ABSTRACT
Insomnia, a habitual yet vicious disorder characterized by depriving of sleep resulting in patients to consume medications for relieving their minds. Of these medications, a few may possess the aptitude to harm the biochemical receptors of the human body, resulting in mutagenicity, and the body may manifest acute toxicological symptoms. Execution of quantitative analysis by QSAR (quantitative structure-activity relationship) methods forms a reliable platform for interpreting the toxicological status of insomnia medicines. Further molecular docking software was utilized for determining the extent binding affinity of the molecules on the protein structures
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