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Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities

Five new cucurbitane-typetriterpenoid glycosides, named Xuedanoside F–J (1–5), were obtained from the rhizomes of Hemsleya penxianensis (Xue dan), which belongs to the family of Cucurbitaceae. These new compounds were elucidated byspectroscopic analysis, including 1D, 2D NMR, and HR-ESI-MS spectra....

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Autores principales: Chen, De-Li, Xu, Xu-Dong, Li, Rong-Tao, Wang, Bo-Wen, Yu, Meng, Liu, Yang-Yang, Ma, Guo-Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720345/
https://www.ncbi.nlm.nih.gov/pubmed/31412677
http://dx.doi.org/10.3390/molecules24162937
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author Chen, De-Li
Xu, Xu-Dong
Li, Rong-Tao
Wang, Bo-Wen
Yu, Meng
Liu, Yang-Yang
Ma, Guo-Xu
author_facet Chen, De-Li
Xu, Xu-Dong
Li, Rong-Tao
Wang, Bo-Wen
Yu, Meng
Liu, Yang-Yang
Ma, Guo-Xu
author_sort Chen, De-Li
collection PubMed
description Five new cucurbitane-typetriterpenoid glycosides, named Xuedanoside F–J (1–5), were obtained from the rhizomes of Hemsleya penxianensis (Xue dan), which belongs to the family of Cucurbitaceae. These new compounds were elucidated byspectroscopic analysis, including 1D, 2D NMR, and HR-ESI-MS spectra. Additionally, all the isolates were evaluated for cytotoxicity against three human cancer cell lines (Hela, MCF-7, and A-549) with the IC(50) ranging from 2.25 to 49.44 µM in vitro with treatment 48 h and showed low cytotoxicity in human normal liver L-02 cells (IC(50) > 50 µM). Compound 5 showed the most significant cytotoxic activity with the IC(50) value of 2.25, 4.72, and 5.33 µM in 48 h, respectively.
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spelling pubmed-67203452019-10-30 Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities Chen, De-Li Xu, Xu-Dong Li, Rong-Tao Wang, Bo-Wen Yu, Meng Liu, Yang-Yang Ma, Guo-Xu Molecules Article Five new cucurbitane-typetriterpenoid glycosides, named Xuedanoside F–J (1–5), were obtained from the rhizomes of Hemsleya penxianensis (Xue dan), which belongs to the family of Cucurbitaceae. These new compounds were elucidated byspectroscopic analysis, including 1D, 2D NMR, and HR-ESI-MS spectra. Additionally, all the isolates were evaluated for cytotoxicity against three human cancer cell lines (Hela, MCF-7, and A-549) with the IC(50) ranging from 2.25 to 49.44 µM in vitro with treatment 48 h and showed low cytotoxicity in human normal liver L-02 cells (IC(50) > 50 µM). Compound 5 showed the most significant cytotoxic activity with the IC(50) value of 2.25, 4.72, and 5.33 µM in 48 h, respectively. MDPI 2019-08-13 /pmc/articles/PMC6720345/ /pubmed/31412677 http://dx.doi.org/10.3390/molecules24162937 Text en © 2019 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
Chen, De-Li
Xu, Xu-Dong
Li, Rong-Tao
Wang, Bo-Wen
Yu, Meng
Liu, Yang-Yang
Ma, Guo-Xu
Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title_full Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title_fullStr Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title_full_unstemmed Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title_short Five New Cucurbitane-Type Triterpenoid Glycosides from the Rhizomes of Hemsleya penxianensis with Cytotoxic Activities
title_sort five new cucurbitane-type triterpenoid glycosides from the rhizomes of hemsleya penxianensis with cytotoxic activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720345/
https://www.ncbi.nlm.nih.gov/pubmed/31412677
http://dx.doi.org/10.3390/molecules24162937
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