Toward the Development of Dual-Targeted Glyceraldehyde-3-phosphate Dehydrogenase/ Trypanothione Reductase Inhibitors against Trypanosoma brucei and Trypanosoma cruzi

摘要

A significant improvement in the treatment of trypanosomiases has been achieved with the recent development of nifurti-mox-eflornithine combination therapy (NECT). As an alternative to drug combinations and as a means to overcome most of the antitrypanosomatid drug discovery challenges, a multi-target drug design strategy has been envisaged. To begin testing this hypothesis, we designed and developed a series of quinone-coumarin hybrids against glyceraldehyde-3-phos-phate dehydrogenase/trypanothione reductase (GAPDH/TR). These enzymes belong to metabolic pathways that are vital to Trypanosoma brucei and Trypanosoma cruzi, and have thus been considered promising drug targets. The synthesized molecules were characterized for their dual-target antitrypanoso-mal profile, both in enzyme assays and in in vitro parasite cultures. The merged derivative 2-{[3-(3-dimethylaminopropoxy)-2-oxo-2/-/-chromen-7-yl]oxy}anthracene-1,4-dione (10) showed an IC_(50) value of 5.4 μm against TbGAPDH and a concomitant K_I value of 2.32 μim against TcTR. Notably, 2-{4-[6-(2-dimethylami-noethoxy)-2-oxo-2H-chromen-3-yl]phenoxy}anthracene-1,4-dione (compound 6) displayed a remarkable EC_(50) value for T. brucei parasites (0.026 hm) combined with a very low cytotoxicity toward mammalian L6 cells (7.95 μm). This promising low toxicity of compound 6 might be at least partially due to the fact that it does not interfere with human glutathione reductase.