Synthesis of glycosylated cationic porphyrins as potential agents in photodynamic therapy

Autor: Driaf, Khalid, Granet, Robert, krausz, Pierre, Kaouadji, Mourad, Verneuil, Bernard, Thomasson, François, Chulia, Albert José, Spiro, Marenglen, Biais, Jean-Claude, Bolbach, Gérard
Zdroj: Canadian Journal of Chemistry; August 1996, Vol. 74 Issue: 8 p1550-1563, 14p
Abstrakt: Trisalkylpyridinium porphyrins substituted by one glycosyl (glucosyl, maltosyl, and lactosyl) moiety have been prepared in acceptable yields. These glycosylated cationic porphyrins have been synthesized from pyrrole condensed with 4-pyridinecarboxaldehyde, and suitable ortho- or paraperacetylglycosyloxybenzaldehyde derivatives in refluxing propionic acid –Ac2O followed by action of alkyliodide in DMF. Deprotection of the glycosylated moieties led to a new class of representative glycosylated porphyrins. Keywords: porphyrins, cationic, glycosylated; phototherapy, cancer.
Databáze: Supplemental Index