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Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook

A new flavone, named crotoncaudatin (1), was isolated from the stems of Croton caudatus Geisel. var. tomentosus Hook., together with nine known analogues: 3,5,6,7,8,3′,4′-heptamethoxyflavone (2), tangeretin (3), nobiletin (4), 5,6,7,4′-tetramethoxy-flavone (5), sinensetin (6), kaempferol (7), tiliro...

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Detalles Bibliográficos
Autores principales: Zou, Guo-An, Su, Zhi-Heng, Zhang, Hong-Wu, Wang, Yuan, Yang, Jun-Shan, Zou, Zhong-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257243/
https://www.ncbi.nlm.nih.gov/pubmed/20335965
http://dx.doi.org/10.3390/molecules15031097
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author Zou, Guo-An
Su, Zhi-Heng
Zhang, Hong-Wu
Wang, Yuan
Yang, Jun-Shan
Zou, Zhong-Mei
author_facet Zou, Guo-An
Su, Zhi-Heng
Zhang, Hong-Wu
Wang, Yuan
Yang, Jun-Shan
Zou, Zhong-Mei
author_sort Zou, Guo-An
collection PubMed
description A new flavone, named crotoncaudatin (1), was isolated from the stems of Croton caudatus Geisel. var. tomentosus Hook., together with nine known analogues: 3,5,6,7,8,3′,4′-heptamethoxyflavone (2), tangeretin (3), nobiletin (4), 5,6,7,4′-tetramethoxy-flavone (5), sinensetin (6), kaempferol (7), tiliroside (8), kaempferol-3-O-rutinoside (9) and rutin (10). The structures of the above compounds were established by a combination of spectroscopic methods, including HR-ESI-MS, (1)H-NMR,( 13C)-NMR, HMQC and HMBC spectra. All compounds were isolated from and identified in this species for the first time and compounds 1-6 are new for the genus Croton.
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spelling pubmed-62572432018-12-04 Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook Zou, Guo-An Su, Zhi-Heng Zhang, Hong-Wu Wang, Yuan Yang, Jun-Shan Zou, Zhong-Mei Molecules Article A new flavone, named crotoncaudatin (1), was isolated from the stems of Croton caudatus Geisel. var. tomentosus Hook., together with nine known analogues: 3,5,6,7,8,3′,4′-heptamethoxyflavone (2), tangeretin (3), nobiletin (4), 5,6,7,4′-tetramethoxy-flavone (5), sinensetin (6), kaempferol (7), tiliroside (8), kaempferol-3-O-rutinoside (9) and rutin (10). The structures of the above compounds were established by a combination of spectroscopic methods, including HR-ESI-MS, (1)H-NMR,( 13C)-NMR, HMQC and HMBC spectra. All compounds were isolated from and identified in this species for the first time and compounds 1-6 are new for the genus Croton. Molecular Diversity Preservation International 2010-02-26 /pmc/articles/PMC6257243/ /pubmed/20335965 http://dx.doi.org/10.3390/molecules15031097 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Zou, Guo-An
Su, Zhi-Heng
Zhang, Hong-Wu
Wang, Yuan
Yang, Jun-Shan
Zou, Zhong-Mei
Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title_full Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title_fullStr Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title_full_unstemmed Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title_short Flavonoids from the Stems of Croton caudatus Geisel. var. tomentosus Hook
title_sort flavonoids from the stems of croton caudatus geisel. var. tomentosus hook
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257243/
https://www.ncbi.nlm.nih.gov/pubmed/20335965
http://dx.doi.org/10.3390/molecules15031097
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