In Vitro Antileishmanial, Trypanocidal, and Mammalian Cell Activities of Diverse N,N′ -Dihetaryl Substituted Diamines and Related Compounds

The leishmaniasis and Chagas diseases constitute a serious public health problem worldwide with few and ineffective treatment options. The search for new antiparasitic candidates at the initial steps of drug discovery and development is still necessary. The synthesis of 22 de novo synthetized N,N′-dihetaryl-alkyldiamine derivatives and in vitro antiparasitic activity were evaluated for the first time against intracellular and extracellular forms of Leishmania (Leishmania) infantum, L. (Viannia) panamensis, L. (Leishmania) amazonensis, and Trypanosoma cruzi. Additionally, the toxicity on mammalian cells was determined. Some of these substituted N,N′-diamines (25–35 % of the tested compounds) showed interesting results against free-living forms of parasites with activities at the inhibitory concentration (IC(50)) level of 1.96 to 28.83 μM for L. (L.) infantum promastigotes and IC(50) of 0.02 to 5.31 μM for T. cruzi epimastigotes. No activity at the IC(50) level on intracellular amastigotes of T. cruzi was observed. However, N(1),N(2)-dibenzylethane-1,2-diamine 5a revealed an important activity against the intracellular amastigotes of L. infantum (IC(50) 25.42 μM ±0.33) and L. panamensis (IC(50) 58.20 μM ±3.23), while their analogue N(1),N(4)-dibenzylbutane-1,4-diamine 5c resulted in activity only against L. panamensis (IC(50) 11.19 μM ±0.20) without toxicity on Vero and THP-1 mammalian cells. The active compounds against intracellular parasites with low toxicity in mammalian cells may be considered for future studies in experimental models.