HYACINTHACINE-A2;(1R,2R,3R,7AR)-3-(HYDROXYMETHYL)-HEXAHYDRO-1H-PYRROLIZINE-1,2-DIOL
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 6aAJG7QH44D |
|---|---|
| InChI | InChI=1S/C8H15NO3/c10-4-6-8(12)7(11)5-2-1-3-9(5)6/h5-8,10-12H,1-4H2/t5-,6-,7-,8-/m1/s1 |
| InChIKey | STFSMGASTIYWRS-WCTZXXKLSA-N |
| Mol Weight | 173.21 g/mol |
| Molecular Formula | C8H15NO3 |
| Exact Mass | 173.105193 g/mol |
| Enantiomer InChIKey | STFSMGASTIYWRS-XAMCCFCMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
- (+)-HYACINTHACINE-A2
Octahydro-5-pentylindolizin-8-ol
(1R,2S,7R,8aS)-indolizidine-1,2,7-triol
(1S,2S,7S,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,7-triol
(1S,2S,7R,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,7-triol
(1R,2S,7S,8aR)-indolizidine-1,2,7-triol
1.beta.-(N-Octyl)-deoxynojirimycin
1.alpha.-(N-Octyl)-deoxynojirimycin
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis, Biological Evaluation and Docking Studies of Casuarine Analogues: Effects of Structural Modifications at Ring B on Inhibitory Activity Towards Glucoamylase | European Journal of Organic Chemistry | 2010 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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