The Design and Synthesis of Potent and Selective Inhibitors of Trypanosoma brucei Glycogen Synthase Kinase 3 for the Treatment of Human African Trypanosomiasis
Author(s) -
R. Urich,
Raffaella Grimaldi,
Torsten Luksch,
Julie A. Frearson,
Ruth Brenk,
Paul G. Wyatt
Publication year - 2014
Publication title -
journal of medicinal chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.01
H-Index - 261
eISSN - 1520-4804
pISSN - 0022-2623
DOI - 10.1021/jm500239b
Subject(s) - trypanosoma brucei , gsk 3 , african trypanosomiasis , chemistry , biochemistry , enzyme , gsk3b , enzyme inhibitor , glycogen synthase , trypanocidal agent , trypanosoma brucei rhodesiense , trypanosomiasis , kinase , virology , biology , gene
Glycogen synthase kinase 3 (GSK3) is a genetically validated drug target for human African trypanosomiasis (HAT), also called African sleeping sickness. We report the synthesis and biological evaluation of aminopyrazole derivatives as Trypanosoma brucei GSK3 short inhibitors. Low nanomolar inhibitors, which had high selectivity over the off-target human CDK2 and good selectivity over human GSK3β enzyme, have been prepared. These potent kinase inhibitors demonstrated low micromolar levels of inhibition of the Trypanosoma brucei brucei parasite grown in culture.
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