, Ji Min
Kim, Sanghee
author_facet Jeon, Hongjun
Lim, Chaemin
Lee, Ji Min
Kim, Sanghee
author_sort Jeon, Hongjun
collection PubMed
description As a new model of chemical assay-guided natural product isolation, an effective chemodosimetric assay system was devised. Our chemical assay system features a fluorogenic chemodosimeter immobilized on a solid support, which offers advantages in identifying the desired compounds in complex natural product mixtures. To isolate only compounds with the target functional groups, the click chemistry concept was adopted. The model system presented here was developed for natural products with a terminal alkyne. Using our newly designed alkyne sensing beads with the aforementioned features, we have readily identified, quantified, and isolated compounds with a terminal alkyne group from plant extracts.
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spelling pubmed-54890242017-07-13 Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe Jeon, Hongjun Lim, Chaemin Lee, Ji Min Kim, Sanghee Chem Sci Chemistry As a new model of chemical assay-guided natural product isolation, an effective chemodosimetric assay system was devised. Our chemical assay system features a fluorogenic chemodosimeter immobilized on a solid support, which offers advantages in identifying the desired compounds in complex natural product mixtures. To isolate only compounds with the target functional groups, the click chemistry concept was adopted. The model system presented here was developed for natural products with a terminal alkyne. Using our newly designed alkyne sensing beads with the aforementioned features, we have readily identified, quantified, and isolated compounds with a terminal alkyne group from plant extracts. Royal Society of Chemistry 2015-05-01 2015-03-25 /pmc/articles/PMC5489024/ /pubmed/28706669 http://dx.doi.org/10.1039/c5sc00360a Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Jeon, Hongjun
Lim, Chaemin
Lee, Ji Min
Kim, Sanghee
Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title_full Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title_fullStr Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title_full_unstemmed Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title_short Chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
title_sort chemical assay-guided natural product isolation via solid-supported chemodosimetric fluorescent probe
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489024/
https://www.ncbi.nlm.nih.gov/pubmed/28706669
http://dx.doi.org/10.1039/c5sc00360a
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