1. Academic Validation
  2. The evaluation of quinonoid compounds against Trypanosoma cruzi: synthesis of imidazolic anthraquinones, nor-beta-lapachone derivatives and beta-lapachone-based 1,2,3-triazoles

The evaluation of quinonoid compounds against Trypanosoma cruzi: synthesis of imidazolic anthraquinones, nor-beta-lapachone derivatives and beta-lapachone-based 1,2,3-triazoles

  • Bioorg Med Chem. 2010 May 1;18(9):3224-30. doi: 10.1016/j.bmc.2010.03.029.
Eufrânio N da Silva Jr 1 Tiago T Guimarães Rubem F S Menna-Barreto Maria do Carmo F R Pinto Carlos A de Simone Claudia Pessoa Bruno C Cavalcanti José R Sabino Carlos Kleber Z Andrade Marilia O F Goulart Solange L de Castro Antônio V Pinto
Affiliations

Affiliation

  • 1 Núcleo de Pesquisas de Produtos Naturais, UFRJ, 21941-971, Rio de Janeiro, RJ, Brazil.
Abstract

In continuing our screening program of naphthoquinone activity against Trypanosoma cruzi, the aetiological agent of Chagas' disease, new beta-lapachone-based 1,2,3-triazoles, 3-arylamino-nor-beta-lapachones, 3-alkoxy-nor-beta-lapachones and imidazole Anthraquinones were synthesised and evaluated against bloodstream trypomastigote forms of the Parasite. Compounds 2,2-dimethyl-3-(2,4-dibromophenylamino)-2,3-dihydro-naphtho[1,2-b]furan-4,5-dione, IC(50)/24h 24.9+/-7.4 and 4-azido-3-bromo-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromene-5,6-dione with 23.4+/-3.8 microM showed a trypanosomicidal activity higher than benznidazole. These results demonstrate the potential of naphthoquinone derivatives as novel structures for the development of alternative drugs for Chagas' disease.

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