Oduor, R.O.Kayode, K. OjoGareth, P. WilliamsFrancois, BertelliJames, MillsLouis, MaesDavid, C. PrydeTanya, ParkinsonWesley, C. Van VoorhisTod P., Holler2012-09-212012-09-212012-09-21http://ir-library.ku.ac.ke/handle/123456789/5520PLoS Neglected Tropical DiseaseBackground: Trypanosoma brucei, the causative agent of Human African Trypanosomiasis (HAT), expresses two proteins with homology to human glycogen synthase kinase 3b (HsGSK-3) designated TbruGSK-3 short and TbruGSK-3 long. TbruGSK- 3 short has previously been validated as a potential drug target and since this enzyme has also been pursued as a human drug target, a large number of inhibitors are available for screening against the parasite enzyme. A collaborative industrial/ academic partnership facilitated by the World Health Organisation Tropical Diseases Research division (WHO TDR) was initiated to stimulate research aimed at identifying new drugs for treating HAT. Methodology/Principal Findings: A subset of over 16,000 inhibitors of HsGSK-3 b from the Pfizer compound collection was screened against the shorter of two orthologues of TbruGSK-3. The resulting active compounds were tested for selectivity versus HsGSK-3b and a panel of human kinases, as well as in vitro anti-trypanosomal activity. Structural analysis of the human and trypanosomal enzymes was also performed. Conclusions/Significance: We identified potent and selective compounds representing potential attractive starting points for a drug discovery program. Structural analysis of the human and trypanosomal enzymes also revealed hypotheses for further improving selectivity of the compounds.enArticle