A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs

Immuno-conjugates obtained by linking enzymes with appropriate monoclonal a ntibodies, which bind to tumor-associated antigens, can be employed in a tu mor-selective antibody directed enzyme prodrug therapy (ADEPT). For this st rategy the glycosides 17a-c were prepared as prodrugs of CI-TMI 14 which is a structurally simplified analogue of the highly potent antitumor agent du ocarmycin SA 2. Exposure of 17a-c to cultured carcinoma cells of line A549 displayed a very low toxicity; however, after addition of the corresponding enzymes and exposure for 24 h at prodrug concentrations of <0.1 <mu>M the proliferation of the carcinoma cells was inhibited almost completely with E D50prodrug/ED50drug of UP to 270 in the presence and in the absence of the enzyme. The synthesis of 17a-c was achieved by transformation of nitroanisi dine 6 into 12 which was glycosidated to give 16a-c. Removal of the silyl g roups, introduction of a chlorine atom and solvolysis of the acetal groups led to 17a-c, of which 17a and 17c are promising candidates for further ela boration. (C) 2001 Elsevier Science Ltd. All rights reserved.