A fluorine-19 NMR study of 2-deoxy-2-fluoro-D-galactose in mice was written by Kanazawa, Yoko; Kuribayashi, Satoru; Kojima, Masaharu; Haradahira, Terushi. And the article was included in Chemical & Pharmaceutical Bulletin on October 25,1988.Application of 67341-43-9 The following contents are mentioned in the article:
The metabolic pathway of 2-deoxy-2-fluoro-D-galactose (FDGal), a potential reagent for diagnosis by position emission tomog., in mice was studied by 19F NMR. Efficient accumulation of FDGal in liver was demonstrated by NMR. This fluorinated hexose was converted to 2-deoxy-2-fluoro-D-glucose (FDG) through UDP-FDGal and UDP-FDG apparently by the action of UDP-Gal epimerase. This study involved multiple reactions and reactants, such as Uridine 5′-(trihydrogen diphosphate) P’-(2-deoxy-2-fluoro-α-D-glucopyranosyl) ester (cas: 67341-43-9Application of 67341-43-9).
Uridine 5′-(trihydrogen diphosphate) P’-(2-deoxy-2-fluoro-α-D-glucopyranosyl) ester (cas: 67341-43-9) belongs to tetrahydrofuran derivatives. Tetrahydrofuran (THF) is a Lewis base that bonds to a variety of Lewis acids such as I2, phenols, triethylaluminum and bis(hexafluoroacetylacetonato)copper(II). It is more basic than diethyl ether and forms stronger complexes with Li+, Mg2+, and boranes. It is a popular solvent for hydroboration reactions and for organometallic compounds such as organolithium and Grignard reagents.Application of 67341-43-9
67341-43-9;Uridine 5′-(trihydrogen diphosphate) P’-(2-deoxy-2-fluoro-α-D-glucopyranosyl) ester;The future of 67341-43-9;New trend of C15H23FN2O16P2 ;function of 67341-43-9