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Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities

The roots of Euphorbia fischeriana have been used as a traditional Chinese medicine for the treatment of tuberculosis and ringworm. In the current study, diterpenoids from the ethyl acetate extract of the roots E. fischeriana and their cytotoxic effects against five cancer lines were investigated. T...

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Autores principales: Zhu, Qin-Feng, Xu, Guo-Bo, Liao, Shang-Gao, Yan, Xue-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653608/
https://www.ncbi.nlm.nih.gov/pubmed/36364087
http://dx.doi.org/10.3390/molecules27217258
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author Zhu, Qin-Feng
Xu, Guo-Bo
Liao, Shang-Gao
Yan, Xue-Long
author_facet Zhu, Qin-Feng
Xu, Guo-Bo
Liao, Shang-Gao
Yan, Xue-Long
author_sort Zhu, Qin-Feng
collection PubMed
description The roots of Euphorbia fischeriana have been used as a traditional Chinese medicine for the treatment of tuberculosis and ringworm. In the current study, diterpenoids from the ethyl acetate extract of the roots E. fischeriana and their cytotoxic effects against five cancer lines were investigated. Two new ent-abietane diterpenoids, euphonoids H and I (1–2), as well as their two analogues (3–4) were first isolated from this source. The structures of the two new compounds were elucidated on the basis of spectroscopic data and quantum chemical calculation. Their absolute configurations were assigned via ECD spectrum calculation. The isolated compounds were evaluated for their antiproliferative activities against five cancer cell lines. Compounds 1 and 2 exhibited significant inhibitory effects against human prostate cancers C4-2B and C4-2B/ENZR cell lines with IC(50) values ranging from 4.16 ± 0.42 to 5.74 ± 0.45 μM.
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spelling pubmed-96536082022-11-15 Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities Zhu, Qin-Feng Xu, Guo-Bo Liao, Shang-Gao Yan, Xue-Long Molecules Article The roots of Euphorbia fischeriana have been used as a traditional Chinese medicine for the treatment of tuberculosis and ringworm. In the current study, diterpenoids from the ethyl acetate extract of the roots E. fischeriana and their cytotoxic effects against five cancer lines were investigated. Two new ent-abietane diterpenoids, euphonoids H and I (1–2), as well as their two analogues (3–4) were first isolated from this source. The structures of the two new compounds were elucidated on the basis of spectroscopic data and quantum chemical calculation. Their absolute configurations were assigned via ECD spectrum calculation. The isolated compounds were evaluated for their antiproliferative activities against five cancer cell lines. Compounds 1 and 2 exhibited significant inhibitory effects against human prostate cancers C4-2B and C4-2B/ENZR cell lines with IC(50) values ranging from 4.16 ± 0.42 to 5.74 ± 0.45 μM. MDPI 2022-10-26 /pmc/articles/PMC9653608/ /pubmed/36364087 http://dx.doi.org/10.3390/molecules27217258 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhu, Qin-Feng
Xu, Guo-Bo
Liao, Shang-Gao
Yan, Xue-Long
Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title_full Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title_fullStr Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title_full_unstemmed Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title_short Ent-Abietane Diterpenoids from Euphorbia fischeriana and Their Cytotoxic Activities
title_sort ent-abietane diterpenoids from euphorbia fischeriana and their cytotoxic activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653608/
https://www.ncbi.nlm.nih.gov/pubmed/36364087
http://dx.doi.org/10.3390/molecules27217258
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