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Intramolecular rearrangement of the monosaccharide esters of an opioid pentapeptide: formation and identification of novel Amadori compounds related to fructose and tagatose


Horvat, Štefica; Roščić, Maja; Varga-Defterdarović, Lidija; Horvat, Jaroslav
Intramolecular rearrangement of the monosaccharide esters of an opioid pentapeptide: formation and identification of novel Amadori compounds related to fructose and tagatose // Journal of the Chemical Society. Perkin transactions. I, 5 (1998), 909-913 doi:10.1039/A707509J (međunarodna recenzija, članak, znanstveni)


Naslov
Intramolecular rearrangement of the monosaccharide esters of an opioid pentapeptide: formation and identification of novel Amadori compounds related to fructose and tagatose

Autori
Horvat, Štefica ; Roščić, Maja ; Varga-Defterdarović, Lidija ; Horvat, Jaroslav

Izvornik
Journal of the Chemical Society. Perkin transactions. I (0300-922X) 5 (1998); 909-913

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Monosaccharide ; ester ; rearrangement ; Amadori ; glycation

Sažetak
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.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
00980704

Ustanove
Institut "Ruđer Bošković", Zagreb

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


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