(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-2-methylol-6-[4-(4-nitrophenyl)butoxy]tetrahydropyran-4-yl]oxy-6-methyl-tetrahydropyran-3,4,5-triol
Compound with spectra: 1 NMR
![(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-2-methylol-6-[4-(4-nitrophenyl)butoxy]tetrahydropyran-4-yl]oxy-6-methyl-tetrahydropyran-3,4,5-triol](/api/compound/C7MLaKg4rfG.png?ph=true&h=300&w=458 "(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-3,5-dihydroxy-2-methylol-6-[4-(4-nitrophenyl)butoxy]tetrahydropyran-4-yl]oxy-6-methyl-tetrahydropyran-3,4,5-triol")
| SpectraBase Compound ID | C7MLaKg4rfG |
|---|---|
| InChI | InChI=1S/C22H33NO12/c1-11-15(25)17(27)18(28)22(33-11)35-20-16(26)14(10-24)34-21(19(20)29)32-9-3-2-4-12-5-7-13(8-6-12)23(30)31/h5-8,11,14-22,24-29H,2-4,9-10H2,1H3/t11-,14+,15-,16-,17+,18+,19+,20-,21+,22-/m0/s1 |
| InChIKey | GFCMLUJVHZKTGT-VZWSXCNISA-N |
| Mol Weight | 503.5 g/mol |
| Molecular Formula | C22H33NO12 |
| Exact Mass | 503.200275 g/mol |
| Enantiomer InChIKey | GFCMLUJVHZKTGT-SQUSMOATSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
2-PHENYLETHYL-3-O-(6-DEOXY-ALPHA-L-MANNOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE
LIGUROBUSTOSIDE-A;GERANIOL-(3'-O-ALPHA-L-RHAMNOPYRANOSYL-BETA-D-GLUCOPYRANOSIDE)
(2-ACRYLAMIDOETHYL)-3-O-(ALPHA-D-GLUCOPYRANOSYL)-ALPHA-D-MANNOPYRANOSIDE
ENTADAMIDE-A-BETA-D-GLUCOPYRANOSYL-(1->3)-BETA-D-GLUCOPYRANOSIDE
RHODIOLOSIDE-C;(2-E,4-R)-4-HYDROXY-3,7-DIMETHYL-2,6-OCTADIENYL-BETA-D-GLUCOPYRANOSYL-(1->3)-BETA-D-GLUCOPYRANOSIDE
PHENYL-BETA-D-GALACTOPYRANOSYL-(1->3)-BETA-D-GLUCOPYRANOSIDE
(2-E,6-Z)-2,6-DIMETHYL-8-[(O-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-ALPHA-L-RHAMNOPYRANOSYL)-OXY]-OCTADIEN-1-YL-ALPHA-L-RHAMNOPYRANOSIDE
ALPHA-D-GLUCURONOPYRANOSYL-(1->3)-ALPHA-L-GALACTOSE
(-)-CENTROLOBOL-DIGLYCOSIDE;(3R)-1,7-BIS-(4-DIHYDROXYPHENYL)-3-HEPTANOL-3-O-BETA-D-GLUCOPYRANOSYL-(1->3)-BETA-D-XYLOPYRANOSIDE
3-AMINOPROPYL-2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Chemoenzymatic synthesis of the Salmonella group E1 core trisaccharide using a recombinant β-(1→4)-mannosyltransferase | Carbohydrate Research | 1999 |