Pregled bibliografske jedinice broj: 12659
Synthesis and cis-trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues
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 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 12659 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and cis-trans isomerism in novel Leu-enkephalin-related peptidomimetics containing N-glycated glycine residues
Autori
Čudić, Mare ; Horvat, Jaroslav ; Elofsson, Mikael ; Bergquist, Karl-Erik ; Kihlberg, Jan ; Horvat, Štefica
Izvornik
Journal of the Chemical Society. Perkin transactions. I (0300-922X) 11
(1998);
1789-1795
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
cis/trans ; isomerism ; opioid ; peptidomimetic ; glycation
Sažetak
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.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
