Synthesis and cis-trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues (CROSBI ID 80424)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Čudić, Mare ; Horvat, Jaroslav ; Elofsson, Mikael ; Bergquist, Karl-Erik ; Kihlberg, Jan ; Horvat, Štefica
engleski
Synthesis and cis-trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues
The influence of a new peptoid residue on amide bond stereochemistry has been explored via the synthesis and NMR analysis of novel peptidomimetics related to the endogenous opioid pentapeptide Leu-enkephalin. The compounds studied include enkephalin analogues N-alkylated at either the second or both the second and the third amino acid residues with 6-deoxy-D-galactose moiety.
cis/trans ; isomerism ; opioid ; peptidomimetic ; glycation
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Podaci o izdanju
11
1998.
1789-1795
objavljeno
0300-922X
10.1039/A801472H