3-H-[1,2]Dithiole as a New Anti-Trypanosoma cruzi Chemotype: Biological and Mechanism of Action Studies

• Main Authors: Marcos Couto, Carina Sánchez, Belén Dávila, Valentina Machín, Javier Varela, Guzmán Álvarez, Mauricio Cabrera, Laura Celano, Beatriz Aguirre-López, Nallely Cabrera, Marieta Tuena de Gómez-Puyou, Armando Gómez-Puyou, Ruy Pérez-Montfort, Hugo Cerecetto, Mercedes González
• Format: Article
• Language: English
• Published: MDPI AG 2015-08-01
• Series: Molecules
• Subjects: anti-T. cruzi activity; 3H-1,2-dithiole; triosephosphate isomerase; cruzipain; membrane sterol biosynthesis; 1H-NMR metabolomics
• Online Access: http://www.mdpi.com/1420-3049/20/8/14595

The current pharmacological Chagas disease treatments, using Nifurtimox or Benznidazole, show limited therapeutic results and are associated with potential side effects, like mutagenicity. Using random screening we have identified new chemotypes that were able to inhibit relevant targets of the Trypanosoma cruzi. We found 3H-[1,2]dithioles with the ability to inhibit Trypanosoma cruzi triosephosphate isomerase (TcTIM). Herein, we studied the structural modifications of this chemotype to analyze the influence of volume, lipophilicity and electronic properties in the anti-T. cruzi activity. Their selectivity to parasites vs. mammalian cells was also examined. To get insights into a possible mechanism of action, the inhibition of the enzymatic activity of TcTIM and cruzipain, using the isolated enzymes, and the inhibition of membrane sterol biosynthesis and excreted metabolites, using the whole parasite, were achieved. We found that this structural framework is interesting for the generation of innovative drugs for the treatment of Chagas disease.