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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...

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Autores principales: Ding, Wenbing, Huang, Rui, Zhou, Zhongshi, Li, Youzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
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.
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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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