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izvor podataka: crosbi

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

Čudić, Mare ; Horvat, Jaroslav ; Elofsson, Mikael ; Bergquist, Karl-Erik ; Kihlberg, Jan ; Horvat, Štefica Synthesis and cis-trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues // Journal of the Chemical Society. Perkin transactions. I, 11 (1998), 1789-1795. doi: 10.1039/A801472H

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

Povezanost rada

Kemija

Poveznice
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