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 |