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Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus
A new cycloartane-type triterpene glycoside, agroastragaloside V (1) was isolated from the roots of Astragalus membranaceus. The structure was identified as 3-O-β-(2'-O-acetyl)-d-xylopyranosyl-6-O-β-d-glucopyranosyl-(24S)-3β,6α,24α,25-tetrahydroxy-9,19-cyclolanostane, by means of spectroscopic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269660/ https://www.ncbi.nlm.nih.gov/pubmed/23529032 http://dx.doi.org/10.3390/molecules18043725 |
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author | Lee, Dae-Young Noh, Hyung-Jun Choi, Jehun Lee, Kyeong-Hee Lee, Min-Ho Lee, Ji-Hyun Hong, Yoonpyo Lee, Seung-Eun Kim, Seung-Yu Kim, Geum-Soog |
author_facet | Lee, Dae-Young Noh, Hyung-Jun Choi, Jehun Lee, Kyeong-Hee Lee, Min-Ho Lee, Ji-Hyun Hong, Yoonpyo Lee, Seung-Eun Kim, Seung-Yu Kim, Geum-Soog |
author_sort | Lee, Dae-Young |
collection | PubMed |
description | A new cycloartane-type triterpene glycoside, agroastragaloside V (1) was isolated from the roots of Astragalus membranaceus. The structure was identified as 3-O-β-(2'-O-acetyl)-d-xylopyranosyl-6-O-β-d-glucopyranosyl-(24S)-3β,6α,24α,25-tetrahydroxy-9,19-cyclolanostane, by means of spectroscopic methods, including HR-FAB/MS, 1D NMR ((1)H, (13)C, DEPT), 2D NMR (gCOSY, gHSQC, gHMBC, NOESY), and IR spectroscopy. Four known cycloartane glycosides, namely, agroastragaloside I (2), agroastragaloside II (3), isoastragaloside II (4) and astragaloside IV (5) were also isolated. All isolated compounds were tested for the ability to inhibit LPS-induced nitric oxide production in RAW264.7 macrophages. |
format | Online Article Text |
id | pubmed-6269660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62696602018-12-14 Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus Lee, Dae-Young Noh, Hyung-Jun Choi, Jehun Lee, Kyeong-Hee Lee, Min-Ho Lee, Ji-Hyun Hong, Yoonpyo Lee, Seung-Eun Kim, Seung-Yu Kim, Geum-Soog Molecules Communication A new cycloartane-type triterpene glycoside, agroastragaloside V (1) was isolated from the roots of Astragalus membranaceus. The structure was identified as 3-O-β-(2'-O-acetyl)-d-xylopyranosyl-6-O-β-d-glucopyranosyl-(24S)-3β,6α,24α,25-tetrahydroxy-9,19-cyclolanostane, by means of spectroscopic methods, including HR-FAB/MS, 1D NMR ((1)H, (13)C, DEPT), 2D NMR (gCOSY, gHSQC, gHMBC, NOESY), and IR spectroscopy. Four known cycloartane glycosides, namely, agroastragaloside I (2), agroastragaloside II (3), isoastragaloside II (4) and astragaloside IV (5) were also isolated. All isolated compounds were tested for the ability to inhibit LPS-induced nitric oxide production in RAW264.7 macrophages. MDPI 2013-03-25 /pmc/articles/PMC6269660/ /pubmed/23529032 http://dx.doi.org/10.3390/molecules18043725 Text en © 2013 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Communication Lee, Dae-Young Noh, Hyung-Jun Choi, Jehun Lee, Kyeong-Hee Lee, Min-Ho Lee, Ji-Hyun Hong, Yoonpyo Lee, Seung-Eun Kim, Seung-Yu Kim, Geum-Soog Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title | Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title_full | Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title_fullStr | Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title_full_unstemmed | Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title_short | Anti-Inflammatory Cycloartane-Type Saponins of Astragalus membranaceus |
title_sort | anti-inflammatory cycloartane-type saponins of astragalus membranaceus |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269660/ https://www.ncbi.nlm.nih.gov/pubmed/23529032 http://dx.doi.org/10.3390/molecules18043725 |
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