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Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities

One new pentacyclic triterpenoid, 3β-carboxylicfilic-4(23)-ene (1), and three known pentacyclic triterpenoids, adian-5-en-3α-ol (2), fernenol (3), and fern-7-en-3β-ol (4) were isolated from the petroleum ether phase of the ethanolic extract of Ainsliaea yunnanensis Franch. Their structures were esta...

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Detalles Bibliográficos
Autores principales: Li, Jinjie, Zhang, Bo, Liu, Hailing, Zhang, Xuan, Shang, Xiaoya, Zhao, Changqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273999/
https://www.ncbi.nlm.nih.gov/pubmed/27827998
http://dx.doi.org/10.3390/molecules21111481
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author Li, Jinjie
Zhang, Bo
Liu, Hailing
Zhang, Xuan
Shang, Xiaoya
Zhao, Changqi
author_facet Li, Jinjie
Zhang, Bo
Liu, Hailing
Zhang, Xuan
Shang, Xiaoya
Zhao, Changqi
author_sort Li, Jinjie
collection PubMed
description One new pentacyclic triterpenoid, 3β-carboxylicfilic-4(23)-ene (1), and three known pentacyclic triterpenoids, adian-5-en-3α-ol (2), fernenol (3), and fern-7-en-3β-ol (4) were isolated from the petroleum ether phase of the ethanolic extract of Ainsliaea yunnanensis Franch. Their structures were established by spectroscopic methods including 1-D and 2-D NMR, and MS experiments. Compounds 1, 2, 3, and 4 showed significant selective cytotoxicity against human acute monocytic leukemia cell line (THP-1) with IC(50) values of 5.12 μM, 1.78 μM, 1.74 μM, and 1.75 μΜ, respectively. Compound 1 also showed an anti-inflammatory effect through the inhibition of the activity of NF-κB by blocking the nuclear translocation of p65.
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spelling pubmed-62739992018-12-28 Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities Li, Jinjie Zhang, Bo Liu, Hailing Zhang, Xuan Shang, Xiaoya Zhao, Changqi Molecules Article One new pentacyclic triterpenoid, 3β-carboxylicfilic-4(23)-ene (1), and three known pentacyclic triterpenoids, adian-5-en-3α-ol (2), fernenol (3), and fern-7-en-3β-ol (4) were isolated from the petroleum ether phase of the ethanolic extract of Ainsliaea yunnanensis Franch. Their structures were established by spectroscopic methods including 1-D and 2-D NMR, and MS experiments. Compounds 1, 2, 3, and 4 showed significant selective cytotoxicity against human acute monocytic leukemia cell line (THP-1) with IC(50) values of 5.12 μM, 1.78 μM, 1.74 μM, and 1.75 μΜ, respectively. Compound 1 also showed an anti-inflammatory effect through the inhibition of the activity of NF-κB by blocking the nuclear translocation of p65. MDPI 2016-11-07 /pmc/articles/PMC6273999/ /pubmed/27827998 http://dx.doi.org/10.3390/molecules21111481 Text en © 2016 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
Li, Jinjie
Zhang, Bo
Liu, Hailing
Zhang, Xuan
Shang, Xiaoya
Zhao, Changqi
Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title_full Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title_fullStr Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title_full_unstemmed Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title_short Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities
title_sort triterpenoids from ainsliaea yunnanensis franch. and their biological activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273999/
https://www.ncbi.nlm.nih.gov/pubmed/27827998
http://dx.doi.org/10.3390/molecules21111481
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