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Four New Pterosins from Pteris cretica and Their Cytotoxic Activities

Phytochemical investigation of the aerial parts of Pteris cretica led to the isolation and elucidation of nine pterosins, including four new pterosins, creticolacton A (1), 13-hydroxy-2(R),3(R)-pterosin L (2), creticoside A (3), and spelosin 3-O-β-d-glucopyranoside (4), together with five known pter...

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Detalles Bibliográficos
Autores principales: Lu, Jian, Peng, Caiying, Cheng, Shuang, Liu, Jianqun, Ma, Qinge, Shu, Jicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696042/
https://www.ncbi.nlm.nih.gov/pubmed/31366093
http://dx.doi.org/10.3390/molecules24152767
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author Lu, Jian
Peng, Caiying
Cheng, Shuang
Liu, Jianqun
Ma, Qinge
Shu, Jicheng
author_facet Lu, Jian
Peng, Caiying
Cheng, Shuang
Liu, Jianqun
Ma, Qinge
Shu, Jicheng
author_sort Lu, Jian
collection PubMed
description Phytochemical investigation of the aerial parts of Pteris cretica led to the isolation and elucidation of nine pterosins, including four new pterosins, creticolacton A (1), 13-hydroxy-2(R),3(R)-pterosin L (2), creticoside A (3), and spelosin 3-O-β-d-glucopyranoside (4), together with five known pterosins 5–9. Their structures were identified mainly on the basis of 1D and 2D NMR spectral data, ESI-MS and literature comparisons. Compounds 1 and 3 were new type of petrosins with a six membered ring between C-14 and C-15. The new compounds were tested in vitro for their cytotoxic activities against four human tumor cell lines (SH-SY5Y, SGC-7901, HCT-116, Lovo). Results showed that compounds 1 and 2 exhibited cytotoxic activity against HCT-116 cells with IC(50) value of 22.4 μM and 15.8 μM, respectively.
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spelling pubmed-66960422019-09-05 Four New Pterosins from Pteris cretica and Their Cytotoxic Activities Lu, Jian Peng, Caiying Cheng, Shuang Liu, Jianqun Ma, Qinge Shu, Jicheng Molecules Article Phytochemical investigation of the aerial parts of Pteris cretica led to the isolation and elucidation of nine pterosins, including four new pterosins, creticolacton A (1), 13-hydroxy-2(R),3(R)-pterosin L (2), creticoside A (3), and spelosin 3-O-β-d-glucopyranoside (4), together with five known pterosins 5–9. Their structures were identified mainly on the basis of 1D and 2D NMR spectral data, ESI-MS and literature comparisons. Compounds 1 and 3 were new type of petrosins with a six membered ring between C-14 and C-15. The new compounds were tested in vitro for their cytotoxic activities against four human tumor cell lines (SH-SY5Y, SGC-7901, HCT-116, Lovo). Results showed that compounds 1 and 2 exhibited cytotoxic activity against HCT-116 cells with IC(50) value of 22.4 μM and 15.8 μM, respectively. MDPI 2019-07-30 /pmc/articles/PMC6696042/ /pubmed/31366093 http://dx.doi.org/10.3390/molecules24152767 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
Lu, Jian
Peng, Caiying
Cheng, Shuang
Liu, Jianqun
Ma, Qinge
Shu, Jicheng
Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title_full Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title_fullStr Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title_full_unstemmed Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title_short Four New Pterosins from Pteris cretica and Their Cytotoxic Activities
title_sort four new pterosins from pteris cretica and their cytotoxic activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696042/
https://www.ncbi.nlm.nih.gov/pubmed/31366093
http://dx.doi.org/10.3390/molecules24152767
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