3-AMINO-3-DEOXY-D-GLUOCOSE-6-PHOSPHATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 22B9YTcaUUD |
|---|---|
| InChI | InChI=1S/2C6H14NO8P/c2*7-3-4(8)2(1-14-16(11,12)13)15-6(10)5(3)9/h2*2-6,8-10H,1,7H2,(H2,11,12,13)/t2-,3+,4-,5-,6+;2-,3+,4-,5-,6-/m11/s1 |
| InChIKey | HJUDVKROFDFIFA-KFNDIKROSA-N |
| Mol Weight | 518.3 g/mol |
| Molecular Formula | C12H28N2O16P2 |
| Exact Mass | 518.091407 g/mol |
| Enantiomer InChIKey | HJUDVKROFDFIFA-MABNHWOWSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
MANNOSE, 6-MONO(DIHYDROGEN PHOSPHATE), BARIUM SALT
D-GALACTOSE, 6-(DIHYDROGEN PHOSPHATE), BARIUM SALT
D-Glucose 6-phosphate
ALPHA-D-GLUCOPYRANOSE-6-O-PHOSPHATE
ALPHA/BETA-D-MANNOPYRANOSIYL-6-O-PHOSPHATE
(MANNOSE-6)PHOSPHATE, DIANION
(MANNOSE-6)PHOSPHATE, MONOANION
D-Glucose 6-phosphate sodium salt
BETA-D-MANNOPYRANOSIYL-6-O-MONOTHIOPHOSPHATE
ALPHA-D-MANNOPYRANOSIYL-6-O-MONOTHIOPHOSPHATE
| Title | Journal or Book | Year |
|---|---|---|
| Importance of Specific Hydrogen-Bond Donor−Acceptor Interactions for the Key Carbocycle-Forming Reaction Catalyzed by 2-Deoxy-scyllo-inosose Synthase in the Biosynthesis of 2-Deoxystreptamine-Containing Aminocyclitol Antibiotics | The Journal of Organic Chemistry | 2002 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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