2,6-DIDEOXY-2,6-IMINO-D-GLYCERO-L-GALACTO-HEPTITOL;ALPHA-HOMOGALACTONOJINIMYCIN
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 1XGnifONwVS |
|---|---|
| InChI | InChI=1S/C7H15NO5/c9-1-3-5(11)7(13)6(12)4(2-10)8-3/h3-13H,1-2H2/t3-,4-,5+,6+/m1/s1 |
| InChIKey | CLVUFWXGNIFGNC-ZXXMMSQZSA-N |
| Mol Weight | 193.2 g/mol |
| Molecular Formula | C7H15NO5 |
| Exact Mass | 193.095023 g/mol |
| Enantiomer InChIKey | CLVUFWXGNIFGNC-UNTFVMJOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
ALPHA-1-C-HYDROXYMETHYLFAGOMINE
2,5-IMINO-2,5,6-TRIDEOXY-D-MANNO-HEPTITOL;6-DEOXY-HOMO-2R,5R-BIS-(HYDROXYMETHYL)-3R,4R-DIHYDROXYPYRROLIDINE
2,5-IMINO-2,5,6-TRIDEOXY-D-GULO-HEPTITOL
(2R,3R,4S,5S)-2-(HYDROXYMETHYL)-5-PROPYL-PYRROLIDINE-3,4-DIOL
(2R,3R,4R,5R)-2-(HYDROXYMETHYL)-5-PROPYL-PYRROLIDINE-3,4-DIOL
| Title | Journal or Book | Year |
|---|---|---|
| Piperidine analogues of D-galactose as potent inhibitors of α-galactosidase: Synthesis by stannane-mediated hydroxymethylation of 5-azido-1,4-lactones. Structural relationships between D-galactosidase and L-rhamnosidase inhibitors | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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