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New Triterpenoid Saponins from the Herb Hylomecon japonica
Background: Hylomecon japonica, a plant of the Papaveraceae family which is well-known for the alkaloids they produce, is a perennial plant widely distributed in the northeast, central and east regions of China. Although a variety of chemical constituents, including alkaloids, flavonoids, and megast...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151478/ https://www.ncbi.nlm.nih.gov/pubmed/29065554 http://dx.doi.org/10.3390/molecules22101731 |
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author | Qu, Yan-Fei Gao, Jing-Yu Wang, Jing Geng, Yan-Mei Zhou, Yu Sun, Cheng-Xin Li, Fei Feng, Lei Yu, Meng-Juan Wang, Guang-Shu |
author_facet | Qu, Yan-Fei Gao, Jing-Yu Wang, Jing Geng, Yan-Mei Zhou, Yu Sun, Cheng-Xin Li, Fei Feng, Lei Yu, Meng-Juan Wang, Guang-Shu |
author_sort | Qu, Yan-Fei |
collection | PubMed |
description | Background: Hylomecon japonica, a plant of the Papaveraceae family which is well-known for the alkaloids they produce, is a perennial plant widely distributed in the northeast, central and east regions of China. Although a variety of chemical constituents, including alkaloids, flavonoids, and megastigmoids, have been isolated from H. japonica, the investigation of saponins in H. japonica has not been reported until now. Methods: Various separation techniques, including polyporous resin column chromatography, silica gel column chromatography and hemi-preparative HPLC were applied to the isolation of triterpenoid saponins, and chemical methods such as acid hydrolysis and spectroscopic methods including HRESIMS and NMR were applied to their structure elucidation, and the XTT reduction method was used to assay cytotoxicity. Results: Two new triterpenoid saponins, named hylomeconoside A (1) and B (2) which were identified as 3-O-β-d-galactopyranosyl-(1→2)-β-d-glucuronopyranosyl-gypsogenin-28-O-β-d-xylopyranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-α-l-rhamnopyranosyl-(1→2)-β-d-quinovopyranoside (1) and 3-O-β-d-galactopyranosyl-(1→2)-β-d-glucuronopyranosyl-gypsogenin-28-O-β-d-xylopyranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranoside (2), and two known triterpenoid saponins identified as dubioside C (3) and lucyoside P (4) on the basis of spectroscopic and chemical evidence, were isolated from H. japonica. Compound 1 exhibited moderate cytotoxicity on MGC-803 and HL-60 cells, with IC(50) values of 43.8 and 32.4 μg·mL(−1), respectively. Conclusions: Compounds 1 and 2 are new saponins, and 1 is considered to be one of the antitumor principles in this plant. This is the first time that triterpenoid saponins have been isolated from plants of the Papaveraceae family. |
format | Online Article Text |
id | pubmed-6151478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61514782018-11-13 New Triterpenoid Saponins from the Herb Hylomecon japonica Qu, Yan-Fei Gao, Jing-Yu Wang, Jing Geng, Yan-Mei Zhou, Yu Sun, Cheng-Xin Li, Fei Feng, Lei Yu, Meng-Juan Wang, Guang-Shu Molecules Article Background: Hylomecon japonica, a plant of the Papaveraceae family which is well-known for the alkaloids they produce, is a perennial plant widely distributed in the northeast, central and east regions of China. Although a variety of chemical constituents, including alkaloids, flavonoids, and megastigmoids, have been isolated from H. japonica, the investigation of saponins in H. japonica has not been reported until now. Methods: Various separation techniques, including polyporous resin column chromatography, silica gel column chromatography and hemi-preparative HPLC were applied to the isolation of triterpenoid saponins, and chemical methods such as acid hydrolysis and spectroscopic methods including HRESIMS and NMR were applied to their structure elucidation, and the XTT reduction method was used to assay cytotoxicity. Results: Two new triterpenoid saponins, named hylomeconoside A (1) and B (2) which were identified as 3-O-β-d-galactopyranosyl-(1→2)-β-d-glucuronopyranosyl-gypsogenin-28-O-β-d-xylopyranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-α-l-rhamnopyranosyl-(1→2)-β-d-quinovopyranoside (1) and 3-O-β-d-galactopyranosyl-(1→2)-β-d-glucuronopyranosyl-gypsogenin-28-O-β-d-xylopyranosyl-(1→3)-β-d-xylopyranosyl-(1→4)-α-l-rhamnopyranosyl-(1→2)-α-l-arabinopyranoside (2), and two known triterpenoid saponins identified as dubioside C (3) and lucyoside P (4) on the basis of spectroscopic and chemical evidence, were isolated from H. japonica. Compound 1 exhibited moderate cytotoxicity on MGC-803 and HL-60 cells, with IC(50) values of 43.8 and 32.4 μg·mL(−1), respectively. Conclusions: Compounds 1 and 2 are new saponins, and 1 is considered to be one of the antitumor principles in this plant. This is the first time that triterpenoid saponins have been isolated from plants of the Papaveraceae family. MDPI 2017-10-23 /pmc/articles/PMC6151478/ /pubmed/29065554 http://dx.doi.org/10.3390/molecules22101731 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Qu, Yan-Fei Gao, Jing-Yu Wang, Jing Geng, Yan-Mei Zhou, Yu Sun, Cheng-Xin Li, Fei Feng, Lei Yu, Meng-Juan Wang, Guang-Shu New Triterpenoid Saponins from the Herb Hylomecon japonica |
title | New Triterpenoid Saponins from the Herb Hylomecon japonica |
title_full | New Triterpenoid Saponins from the Herb Hylomecon japonica |
title_fullStr | New Triterpenoid Saponins from the Herb Hylomecon japonica |
title_full_unstemmed | New Triterpenoid Saponins from the Herb Hylomecon japonica |
title_short | New Triterpenoid Saponins from the Herb Hylomecon japonica |
title_sort | new triterpenoid saponins from the herb hylomecon japonica |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151478/ https://www.ncbi.nlm.nih.gov/pubmed/29065554 http://dx.doi.org/10.3390/molecules22101731 |
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