New copper-based complexes with quinoxaline N1,N4-dioxide derivatives, potential antitumoral agents

作者: Carolina Urquiola , Dinorah Gambino , Mauricio Cabrera , María Laura Lavaggi , Hugo Cerecetto

DOI: 10.1016/J.JINORGBIO.2007.07.028

关键词: SubstituentChemistryV79 cellsCytotoxic T cellStereochemistryMedicinal chemistryCopperSuperoxideSelectivityQuinoxalineMetal

摘要: Abstract Taking into account our previous studies on cytotoxic metal compounds, new copper complexes with 3-aminoquinoxaline-2-carbonitrile N 1 , 4 -dioxide derivatives as ligands were synthesized and characterized by different spectroscopic methods. The hypoxic selective cytotoxicity towards V79 cells the superoxide dismutase-like activity of determined related to physicochemical properties compounds. In particular, copper(II) complex 3-amino-6-chloro-7-fluoroquinoxaline-2-carbonitrile showed selectivity in hypoxia being most lipophilic compound series. On contrary, was but not that 3-amino-7-chloro-6-methoxy-quinoxaline-2-carbonitrile neither oxia nor assayed conditions. σ m Hammett substituent electronic descriptor effect conditions SOD-like correlated normoxia.

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