Mixed Ligand Cu<sup>II</sup>N<sub>2</sub>O<sub>2</sub> Complexes: Biomimetic Synthesis, Activities in Vitro and Biological
Models, Theoretical Calculations
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Abstract
Three
new mixed ligand Cu<sup>II</sup>N<sub>2</sub>O<sub>2</sub> complexes,
namely, [Cu<sup>II</sup>(2-A-6-MBT)<sub>2</sub>(<i>m</i>-NB)<sub>2</sub>] (<b>1</b>), [Cu<sup>II</sup>(2-ABT)<sub>2</sub>(<i>m</i>-NB)<sub>2</sub>] (<b>2</b>), and
[Cu<sup>II</sup>(2-ABT)<sub>2</sub>(<i>o</i>-NB)<sub>2</sub>] (<b>3</b>), (2-A-6-MBT = 2-amino-6-methoxybenzothiazole, <i>m</i>-NB = <i>m</i>-nitrobenzoate, 2-ABT = 2-aminobenzothiazole,
and <i>o</i>-NB = <i>o</i>-nitrobenzoate), have
been prepared by the biomimetic synthesis strategy, and their structures
were determined by X-ray crystallography studies and spectral methods.
These complexes exhibited the effective superoxide dismutase (SOD)
activity and catecholase
activity. On the basis of the experimental data and computational
studies, the structure–activity relationship for these complexes
was investigated. The results reveal that electron-accepting abilities
of these complexes and coordination geometries have significant effects
on the SOD activity and catecholase activity. Then, we found that <b>1</b> and <b>2</b> exerted potent intracellular antioxidant
capacity in the model of H<sub>2</sub>O<sub>2</sub>-induced oxidative
stress based on HeLa cervical cancer cells, which were screened out
by the cytotoxicity assays of different kinds of cells. Furthermore, <b>1</b>–<b>3</b> showed the favorable biocompatibility
in two different biological models: <i>Saccharomyces cerevisiae</i> and human vascular endothelial cells. These biological experimental
data are indicative of the promising application potential of these
complexes in biology and pharmacology