Carbocyclic thymidine derivatives efficiently inhibit Plasmodium falciparum thymidylate kinase (PfTMK)

Abstract During the course of our research into new anti-malaria drugs, Plasmodium falciparum thymidylate kinase ( Pf TMK) has emerged as an important drug target because of its unique substrate specificity. Compared with human thymidylate kinase ( Hs TMK), Pf TMK shows broader substrate specificity, which includes both purine and pyrimidine nucleotides. Pf TMK accepts both 2′-deoxyguanosine monophosphate (dGMP) and thymidine monosphosphate (TMP) as substrates. We have evaluated the inhibitory activity of seven carbocyclic thymidine analogs and report the first structure‒activity relationship for these inhibitors against Pf TMK. The 2′,3′ dideoxycarbocyclic derivative of thymidine showed the most potent inhibition of the enzyme. The K i dTMP and K i dGMP values were 20 and 7 μM respectively. Thus, further modifications of carbocyclic thymidine analogs represent a good strategy for developing more powerful thymidylate kinase inhibitors.