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New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata

Inflammation is related to many diseases. Lindera akoensis Hayata was often used in folk therapy in Taiwan for inflammation. In this study, three new flavonol acyl glycosides, namely kaempferol-3-O-β-D-4′′,6′′-di-(E)-p-coumaroylglucoside (1), 3′′-(E)-p-coumaroylafzelin (2) and 4′-O- methyl-2′′,4′′-d...

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Autores principales: Yang, Chung-Ping, Shie, Pei-Hsin, Huang, Guan-Jhong, Chien, Shih-Chang, Kuo, Yueh-Hsiung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384965/
https://www.ncbi.nlm.nih.gov/pubmed/30720720
http://dx.doi.org/10.3390/molecules24030563
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author Yang, Chung-Ping
Shie, Pei-Hsin
Huang, Guan-Jhong
Chien, Shih-Chang
Kuo, Yueh-Hsiung
author_facet Yang, Chung-Ping
Shie, Pei-Hsin
Huang, Guan-Jhong
Chien, Shih-Chang
Kuo, Yueh-Hsiung
author_sort Yang, Chung-Ping
collection PubMed
description Inflammation is related to many diseases. Lindera akoensis Hayata was often used in folk therapy in Taiwan for inflammation. In this study, three new flavonol acyl glycosides, namely kaempferol-3-O-β-D-4′′,6′′-di-(E)-p-coumaroylglucoside (1), 3′′-(E)-p-coumaroylafzelin (2) and 4′-O- methyl-2′′,4′′-di-(E)-p-coumaroylquercitrin (3), and three components, 3β-dodecyl-4β-hydroxy- 5β-methyldihydrofuran-2-one (4), 2β-acetoxyclovan-9α-ol (5), (1α,4β,6β)-trihydroxyeudesmane (6) that were isolated from the natural product for the first time were obtained along with 25 known compounds from L. akoensis. Their structures were determined by comprehensive spectroscopic analyses (1D and 2D NMR, EI-, ESI- and HRESI-MS). The ability of 1 to decrease the LPS-stimulated production of nitrite in RAW264.7 cell was evaluated, showing an IC(50) value of 36.3 ± 3.2 μM. This result supports the value of L. akoensis as a traditional medicine resource.
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spelling pubmed-63849652019-02-23 New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata Yang, Chung-Ping Shie, Pei-Hsin Huang, Guan-Jhong Chien, Shih-Chang Kuo, Yueh-Hsiung Molecules Article Inflammation is related to many diseases. Lindera akoensis Hayata was often used in folk therapy in Taiwan for inflammation. In this study, three new flavonol acyl glycosides, namely kaempferol-3-O-β-D-4′′,6′′-di-(E)-p-coumaroylglucoside (1), 3′′-(E)-p-coumaroylafzelin (2) and 4′-O- methyl-2′′,4′′-di-(E)-p-coumaroylquercitrin (3), and three components, 3β-dodecyl-4β-hydroxy- 5β-methyldihydrofuran-2-one (4), 2β-acetoxyclovan-9α-ol (5), (1α,4β,6β)-trihydroxyeudesmane (6) that were isolated from the natural product for the first time were obtained along with 25 known compounds from L. akoensis. Their structures were determined by comprehensive spectroscopic analyses (1D and 2D NMR, EI-, ESI- and HRESI-MS). The ability of 1 to decrease the LPS-stimulated production of nitrite in RAW264.7 cell was evaluated, showing an IC(50) value of 36.3 ± 3.2 μM. This result supports the value of L. akoensis as a traditional medicine resource. MDPI 2019-02-04 /pmc/articles/PMC6384965/ /pubmed/30720720 http://dx.doi.org/10.3390/molecules24030563 Text en © 2019 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
Yang, Chung-Ping
Shie, Pei-Hsin
Huang, Guan-Jhong
Chien, Shih-Chang
Kuo, Yueh-Hsiung
New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title_full New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title_fullStr New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title_full_unstemmed New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title_short New Anti-inflammatory Flavonol Glycosides from Lindera akoensis Hayata
title_sort new anti-inflammatory flavonol glycosides from lindera akoensis hayata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384965/
https://www.ncbi.nlm.nih.gov/pubmed/30720720
http://dx.doi.org/10.3390/molecules24030563
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