Synthesis of novel β-lactams: Antioxidant activity, acetylcholinesterase inhibition and computational studies

被引:50
作者
Fahim, Asmaa M. [1 ]
Farag, Ahmad M. [2 ]
Mermer, Arif [3 ]
Bayrak, Hacer [4 ]
Sirin, Yakup [5 ]
机构
[1] Natl Res Ctr Dokki, Green Chem Dept, POB 12622, Cairo, Egypt
[2] Cairo Univ, Dept Chem, Fac Sci, Giza 12613, Egypt
[3] Univ Hlth Sci Istanbul, Dept Biotechnol, TR-34660 Istanbul, Turkey
[4] Karadeniz Tech Univ, Dept Chem & Chem Proc Technol, TR-61080 Trabzon, Turkey
[5] Karadeniz Tech Univ, Dept Chem, TR-61080 Trabzon, Turkey
关键词
beta-Lactams; Antioxidant activities; Acetylcholinesterase inhibition; Molecular docking; Computational studies; DENSITY-FUNCTIONAL THEORY; BIOLOGICAL EVALUATION; EQUILIBRIUM GEOMETRIES; MOLECULAR DOCKING; REACTIVITY; DFT; OPTIMIZATION; DERIVATIVES; MECHANISMS; SPECTRA;
D O I
10.1016/j.molstruc.2021.130092
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A convenient synthesis of some novel beta-lactam derivatives with interesting pharmacological activities was described. Some of the synthesized compounds exhibited excellent antioxidant activity and showed acetylcholinesterase inhibition. Theoretical studies were carried out on the most potent compounds 5a and 5b to compare their potential interaction with crystal structure of recombinant human acetyl cholinesterase in complex with Donepezil (PDB ID: 4EY7) and binary complex of native hAChE with Donepezil (PDBID:6O4W). The comprehensive theoretical and experimental mechanical studies of compounds 5b were compatible with its FT-IR, H-1 NMR,C-13 NMR and Mass spectral data. The optimized molecular structure and the harmonic vibrational frequencies were examined DFT/B3LYP/6-31G(d) and Hartree-Fock HF/6-31G(d) energies and the difference in bond length and energies between compounds 5a and 5b was confirmed via theoretical studies. (C) 2021 Elsevier B.V. All rights reserved.
引用
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页数:16
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