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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6696042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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