Synthesis and cytotoxicity of podophyllotoxin analogues modified in the A ring.
Angeles Castro, José M Miguel del Corral, Marina Gordaliza, Concepción Grande, Antonia Gómez-Zurita, Dolores García-Grávalos, Arturo San Feliciano, Angeles Castro, José M.Miguel del Corral, Marina Gordaliza, Concepción Grande, Antonia Gómez-Zurita, Dolores Garcı́a-Grávalos, Arturo San Feliciano
Index: Eur. J. Med. Chem. 38(1) , 65-74, (2003)
Full Text: HTML
Abstract
Several podophyllotoxin derivatives lacking the methylenedioxy group or with different functionalization of the A-ring of the cyclolignan skeleton have been prepared and evaluated for their cytotoxic activities on four neoplastic cell lines (P-388, A-549, HT-29 and MEL-28). Most of them maintained their cytotoxicity at the microM level.Copyright 2002 Editions scienctifiques et médicales Elsevier SAS
Related Compounds
Related Articles:
2011-01-10
[Chemistry 17(2) , 572-9, (2011)]
1995-02-01
[Toxicol. Lett. 76(1) , 39-45, (1995)]
1997-06-01
[Lipids 32(6) , 605-10, (1997)]
2007-07-01
[J. Biomed. Mater. Res. B. Appl. Biomater. 82(1) , 44-50, (2007)]
2012-02-01
[Anal. Biochem. 421(1) , 327-9, (2012)]