Cytotoxic activity of semi-synthetic derivatives of elatol and isoobtusol
; Silva, Izabella T.
; Zimmermann, Lara A. ; Lhullier, Cíntia ; Mañalich Arana, María Victoria
; Palermo, Jorge Alejandro
; Falkenberg, Miriam ; Simoes, Cláudia M. O.
; Schenkel, Eloir P.
; Duran, Fernando Javier 
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Fecha
10/2012
Editorial
Molecular Diversity Preservation International
Revista
Marine Drugs
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ISSN
1660-3397
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Inglés
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Resumen
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 CC50 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. © 2012 by the authors; licensee MDPI, Basel, Switzerland.
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