Abstract
1-(Beta-d-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) corresponds structurally to cytidine minus the exocyclic 4-amino group. The increased electrophilic character of its simple aglycon endows the molecule with unique biologic properties as a potent inhibitor of both cytidine deaminase and DNA cytosine methyltransferase. The latter activity makes zebularine a promising antitumor agent that is hydrolytically stable, preferentially targets cancer cells, and shows activity both in vitro and in experimental animals, even after oral administration.
| Original language | English |
|---|---|
| Pages (from-to) | 246-254 |
| Number of pages | 9 |
| Journal | Annals of the New York Academy of Sciences |
| Volume | 1058 |
| DOIs | |
| State | Published - 1 Jan 2005 |
| Externally published | Yes |
ASJC Scopus subject areas
- General Neuroscience
- General Biochemistry, Genetics and Molecular Biology
- History and Philosophy of Science