Abstract
Recently Chloroquine and its derivative Hydroxychloroquine have garnered enormous interest amongst the clinicians and health authorities’ world over as a potential treatment to contain COVID-19 pandemic. The present research aims at investigating the therapeutic potential of Chloroquine and its potent derivative Hydroxychloroquine against SARS-CoV-2 viral proteins. At the same time screening was performed for some chemically synthesized derivatives of Chloroquine and compared their binding efficacy with chemically synthesized Chloroquine derivatives through in silico approaches. For the purpose of the study, some essential viral proteins and enzymes were selected that are implicated in SARS-CoV-2 replication and multiplication as putative drug targets. Chloroquine, Hydroxychloroquine, and some of their chemically synthesized derivatives, taken from earlier published studies were selected as drug molecules. We have conducted molecular docking and related studies between Chloroquine and its derivatives and SARS-CoV-2 viral proteins, and the findings show that both Chloroquine and Hydroxychloroquine can bind to specific structural and non-structural proteins implicated in the pathogenesis of SARS-CoV-2 infection with different efficiencies. Our current study also shows that some of the chemically synthesized Chloroquine derivatives can also potentially inhibit various SARS-CoV-2 viral proteins by binding to them and concomitantly effectively disrupting the active site of these proteins. These findings bring into light another possible mechanism of action of Chloroquine and Hydroxychloroquine and also pave the way for further drug repurposing and remodeling.Communicated by Ramaswamy H. Sarma.
Keywords: COVID-19; Chloroquine derivatives; Hydroxychloroquine; SARS-CoV-2; molecular docking.
【저자키워드】 COVID-19, SARS-CoV-2, Hydroxychloroquine, molecular docking, Chloroquine derivatives, 【초록키워드】 Efficacy, Pathogenesis, Chloroquine, Hydroxychloroquine, SARS-COV-2 infection, COVID-19 pandemic, Infection, molecular docking, Viral proteins, Proteins, non-structural proteins, Protein, Viral, Research, non-structural protein, targets, Enzymes, mechanism of action, SARS-CoV-2 replication, binding, Potential treatment, active site, Health authority, Viral protein, clinician, enzyme, therapeutic potential, multiplication, remodeling, derivative, derivatives, pathogenesis of SARS-CoV-2, SARS-CoV-2 viral, selected, inhibit, conducted, was performed, implicated, disrupting, in silico approaches, 【제목키워드】 Hydroxychloroquine, binding affinity, Screening, drug target, SARS-CoV-2 protein, derivative,