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New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng
BACKGROUND: Root rot is a serious destructive disease of Panax notoginseng, a famous cultivated araliaceous herb called Sanqi or Tianqi in Southwest China. METHODS: The chemical substances of Sanqi rot roots were explored by chromatographic techniques. MS, 1D/2D-NMR, and single crystal X-ray diffrac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195571/ https://www.ncbi.nlm.nih.gov/pubmed/32372862 http://dx.doi.org/10.1016/j.jgr.2019.01.008 |
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author | Shang, Jia-Huan Sun, Wen-Jie Zhu, Hong-Tao Wang, Dong Yang, Chong-Ren Zhang, Ying-Jun |
author_facet | Shang, Jia-Huan Sun, Wen-Jie Zhu, Hong-Tao Wang, Dong Yang, Chong-Ren Zhang, Ying-Jun |
author_sort | Shang, Jia-Huan |
collection | PubMed |
description | BACKGROUND: Root rot is a serious destructive disease of Panax notoginseng, a famous cultivated araliaceous herb called Sanqi or Tianqi in Southwest China. METHODS: The chemical substances of Sanqi rot roots were explored by chromatographic techniques. MS, 1D/2D-NMR, and single crystal X-ray diffraction were applied to determine the structures. Murine macrophage RAW264.7 and five human cancer cell lines were used separately for evaluating the antiinflammatory and cytotoxic activities. RESULTS AND CONCLUSION: Thirty dammarane-type triterpenes and saponins were isolated from the rot roots of P. notoginseng. Among them, seven triterpenes, namely, 20(S)-dammar-25-ene-24(S)-hydroperoxyl-3β,6α,12β,20-tetrol (1), 20(S)-dammar-3-oxo-23-ene-25-hydroperoxyl-6α,12β,20-triol (2), 20(S)-dammar-12-oxo-23-ene-25-hydroperoxyl-3β,6α,20-triol (3), 20(S)-dammar-3-oxo-23-ene-25-hydroperoxyl-12β,20-diol (4), 20(S),24(R)-epoxy-3,4-seco-dammar-25-hydroxy-12-one-3-oic acid (5), 20(S),24(R)-epoxy-3,4-seco-dammar-25-hydroxy-12-one-3-oic acid methyl ester (6), and 6α-hydroxy-22,23,24,25,26,27-hexanordammar-3,12,20-trione (7), are new compounds. In addition, 12 known ones (12–16 and 19–25) were reported in Sanqi for the first time. The new Compound 1 showed comparable antiinflammatory activity on inhibition of NO production to the positive control, whereas the known compounds 9, 12, 13, and 16 displayed moderate cytotoxicities against five human cancer cell lines. The results will provide scientific basis for understanding the chemical constituents of Sanqi rot roots and new candidates for searching antiinflammatory and antitumor agents. |
format | Online Article Text |
id | pubmed-7195571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-71955712020-05-05 New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng Shang, Jia-Huan Sun, Wen-Jie Zhu, Hong-Tao Wang, Dong Yang, Chong-Ren Zhang, Ying-Jun J Ginseng Res Chemistry BACKGROUND: Root rot is a serious destructive disease of Panax notoginseng, a famous cultivated araliaceous herb called Sanqi or Tianqi in Southwest China. METHODS: The chemical substances of Sanqi rot roots were explored by chromatographic techniques. MS, 1D/2D-NMR, and single crystal X-ray diffraction were applied to determine the structures. Murine macrophage RAW264.7 and five human cancer cell lines were used separately for evaluating the antiinflammatory and cytotoxic activities. RESULTS AND CONCLUSION: Thirty dammarane-type triterpenes and saponins were isolated from the rot roots of P. notoginseng. Among them, seven triterpenes, namely, 20(S)-dammar-25-ene-24(S)-hydroperoxyl-3β,6α,12β,20-tetrol (1), 20(S)-dammar-3-oxo-23-ene-25-hydroperoxyl-6α,12β,20-triol (2), 20(S)-dammar-12-oxo-23-ene-25-hydroperoxyl-3β,6α,20-triol (3), 20(S)-dammar-3-oxo-23-ene-25-hydroperoxyl-12β,20-diol (4), 20(S),24(R)-epoxy-3,4-seco-dammar-25-hydroxy-12-one-3-oic acid (5), 20(S),24(R)-epoxy-3,4-seco-dammar-25-hydroxy-12-one-3-oic acid methyl ester (6), and 6α-hydroxy-22,23,24,25,26,27-hexanordammar-3,12,20-trione (7), are new compounds. In addition, 12 known ones (12–16 and 19–25) were reported in Sanqi for the first time. The new Compound 1 showed comparable antiinflammatory activity on inhibition of NO production to the positive control, whereas the known compounds 9, 12, 13, and 16 displayed moderate cytotoxicities against five human cancer cell lines. The results will provide scientific basis for understanding the chemical constituents of Sanqi rot roots and new candidates for searching antiinflammatory and antitumor agents. Elsevier 2020-05 2019-02-06 /pmc/articles/PMC7195571/ /pubmed/32372862 http://dx.doi.org/10.1016/j.jgr.2019.01.008 Text en © 2019 The Korean Society of Ginseng, Published by Elsevier Korea LLC. 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 | Chemistry Shang, Jia-Huan Sun, Wen-Jie Zhu, Hong-Tao Wang, Dong Yang, Chong-Ren Zhang, Ying-Jun New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title | New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title_full | New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title_fullStr | New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title_full_unstemmed | New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title_short | New hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of Panax notoginseng |
title_sort | new hydroperoxylated and 20,24-epoxylated dammarane triterpenes from the rot roots of panax notoginseng |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195571/ https://www.ncbi.nlm.nih.gov/pubmed/32372862 http://dx.doi.org/10.1016/j.jgr.2019.01.008 |
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