3-O-(BETA-D-GALACTOPYRANOSYL)-N-(TETRADECANOYL)-L-SERINE-SODIUM-SALT;I-GAL-SER-[CO2NA]-[C14]
Compound with spectra: 1 NMR
![3-O-(BETA-D-GALACTOPYRANOSYL)-N-(TETRADECANOYL)-L-SERINE-SODIUM-SALT;I-GAL-SER-[CO2NA]-[C14]](/api/compound/GEFZfO5U9Ri.png?ph=true&h=300&w=458 "3-O-(BETA-D-GALACTOPYRANOSYL)-N-(TETRADECANOYL)-L-SERINE-SODIUM-SALT;I-GAL-SER-[CO2NA]-[C14]")
| SpectraBase Compound ID | GEFZfO5U9Ri |
|---|---|
| InChI | InChI=1S/C23H43NO9.Na/c1-2-3-4-5-6-7-8-9-10-11-12-13-18(26)24-16(22(30)31)15-32-23-21(29)20(28)19(27)17(14-25)33-23;/h16-17,19-21,23,25,27-29H,2-15H2,1H3,(H,24,26)(H,30,31);/q;+1/p-1/t16?,17-,19+,20+,21-,23-;/m0./s1 |
| InChIKey | LTELIPWTBUFVJO-VUFINAHXSA-M |
| Mol Weight | 499.6 g/mol |
| Molecular Formula | C23H42NNaO9 |
| Exact Mass | 499.275726 g/mol |
| Parent InChIKey | OWCLTFSGQKRODN-SQLNJODVSA-M |
| Enantiomer InChIKey | LTELIPWTBUFVJO-XMJPMYEQSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:CD3OD |
N-Allyloxycarbonyl-B-galactosyl-L-serine
N-Allyloxycarbonyl-B-galactosyl-L-serine methyl ester
1,4-DIDEOXY-1,4-IMINO-(5-O-BETA-D-GLUCOPYRANOSYL)-D-ARABINITOL
N-[TRIS-(ALPHA-D-MANNOPYRANOSYL-OXYMETHYL)]-METHYL-(5-METHOXYCARBONYL)-PENTANOAMIDE
N-[TRIS-(ALPHA-D-MANNOPYRANOSYL-OXYMETHYL)]-METHYL-5-CARBOXYPENTANOAMIDE
1-O-BEHENOYL-2-O-LAUROYL-3-O-BETA-D-GALACTOPYRANOSYL-RAC-GLYCEROL;DIASTEREOISOMER-1-AND-2
(2-S)-1,2-DIPALMITOYL-3-O-BETA-D-GALACTOPYRANOSYL-GLYCEROL
1,2-O-DILAUROYL-3-O-BETA-D-GLUCOPYRANOSYL-RAC-GLYCEROL;DIASTEREOISOMER-1-AND-2
1,2-O-DIBEHENOYL-3-O-BETA-D-GLUCOPYRANOSYL-RAC-GLYCEROL;DIASTEREOISOMER-1
1,2-DI-O-PALMITOYL-3-O-(BETA-D-GALACTOPYRANOSYL)-RAC-GLYCEROL
| Title | Journal or Book | Year |
|---|---|---|
| Amphiphilic Anionic Analogues of Galactosylceramide: Synthesis, Anti-HIV-1 Activity, and gp120 Binding | Journal of Medicinal Chemistry | 2001 |