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Acta Pharmaceutica Sinica ; (12): 754-757, 2009.
Article in Chinese | WPRIM | ID: wpr-344111

ABSTRACT

Six naphthalimide polyamine conjugates were synthesized and their structures were confirmed by elemental analysis, 1H NMR, 13C NMR and MS. Antitumor activities were evaluated in vitro using MTT assay on Leukemia cells (K562), human breast cancer cells (MB-231) and prostate cancer cells (Ln cap cell). The results showed that most of the six compounds were superior to the control (amonafide), 6d, 6e, and 6f exhibited nice selectivity in a screen of hepatoma cells (BEL-7402) and human normal hepatocytes (QSG-7701).


Subject(s)
Humans , Male , Antineoplastic Agents , Pharmacology , Cell Line, Tumor , Molecular Structure , Naphthalimides , Pharmacology , Polyamines , Pharmacology
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