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Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol

In the present study, the in vitro cytotoxic effects of six semi-synthetic derivatives of elatol (1) and isoobtusol (2) were investigated. Chemical modifications were performed on the hydroxyl groups aiming to get derivatives of different polarity, namely the hemisuccinate, carbamate and sulfamate....

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Autores principales: Lang, Karen L., Silva, Izabella T., Zimmermann, Lara A., Lhullier, Cíntia, Mañalich Arana, Maria V., Palermo, Jorge A., Falkenberg, Miriam, Simões, Cláudia M. O., Schenkel, Eloir P., Durán, Fernando J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497021/
https://www.ncbi.nlm.nih.gov/pubmed/23170082
http://dx.doi.org/10.3390/md10102254
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author Lang, Karen L.
Silva, Izabella T.
Zimmermann, Lara A.
Lhullier, Cíntia
Mañalich Arana, Maria V.
Palermo, Jorge A.
Falkenberg, Miriam
Simões, Cláudia M. O.
Schenkel, Eloir P.
Durán, Fernando J.
author_facet Lang, Karen L.
Silva, Izabella T.
Zimmermann, Lara A.
Lhullier, Cíntia
Mañalich Arana, Maria V.
Palermo, Jorge A.
Falkenberg, Miriam
Simões, Cláudia M. O.
Schenkel, Eloir P.
Durán, Fernando J.
author_sort Lang, Karen L.
collection PubMed
description In the present study, the in vitro cytotoxic effects of six semi-synthetic derivatives of elatol (1) and isoobtusol (2) were investigated. Chemical modifications were performed on the hydroxyl groups aiming to get derivatives of different polarity, namely the hemisuccinate, carbamate and sulfamate. The structural elucidation of the new derivatives was based on detailed NMR and MS spectroscopic analyses. The in vitro cytotoxicity of compounds 1 to 8 was evaluated against A459 and RD tumor cell lines with CC(50) values ranging from 4.93 to 41.53 µM. These results suggest that the structural modifications performed on both compounds could be considered a good strategy to obtain more active derivatives.
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spelling pubmed-34970212012-11-20 Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol Lang, Karen L. Silva, Izabella T. Zimmermann, Lara A. Lhullier, Cíntia Mañalich Arana, Maria V. Palermo, Jorge A. Falkenberg, Miriam Simões, Cláudia M. O. Schenkel, Eloir P. Durán, Fernando J. Mar Drugs Article In the present study, the in vitro cytotoxic effects of six semi-synthetic derivatives of elatol (1) and isoobtusol (2) were investigated. Chemical modifications were performed on the hydroxyl groups aiming to get derivatives of different polarity, namely the hemisuccinate, carbamate and sulfamate. The structural elucidation of the new derivatives was based on detailed NMR and MS spectroscopic analyses. The in vitro cytotoxicity of compounds 1 to 8 was evaluated against A459 and RD tumor cell lines with CC(50) values ranging from 4.93 to 41.53 µM. These results suggest that the structural modifications performed on both compounds could be considered a good strategy to obtain more active derivatives. MDPI 2012-10-18 /pmc/articles/PMC3497021/ /pubmed/23170082 http://dx.doi.org/10.3390/md10102254 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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
Lang, Karen L.
Silva, Izabella T.
Zimmermann, Lara A.
Lhullier, Cíntia
Mañalich Arana, Maria V.
Palermo, Jorge A.
Falkenberg, Miriam
Simões, Cláudia M. O.
Schenkel, Eloir P.
Durán, Fernando J.
Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title_full Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title_fullStr Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title_full_unstemmed Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title_short Cytotoxic Activity of Semi-Synthetic Derivatives of Elatol and Isoobtusol
title_sort cytotoxic activity of semi-synthetic derivatives of elatol and isoobtusol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3497021/
https://www.ncbi.nlm.nih.gov/pubmed/23170082
http://dx.doi.org/10.3390/md10102254
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