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Repositioning of a Diaminothiazole Series Confirmed to Target the Cyclin-Dependent Kinase CRK12 for Use in the Treatment of African Animal Trypanosomiasis.

Alasdair SmithRichard J WallStephen PattersonTim RowanEva Rico VidalLaste StojanovskiMargaret HuggettShahienaz E HamptonMichael G ThomasVictoriano Corpas LopezKirsten GillingwaterJeff DukeGrant NapierRose PeterHervé S VitouleyJustin R HarrisonRachel MilneLaura JeacockNicola BakerSusan H DavisFrederick SimeonsJennifer RileyDavid HornReto BrunFabio ZuccottoMichael J WittySusan WyllieKevin D ReadIan H Gilbert
Published in: Journal of medicinal chemistry (2022)
African animal trypanosomiasis or nagana, caused principally by infection of the protozoan parasites Trypanosoma congolense and Trypanosoma vivax , is a major problem in cattle and other livestocks in sub-Saharan Africa. Current treatments are threatened by the emergence of drug resistance and there is an urgent need for new, effective drugs. Here, we report the repositioning of a compound series initially developed for the treatment of human African trypanosomiasis. A medicinal chemistry program, focused on deriving more soluble analogues, led to development of a lead compound capable of curing cattle infected with both T. congolense and T. vivax via intravenous dosing. Further optimization has the potential to yield a single-dose intramuscular treatment for this disease. Comprehensive mode of action studies revealed that the molecular target of this promising compound and related analogues is the cyclin-dependent kinase CRK12.
Keyphrases
  • cell cycle
  • low dose
  • plasmodium falciparum
  • combination therapy
  • risk assessment
  • cell death
  • climate change
  • pluripotent stem cells