18O-LABELED-UDP-GLC-N-AC;URIDINE-5'-(2''-ACETAMIDO-2''-DEOXY-[1-18O]-ALPHA-D-GLUCOPYRANOSYL)-DIPHOSPHATE
Compound with spectra: 1 NMR
![18O-LABELED-UDP-GLC-N-AC;URIDINE-5'-(2''-ACETAMIDO-2''-DEOXY-[1-18O]-ALPHA-D-GLUCOPYRANOSYL)-DIPHOSPHATE](/api/compound/KHOS5vjDzbF.png?ph=true&h=300&w=458 "18O-LABELED-UDP-GLC-N-AC;URIDINE-5'-(2''-ACETAMIDO-2''-DEOXY-[1-18O]-ALPHA-D-GLUCOPYRANOSYL)-DIPHOSPHATE")
| SpectraBase Compound ID | KHOS5vjDzbF |
|---|---|
| InChI | InChI=1S/C17H27N3O17P2/c1-6(22)18-10-13(26)11(24)7(4-21)35-16(10)36-39(31,32)37-38(29,30)33-5-8-12(25)14(27)15(34-8)20-3-2-9(23)19-17(20)28/h2-3,7-8,10-16,21,24-27H,4-5H2,1H3,(H,18,22)(H,29,30)(H,31,32)(H,19,23,28)/t7-,8+,10-,11-,12+,13-,14+,15+,16-/m1/s1 |
| InChIKey | LFTYTUAZOPRMMI-VZRSNIEFSA-N |
| Mol Weight | 607.35 g/mol |
| Molecular Formula | C17H27N3O17P2 |
| Exact Mass | 607.08157 g/mol |
| Enantiomer InChIKey | LFTYTUAZOPRMMI-SBHKVJLYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
URIDINE-5'-DIPHOSPHONO-N-ACETYLGLUCOSAMINE;UDP-GLCNAC
URIDINE-5'-DIPHOSPHONO-N-ACETYLGALACTOSAMINE;UDP-GALNAC
P-(1)-[BETA-D-GLUCOPYRANOSYL-(1->4)-2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL]-P-(2)-DOLICHYL-PYROPHOSPHATE;MIXTURE
CYTIDYLYL-(5' TO 3')-URIDINE
PARA-NITROPHENYL 2-ACETAMIDO-3-{2-ACETAMIDO-3-[2-ACETAMIDO-3-(2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYLPHOSPHO)-2-DEOXY-ALPHA-D-GLUCOPYRANOSYLPHOSPHO]-2-DEOXY-ALPHA-D-GLUCOPYRANOSYLPHOSPHO}-2-DEOXY-B
2',5'-Di(tert-butyldimethylsilyl)-3'-(1-bromovinyl ethylphosphate)uridine
A-500359-F-AMIDE
5'-O-TRITYLURIDINE-2',3'-CYCLOPHOSPHATE
2'-O-(ORTHO-CHLOROBENZOYL)-5'-O-(TERT.-BUTYLDIPHENYLSILYL)-3'-O-[(METHYLTHIO)-METHYL]-URIDINE
| Title | Journal or Book | Year |
|---|---|---|
| Sialic Acid Biosynthesis: Stereochemistry and Mechanism of the Reaction Catalyzed by the Mammalian UDP-N-Acetylglucosamine 2-Epimerase | Journal of the American Chemical Society | 2003 |