Chiral ligand induced geometrical type of isomerism in Schiff-base Copper(II) complexes with urease inhibitory activities

• Published in: Inorganica Chimica Acta 2023-12, Vol.558, p.121707, Article 121707
• Main Authors: Valentová, Jindra, Lintnerová, Lucia, Sláviková, Barbora, Baran, Peter
• Format: Article
• Language: English
• Subjects: 2-Formylphenoxyacetic acid; Amino acids; Antiurease activity; Copper(II); Schiff-base complexes; Stereoisomerism
• ISSN: 0020-1693; 1873-3255
• DOI: 10.1016/j.ica.2023.121707

[Display omitted] •Novel copper(II) complexes with Schiff-base ligands derived from 2-formylphenoxyacetic acid (fphaa) and DL-α-alanine, β-alanine, taurine, and γ-aminobutanoic acid.•New type of stereoisomerism arising from a different molecular arrangement of the apical ligand in square-pyramidal or square-bipyramidal complexes with respect to the conformation of a multidentate equatorial ligand.•Complexes with excellent inhibitory properties against jack bean urease. Enzyme urease plays a significant role in the pathogenesis of several diseases and has practical implications in fields such as agriculture and chemical analysis. Four new copper(II) complexes with Schiff-base ligands obtained from the template synthesis of 2-formylphenoxyacetic acid (fphaa) with DL-α-alanine, β-alanine, taurine, and γ-aminobutanoic acid were synthesized in addition to the previously described [Cu(fphaa-gly)(H2O)] derived from glycine. Crystallographic study of two solvates of Cu(fphaa-α-ala)⋅S (where S = H2O or DMSO) showed similarity of these complexes with the one derived from glycine. In addition, an E/Z isomerism originating in a different molecular arrangement of the aqua ligand with respect to the methyl group from alanine was described in the aqua complex. Only Z isomers were found in the complex with DMSO. All prepared complexes showed excellent inhibitory properties against jack bean urease (IC50 = 0.53–0.71 μmol/dm3), considerably better than the standard inhibitor acetohydroxamic acid (IC50 = 185 μmol/dm3).