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 / Malachowska, M; Sperduto, C; Darmostuk, M; Monti, D; Venanzi, M; Mancini, G; D'Acunto, Cw; Králová, J; Ruml, T; Wimmer, Z; Drašar, Pb. - In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES. - ISSN 1088-4246. - 20:7(2016), pp. 773-784. [10.1142/S1088424616500875]

Porphyrins with directly meso -attached disaccharide moieties: Synthesis, self-assembly and cellular study

Monti D;
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.
2016
01 Pubblicazione su rivista::01a Articolo in rivista
Porphyrins with directly meso -attached disaccharide moieties: Synthesis, self-assembly and cellular study / Malachowska, M; Sperduto, C; Darmostuk, M; Monti, D; Venanzi, M; Mancini, G; D'Acunto, Cw; Králová, J; Ruml, T; Wimmer, Z; Drašar, Pb. - In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES. - ISSN 1088-4246. - 20:7(2016), pp. 773-784. [10.1142/S1088424616500875]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1468876
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