A comparative study of mesoionic compounds in Leishmania sp. and toxicity evaluation

In this first study, a series of mesoionic compounds like 1,3,4-thiadiazolium-2-phenylamine derivatives were synthesized and studied in Leishmania amazonensis. The cytotoxic effects of these compounds on the host cells were investigated and the antileishmanial in vitro activity was compared with other species of Leishmania (Leishmania chagasi and Leishmania braziliensis). The compounds presented lower toxicity in murine macrophages than the reference drug pentamidine. The halogen derivatives 5, 6, 8 and 13 (4-F, 4-Cl, 4-Br and 3-Cl) were the most active compounds among all the species tested.

Chemical structure of the mesoionic salt derivatives, 4-phenyl-5-(3- or 4-R-cinnamoyl)-1,3,4-thiadiazolium-2-phenylamine chlorides.Figure optionsDownload as PowerPoint slide