Kinetics and substrate specificity of human and canine cytidine deaminase was written by Fanucchi, Michael P.; Watanabe, Kyoichi A.; Fox, Jack J.; Chou, Ting Chao. And the article was included in Biochemical Pharmacology on April 1,1986.Name: 4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one The following contents are mentioned in the article:
The reaction kinetics and specificity of human and canine liver cytidine deaminase (I) for the virucide 1-(2′-deoxy-2′-fluoro-β-D-arabinofuranosyl)-5-iodocytosine (FIAC) and some other 5-substituted arabinofuranosylcytosine analogs are reported. The Km and Vmax values of human and canine I for FIAC differed significantly; marked kinetic differences of human and canine I were also observed with cytidine, deoxycytidine, arabinofuranosylcytidine, and deoxyfluoroarabinofuranosylcytosine. Studies with human I showed that substitution at the 5-position affected enzyme activity. Thus, although deoxyfluoroarabinofuranosylethylcytosine is a potent antiviral compound in vitro, it was not deaminated by human I. This study involved multiple reactions and reactants, such as 4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one (cas: 56632-83-8Name: 4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one).
4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one (cas: 56632-83-8) belongs to pyrimidine derivatives. Pyrimidine also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. As nucleotides in DNA and RNA, pyrimidine nucleotide derivatives have a wide range of biological applications. For example, pyrimidine derivatives are useful in DNA repair studies involving cancer and epigenetics.Name: 4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one
56632-83-8;4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidin-2(1H)-one;The future of 56632-83-8;New trend of C9H12FN3O4;function of 56632-83-8