FTIR, NMR and UV-Visible Spectral Investigations, Theoretical Calculations, Topological Analysis, Chemical Stablity, and Molecular Docking Study on Novel Bioactive Compound: The 5-(5-Nitro Furan-2-Ylmethylen), 3-N-(2-Methoxy Phenyl),2-N′- (2-Methoxyphenyl) Imino Thiazolidin-4-One

• Published in: Polycyclic aromatic compounds Vol. 43; no. 5; pp. 4685 - 4706
• Main Authors: Rahmani, Rachida, Perveen, Fouzia, Benhalima, Nadia, Djafri, Ahmed, Khelloul, Nawel, Chouaih, Abdelkader, Djafri, Ayada, Kanoun, Mohammed Benali, Goumri-Said, Souraya
• Format: Journal Article
• Language: English
• Published: Philadelphia Taylor & Francis 28-05-2023; Taylor & Francis Ltd
• Subjects: Acetylcholinesterase; Binding sites; Bioactive compounds; Biological activity; Chemical bonds; Chemical reactions; Chloroform; Continuum modeling; Density distribution; Density functional theory; Electron density; Electron transitions; Electrons; Electrostatic properties; Fourier transforms; furan; Hydrogen bonds; Molecular docking; Molecular orbitals; Molecular properties; NMR; NMR spectroscopy; Nuclear magnetic resonance; RDG/AIM; Spectroscopy; thiazolidinones
• ISSN: 1040-6638; 1563-5333
• DOI: 10.1080/10406638.2022.2094971

In this work, a thiazole derivative, 5-(5-nitro furan-2-ylmethylen), 3-N-(2-methoxy phenyl),2-N'-(2-methoxyphenyl) imino thiazolidin-4-one (abbreviated by NF2MT), was characterized through Fourier transform infrared, UV-vis,
1
H and
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C nuclear magnetic resonance (NMR) spectroscopy. Besides, a complete and detailed vibrational assignment have been achieved by means of density functional theory (DFT) calculations using the B3LYP theory and the 6 311G(d,p) basis set. Based on the electron density distribution, reduced density gradient and atoms-in molecules analyses have been performed to describe and identify the intra- and intermolecular interactions within the molecule. Non-covalent interactivities between non-bonded atoms were also characterized. In addition, the frontier molecular orbitals and global chemical reactivity descriptors of NF2MT were further investigated using DFT, revealing the most important electronic properties of the compound. The TD-DFT method at CAM-B3LYP/6-311G(d,p) level with the chloroform solvent and polarized continuum model was applied to obtain optical behavior as well as the electronic transitions for the molecule. On the other hand, molecular properties such as atomic charges (Mulliken and NBO) and molecular electrostatic potential were calculated to locate the most reactive sites in the molecule that promote hydrogen bond formation. Molecular docking studies were also carried out to predict and display binding sites of NF2MT with its target protein. The biological activity was tested with acetylcholinesterase and butyrylcholinesterase.