Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme. Irreversible inhibitors are therefore the equivalent of poisons in heterogeneous catalysis. 73464-50-3, C13H18O10. A document type is Article, introducing its new discovery., Related Products of 73464-50-3
Reaction of methyl 2,3,4-tri-O-acetyl-1-O-(trichloroacetimidoyl)-alpha-d- glucopyranuronate with 3?-deoxy-3?-fluorothymidine in the presence of trimethylsilyl trifluoromethanesulfonate gave (2R,3R,4S,5S,6S)-2-(((2R,3S,5R) -3-fluoro-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl) tetrahydrofuran-2-yl)methoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4, 5-triyl triacetate, which was hydrolysed to 3?-deoxy-3?- fluorothymidine-5?-glucuronide. Analysis of this reference standard by high performance liquid chromatography enabled the identification of [ 18F]3?-deoxy-3?-fluorothymidine-5?-glucuronide in blood samples from six human patients who had been administered [ 18F]3?-deoxy-3?-fluorothymidine.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 73464-50-3. This is the end of this tutorial post, and I hope it has helped your research about 73464-50-3
Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics