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Flavonoids from Symplocos racemosa

A novel isoflavone glycoside, peseudobatigenin 7-O-[β-d-apiofuranosyl-(1''''→5''')-O-β-d-apiofuranosyl-(1'''→6'')]-β-d-glucopyranoside, namely sympracemoside (1), was isolated from the aerial parts of Symplocos racemosa along with 15 known...

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Autores principales: Jung, Mila, Choi, Janggyoo, Chae, Hee-Sung, Cho, Jae Youl, Kim, Young-Dong, Htwe, Khin Myo, Lee, Woo-Shin, Chin, Young-Won, Kim, Jinwoong, Yoon, Kee Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272286/
https://www.ncbi.nlm.nih.gov/pubmed/25549060
http://dx.doi.org/10.3390/molecules20010358
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author Jung, Mila
Choi, Janggyoo
Chae, Hee-Sung
Cho, Jae Youl
Kim, Young-Dong
Htwe, Khin Myo
Lee, Woo-Shin
Chin, Young-Won
Kim, Jinwoong
Yoon, Kee Dong
author_facet Jung, Mila
Choi, Janggyoo
Chae, Hee-Sung
Cho, Jae Youl
Kim, Young-Dong
Htwe, Khin Myo
Lee, Woo-Shin
Chin, Young-Won
Kim, Jinwoong
Yoon, Kee Dong
author_sort Jung, Mila
collection PubMed
description A novel isoflavone glycoside, peseudobatigenin 7-O-[β-d-apiofuranosyl-(1''''→5''')-O-β-d-apiofuranosyl-(1'''→6'')]-β-d-glucopyranoside, namely sympracemoside (1), was isolated from the aerial parts of Symplocos racemosa along with 15 known flavonoids (2–16). Their structures were characterized by Q-TOF mass, optical rotation, UV, 1D and 2D-NMR spectroscopic data. Compounds 3, 9, 16 showed moderate inhibitory activities against NO production with IC(50) value of 88.2, 42.1 and 74.3 μM, respectively.
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spelling pubmed-62722862018-12-28 Flavonoids from Symplocos racemosa Jung, Mila Choi, Janggyoo Chae, Hee-Sung Cho, Jae Youl Kim, Young-Dong Htwe, Khin Myo Lee, Woo-Shin Chin, Young-Won Kim, Jinwoong Yoon, Kee Dong Molecules Communication A novel isoflavone glycoside, peseudobatigenin 7-O-[β-d-apiofuranosyl-(1''''→5''')-O-β-d-apiofuranosyl-(1'''→6'')]-β-d-glucopyranoside, namely sympracemoside (1), was isolated from the aerial parts of Symplocos racemosa along with 15 known flavonoids (2–16). Their structures were characterized by Q-TOF mass, optical rotation, UV, 1D and 2D-NMR spectroscopic data. Compounds 3, 9, 16 showed moderate inhibitory activities against NO production with IC(50) value of 88.2, 42.1 and 74.3 μM, respectively. MDPI 2014-12-26 /pmc/articles/PMC6272286/ /pubmed/25549060 http://dx.doi.org/10.3390/molecules20010358 Text en © 2014 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Jung, Mila
Choi, Janggyoo
Chae, Hee-Sung
Cho, Jae Youl
Kim, Young-Dong
Htwe, Khin Myo
Lee, Woo-Shin
Chin, Young-Won
Kim, Jinwoong
Yoon, Kee Dong
Flavonoids from Symplocos racemosa
title Flavonoids from Symplocos racemosa
title_full Flavonoids from Symplocos racemosa
title_fullStr Flavonoids from Symplocos racemosa
title_full_unstemmed Flavonoids from Symplocos racemosa
title_short Flavonoids from Symplocos racemosa
title_sort flavonoids from symplocos racemosa
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272286/
https://www.ncbi.nlm.nih.gov/pubmed/25549060
http://dx.doi.org/10.3390/molecules20010358
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