2-[N-[(TERT.-BUTYLOXY)-CARBONYL]-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-ALPHA-D-GLUCOPYRANOSE
Compound with spectra: 1 NMR
![2-[N-[(TERT.-BUTYLOXY)-CARBONYL]-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-ALPHA-D-GLUCOPYRANOSE](/api/compound/Lk4sFT1IR66.png?ph=true&h=300&w=458 "2-[N-[(TERT.-BUTYLOXY)-CARBONYL]-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-ALPHA-D-GLUCOPYRANOSE")
| SpectraBase Compound ID | Lk4sFT1IR66 |
|---|---|
| InChI | InChI=1S/C26H41N3O9/c1-14(2)11-16(23(34)29-19-21(32)20(31)18(13-30)37-24(19)35)27-22(33)17(12-15-9-7-6-8-10-15)28-25(36)38-26(3,4)5/h6-10,14,16-21,24,30-32,35H,11-13H2,1-5H3,(H,27,33)(H,28,36)(H,29,34)/t16-,17-,18-,19-,20-,21-,24-/m0/s1 |
| InChIKey | WMVSOVXHMFWBFY-RGEBKRNOSA-N |
| Mol Weight | 539.6 g/mol |
| Molecular Formula | C26H41N3O9 |
| Exact Mass | 539.28428 g/mol |
| Enantiomer InChIKey | WMVSOVXHMFWBFY-JZUHGBKFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
6-O-(L-TYROSILGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYL)-ALPHA-D-MANNOPYRANOSE
6-O-(L-TYROSILGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYL)-BETA-D-MANOPYRANOSE
BOC-GLU-(O-TERT.-BUTYL)-TYR-[SO2C6H4(4-COOH)]-LEU-OBZL
PYLORICIDIN-A;3-[5-(VALYL-VALYL-LEUCYL)-AMINO-2,3,4,6-TETRAHYDROXYHEXANOYL]-AMINO-3-PHENYLPROPIONIC-ACID
3-O-PALMITOYL-6-O-(BENZYLOXY-METHYL)-2-DEOXY-2-PALMITAMIDO-ALPHA-D-GLUCOPYRANOSIDE
CONOIDEOCRELLIDE_A
CHEVALIERIN_C
2-BENZAMIDO-3-0-(L-1-CARBOXYPROPYL)-2-DEOXY-D-GLUCOSE
N-[(3R,4R,5S,6R)-4,5-dihydroxy-2-[(5-keto-3-methyl-2H-furan-2-yl)oxy]-6-methylol-tetrahydropyran-3-yl]acetamide
beta-D-glucopyranoside, 2,5-dimethylphenyl 2-(acetylamino)-2-deoxy-
| Title | Journal or Book | Year |
|---|---|---|
| [5-Leucin]enkephalin-Related Glycoconjugates: Structurally Novel Agents Effective against HIV-1 | Helvetica Chimica Acta | 1991 |