Artículo de revista
Rhenium(I) tricarbonyl compounds of bioactive thiosemicarbazones: Synthesis, characterization and activity against Trypanosoma cruzi
Fecha
2017Registro en:
Journal of Inorganic Biochemistry, Volumen 170,
18733344
01620134
10.1016/j.jinorgbio.2017.01.011
Autor
Rodríguez Arce, Esteban
Machado, Ignacio
Rodríguez, Belén
Lapier, Michel
Zúñiga, María Carolina
Maya Arango, Juan
Olea Azar, Claudio
Otero, Lucía
Gambino, Dinorah
Institución
Resumen
© 2017 Elsevier Inc. American Trypanosomiasis is a chronic infection discovered and described in 1909 by the Brazilian scientist Carlos Chagas. It is caused by the protozoan parasite Trypanosoma cruzi. Although it affects about 10 million people in Latin America, the current chemotherapy is still inadequate. The discovery of new drugs is urgently needed. Our group is focused on the development of prospective metal-based drugs mainly based on bioactive ligands and pharmacologically interesting metal ions. In this work three new rhenium(I) tricarbonyl compounds fac-[ReI(CO)3Br(HL)] where HL = 5-nitrofuryl containing thiosemicarbazones were synthesized and fully characterized in solution and in the solid state. The in vitro evaluation of the compounds on T. cruzi trypomastigotes (Dm28c strain) showed that the Re(I) compounds are 8 to 15 times more active than the reference drug Nifurtimox and show a 4 to 17 fold increase in activity in respect to the free (HL) ligands. Obtained compounds