Investigation of berberine and its derivatives in Sars Cov-2 main protease structure by molecular docking, PROTOX-II and ADMET methods: in machine learning and in silico study.

Autor: Oner E; Departmant of Biochemistry, Faculty of Pharmacy, Mersin University, Mersin, Turkey., Al-Khafaji K; Department of Biochemistry, Faculty of Science, Kastsart University, Bangkok, Thailand.; College of Dentistry, The University of Mashreq, Baghdad, Iraq., Mezher MH; Department of Computer Technique Engineering, Islamic university, Babel, Iraq., Demirhan I; Department of Electronic-Automation, Vocational School of Health Sciences, HarranUniversity, Sanlıurfa, Turkey., Suhail Wadi J; Pharmacy Department, AL-Rafidain University College, Baghdad, Iraq., Belge Kurutas E; Department of Biochemistry, Faculty of Medicine, Sutcu Imam University, Kahramanmaras, Turkey., Yalin S; Departmant of Biochemistry, Faculty of Pharmacy, Mersin University, Mersin, Turkey., Choowongkomon K; Department of Biochemistry, Faculty of Science, Kastsart University, Bangkok, Thailand.
Jazyk: angličtina
Zdroj: Journal of biomolecular structure & dynamics [J Biomol Struct Dyn] 2023 Nov; Vol. 41 (19), pp. 9366-9381. Date of Electronic Publication: 2022 Nov 11.
DOI: 10.1080/07391102.2022.2142848
Abstrakt: Bioactive compounds found in plants also have pharmacological antiviral effects. Berberine (BBR), an alkaloid found naturally in plants, is one of the phytochemicals with a wide range of biological activities, including antiviral, anticancer, anti-inflammatory and anti-inflammatory. In this study, we firstly aimed to predict pIC50 values for selcted compounds and then extract the binding patterns of berberine and its derivatives in the Sars Cov-2 Master Protease structure via employing molecular docking approache. Our results showed that berberine and its derivatives have good binding affinities towared Sars Cov2 main protease protein. Based on docking results the pharamaccokinetic studies for berberine, berberrubine, demethylen-berberine, jatrorrhizin, and thalifendine, were conducted and showed a good pharamacokinetic properties as an oral drugs. For deep inspection, we utiilized molecular dynmaics simulation to examine the Sars Cov2 main protease-ligand stabilities. The molecular dynamics simulation and PCA investigations revealed that thalifendine have a strong willing to act as good bindinder to SARS-CoV-2 protease. Further, the network based pharamacology showed that these drugs mediate different pathways such as human T-cell leukemia virus 1 infection, viral carcinogenesis, human immunodeficiency virus 1 infection, kaposi sarcoma-associated herpesvirus infection and epstein-Barr virus infection.The findings of this study have an important recomendation for thalifendine for more in vivo and in vitro studies to work.Communicated by Ramaswamy H. Sarma.
Databáze: MEDLINE