Cargando…
Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid
Dehydroabietic acid (DHA) is a naturally occurring diterpene with different and relevant biological activities. Previous studies have shown that some DHA derivatives display antiproliferative activity. However, the reported compounds did not include triazole derivatives. Starting from DHA (8,11,13-a...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271890/ https://www.ncbi.nlm.nih.gov/pubmed/24566318 http://dx.doi.org/10.3390/molecules19022523 |
_version_ | 1783377031681015808 |
---|---|
author | Pertino, Mariano Walter Verdugo, Valery Theoduloz, Cristina Schmeda-Hirschmann, Guillermo |
author_facet | Pertino, Mariano Walter Verdugo, Valery Theoduloz, Cristina Schmeda-Hirschmann, Guillermo |
author_sort | Pertino, Mariano Walter |
collection | PubMed |
description | Dehydroabietic acid (DHA) is a naturally occurring diterpene with different and relevant biological activities. Previous studies have shown that some DHA derivatives display antiproliferative activity. However, the reported compounds did not include triazole derivatives. Starting from DHA (8,11,13-abietatrien-18-oic acid), and its alcohol dehydroabietinol (8,11,13-abietatrien-18-ol), four alkyl esters were prepared. The alkyl terpenes were treated with different aromatic azides to synthesize hybrid compounds using click chemistry. Some 16 new DHA hybrids were thus synthesized and their structures were confirmed by spectroscopic and spectrometric means. The antiproliferative activity of the new compounds was assessed towards human cell lines, namely normal lung fibroblasts (MRC-5), gastric epithelial adenocarcinoma (AGS), lung cancer (SK-MES-1) and bladder carcinoma (J82) cells. Better antiproliferative effect was found for compound 5, with an IC(50) of 6.1 μM and selectivity on SK-MES-1 cells. Under the same experimental conditions, the IC(50) of etoposide, was 1.83 µM. |
format | Online Article Text |
id | pubmed-6271890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62718902018-12-20 Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid Pertino, Mariano Walter Verdugo, Valery Theoduloz, Cristina Schmeda-Hirschmann, Guillermo Molecules Article Dehydroabietic acid (DHA) is a naturally occurring diterpene with different and relevant biological activities. Previous studies have shown that some DHA derivatives display antiproliferative activity. However, the reported compounds did not include triazole derivatives. Starting from DHA (8,11,13-abietatrien-18-oic acid), and its alcohol dehydroabietinol (8,11,13-abietatrien-18-ol), four alkyl esters were prepared. The alkyl terpenes were treated with different aromatic azides to synthesize hybrid compounds using click chemistry. Some 16 new DHA hybrids were thus synthesized and their structures were confirmed by spectroscopic and spectrometric means. The antiproliferative activity of the new compounds was assessed towards human cell lines, namely normal lung fibroblasts (MRC-5), gastric epithelial adenocarcinoma (AGS), lung cancer (SK-MES-1) and bladder carcinoma (J82) cells. Better antiproliferative effect was found for compound 5, with an IC(50) of 6.1 μM and selectivity on SK-MES-1 cells. Under the same experimental conditions, the IC(50) of etoposide, was 1.83 µM. MDPI 2014-02-21 /pmc/articles/PMC6271890/ /pubmed/24566318 http://dx.doi.org/10.3390/molecules19022523 Text en © 2014 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 Verdugo, Valery Theoduloz, Cristina Schmeda-Hirschmann, Guillermo Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title | Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title_full | Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title_fullStr | Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title_full_unstemmed | Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title_short | Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid |
title_sort | synthesis and antiproliferative activity of some novel triazole derivatives from dehydroabietic acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271890/ https://www.ncbi.nlm.nih.gov/pubmed/24566318 http://dx.doi.org/10.3390/molecules19022523 |
work_keys_str_mv | AT pertinomarianowalter synthesisandantiproliferativeactivityofsomenoveltriazolederivativesfromdehydroabieticacid AT verdugovalery synthesisandantiproliferativeactivityofsomenoveltriazolederivativesfromdehydroabieticacid AT theodulozcristina synthesisandantiproliferativeactivityofsomenoveltriazolederivativesfromdehydroabieticacid AT schmedahirschmannguillermo synthesisandantiproliferativeactivityofsomenoveltriazolederivativesfromdehydroabieticacid |