Abstract

Two new metallocene complexes with formulation [Fe(eta 5-C5H5){(eta 5-C5H4)-N--CH-2-C4H2O-(5-C6H4-2-NO2)}] (3) and [Fe(eta 5-C5H5){(eta 5-C5H4)-N--CH-2-C4H2O-(5-C6H4-4-NO2)}] (4) have been synthesized and their antitrypanosomal activity has been evaluated. Complexes 3 and 4 were obtained by condensation reaction of ferrocenylamine (1) with respective 5-(2-nitrophenyl)-2-furancarboxaldehyde (2a) or 5-(4-nitrophenyl)-2furancarboxaldehyde (2b). The complexes were fully characterized by spectroscopic techniques (FT-IR, 1H and 13C{1H} NMR, and HRMS), which confirm their correct obtainment. The crystal structures of 3 and 4 were also determined by single crystal X-ray diffraction. Furthermore, UV-visible studies revealed that compounds 3 and 4 exhibited suitable stability in DMSO:HEPES buffer solution (80:20) throughout 24 h. The in vitro antiparasitic activities of ferrocenyl imine derivatives 3 and 4 were assessed against two species of parasites, Trypanosoma cruzi (T. cruzi) and Trypanosoma brucei (T. brucei). The obtained results revealed that compound 3 (EC50 = 0.44 mu M) exhibited nearly a 40 -fold greater efficacy as an anti -T. brucei agent compared to derivative 4 (EC50 = 16.0 mu M). Moreover, compound 3 demonstrated superior potency when compared with its organometallic analogs (EC50 = 2.42-13.3 mu M), which were previously reported by our research group. Interestingly, the EC50 value of 3 was found to be 8 times greater than that of nifurtimox (EC50 = 3.56 mu M). The cytotoxicity of the ferrocenyl imines was also evaluated on the L6 rat skeletal myoblast cell line.