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Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells

Several simple and prenylated coumarin derivatives were isolated from the dichloromethane extract of the root of Neocryptodiscus papillaris based on moderate cytotoxic activity of the extract in COLO205, KM12 and MCF7 cancer cells. While the major prenylated furanocoumarin derivatives and osthol iso...

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Autores principales: Tosun, Fatma, Mıhoğlugil, Feyyaz, Beutler, John A., Eroğlu Özkan, Esra, Miski, Mahmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7420726/
https://www.ncbi.nlm.nih.gov/pubmed/32635247
http://dx.doi.org/10.3390/molecules25133040
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author Tosun, Fatma
Mıhoğlugil, Feyyaz
Beutler, John A.
Eroğlu Özkan, Esra
Miski, Mahmut
author_facet Tosun, Fatma
Mıhoğlugil, Feyyaz
Beutler, John A.
Eroğlu Özkan, Esra
Miski, Mahmut
author_sort Tosun, Fatma
collection PubMed
description Several simple and prenylated coumarin derivatives were isolated from the dichloromethane extract of the root of Neocryptodiscus papillaris based on moderate cytotoxic activity of the extract in COLO205, KM12 and MCF7 cancer cells. While the major prenylated furanocoumarin derivatives and osthol isolated from the dichloromethane extract were responsible for the activity in the colon and breast cancer cell lines, the 4′-acylated osthol derivatives including a novel coumarino-alkaloid; neopapillarine) demonstrated selective cytotoxic activity in A498 and UO31 renal cancer cell lines.
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spelling pubmed-74207262020-08-18 Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells Tosun, Fatma Mıhoğlugil, Feyyaz Beutler, John A. Eroğlu Özkan, Esra Miski, Mahmut Molecules Article Several simple and prenylated coumarin derivatives were isolated from the dichloromethane extract of the root of Neocryptodiscus papillaris based on moderate cytotoxic activity of the extract in COLO205, KM12 and MCF7 cancer cells. While the major prenylated furanocoumarin derivatives and osthol isolated from the dichloromethane extract were responsible for the activity in the colon and breast cancer cell lines, the 4′-acylated osthol derivatives including a novel coumarino-alkaloid; neopapillarine) demonstrated selective cytotoxic activity in A498 and UO31 renal cancer cell lines. MDPI 2020-07-03 /pmc/articles/PMC7420726/ /pubmed/32635247 http://dx.doi.org/10.3390/molecules25133040 Text en © 2020 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
Tosun, Fatma
Mıhoğlugil, Feyyaz
Beutler, John A.
Eroğlu Özkan, Esra
Miski, Mahmut
Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title_full Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title_fullStr Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title_full_unstemmed Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title_short Neopapillarine, an Unusual Coumarino-Alkaloid from the Root Extract of Neocryptodiscus papillaris with Cytotoxic Activity on Renal Cancer Cells
title_sort neopapillarine, an unusual coumarino-alkaloid from the root extract of neocryptodiscus papillaris with cytotoxic activity on renal cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7420726/
https://www.ncbi.nlm.nih.gov/pubmed/32635247
http://dx.doi.org/10.3390/molecules25133040
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