Cargando…
High-Temperature, Solid-Phase Reaction of α-Amino Groups in Peptides with Lactose and Glucose: An Alternative Mechanism Leading to an α-Ketoacyl Derivative
[Image: see text] The reaction of proteins with reducing sugars results in the formation of Amadori products, which involves the N-terminal group and/or ε-amino group of the lysine side chain. However, less attention has been given to the reactivity of the N-terminus of a peptide chain under similar...
Autores principales: | Kijewska, Monika, Zawadzka, Michalina, Stefanowicz, Piotr |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10103172/ https://www.ncbi.nlm.nih.gov/pubmed/37000938 http://dx.doi.org/10.1021/acs.jafc.3c00821 |
Ejemplares similares
-
Studies on the synthesis and stability of α-ketoacyl peptides
por: Sajapin, Johann, et al.
Publicado: (2020) -
Silver-mediated
Room Temperature Reactions for the
Synthesis of N-α-Ketoacyl Sulfoximines
and N-α,β-Unsaturated Acyl Sulfoximines
por: Gupta, Ria, et al.
Publicado: (2023) -
Site-selective solid phase synthesis of carbonylated peptides
por: Waliczek, Mateusz, et al.
Publicado: (2015) -
Selenium in Peptide Chemistry
por: Pehlivan, Özge, et al.
Publicado: (2023) -
One-pot efficient synthesis of N(α)-urethane-protected β- and γ-amino acids
por: Cal, Marta, et al.
Publicado: (2012)