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Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives
New diterpenylquinones, combining a diterpene diacid and a naphthoquinone, were prepared from junicedric acid and lapachol. The new derivatives were assessed as gastroprotective agents by the HCl-EtOH-induced gastric lesions model in mice as well as for basal cytotoxicity on the following human cell...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264310/ https://www.ncbi.nlm.nih.gov/pubmed/21996716 http://dx.doi.org/10.3390/molecules16108614 |
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author | Pertino, Mariano Walter Theoduloz, Cristina Palenzuela, Jose Antonio del Mar Afonso, Maria Yesilada, Erdem Monsalve, Francisco González, Paulo Droguett, Daniel Schmeda-Hirschmann, Guillermo |
author_facet | Pertino, Mariano Walter Theoduloz, Cristina Palenzuela, Jose Antonio del Mar Afonso, Maria Yesilada, Erdem Monsalve, Francisco González, Paulo Droguett, Daniel Schmeda-Hirschmann, Guillermo |
author_sort | Pertino, Mariano Walter |
collection | PubMed |
description | New diterpenylquinones, combining a diterpene diacid and a naphthoquinone, were prepared from junicedric acid and lapachol. The new derivatives were assessed as gastroprotective agents by the HCl-EtOH-induced gastric lesions model in mice as well as for basal cytotoxicity on the following human cell lines: Normal lung fibroblasts (MRC-5), gastric epithelial adenocarcinoma (AGS), and hepatocellular carcinoma (Hep G2). Several of the new compounds were significantly active as antiulcer agents and showed selective cytotoxicity against AGS cells. |
format | Online Article Text |
id | pubmed-6264310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62643102018-12-10 Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives Pertino, Mariano Walter Theoduloz, Cristina Palenzuela, Jose Antonio del Mar Afonso, Maria Yesilada, Erdem Monsalve, Francisco González, Paulo Droguett, Daniel Schmeda-Hirschmann, Guillermo Molecules Article New diterpenylquinones, combining a diterpene diacid and a naphthoquinone, were prepared from junicedric acid and lapachol. The new derivatives were assessed as gastroprotective agents by the HCl-EtOH-induced gastric lesions model in mice as well as for basal cytotoxicity on the following human cell lines: Normal lung fibroblasts (MRC-5), gastric epithelial adenocarcinoma (AGS), and hepatocellular carcinoma (Hep G2). Several of the new compounds were significantly active as antiulcer agents and showed selective cytotoxicity against AGS cells. MDPI 2011-10-13 /pmc/articles/PMC6264310/ /pubmed/21996716 http://dx.doi.org/10.3390/molecules16108614 Text en © 2011 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Pertino, Mariano Walter Theoduloz, Cristina Palenzuela, Jose Antonio del Mar Afonso, Maria Yesilada, Erdem Monsalve, Francisco González, Paulo Droguett, Daniel Schmeda-Hirschmann, Guillermo Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title | Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title_full | Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title_fullStr | Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title_full_unstemmed | Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title_short | Synthesis and Pharmacological Activity of Diterpenylnaphthoquinone Derivatives |
title_sort | synthesis and pharmacological activity of diterpenylnaphthoquinone derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264310/ https://www.ncbi.nlm.nih.gov/pubmed/21996716 http://dx.doi.org/10.3390/molecules16108614 |
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