Senocak_2021_J.Biochem.Mol.Toxicol__e22969

Schiff bases are compounds that have gained importance in the paint industry due to their colorful nature and in the field of chemistry and biochemistry due to their biological activities. Various biological applications of Schiff bases, such as antitumor, antifungal, antibacterial, antioxidant, antituberculosis, and anthelmintic, have been widely studied. Within the scope of the study, 5-bromo-2-hydroxybenzaldehyde and amino acid methyl esters (isoleucine, phenylalanine, and methionine) and amino acid Schiff bases were synthesized first. The synthesis of the new Zn(II) complexes of these Schiff bases was carried out by the reaction of synthesized Schiff bases and Zn(OAc)(2) .2H(2) O. The structures of the synthesized complexes were elucidated using elemental analysis, Fourier transform infrared, nuclear magnetic resonance, UV-visible, and thermal analysis spectroscopy techniques. These synthesized salts were found to be effective inhibitor compounds for the alpha-glycosidase, and acetylcholinesterase enzyme with Ki values in the range of 30.50 +/- 3.82-38.17 +/- 6.26 microM for alpha-glycosidase, 3.68 +/- 0.54-10.27 +/- 1.68 microM for butyrylcholinesterase, and 6.26 +/- 0.83-15.73 +/- 4.73 microM for acetylcholinesterase, respectively.