| Literature DB >> 28110521 |
William G Devine1, Rosario Diaz-Gonzalez2, Gloria Ceballos-Perez2, Domingo Rojas2, Takashi Satoh1, Westley Tear1, Ranae M Ranade, Ximena Barros-Álvarez3, Wim G J Hol, Frederick S Buckner, Miguel Navarro2, Michael P Pollastri1.
Abstract
Human African trypanosomiasis is a neglected tropical disease that is lethal if left untreated. Existing therapeutics have limited efficacy and severe associated toxicities. 2-(2-(((3-((1H-Benzo[d]imidazol-2-yl)amino)propyl)amino)methyl)-4,6-dichloro-1H-indol-1-yl)ethan-1-ol (NEU-1053) has recently been identified from a high-throughput screen of >42,000 compounds as a highly potent and fast-acting trypanocidal agent capable of curing a bloodstream infection of Trypanosoma brucei in mice. We have designed a library of analogues to probe the structure-activity relationship and improve the predicted central nervous system (CNS) exposure of NEU-1053. We report the activity of these inhibitors of T. brucei, the efficacy of NEU-1053 in a murine CNS model of infection, and identification of the target of NEU-1053 via X-ray crystallography.Entities:
Keywords: Trypanosoma brucei; medicinal chemistry; methionyl-tRNA synthetase
Mesh:
Substances:
Year: 2017 PMID: 28110521 PMCID: PMC5346068 DOI: 10.1021/acsinfecdis.6b00202
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084