| Literature DB >> 29197735 |
Muthusamy Venkatraj1, Irene G Salado1, Jan Heeres1, Jurgen Joossens1, Paul J Lewi1, Guy Caljon2, Louis Maes2, Pieter Van der Veken1, Koen Augustyns3.
Abstract
Human African trypanosomiasis (HAT), also known as sleeping sickness is a parasitic disease transmitted by the bite of the 'Glossina' insect, commonly known as the tsetse fly. This disease affects mostly poor populations living in remote rural areas of Africa. Untreated, it is usually fatal. Currently, safe and effective treatments against this disease are lacking. Phenotypic screening of triazine non-nucleoside HIV-1 reverse transcriptase inhibitors (monomers) resulted in potent and selective antitrypanosomal compounds. This serendipitous discovery and the presence of dimers in many compounds active against these neglected tropical diseases prompted us to investigate antitrypanosomal activity of triazine dimers. Optimization of the triazine dimers resulted in 3,3'-(((ethane-1,2-diylbis(azanediyl))bis(4-(mesityloxy)-1,3,5-triazine-6,2-diyl))bis(azanediyl))dibenzonitrile (compound 38), a compound with very potent in vitro and moderate in vivo antitrypanosomal activity.Entities:
Keywords: Dimer; Microsomal stability; Phenotypic screening; Trypanosoma brucei
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Year: 2017 PMID: 29197735 DOI: 10.1016/j.ejmech.2017.11.075
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514