Intramolecular rearrangement of the monosaccharide esters of an opioid pentapeptide: formation and identification of novel Amadori compounds related to fructose and tagatose (CROSBI ID 80423)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Horvat, Štefica ; Roščić, Maja ; Varga-Defterdarović, Lidija ; Horvat, Jaroslav
engleski
Intramolecular rearrangement of the monosaccharide esters of an opioid pentapeptide: formation and identification of novel Amadori compounds related to fructose and tagatose
Intramolecular rearrangements leading to Amadori adducts from monosaccharide esters in which either glucose, mannose or galactose is linked through its C-6 hydroxy groups to the C-terminal group of the endogenous opioid pentapeptide leucine-enkephalin are reported.
monosaccharide ; ester ; rearrangement ; Amadori ; glycation
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Podaci o izdanju
5
1998.
909-913
objavljeno
0300-922X
10.1039/A707509J