Synthesis and antitumor activities of 10-hydroxy camptothecin derivatives
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Abstract
AimTo find new anticancer drug based on the structure of 10-hydroxy camptothecin. MethodsSeven camptothecin derivatives (3-9) were synthesized and the antitumor activities of these derivatives were evaluated. ResultsStructures of seven new compounds were determined by 1HNMR, IR, MS. Seven compounds showed inhibitory effects on Hela, BEL-7402, 7901 cell lines in vitro. Especially, compound 4 showed high bioactivities to all of the tumor cells in vitro, its anticancer activity against human cervical carcinoma Hela was much higher than that of 10-hydroxy camptothecin. ConclusionSome compounds are worth further studying.
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