[2-[BETA-D-GALACTOPYRANOSYL-(3-BETA-D-GALACTOPYRANOSYL-CARBAMOYLPROPIONYL)-AMINO]-ACETYLAMINO]-ACETIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
![[2-[BETA-D-GALACTOPYRANOSYL-(3-BETA-D-GALACTOPYRANOSYL-CARBAMOYLPROPIONYL)-AMINO]-ACETYLAMINO]-ACETIC-ACID-METHYLESTER](/api/compound/4x0Qv4BR4Bq.png?ph=true&h=300&w=458 "[2-[BETA-D-GALACTOPYRANOSYL-(3-BETA-D-GALACTOPYRANOSYL-CARBAMOYLPROPIONYL)-AMINO]-ACETYLAMINO]-ACETIC-ACID-METHYLESTER")
| SpectraBase Compound ID | 4x0Qv4BR4Bq |
|---|---|
| InChI | InChI=1S/2C21H35N3O15/c2*1-37-13(30)4-22-11(28)5-24(21-19(36)17(34)15(32)9(7-26)39-21)12(29)3-2-10(27)23-20-18(35)16(33)14(31)8(6-25)38-20/h2*8-9,14-21,25-26,31-36H,2-7H2,1H3,(H,22,28)(H,23,27)/t8-,9+,14+,15-,16+,17-,18-,19+,20-,21+;8-,9-,14+,15+,16+,17+,18-,19-,20-,21-/m00/s1 |
| InChIKey | PEMYKMHPDSCFTN-BZJQAKTKSA-N |
| Mol Weight | 1139.0 g/mol |
| Molecular Formula | C42H70N6O30 |
| Exact Mass | 1138.413635 g/mol |
| Enantiomer InChIKey | PEMYKMHPDSCFTN-SVCCCXMGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
N-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHLENYLALANYL-L-LEUCYL]-BETA-D-GLUCOPYRANOSYLAMINE
N-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-SUCCINAMIC-ACID
TERT.-BUTYL_N-[2-OXO-2-[(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-AMINO]-ETHYL]-GLYCYLGLYCINATE
TERT.-BUTYL_N-[2-OXO-2-[(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)-AMINO]-ETHYL]-GLICYLGLYCINATE
N-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)-3-(2,2,2-TRIFLUORO-1-TRIFLUOROMETHYLETHYLAMINO)-ACRYLAMIDE
N-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)-BENZAMIDE
2,3,4,6-TETRA-O-ACETYL-N-(ISOTHIOURONIUM-ACETYL)-BETA-D-GALACTOPYRANOSYLAMINE-HYDROCHLORIDE
2,3,4,6-TETRA-O-ACETYL-N-(ISOTHIOURONIUM-ACETYL)-BETA-D-GLUCOPYRANOSYLAMINE-HYDROCHLORIDE
2,3,4,6-TETRA-O-ACETYL-N-(S-ACETYLMERCAPTOACETYL)-BETA-D-GALACTOPYRANOSYLAMINE
2,3,4,6-TETRA-O-ACETYL-N-(ISOTHIOURONIUM-ACETYL)-ALPHA-D-MANNOPYRANOSYLAMINE-HYDROCHLORIDE
| Title | Journal or Book | Year |
|---|---|---|
| Development of Carbohydrate-Based Scaffolds for Restricted Presentation of Recognition Groups. Extension to Divalent Ligands and Implications for the Structure of Dimerized Receptors | The Journal of Organic Chemistry | 2003 |