Identification of new biologically active synthetic molecules: comparative experimental and theoretical studies on the structure-antioxidant activity relationship of cyclic 1,3-ketoamides

• Published in: Journal of molecular modeling 2021-04, Vol.27 (4), p.109-109, Article 109
• Main Authors: Kerbadou, Riad Mustapha, Hadjadj Aoul, Ratiba, Benmaati, Aouicha, Taleb, Assya, Hacini, Salih, Habib Zahmani, Hadjira
• Format: Article
• Language: English
• Subjects: Affinity; Antioxidants; Characterization and Evaluation of Materials; Chemistry; Chemistry and Materials Science; Computer Appl. in Life Sciences; Computer Applications in Chemistry; Density functional theory; Electron transfer; Enthalpy; Ethanol; Free radicals; Hydrogen bonds; Ionization potentials; Molecular Medicine; Original Paper; Oxidation; Selectivity; Theoretical and Computational Chemistry; Vapor phases
• ISSN: 1610-2940; 0948-5023
• DOI: 10.1007/s00894-021-04705-4

Antioxidant agent is a chemical that prevents the oxidation of other chemical substances. Its use is the most effective means of protecting the organism by neutralizing the harmful effects of free radicals caused by oxidative stress. In the present work, a series of β-ketoamides containing a variety of monosubstituted amide groups were synthesized and tested as antioxidant agents. In order to establish a possible structure-antioxidant activity relationship, we are presenting a systematic theoretical study of these molecules with the aim of clarifying the active sites. In particular, we discuss the selectivity resulting from the choice of a free radical/antioxidant system. The theoretical study of these molecules was carried out using density functional theory (DFT) calculations at the B3LYP/6-311G (d,p) level of theory. In order to shed light on the antioxidant properties of β-ketoamides, O–H bond dissociation enthalpies (BDEs), ionization potentials (IPs), electron affinities (EAs), proton affinities (PAs), and electron transfer enthalpies (ETEs) are performed in the gas phase and in ethanol. The results obtained show that the HAT mechanism is thermodynamically more favored in the gas phase, while the SPLET is preferred in the polar solvent.