Global ETD Search
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Showing 1 to 2 of 2 for “"Anti-cancer prodrugs"”.
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Synthesis of Novel CYP1 Activated Heterocyclic Anticancer Prodrugs
… presented a novel target for the development of anti-cancer prodrugs, which would remain non-toxic until undergoing metabolism to toxic species by CYP1 enzymes over-expressed at tumour sites. The chalcones have been shown to exhibit effective anti-cancer prodrug activity, but are labile to …