PMID

Data

Article Title

Organization

Design, synthesis, and pharmacological evaluation of fluorinated tetrahydrouridine derivatives as inhibitors of cytidine deaminase.

Eisai

Structure of human cytidine deaminase bound to a potent inhibitor.

Harvard University

Synthesis and anticancer and antiviral activities of various 2'- and 3'-methylidene-substituted nucleoside analogues and crystal structure of 2'-deoxy-2'-methylidenecytidine hydrochloride.

Yale University

Cyclic urea nucleosides. Cytidine deaminase activity as a function of aglycon ring size.

TBA

Synthesis of 1,3-diazepin-2-one nucleosides as transition-state inhibitors of cytidine deaminase.

TBA

Carbocyclic analogues of the potent cytidine deaminase inhibitor 1-(beta-D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine).

National Cancer Institute-Bethesda

Compositions and methods for treating cancer

Otsuka Pharmaceutical

Certain compounds, compositions and methods

Eisai