14 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
23916149	14	Investigation of acyclic uridine amide and 5'-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase.	University of Dundee
21600680	9	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
22715973	32	1,2,3-Triazole-containing uracil derivatives with excellent pharmacokinetics as a novel class of potent human deoxyuridine triphosphatase inhibitors.	Taiho Pharmaceutical
22607122	38	Discovery of highly potent human deoxyuridine triphosphatase inhibitors based on the conformation restriction strategy.	Taiho Pharmaceutical
22339362	20	Discovery of a novel class of potent human deoxyuridine triphosphatase inhibitors remarkably enhancing the antitumor activity of thymidylate synthase inhibitors.	Taiho Pharmaceutical
22404301	44	Synthesis and discovery of N-carbonylpyrrolidine- or N-sulfonylpyrrolidine-containing uracil derivatives as potent human deoxyuridine triphosphatase inhibitors.	Taiho Pharmaceutical
16161998	143	Deoxyuridine triphosphate nucleotidohydrolase as a potential antiparasitic drug target.	Cardiff University
21411327	19	β-Branched acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.	University of Dundee
18619713	28	Design, synthesis and evaluation of novel uracil acetamide derivatives as potential inhibitors of Plasmodium falciparum dUTP nucleotidohydrolase.	University of Wales Cardiff
16821778	80	Acyclic nucleoside analogues as inhibitors of Plasmodium falciparum dUTPase.	Cardiff University
23463940	4	Synthesis and evaluation of 18F-labeled carbonic anhydrase IX inhibitors for imaging with positron emission tomography.	Bc Cancer Agency