2950-83-6Relevant articles and documents
Investigation of acyclic uridine amide and 5′-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase
Hampton, Shahienaz E.,Schipani, Alessandro,Bosch-Navarrete, Cristina,Recio, Eliseo,Kaiser, Marcel,Kahnberg, Pia,González-Pacanowska, Dolores,Johansson, Nils Gunnar,Gilbert, Ian H.
, p. 5876 - 5885 (2013/09/12)
Previously we have shown that trityl and diphenyl deoxyuridine derivatives and their acyclic analogues can inhibit Plasmodium falciparum dUTPase (PfdUTPase). We report the synthesis of conformationally restrained amide derivatives as inhibitors PfdUTPase,
Oligopyrrole carboxamides linked with a nucleobase as potential DNA minor groove binding ligands: Synthesis, DNA binding and biological evaluation
Keuser,Pindur, Ulf
, p. 261 - 268 (2007/10/03)
The synthesis of a series of new oligopyrrole carboxamides closely related to netropsin and distamycin A, linked with a nucleobase is reported. The new compounds possess similar structure elements as the known peptide nucleic acids which are interesting s