(1S)-(1-(OH),2,4,5/1,3)-5-([(2-HYDROXY-1-(HYDROXYMETHYL)-ETHYL]-AMINO)-1-C-(HYDROXYMETHYL)-1,2,3,4-CYCLOHEXANETETROL;AO-128
Compound with spectra: 1 NMR
![(1S)-(1-(OH),2,4,5/1,3)-5-([(2-HYDROXY-1-(HYDROXYMETHYL)-ETHYL]-AMINO)-1-C-(HYDROXYMETHYL)-1,2,3,4-CYCLOHEXANETETROL;AO-128](/api/compound/JffOPn4SrD4.png?ph=true&h=300&w=458 "(1S)-(1-(OH),2,4,5/1,3)-5-([(2-HYDROXY-1-(HYDROXYMETHYL)-ETHYL]-AMINO)-1-C-(HYDROXYMETHYL)-1,2,3,4-CYCLOHEXANETETROL;AO-128")
| SpectraBase Compound ID | JffOPn4SrD4 |
|---|---|
| InChI | InChI=1S/C10H21NO7/c12-2-5(3-13)11-6-1-10(18,4-14)9(17)8(16)7(6)15/h5-9,11-18H,1-4H2/t6-,7-,8+,9-,10-/m0/s1 |
| InChIKey | FZNCGRZWXLXZSZ-CIQUZCHMSA-N |
| Mol Weight | 267.28 g/mol |
| Molecular Formula | C10H21NO7 |
| Exact Mass | 267.131802 g/mol |
| Enantiomer InChIKey | FZNCGRZWXLXZSZ-HOTMZDKISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
(1S,2R,3S,4R,5S)-1,2,3,4-TETRAHYDROXY-9-AZA-BICYCLO-[3.3.1]-NONANE
(1-S,2-R,3-S,4-S,5-S,6-R)-5-AMINO-1-(HYDROXYMETHYL)-BICYCLO-[4.1.0]-2,3,4-HEPTANETRIOL
Transaldolase from baker's yeast (S. cerevisiae)
(+)-CASUARINE
ARP GLUCTHR(beta F)
#14A;(2R,3R,4R,5R)-1-BENZYL-2-CARBOXY-3,4,5-TRIHYDROXY-PIPERIDINIUM-CHLORIDE;(2R,3R,4R,5R)-1-BENZYL-3,4,5-TRIHYDROXY-PIPECOLID-ACID-HYDROCHLORIDE-SALT
QEGKMWNUSCPRPO-PTOURQPESA-N
ARP GLUCASP(beta F)
N-[META-(TRIFLUOROMETHYL)-BENZYL]-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
BETA-D-GALACTOFURANOSYL-(1->6)-2-ACETAMIDO-2-DEOXY-D-GLUCITOL
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of valiolamine and its N-substituted derivatives AO-128, validoxylamine G, and validamycin G via branched-chain inosose derivatives | The Journal of Organic Chemistry | 1992 |