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Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix

A new phenolic compound, 2-O-β-laminaribiosyl-4-hydroxyacetophenone (1), was isolated from Cynanchi Wilfordii Radix (CWR, the root of Cynanchum wilfordii Hemsley), along with 10 known aromatic compounds, including cynandione A (2), bungeisides-C (7) and –D (8), p-hydroxyacetophenone (9), 2′,5′-dihyd...

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Autores principales: Uchikura, Takashi, Tanaka, Hiroaki, Sugiwaki, Hidemi, Yoshimura, Morio, Sato-Masumoto, Naoko, Tsujimoto, Takashi, Uchiyama, Nahoko, Hakamatsuka, Takashi, Amakura, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017071/
https://www.ncbi.nlm.nih.gov/pubmed/29538318
http://dx.doi.org/10.3390/molecules23030656
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author Uchikura, Takashi
Tanaka, Hiroaki
Sugiwaki, Hidemi
Yoshimura, Morio
Sato-Masumoto, Naoko
Tsujimoto, Takashi
Uchiyama, Nahoko
Hakamatsuka, Takashi
Amakura, Yoshiaki
author_facet Uchikura, Takashi
Tanaka, Hiroaki
Sugiwaki, Hidemi
Yoshimura, Morio
Sato-Masumoto, Naoko
Tsujimoto, Takashi
Uchiyama, Nahoko
Hakamatsuka, Takashi
Amakura, Yoshiaki
author_sort Uchikura, Takashi
collection PubMed
description A new phenolic compound, 2-O-β-laminaribiosyl-4-hydroxyacetophenone (1), was isolated from Cynanchi Wilfordii Radix (CWR, the root of Cynanchum wilfordii Hemsley), along with 10 known aromatic compounds, including cynandione A (2), bungeisides-C (7) and –D (8), p-hydroxyacetophenone (9), 2′,5′-dihydroxyacetophenone (10), and 2′,4′-dihydroxyacetophenone (11). The structure of the new compound (1) was elucidated using spectroscopic methods and chemical methods. The structure of cynandione A (2), including a linkage mode of the biphenyl parts that remained uncertain, was unambiguously confirmed using the 2D (13)C–(13)C incredible natural abundance double quantum transfer experiment (INADEQUATE) spectrum. Additionally, health issues related to the use of Cynanchi Auriculati Radix (CAR, the root of Cynanchum auriculatum Royle ex Wight) instead of CWR have emerged. Therefore, constituents present in methanolic extracts of commercially available CWRs and CARs were examined using UV-sensitive high-performance liquid chromatography (HPLC), resulting in common detection of three major peaks ascribed to cynandione A (2), p-hydroxyacetophenone (9), and 2′,4′-dihydroxyacetophenone (11). Thus, to distinguish between these ingredients, a thin-layer chromatography (TLC) method, combined with only UV irradiation detection, focusing on wilfosides C1N (12) and K1N (13) as marker compounds characteristic of CAR, was performed. Furthermore, we propose this method as a simple and convenient strategy for the preliminary distinction of CWR and CAR to ensure the quality and safety of their crude drugs.
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spelling pubmed-60170712018-11-13 Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix Uchikura, Takashi Tanaka, Hiroaki Sugiwaki, Hidemi Yoshimura, Morio Sato-Masumoto, Naoko Tsujimoto, Takashi Uchiyama, Nahoko Hakamatsuka, Takashi Amakura, Yoshiaki Molecules Article A new phenolic compound, 2-O-β-laminaribiosyl-4-hydroxyacetophenone (1), was isolated from Cynanchi Wilfordii Radix (CWR, the root of Cynanchum wilfordii Hemsley), along with 10 known aromatic compounds, including cynandione A (2), bungeisides-C (7) and –D (8), p-hydroxyacetophenone (9), 2′,5′-dihydroxyacetophenone (10), and 2′,4′-dihydroxyacetophenone (11). The structure of the new compound (1) was elucidated using spectroscopic methods and chemical methods. The structure of cynandione A (2), including a linkage mode of the biphenyl parts that remained uncertain, was unambiguously confirmed using the 2D (13)C–(13)C incredible natural abundance double quantum transfer experiment (INADEQUATE) spectrum. Additionally, health issues related to the use of Cynanchi Auriculati Radix (CAR, the root of Cynanchum auriculatum Royle ex Wight) instead of CWR have emerged. Therefore, constituents present in methanolic extracts of commercially available CWRs and CARs were examined using UV-sensitive high-performance liquid chromatography (HPLC), resulting in common detection of three major peaks ascribed to cynandione A (2), p-hydroxyacetophenone (9), and 2′,4′-dihydroxyacetophenone (11). Thus, to distinguish between these ingredients, a thin-layer chromatography (TLC) method, combined with only UV irradiation detection, focusing on wilfosides C1N (12) and K1N (13) as marker compounds characteristic of CAR, was performed. Furthermore, we propose this method as a simple and convenient strategy for the preliminary distinction of CWR and CAR to ensure the quality and safety of their crude drugs. MDPI 2018-03-14 /pmc/articles/PMC6017071/ /pubmed/29538318 http://dx.doi.org/10.3390/molecules23030656 Text en © 2018 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
Uchikura, Takashi
Tanaka, Hiroaki
Sugiwaki, Hidemi
Yoshimura, Morio
Sato-Masumoto, Naoko
Tsujimoto, Takashi
Uchiyama, Nahoko
Hakamatsuka, Takashi
Amakura, Yoshiaki
Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title_full Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title_fullStr Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title_full_unstemmed Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title_short Preliminary Quality Evaluation and Characterization of Phenolic Constituents in Cynanchi Wilfordii Radix
title_sort preliminary quality evaluation and characterization of phenolic constituents in cynanchi wilfordii radix
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017071/
https://www.ncbi.nlm.nih.gov/pubmed/29538318
http://dx.doi.org/10.3390/molecules23030656
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