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/DgoR9Z7UyS.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 | DgoR9Z7UyS |
|---|---|
| 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/i36+2 |
| InChIKey | LFTYTUAZOPRMMI-QNFJKIJZSA-N |
| Mol Weight | 609.35 g/mol |
| Molecular Formula | C17H27N3O1618OP2 |
| Exact Mass | 609.085815 g/mol |
| Enantiomer InChIKey | LFTYTUAZOPRMMI-ZHEJQMEYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
DISODIUM-URIDINE-5'-(3-ACETAMIDO-3-DEOXY-2-O-METHYL-ALPHA-D-GLUCOHEPT-2-ULOPYRANOS-1-YL-DIPHOSPATE)
DISODIUM-URIDINE-5'-(3-ACETAMIDO-3-DEOXY-2-O-METHYL-ALPHA-D-MANNOHEPT-2-ULOPYRANOS-1-YL-DIPHOSPATE)
URIDINE-5'-DIPHOSPHONO-N-ACETYLGLUCOSAMINE;UDP-GLCNAC
URIDINE-5'-DIPHOSPHONO-N-ACETYLGALACTOSAMINE;UDP-GALNAC
DISODIUM-URIDINE-5'-[3-ACETAMIDO-2,6-ANHYDRO-1,3-DIDEOXY-D-ARABINOHEPT-2-ENITOL-1-YL-PHOSPHONO]-PHOSPHATE
BRWCTAUOVYRBOB-LYANNJDESA-N
3,4-DICHLOROPHENOXYMETHYL_METHYL_2',5'-DI-O-TETRAHYDROPYRAN-2-YL-3'-O-URIDINE_PHOSPHATE
5'-O-METHOXYTRITYL-2'-O-ACETYLURIDINE-3'-CYANOETHYL(2,2,2-TRICHLOROETHYL)PHOSPHATE
5'-(PARA,PARA'-DIMETHOXYTRITYL)-2'-(2-CHLOROBENZOYL)URIDIN-3'-PHOSPHITE, TRIETHYLAMMONIUM SALT
| 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 |