Journal
INFECTION GENETICS AND EVOLUTION
Volume 88, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.meegid.2020.104699
Keywords
ADMET; Molecular docking; Importin alpha/beta; Drug-resistance; Drug-designing
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In this study, pharmaco-informatics approaches were used to screen 15 lead-like compounds with potential anti-malarial activity from the PubChem database. A novel inhibitor was designed, showing higher bioavailability and drug-likeness scores compared to existing lead compounds. Molecular dynamics simulations confirmed the stability of the complex with promising ADMET properties.
Plasmodium falciparum, the prime causative agent of malaria, is responsible for 4, 05,000 deaths per year and fatality rates are higher among the children aged below 5 years. The emerging distribution of the multi-drug resistant P. falciparum becomes a worldwide concern, so the identification of unique targets and novel inhibitors is a prime need now. In the present study, we have employed pharmaco-informatics approaches to analyze 265 lead-like compounds from PubChem databases for virtual screening. Thereafter, 15 lead-like compounds were docked within the active side pocket of importin alpha. Comparative ligand properties and absorption, distribution, metabolism, excretion, and toxicity (ADMET) profile were also assessed. Finally, a novel inhibitor was designed and assessed computationally for its efficacy. From the comparative analysis we have found that our screened compounds possess better results than the existing lead ivermectin; having the highest binding energy of -15.6 kcal/mol, whereas ivermectin has -12.4 kcal/mol. The novel lead compound possessed more fascinating output without deviating any of the rules of Lipinski. It also possessed higher bioavailability and the drug-likeness score of 0.55 and 0.71, respectively compared to ivermectin. Furthermore, the binding study was confirmed by molecular dynamics simulation over 25 ns by evaluating the stability of the complex. Finally, all the screened compounds and the novel compound showed promising ADMET properties likewise. To end, we hope that our proposed screened compounds, as well as the novel compound, might give some advances to treat malaria efficiently in vitro and in vivo.
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