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Merck

Zebularine: a unique molecule for an epigenetically based strategy in cancer chemotherapy.

Annals of the New York Academy of Sciences (2006-01-06)
Victor E Marquez, James A Kelley, Riad Agbaria, Tisipi Ben-Kasus, Jonathan C Cheng, Christine B Yoo, Peter A Jones
RESUMEN

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.

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Sigma-Aldrich
Zebularine, ≥98% (HPLC), solid