[Synthesis of camptothecin glycosides by phase transfer-catalysis and its inhibitory activity against topo I].

Autor:	Li QY; Key Laboratory of Forest Plant Ecology of Northeast Forestry University, Ministry of Education, Harbin 150040, China., Zhang Y, Yao LP, Fu YJ, Zu YG, Chen XQ, Zheng CY
Jazyk:	čínština
Zdroj:	Yao xue xue bao = Acta pharmaceutica Sinica [Yao Xue Xue Bao] 2005 Dec; Vol. 40 (12), pp. 1116-21.
Abstrakt:	Aim: To find new anticancer drug based on the structure of 10-hydroxy camptothecin. Methods: Six camptothecin glycosides (7-12) were synthesized by phase transfer catalysis. The structures of all compounds synthesized were determined by 1H NMR, IR and MS. Their antitumor activity was evaluated on cancer cells in vitro, and inhibitory activity against Topo I was evaluated by molecular biologic method. Results and Conclusion: The result indicated that the yield of camptothecin glycosides by phase transfer catalysis is much higher than by the method from literature, camptothecin glycosides have much lower cytotoxicities on cancer cell in vitro, but have better inhibitory activity of topo I.
Databáze:	MEDLINE
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