New Coumarin−Thiosemicarbazone Based Zn(II), Ni(II) and Co(II) Metal Complexes: Investigation of Cholinesterase, α‐Amylase, and α‐Glucosidase Enzyme Activities, and Molecular Docking Studies
Esra Nurten Yer Çelik, Mücahit Özdemir, Baybars Köksoy, Tuğba Taşkın‐Tok, Parham Taslımı, Nastaran Sadeghian, Bahattin Yalçın
Abstract
Abstract New coumarin−thiosemicarbazone compounds and their zinc(II), nickel(II), and copper(II) metal complexes were synthesized and characterized. The inhibitory activities of these new coumarin−thiosemicarbazone‐based metal complexes against butyrylcholinesterase (BChE), acetylcholinesterase (AChE), α‐amylase, and α‐glucosidase were determined. The results showed that all the synthetic compounds exhibited potent inhibitory activities against all targets, as compared to the standard inhibitors, as revealed by the half‐maximal inhibitory concentration (IC 50 ) and the inhibitory constant ( K i) values. The K i values of the new complexes for BChE, AChE, and α‐glucosidase enzymes were obtained in the ranges of 115.84–276.07, 31.68–117.08, and 22.56–47.82 μM, respectively. Moreover, molecular docking studies provided support for the conclusion that coumarin−thiosemicarbazone zinc(II) (−102.34; −10.41 kcal/mol) and coumarin−thiosemicarbazone cobalt(II) complexes (−25.46; −9.49 kcal/mol) act as dual inhibitors for both AChE and α‐amylase species. Furthermore, coumarin−thiosemicarbazone cobalt(II) (−39.46 kcal/mol) and coumarin−thiosemicarbazone nickel(II) complexes (−39.41 kcal/mol) demonstrated potential as inhibitors of α‐glucosidase. Of all the compounds studied, bis‐3‐benzyl‐7,8‐dimethoxycoumarin−thiosemicarbazonato zinc(II) is the most potent drug against AChE.