Synthesis and crystal structure of new dicopper(II) complexes having asymmetric N,Nâ²-bis(substituted)oxamides with DNA/protein binding ability: In vitro anticancer activity and molecular docking studies
Keywords: مجتمع Dicopper (II); Dicopper(II) complexes; Asymmetric N,Nâ²-bis(substituted)oxamides; Crystal structure; Molecular docking; DNA-binding; Protein BSA interaction; In vitro cytotoxicity;