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Synthesis and in vitro cytotoxicity of hexacyclic camptothecin analogues
Authors:Jew S  Kim H J  Kim M G  Roh E Y  Hong C I  Kim J K  Lee J H  Lee H  Park H
Affiliation:College of Pharmacy, Seoul National University, Korea.
Abstract:A series of C(7)-N-alkylaminoethyl-C(10), C(11)-methylenedioxy- and ethylenedioxy-camptothecin (3a-g, 4a-b) were prepared. Their syntheses and in vitro cytotoxicity were reported. Among 15 derivatives, 3a and 3b showed more potent cytotoxicity than Camptothecin, especially in CAOV-3 cell line.
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