14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Investigation of acyclic uridine amide and 5'-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase.
University of Dundee
Site-directed mutagenesis provides insights into the selective binding of trityl derivatives to Plasmodium falciparum dUTPase.
Instituto De Parasitolog£A Y Biomedicina L£Pez-Neyra
1,2,3-Triazole-containing uracil derivatives with excellent pharmacokinetics as a novel class of potent human deoxyuridine triphosphatase inhibitors.
Taiho Pharmaceutical
Discovery of highly potent human deoxyuridine triphosphatase inhibitors based on the conformation restriction strategy.
Taiho Pharmaceutical
Discovery of a novel class of potent human deoxyuridine triphosphatase inhibitors remarkably enhancing the antitumor activity of thymidylate synthase inhibitors.
Taiho Pharmaceutical
Synthesis and discovery of N-carbonylpyrrolidine- or N-sulfonylpyrrolidine-containing uracil derivatives as potent human deoxyuridine triphosphatase inhibitors.
Taiho Pharmaceutical
Deoxyuridine triphosphate nucleotidohydrolase as a potential antiparasitic drug target.
Cardiff University
β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.
University of Dundee
Design, synthesis and evaluation of novel uracil acetamide derivatives as potential inhibitors of Plasmodium falciparum dUTP nucleotidohydrolase.
University of Wales Cardiff
Acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.
Cardiff University
