Recently, it has demonstrated that TSC and analogue compounds, 4-thiazolidinones (4-TZN), decreased in vitro infection and induced intracellular elimination of T. gondii [9,10]. This study also used TSC substituted at the aryl hydrazone moiety with a nitro substituent at the ortho, meta and para positions, and 4-thiazolidinones (TZN) substituted at the N-3 position with a phenyl, methyl and hydrogen substituent, and with the same groups at the arylhydrazone moiety. These molecular structures have a good cellular perfusion where they target the parasite and interrupt its multiplication. Carvalho et al. [11] showed that after the arrest of intracellular proliferating parasite, the death of T.gondii and its digestion by lysosomes fusion occurs. Thus, the aim of the present study was to evaluate the effects of these TSC and TZN compounds against extra-and intracellular T. cruzi. Furthermore, we also report the morphological and ultrastructural features of the parasite in the presence of these drugs.