2-(TRIMETHYLSILYL)-ETHYL-2,3,4-TRI-O-ACETYL-ALPHA-D-FUCOPYRANOSYL-(1->4)-2-ACETAMIDO-3,6-DI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 159ZG2qHkRd |
|---|---|
| InChI | InChI=1S/C29H47NO15Si/c1-14-23(40-17(4)33)26(42-19(6)35)27(43-20(7)36)29(39-14)45-24-21(13-38-16(3)32)44-28(37-11-12-46(8,9)10)22(30-15(2)31)25(24)41-18(5)34/h14,21-29H,11-13H2,1-10H3,(H,30,31)/t14-,21-,22-,23+,24-,25-,26+,27-,28-,29-/m1/s1 |
| InChIKey | YIGGPZWWYPRXJP-FSSLVCKKSA-N |
| Mol Weight | 677.8 g/mol |
| Molecular Formula | C29H47NO15Si |
| Exact Mass | 677.271496 g/mol |
| Enantiomer InChIKey | YIGGPZWWYPRXJP-LKQMVCJPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL-(1->4)-2-ACETAMIDO-1,3,6-TRI-O-ACETYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSE
5-AZIDO-3-OXAPENTYL_(2,3-DI-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-(1->4)-2-ACETAMIDO-3-O-ACETYL-6-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
2-(TRIMETHYLSILYL)-ETHYL-2,3,4-TRI-O-ACETYL-ALPHA-D-FUCOPYRANOSYL-(1->3)-2-ACETAMIDO-4,6-DI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE
#B5;1,13-BIS-[4-[2-ACETAMIDO-3,6-DI-O-ACETYL-2-DEOXY-4-O-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-BETA-D-GLUCOPYRANOSYL-OXYMETHYL]
Alanine, 3-[[2-acetamido-4-O-(2-acetamido-2-deoxy-.beta.-D-glucopyranosyl)-2-deoxy-.beta.-D-glucopyranosyl]oxy]-N-carboxy-, N-benzyl methyl ester, pentaacetate (ester), L-
2-ACETAMIDO-3,6-DI-O-BENZOYL-2-DEOXY-4-O-(2,3,5,6-TETRA-O-BENZOYL-1-BETA-D-GALACTOFURANOSYL)-ALPHA/BETA-D-GLUCOPYRANOSE
2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL-(1->4)-1,3,6-TRI-O-ACETYL-2-DEOXY-2-TRIFLUOROACETAMIDO-ALPHA-D-GLUCOPYRANOSE
ALPHA-CHITOBIOSE, OCTAACETATE
3-O-ACETYL-2,4-DI-O-(3,4,6-TRI-O-ACETYL-2-N-ALLYLOXYCARBONYLAMINO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-1,6-ANHYDRO-BETA-D-MANNOPYRANOSE
ZPBUJDPIHBCGOU-QOOJXHJWSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis, Inhibitory Effects on Nitric Oxide and Structure-Activity Relationships of a Glycosphingolipid from the Marine Sponge Aplysinella rhax and Its Analogues | Molecules | 2011 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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