We report herein the synthesis and trypanocidal profile of new (E)-cinnamic N- acylhydrazones (NAHs) designed by exploiting molecular hybridization between the potent cruzain inhibitors (E)-1-(benzo [d][1, 3] dioxol-5-yl)-3-(4-bromophenyl) prop-2-en-1-one and (E)-3-hydroxy-N′-((2-hydroxynaphthalen-1-yl) methylene)-7-methoxy-2-naphthohydrazide. These derivatives were evaluated against both amastigote and trypomastigote forms of ...