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Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth

Twenty-four new phenylpropanoid esters of sucrose, phanerosides A–X (1–24), were isolated from an EtOH extract of the rattans of Phanera championii Benth. (Fabaceae). Their structures were elucidated on the basis of comprehensive spectroscopic data analysis. A wide range of structural analogues were...

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Autores principales: Hu, Ya-Jie, Lan, Qian, Su, Bao-Jun, Liang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301492/
https://www.ncbi.nlm.nih.gov/pubmed/37375320
http://dx.doi.org/10.3390/molecules28124767
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author Hu, Ya-Jie
Lan, Qian
Su, Bao-Jun
Liang, Dong
author_facet Hu, Ya-Jie
Lan, Qian
Su, Bao-Jun
Liang, Dong
author_sort Hu, Ya-Jie
collection PubMed
description Twenty-four new phenylpropanoid esters of sucrose, phanerosides A–X (1–24), were isolated from an EtOH extract of the rattans of Phanera championii Benth. (Fabaceae). Their structures were elucidated on the basis of comprehensive spectroscopic data analysis. A wide range of structural analogues were presented due to the different numbers and positions of acetyl substituents and the structures of phenylpropanoid moieties. Phenylpropanoid esters of sucrose were isolated from the Fabaceae family for the first time. Biologically, the inhibitory effects of compounds 6 and 21 on NO production in LPS-induced BV-2 microglial cells were better than that of the positive control, with IC(50) values of 6.7 and 5.2 μM, respectively. The antioxidant activity assay showed that compounds 5, 15, 17, and 24 displayed moderate DPPH radical scavenging activity, with IC(50) values ranging from 34.9 to 43.9 μM.
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spelling pubmed-103014922023-06-29 Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth Hu, Ya-Jie Lan, Qian Su, Bao-Jun Liang, Dong Molecules Article Twenty-four new phenylpropanoid esters of sucrose, phanerosides A–X (1–24), were isolated from an EtOH extract of the rattans of Phanera championii Benth. (Fabaceae). Their structures were elucidated on the basis of comprehensive spectroscopic data analysis. A wide range of structural analogues were presented due to the different numbers and positions of acetyl substituents and the structures of phenylpropanoid moieties. Phenylpropanoid esters of sucrose were isolated from the Fabaceae family for the first time. Biologically, the inhibitory effects of compounds 6 and 21 on NO production in LPS-induced BV-2 microglial cells were better than that of the positive control, with IC(50) values of 6.7 and 5.2 μM, respectively. The antioxidant activity assay showed that compounds 5, 15, 17, and 24 displayed moderate DPPH radical scavenging activity, with IC(50) values ranging from 34.9 to 43.9 μM. MDPI 2023-06-14 /pmc/articles/PMC10301492/ /pubmed/37375320 http://dx.doi.org/10.3390/molecules28124767 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hu, Ya-Jie
Lan, Qian
Su, Bao-Jun
Liang, Dong
Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title_full Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title_fullStr Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title_full_unstemmed Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title_short Phanerosides A–X, Phenylpropanoid Esters of Sucrose from the Rattans of Phanera championii Benth
title_sort phanerosides a–x, phenylpropanoid esters of sucrose from the rattans of phanera championii benth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10301492/
https://www.ncbi.nlm.nih.gov/pubmed/37375320
http://dx.doi.org/10.3390/molecules28124767
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