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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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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. |
format | Online Article Text |
id | pubmed-6256984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
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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