文摘
We recently reported that 1,14-diphenylacetamide derivatives of spermine exhibit potent nM in聽vitro growth inhibition properties of Plasmodium falciparum. In an effort to expand the structure-activity relationship of this compound class towards malaria, we have prepared and biologically tested a library that includes benzamide and 3-phenylpropanamide 鈥榗apping acid鈥?groups, and polyamines that include spermine (PA3-4-3) and chain extended analogues PA3-8-3 and PA3-12-3. 2-Hydroxy and 2,5-dimethoxy analogues were typically found to exhibit the most potent activity towards the dual drug resistant strain K1 of P.聽falciparum with IC50's in the range of 1.3-9.5聽nM, and selectivity indices (SI) of 42,300 to 4880. In聽vivo evaluation of three analogues against Plasmodium berghei was undertaken, with one demonstrating a modest 27.9% reduction in parasitaemia.
