1. Academic Validation
  2. Design, synthesis, electrochemistry and anti-trypanosomatid hit/lead identification of nitrofuranylazines

Design, synthesis, electrochemistry and anti-trypanosomatid hit/lead identification of nitrofuranylazines

  • RSC Med Chem. 2023 Aug 16;14(10):2012-2029. doi: 10.1039/d3md00220a.
Maryna Saayman 1 Christina Kannigadu 1 Janine Aucamp 1 Helena D Janse van Rensburg 1 Cassiem Joseph 2 Andrew J Swarts 2 David D N'Da 1
Affiliations

Affiliations

  • 1 Centre of Excellence for Pharmaceutical Sciences, North-West University Potchefstroom 2520 South Africa David.Nda@nwu.ac.za +27 18 299 4243 +27 18 299 2256.
  • 2 Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand Johannesburg-Braamfontein 2050 South Africa.
Abstract

Chagas disease and leishmaniasis are vector-borne infectious diseases affecting both humans and Animals. These neglected tropical diseases can be fatal if not treated. Hundreds to thousands of new Chagas disease and leishmaniasis cases are being reported by the WHO every year, and currently available treatments are insufficient. Severe adverse effects, impractical administrations and increased pathogen resistance against current clinical treatments underscore a serious need for the development of new drugs to curb these ailments. In search for such drugs, we investigated a series of nitrofuran-based azine derivatives. Herein, we report the design, synthesis, electrochemistry, and biological activity of these derivatives against promastigotes and amastigotes of Leishmania major, and L. donovani strains, as well as epimastigotes and trypomastigotes of Trypanosoma cruzi. Two leishmanicidal early leads and one trypanosomacidal hit with submicromolar activity were uncovered and stand for further in vivo investigation in the search for new antitrypanosomatid drugs. Future objective will focus on the identification of involved biological targets with the parasites.

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