CFGFJVAAZQVWOK-FMDGEEDCSA-N
Compound with spectra: 2 NMR, and 1 MS (GC)
| SpectraBase Compound ID | KpoEGOSHXP |
|---|---|
| InChI | InChI=1S/C8H15NO4/c10-3-6-8(13)7(12)5-1-4(11)2-9(5)6/h4-8,10-13H,1-3H2/t4-,5-,6-,7-,8-/m1/s1 |
| InChIKey | CFGFJVAAZQVWOK-FMDGEEDCSA-N |
| Mol Weight | 189.21 g/mol |
| Molecular Formula | C8H15NO4 |
| Exact Mass | 189.100108 g/mol |
| Enantiomer InChIKey | CFGFJVAAZQVWOK-WXUMCUSRSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | U1-2010-5582-7 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
- 7-DEOXY-CASUARINE;(1R,2R,3R,6R,7AR)-3-(HYDROXYMETHYL)-HEXAHYDRO-1H-PYRROLIZINE-1,2,6-TRIOL
- (1R,2R,3R,6R,7aR)-3-(Hydroxymethyl)hexahydro-1H-pyrrolizine-1,2,6-triol
1-ALPHA-OCTYL-N-NONYL-1,4-DIDEOXY-1,4-IMINO-D-RIBITOL;(1R,2S,3R,4R)-1-OCTYL-N-NONYL-2,3-DIOL-4-HYDROXYMETHYL-PYRROLIDINE
1-ALPHA-NONYL-N-NONYL-1,4-DIDEOXY-1,4-IMINO-D-RIBITOL;(1R,2S,3R,4R)-1-NONYL-N-NONYL-2,3-DIOL-4-HYDROXYMETHYL-PYRROLIDINE
1-BETA-NONYL-N-NONYL-1,4-DIDEOXY-1,4-IMINO-D-RIBITOL;(1R,2S,3R,4R)-1-NONYL-N-NONYL-2,3-DIOL-4-HYDROXYMETHYL-PYRROLIDINE
#8C;1-BETA-NONYL-N-NONYL-1,4-DIDEOXY-1,4-IMINO-L-RIBITOL-TRIFLUOROACETATE-SALT;(1S,2R,3S,4S)-1-NONYL-N-NONYL-2,3-DIOL-4-HYDROXYMETHYL-1-PYRROLIDINE-TRIFLUOROAC
HYACINTHACINE-B1;(1S,2R,3R,5R,7AR)-1,2-DIHYDROXY-3,5-DIHYDROXY-METHYL-PYRROLIZIDINE
HYACINTHACINE-B2;(1S,2R,3R,5S,7AR)-1,2-DIHYDROXY-3,5-DIHYDROXY-METHYL-PYRROLIZIDINE
(2R,3R,4R,5R)-3,4-DIHYDROXY-2-(HYDROXYMETHYL)-5-PROPYL-PYRROLIDINE-1-CARBOXAMIDE
(1S,2S,7R,8S,8aR)-(-)-1,2,7,8-Tetrahydroxyindolizidine
(1S,2R,7R,8R,8AR)-1,2,7,8-TETRAHYDROXYINDOLIZIDINE
(1S,2R,7R,8S,8aR)-(-)-1,2,7,8-Tetrahydroxyindolizidine
| 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 |
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