101814-74-8Relevant articles and documents
NMR-based conformational analysis of 2′,6-disubstituted uridines and antiviral evaluation of new phosphoramidate prodrugs
Da Paix?o Soares, Fábio,Groaz, Elisabetta,Lescrinier, Eveline,Neyts, Johan,Leyssen, Pieter,Herdewijn, Piet
, p. 5809 - 5815 (2015)
Six novel phosphoramidate prodrugs of uridine analogues, with structural modifications introduced at the 6- and 2′,6-positions, have been prepared and evaluated for selective antiviral activity against hepatitis C virus, as well as other positive-stranded RNA viruses. An analysis of the conformational properties of the parent nucleosides was carried out using two-dimensional NMR spectroscopy based experiments, highlighting a 3′-endo (North) sugar puckering preference and syn orientation.
PYRIMIDINE DERIVATIVES AS ANTICANCER AGENTS
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, (2008/12/07)
The present invention includes methods of treating or preventing cancer by administering an effective amount of 6-substituted pyrimidine derivatives of the Formula I to a subject need thereof: