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Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities

A pair of new diphenyl glycerol ether enantiomers (−)-1 and (+)-1 and two new methyl benzamidobenzoates 2 and 3, named (−)-(R)- and (+)-(S)-isatindigotrioic acid [(−)-1 and (+)-1] and isatindigoticamides A (2) and B (3), respectively, were isolated from an aqueous decoction of the roots of Isatis in...

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Detalles Bibliográficos
Autores principales: Liu, Yufeng, Chen, Minghua, Guo, Qinglan, Li, Yuhuan, Jiang, Jiandong, Shi, Jiangong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343108/
https://www.ncbi.nlm.nih.gov/pubmed/28303224
http://dx.doi.org/10.1016/j.apsb.2016.09.004
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author Liu, Yufeng
Chen, Minghua
Guo, Qinglan
Li, Yuhuan
Jiang, Jiandong
Shi, Jiangong
author_facet Liu, Yufeng
Chen, Minghua
Guo, Qinglan
Li, Yuhuan
Jiang, Jiandong
Shi, Jiangong
author_sort Liu, Yufeng
collection PubMed
description A pair of new diphenyl glycerol ether enantiomers (−)-1 and (+)-1 and two new methyl benzamidobenzoates 2 and 3, named (−)-(R)- and (+)-(S)-isatindigotrioic acid [(−)-1 and (+)-1] and isatindigoticamides A (2) and B (3), respectively, were isolated from an aqueous decoction of the roots of Isatis indigotica (ban lan gen). Their structures were elucidated by spectroscopic data analysis including 2D NMR experiments. The absolute configurations of (−)-1 and (+)-1 were assigned based on the CD exciton chirality method. Compounds 2 and 3 exhibited antiviral activities against HSV-1 with IC(50) values of 4.87 and 25.87 μmol/L, respectively. Compound 2 was also found active against Coxsackie virus B3 and LPS-induced NO production.
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spelling pubmed-53431082017-03-16 Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities Liu, Yufeng Chen, Minghua Guo, Qinglan Li, Yuhuan Jiang, Jiandong Shi, Jiangong Acta Pharm Sin B Original Article A pair of new diphenyl glycerol ether enantiomers (−)-1 and (+)-1 and two new methyl benzamidobenzoates 2 and 3, named (−)-(R)- and (+)-(S)-isatindigotrioic acid [(−)-1 and (+)-1] and isatindigoticamides A (2) and B (3), respectively, were isolated from an aqueous decoction of the roots of Isatis indigotica (ban lan gen). Their structures were elucidated by spectroscopic data analysis including 2D NMR experiments. The absolute configurations of (−)-1 and (+)-1 were assigned based on the CD exciton chirality method. Compounds 2 and 3 exhibited antiviral activities against HSV-1 with IC(50) values of 4.87 and 25.87 μmol/L, respectively. Compound 2 was also found active against Coxsackie virus B3 and LPS-induced NO production. Elsevier 2017-03 2016-11-08 /pmc/articles/PMC5343108/ /pubmed/28303224 http://dx.doi.org/10.1016/j.apsb.2016.09.004 Text en © 2017 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Liu, Yufeng
Chen, Minghua
Guo, Qinglan
Li, Yuhuan
Jiang, Jiandong
Shi, Jiangong
Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title_full Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title_fullStr Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title_full_unstemmed Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title_short Aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
title_sort aromatic compounds from an aqueous extract of “ban lan gen” and their antiviral activities
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343108/
https://www.ncbi.nlm.nih.gov/pubmed/28303224
http://dx.doi.org/10.1016/j.apsb.2016.09.004
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