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New Sesquiterpenoids from Ambrosia artemisiifolia L.
A new pseudoguaianolide 1 and two new guaiane-type sesquiterpene glucosides 2 and 3, were isolated from the aerial parts of Ambrosia artemisiifolia L together with two known sesquiterpene dilactones 4 and 5. The new compounds were determined on the basis of spectroscopic and chemical methods to be 3...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272762/ https://www.ncbi.nlm.nih.gov/pubmed/25764487 http://dx.doi.org/10.3390/molecules20034450 |
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author | Ding, Wenbing Huang, Rui Zhou, Zhongshi Li, Youzhi |
author_facet | Ding, Wenbing Huang, Rui Zhou, Zhongshi Li, Youzhi |
author_sort | Ding, Wenbing |
collection | PubMed |
description | A new pseudoguaianolide 1 and two new guaiane-type sesquiterpene glucosides 2 and 3, were isolated from the aerial parts of Ambrosia artemisiifolia L together with two known sesquiterpene dilactones 4 and 5. The new compounds were determined on the basis of spectroscopic and chemical methods to be 3β-acetoxy-4β-hydroxy-1α,7α, 10β,11αH-pseudoguaia-12,8β-olide (1), 1β,7β,9β,10β,13αH-guaia-4(5)-en-12,6β-olide 9-O-β-d-glucoside (2) and 4β-hydroxy-1α,5α,7α,9αH-guaia-10(14),11(13)-dien-12-acid 9-O-β-d-glucoside (3). The isolated compounds were evaluated for cytotoxicity against human promyelocytic leukemia HL-60 cell lines in vitro, but were all inactive. |
format | Online Article Text |
id | pubmed-6272762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62727622018-12-31 New Sesquiterpenoids from Ambrosia artemisiifolia L. Ding, Wenbing Huang, Rui Zhou, Zhongshi Li, Youzhi Molecules Communication A new pseudoguaianolide 1 and two new guaiane-type sesquiterpene glucosides 2 and 3, were isolated from the aerial parts of Ambrosia artemisiifolia L together with two known sesquiterpene dilactones 4 and 5. The new compounds were determined on the basis of spectroscopic and chemical methods to be 3β-acetoxy-4β-hydroxy-1α,7α, 10β,11αH-pseudoguaia-12,8β-olide (1), 1β,7β,9β,10β,13αH-guaia-4(5)-en-12,6β-olide 9-O-β-d-glucoside (2) and 4β-hydroxy-1α,5α,7α,9αH-guaia-10(14),11(13)-dien-12-acid 9-O-β-d-glucoside (3). The isolated compounds were evaluated for cytotoxicity against human promyelocytic leukemia HL-60 cell lines in vitro, but were all inactive. MDPI 2015-03-10 /pmc/articles/PMC6272762/ /pubmed/25764487 http://dx.doi.org/10.3390/molecules20034450 Text en © 2015 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/4.0/). |
spellingShingle | Communication Ding, Wenbing Huang, Rui Zhou, Zhongshi Li, Youzhi New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title | New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title_full | New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title_fullStr | New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title_full_unstemmed | New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title_short | New Sesquiterpenoids from Ambrosia artemisiifolia L. |
title_sort | new sesquiterpenoids from ambrosia artemisiifolia l. |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272762/ https://www.ncbi.nlm.nih.gov/pubmed/25764487 http://dx.doi.org/10.3390/molecules20034450 |
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