Nickel(II), copper(II) and zinc(II) complexes of N2O2 tetradentate Schiff base ligands strongly interact with B-DNA, usually by groove-binding and/or by intercalation [1]. It has been also shown that the presence of aromatic substituents on the N,N’ bridge make them suitable G-quadruplex binders [2]. In this context, we have recently investigated the binding toward duplex and G-quadruplex DNA of nickel(II), copper(II) and zinc(II) complexes of N,N’-bis-5-(triethyl ammonium methyl)-salicylidene-2,3-naphthalendiiminato) (see Figure), by spectroscopic and computational methods [3,4]. The compounds show also biological activity against human cancer cell lines. Different substituents are presently considered on the N,N’-bridge, in order to increase their selectivity towards telomeric and oncogene promoter DNA sequences, rather than toward B-DNA, and to target G-quadruplexes on the grooves rather than by π-π stacking.
Terenzi, A., Bonsignore, R., Spinello, A., Almerico, A.M., Lauria, A., Barone, G. (2014). DNA-Binding of NiII, CuII and ZnII Complexes of Salen Derivatives. In Third Whole Action Meeting of the COST Action CM1105. Zurigo.
DNA-Binding of NiII, CuII and ZnII Complexes of Salen Derivatives
TERENZI, Alessio;Bonsignore, Riccardo;SPINELLO, Angelo;ALMERICO, Anna Maria;LAURIA, Antonino;BARONE, Giampaolo
2014-01-01
Abstract
Nickel(II), copper(II) and zinc(II) complexes of N2O2 tetradentate Schiff base ligands strongly interact with B-DNA, usually by groove-binding and/or by intercalation [1]. It has been also shown that the presence of aromatic substituents on the N,N’ bridge make them suitable G-quadruplex binders [2]. In this context, we have recently investigated the binding toward duplex and G-quadruplex DNA of nickel(II), copper(II) and zinc(II) complexes of N,N’-bis-5-(triethyl ammonium methyl)-salicylidene-2,3-naphthalendiiminato) (see Figure), by spectroscopic and computational methods [3,4]. The compounds show also biological activity against human cancer cell lines. Different substituents are presently considered on the N,N’-bridge, in order to increase their selectivity towards telomeric and oncogene promoter DNA sequences, rather than toward B-DNA, and to target G-quadruplexes on the grooves rather than by π-π stacking.File | Dimensione | Formato | |
---|---|---|---|
cost.pdf
Solo gestori archvio
Dimensione
1.64 MB
Formato
Adobe PDF
|
1.64 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.