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Neoglycolipids in anticancer treatments

The vaccine was incorporated into phospholipid-based liposomes prior to administration the mice that were immunized with the liposome preparations elicited IgM and IgG antibodies against the Tn antigen. [Pg.373]

Synthesis of the vaccine candidate 21 was achieved in high yield by condensation of the C-terminal carboxylic acid of lipopolypeptide (24) and the amine of spacer-containing Tn antigen (25), followed by deprotection of the amino acid side chain. The fully protected lipopolypeptide 24 was produced by coupling the lipid S-[2,3-bis(hexadecanoyloxy)-propyl]-7V-Fmoc-Cys (Pam2FmocCys (3)) to the N-terminal amine of the resin-bound peptide (22), and by subsequent linking of the hexadecanoic add to the free amine of the resin-bound lipopolypeptide (Fig. 14). [Pg.373]


See other pages where Neoglycolipids in anticancer treatments is mentioned: [Pg.353]    [Pg.372]   
See also in sourсe #XX -- [ Pg.372 ]




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