Artículo
Cytotoxic activity of semi-synthetic derivatives of elatol and isoobtusol
Lang, Karen L.; 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
Fecha de publicación:
10/2012
Editorial:
Molecular Diversity Preservation International
Revista:
Marine Drugs
ISSN:
1660-3397
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
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.
Palabras clave:
Cytotoxic Activity
,
Elatol
,
Isoobtusol
,
Sesquiterpenes
,
Synthesis
Archivos asociados
Licencia
Identificadores
Colecciones
Articulos(UMYMFOR)
Articulos de UNID.MICROANAL.Y MET.FISICOS EN QUIM.ORG.(I)
Articulos de UNID.MICROANAL.Y MET.FISICOS EN QUIM.ORG.(I)
Citación
Lang, Karen L.; Silva, Izabella T.; Zimmermann, Lara A.; Lhullier, Cíntia; Mañalich Arana, María Victoria; et al.; Cytotoxic activity of semi-synthetic derivatives of elatol and isoobtusol; Molecular Diversity Preservation International; Marine Drugs; 10; 10; 10-2012; 2254-2264
Compartir
Altmétricas