Design, synthesis and cruzain docking of 3-(4-substituted-aryl)-1,2,4-oxadiazole-N-acylhydrazones as anti-Trypanosoma cruzi agents.
dos Santos Filho JM, Leite AC, de Oliveira BG, Moreira DR, Lima MS, Soares MB, Leite LF, Bioorg Med Chem, 2009 Sep 15 - link

Synthesis, Cruzain docking, and in vitro studies of aryl-4-oxothiazolylhydrazones against Trypanosoma cruzi.
Leite AC, Moreira DR, Cardoso MV, Hernandes MZ, Alves Pereira VR, Silva RO, Kiperstok AC, Lima Mda S, Soares MB, ChemMedChem, 2007 Sep - link

Synthesis, docking, and in vitro activity of thiosemicarbazones, aminoacyl-thiosemicarbazides and acyl-thiazolidones against Trypanosoma cruzi.
Leite AC, de Lima RS, Moreira DR, Cardoso MV, Gouveia de Brito AC, Farias Dos Santos LM, Hernandes MZ, Kiperstok AC, de Lima RS, Soares MB, Bioorg Med Chem, 2006 Jun 1 - link