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2-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-BETA-D-GLUCOPYRANOSE

Compound with spectra: 1 NMR

2-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-BETA-D-GLUCOPYRANOSE
SpectraBase Compound ID FvQvVQKvGpR
InChI InChI=1S/C50H60N6O15/c1-30(2)22-36(47(64)56-42-44(61)43(60)39(27-57)71-48(42)65)54-46(63)38(23-31-12-6-3-7-13-31)53-41(59)26-51-40(58)25-52-45(62)37(55-49(66)68-28-33-14-8-4-9-15-33)24-32-18-20-35(21-19-32)70-50(67)69-29-34-16-10-5-11-17-34/h3-21,30,36-39,42-44,48,57,60-61,65H,22-29H2,1-2H3,(H,51,58)(H,52,62)(H,53,59)(H,54,63)(H,55,66)(H,56,64)/t36-,37-,38-,39-,42-,43-,44-,48-/m0/s1
InChIKey NQSRFENIDCYQJM-BLGDOCRVSA-N
Mol Weight 985.1 g/mol
Molecular Formula C50H60N6O15
Exact Mass 984.411665 g/mol
Enantiomer InChIKey NQSRFENIDCYQJM-DRNVGVKASA-N

View Spectrum of 2-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-BETA-D-GLUCOPYRANOSE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
2-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCYLAMINO]-2-DEOXY-ALPHA-D-GLUCOPYRANOSE
N-[N,O-BIS-[(BENZOYLOXY)-CARBONYL]-L-TRIOSYLGLYCYLGLYCYL-L-PHLENYLALANYL-L-LEUCYL]-BETA-D-GLUCOPYRANOSYLAMINE
L-TYROSYL-N-(6-DEOXY-ALPHA-D-GALACTOS-6-YL)-GLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCINE
L-TYROSYL-N-(6-DEOXY-BETA-D-GALACTOS-6-YL)-GLYCYLGLYCYL-L-PHENYLALANYL-L-LEUCINE
H-TYR-SAA2-PHE-LEU-OME.HCL
BOC-GLU-(O-TERT.-BUTYL)-TYR-[SO2C6H3(3-OH)(4-COOH)]-LEU-OBZL
TAURAMAMIDE_ETHYLESTER
3-[2-[2-[2-[[2-[[1-[2-[[2-[[2-[[2-acetamido-3-(4-hydroxyphenyl)propanoyl]amino]-3-hydroxy-propanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-phenyl-propanoyl]pyrrolidine-2-carbonyl]amino]-3-hydroxy-propanoyl]amino]-3-methyl-butanoyl]oxyethoxy]ethoxy]p
ALPHA-DISACCHARIDE (FROM SHIGELLA BOYDII, TYPE 9)
BETA-DISACCHARIDE (FROM SHIGELLA BOYDII, TYPE 9)
Title Journal or Book Year
[5-Leucin]enkephalin-Related Glycoconjugates: Structurally Novel Agents Effective against HIV-1 Helvetica Chimica Acta 1991
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