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Partition Coefficients (logP) of Hydrolysable Tannins

The partition coefficients (logP) between n-octanol and water of 47 purified and characterized hydrolysable tannins were measured with the shake flask method utilizing UPLC and HPLC with UV detection. Results show that galloyl glucoses and gallotannins are clearly more hydrophobic than ellagitannins...

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Autores principales: Virtanen, Valtteri, Karonen, Maarit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465006/
https://www.ncbi.nlm.nih.gov/pubmed/32823639
http://dx.doi.org/10.3390/molecules25163691
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author Virtanen, Valtteri
Karonen, Maarit
author_facet Virtanen, Valtteri
Karonen, Maarit
author_sort Virtanen, Valtteri
collection PubMed
description The partition coefficients (logP) between n-octanol and water of 47 purified and characterized hydrolysable tannins were measured with the shake flask method utilizing UPLC and HPLC with UV detection. Results show that galloyl glucoses and gallotannins are clearly more hydrophobic than ellagitannins but the differences in hydrophobicity within ellagitannins are more varied than within galloyl glucoses or gallotannins. Most notable structural features that were found to influence the hydrophobicity of ellagitannins were the number of free galloyl groups, acyclic versus cyclic polyol, substitution of the anomeric position of glucose and (4)C(1) versus (1)C(4) conformation of the glucopyranose core.
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spelling pubmed-74650062020-09-04 Partition Coefficients (logP) of Hydrolysable Tannins Virtanen, Valtteri Karonen, Maarit Molecules Article The partition coefficients (logP) between n-octanol and water of 47 purified and characterized hydrolysable tannins were measured with the shake flask method utilizing UPLC and HPLC with UV detection. Results show that galloyl glucoses and gallotannins are clearly more hydrophobic than ellagitannins but the differences in hydrophobicity within ellagitannins are more varied than within galloyl glucoses or gallotannins. Most notable structural features that were found to influence the hydrophobicity of ellagitannins were the number of free galloyl groups, acyclic versus cyclic polyol, substitution of the anomeric position of glucose and (4)C(1) versus (1)C(4) conformation of the glucopyranose core. MDPI 2020-08-13 /pmc/articles/PMC7465006/ /pubmed/32823639 http://dx.doi.org/10.3390/molecules25163691 Text en © 2020 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
Virtanen, Valtteri
Karonen, Maarit
Partition Coefficients (logP) of Hydrolysable Tannins
title Partition Coefficients (logP) of Hydrolysable Tannins
title_full Partition Coefficients (logP) of Hydrolysable Tannins
title_fullStr Partition Coefficients (logP) of Hydrolysable Tannins
title_full_unstemmed Partition Coefficients (logP) of Hydrolysable Tannins
title_short Partition Coefficients (logP) of Hydrolysable Tannins
title_sort partition coefficients (logp) of hydrolysable tannins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465006/
https://www.ncbi.nlm.nih.gov/pubmed/32823639
http://dx.doi.org/10.3390/molecules25163691
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