Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1294, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2023.136348
Keywords
DFT; FT-IR; MESP; ADME; Protein-ligand docking
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In this study, a Schiff base compound was successfully synthesized and characterized, and its properties were comprehensively investigated using computational methods. The results of vibrational analysis and theoretical calculations were in good agreement with experimental data. Furthermore, the compound showed potential pharmaceutical properties.
The Schiff base compound1-(3-((4-(diethylamino)-2-hydroxybenzylidene)amino)phenyl)ethan-1-one (34D2HA) has been synthesized and characterized by FT-IR, XRD techniques. The title compound was optimized. From the calculated perspective, the title compound's Natural bond orbital, Molecular Electrostatic Potential, Electron Localization Function, Localized-Orbital Locator, Frontier Molecular Orbital, Mulliken charges and Fukui function properties were also examined. The vibrational analysis of 34D2HA were investigated by means of computational calculations. The intensity of vibrational bands and the fundamental frequencies were evaluated by the standard B3LYP method on the basis set of 6-311G(d,p) combination with diffusion function + + are done by density functional theory (DFT). In addition to PED, VEDA was utilized to predict vibrational assignment. The absorptions were analyzed theoretically using UV-Vis spectra with different solvents. The experimental and computed bond parameters exhibit a strong agreement. The infrared frequency calculations lead overall agreement with observed spectral patterns. Beside, ADME studies have been carried out and this compound satisfies with Lipinski's rule of five. The results of protein- ligand docking using the Auto Dock method with various proteins suggest that the molecule has pharmaceutical properties against receptors.
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