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Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity

Protopanaxatriol saponins obtained with AB-8 macroporous resin mainly consisted of ginsenosides Rg(1) and Re. A novel mono-ester of ginsenoside-Rh(1) (ginsenoside-ORh(1)) was synthesized through further enzymatic hydrolysis and octanoyl chloride modifications. A 53% yield was obtained by a facile sy...

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Detalles Bibliográficos
Autores principales: Han, Mei, Hou, Jin-Gang, Dong, Cheng-Ming, Li, Wei, Yu, Hao-Lun, Zheng, Yi-Nan, Chen, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256984/
https://www.ncbi.nlm.nih.gov/pubmed/20110899
http://dx.doi.org/10.3390/molecules15010399
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author Han, Mei
Hou, Jin-Gang
Dong, Cheng-Ming
Li, Wei
Yu, Hao-Lun
Zheng, Yi-Nan
Chen, Li
author_facet Han, Mei
Hou, Jin-Gang
Dong, Cheng-Ming
Li, Wei
Yu, Hao-Lun
Zheng, Yi-Nan
Chen, Li
author_sort Han, Mei
collection PubMed
description Protopanaxatriol saponins obtained with AB-8 macroporous resin mainly consisted of ginsenosides Rg(1) and Re. A novel mono-ester of ginsenoside-Rh(1) (ginsenoside-ORh(1)) was synthesized through further enzymatic hydrolysis and octanoyl chloride modifications. A 53% yield was obtained by a facile synthetic method. The structures were identified on the basis of 1D-NMR and 2D-NMR, as well as ESI-TOF-MS mass spectroscopic analyses. The isolated and synthetic compounds were applied in an anti-tumor bioassay, in which ginsenoside ORh(1) showed moderate effects on Murine H22 Hepatoma Cells.
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spelling pubmed-62569842018-12-03 Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity Han, Mei Hou, Jin-Gang Dong, Cheng-Ming Li, Wei Yu, Hao-Lun Zheng, Yi-Nan Chen, Li Molecules Article Protopanaxatriol saponins obtained with AB-8 macroporous resin mainly consisted of ginsenosides Rg(1) and Re. A novel mono-ester of ginsenoside-Rh(1) (ginsenoside-ORh(1)) was synthesized through further enzymatic hydrolysis and octanoyl chloride modifications. A 53% yield was obtained by a facile synthetic method. The structures were identified on the basis of 1D-NMR and 2D-NMR, as well as ESI-TOF-MS mass spectroscopic analyses. The isolated and synthetic compounds were applied in an anti-tumor bioassay, in which ginsenoside ORh(1) showed moderate effects on Murine H22 Hepatoma Cells. Molecular Diversity Preservation International 2010-01-19 /pmc/articles/PMC6256984/ /pubmed/20110899 http://dx.doi.org/10.3390/molecules15010399 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
Han, Mei
Hou, Jin-Gang
Dong, Cheng-Ming
Li, Wei
Yu, Hao-Lun
Zheng, Yi-Nan
Chen, Li
Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title_full Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title_fullStr Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title_full_unstemmed Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title_short Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
title_sort isolation, synthesis and structures of ginsenoside derivatives and their anti-tumor bioactivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256984/
https://www.ncbi.nlm.nih.gov/pubmed/20110899
http://dx.doi.org/10.3390/molecules15010399
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