Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation
A semisynthetic β-glucosidase inhibitor was identified from a chemically engineered extract prepared by reaction with benzenesulfonyl chloride. The structure includes a natural histamine portion and a benzenesulfonyl portion introduced during the diversification step. © 2011 Springer Science+Busines...
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2011
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811991_v15_n3_p713_Salazar http://hdl.handle.net/20.500.12110/paper_13811991_v15_n3_p713_Salazar |
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paper:paper_13811991_v15_n3_p713_Salazar2023-06-08T16:12:22Z Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation Biomolecular properties Chemically engineered extract Sulfonylation benzene beta glucosidase chloride article chemical engineering chemical reaction chemical structure priority journal synthesis beta-Glucosidase Chemical Engineering Enzyme Inhibitors Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Extracts Sulfones Urticaceae A semisynthetic β-glucosidase inhibitor was identified from a chemically engineered extract prepared by reaction with benzenesulfonyl chloride. The structure includes a natural histamine portion and a benzenesulfonyl portion introduced during the diversification step. © 2011 Springer Science+Business Media B.V. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811991_v15_n3_p713_Salazar http://hdl.handle.net/20.500.12110/paper_13811991_v15_n3_p713_Salazar |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Biomolecular properties Chemically engineered extract Sulfonylation benzene beta glucosidase chloride article chemical engineering chemical reaction chemical structure priority journal synthesis beta-Glucosidase Chemical Engineering Enzyme Inhibitors Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Extracts Sulfones Urticaceae |
spellingShingle |
Biomolecular properties Chemically engineered extract Sulfonylation benzene beta glucosidase chloride article chemical engineering chemical reaction chemical structure priority journal synthesis beta-Glucosidase Chemical Engineering Enzyme Inhibitors Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Extracts Sulfones Urticaceae Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
topic_facet |
Biomolecular properties Chemically engineered extract Sulfonylation benzene beta glucosidase chloride article chemical engineering chemical reaction chemical structure priority journal synthesis beta-Glucosidase Chemical Engineering Enzyme Inhibitors Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plant Extracts Sulfones Urticaceae |
description |
A semisynthetic β-glucosidase inhibitor was identified from a chemically engineered extract prepared by reaction with benzenesulfonyl chloride. The structure includes a natural histamine portion and a benzenesulfonyl portion introduced during the diversification step. © 2011 Springer Science+Business Media B.V. |
title |
Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
title_short |
Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
title_full |
Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
title_fullStr |
Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
title_full_unstemmed |
Discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
title_sort |
discovery of a β-glucosidase inhibitor from a chemically engineered extract prepared through sulfonylation |
publishDate |
2011 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811991_v15_n3_p713_Salazar http://hdl.handle.net/20.500.12110/paper_13811991_v15_n3_p713_Salazar |
_version_ |
1768546222869577728 |