A series of porphyrins with directly meso-attached "sucrose" moiety by the carbon C-6? of its "fructose" end was synthesized, and their physico-chemical and aggregation properties studied by spectroscopic (fluorescence, circular dichroism, resonance light scattering) techniques. The effect of selected porphyrins on tumor cells was also evaluated.
Porphyrins with directly meso -attached disaccharide moieties: Synthesis, self-assembly and cellular study
2016
Abstract
A series of porphyrins with directly meso-attached "sucrose" moiety by the carbon C-6? of its "fructose" end was synthesized, and their physico-chemical and aggregation properties studied by spectroscopic (fluorescence, circular dichroism, resonance light scattering) techniques. The effect of selected porphyrins on tumor cells was also evaluated.File in questo prodotto:
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