Design, synthesis and immunostimulating activity of mannosylated desmuramyl peptides (CROSBI ID 681037)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | domaća recenzija
Podaci o odgovornosti
Ribić, Rosana ; Tomić, Srđanka
engleski
Design, synthesis and immunostimulating activity of mannosylated desmuramyl peptides
Muramyl dipeptide (MDP), N-acetylmuramyl-L-alanyl- D-isoglutamine, is the smallest structural unit of bacterial peptidoglycan responsible for eliciting of immune response. It acts as a pathogen- associated molecular pattern and activates nucleotide-binding oligomerization domain- containing protein 2 (NOD2). [1] Desmuramyl peptides possess L-Ala-D-isoGln pharmacophore which is essential for the immunostimulatory properties. We have designed mannosylated desmuramly peptides (Figure 1) using multiple pathogen recognition receptor activation approach. [2] Mannose receptors are C-type lectin receptors expressed on immunocompetent cells and represent additional pattern recognition target for affecting immune system. [3]Adamantane was introduced in order to increase the lipophilicity of L-Ala-D-isoGln peptide and to facilitate the anchoring of the compound to the lipid bilayer.
adamantane, desmuramyl peptides, mannose, immunostimulating activity
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Podaci o prilogu
11-11.
2019.
objavljeno
Podaci o matičnoj publikaciji
Peptide Chemistry Day : book of abstracts
Frkanec, Ruža ; Namjesnik, Danijel
Zagreb: Sveučilište u Zagrebu, Hrvatsko kemijsko društvo
978-953-8250-03-3
Podaci o skupu
Peptide Chemistry Day
predavanje
19.09.2019-19.09.2019
Zagreb, Hrvatska