Journal
HELIYON
Volume 7, Issue 10, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.heliyon.2021.e08209
Keywords
(E)-benzyl-2-(4-hydroxy-2-methoxybenzylidene); Hydrazinecarbodithioate; Mass spectra; Antituberculosis
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A new Schiff base compound was successfully synthesized and characterized through experimental and theoretical studies, showing low chemical reactivity and high kinetic stability. In silico studies predicted the absorption, distribution, metabolism, and excretion profiles of the compound, while molecular docking results suggested its potential as an antituberculosis agent compared to ethambutol.
A new Schiff base, (E)-benzyl-2-(4-hydroxy-2-methoxybenzylidene)hydrazinecarbodithioate (compound 1) has been synthesized and experimentally characterized by the IR, UV-Vis, H-1-NMR and mass spectroscopies. The theoretical study of the synthesized compound was evaluated using the density functional theory (DFT) at B3LYP/6-31G+(d,p) basis set. The electronic absorption spectrum of compound 1 was evaluated using time-dependentdensity functional theory. Besides, in silico studies were done for the prediction of absorption, distribution,metabolism and excretion profiles of compound 1. According to the result, the theoretical data were well fitted with the experimental values. The studied compound has low chemical reactivity and high kinetic stability. In the molecular electrostatic potential map, the negative and positive potential sites were found around electronegative atoms and hydrogen atoms of compound 1, respectively. The 97.75% Lewis and 2.25% non-Lewis structure were present in the studied molecule. The molecular docking results reveal that compound 1 can be used as antituberculosis agent as compare to ethambutol.
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