METHYL-2,3-DIDEOXY-4-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-ERYTHRO-HEXOPYRANOSIDE
Compound with spectra: 1 NMR
![METHYL-2,3-DIDEOXY-4-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-ERYTHRO-HEXOPYRANOSIDE](/api/compound/D8UTkrAmth8.png?ph=true&h=300&w=458 "METHYL-2,3-DIDEOXY-4-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-ERYTHRO-HEXOPYRANOSIDE")
| SpectraBase Compound ID | D8UTkrAmth8 |
|---|---|
| InChI | InChI=1S/C19H34O13/c1-7-12(22)14(24)16(26)18(28-7)32-17-15(25)13(23)10(6-21)31-19(17)30-8-3-4-11(27-2)29-9(8)5-20/h7-26H,3-6H2,1-2H3/t7-,8-,9+,10+,11+,12+,13-,14+,15-,16-,17+,18-,19+/m0/s1 |
| InChIKey | PNWVYPCCFRRLAT-UPKBBCCLSA-N |
| Mol Weight | 470.5 g/mol |
| Molecular Formula | C19H34O13 |
| Exact Mass | 470.199941 g/mol |
| Enantiomer InChIKey | PNWVYPCCFRRLAT-KTFZXFCRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
METHYL-2,3,6-TRIDEOXY-4-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-ERYTHRO-HEXOPYRANOSIDE
CUSCUTIC-ACID-AA;(11S)-JALAPINOLIC-ACID-11-O-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-0-BETA-D-GLUCOPYRANOSYL-(1->2)-BETA-D-FUCOPYRANOSIDE
PORANIC-ACID-A;(11S)-HYDROXYTETRADECANOIC-ACID-11-O-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-O-BETA-D-GLUCOPYRANOSYL-(1->2)-BETA-D-QUINOVOPYRANOSIDE
PORANIC-ACID-B;(3S,11S)-DIHYDROXYTETRADECANOIC-ACID-11-O-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-O-BETA-D-GLUCOPYRANOSYL-(1->2)-BETA-D-QUINOVOPYRANOSIDE
METHYL-ALPHA-L-FUCOPYRANOSYL-(1->2)-BETA-D-GALACTOPYRANOSYL-(1->2)-XYLOPYRANOSIDE
METHYL-O-ALPHA-L-RHAMNOPYRANOSYL-0-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-ALPHA-D-GALACTOPYRANOSIDE
ALPHA-D-MANNOPYRANOSYL-(1->2)-ALPHA-D-MANNOPYRANOSYL-(1->3)-BETA-D-GALACTOPYRANOSE
OCTYL-2-O-[2-O-(ALPHA-D-MANNOPYRANOSYL)-ALPHA-D-MANNOPYRANOSYL]-ALPHA-D-ARABINOFURANOSIDE
Methyl .alpha.-D-glucopyranosyl-(1->2).alpha.-D-glucopyranosyl-(1->3).alpha.-D-glucopyranoside
SIBIRICAPHENONE;4'-O-[ALPHA-L-RHAMNOPYRANOSYL-(1->2)-BETA-D-GLUCOPYRANOSYL]-ACETOPHENONE
| Title | Journal or Book | Year |
|---|---|---|
| Molecular recognition XI. The synthesis of extensively deoxygenated derivatives of the H-type 2 human blood group determinant and their binding by an anti-H-type 2 monoclonal antibody and the lectin 1 of Ulexeuropaeus | Canadian Journal of Chemistry | 1992 |