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Drug Discov Today ; 25(5): 928-941, 2020 05.
Article in English | MEDLINE | ID: covidwho-72302

ABSTRACT

In the past decade we have seen two major Ebola virus outbreaks in Africa, the Zika virus in Brazil and the Americas and the current pandemic of coronavirus disease (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). There is a strong sense of déjà vu because there are still no effective treatments. In the COVID-19 pandemic, despite being a new virus, there are already drugs suggested as active in in vitro assays that are being repurposed in clinical trials. Promising SARS-CoV-2 viral targets and computational approaches are described and discussed. Here, we propose, based on open antiviral drug discovery approaches for previous outbreaks, that there could still be gaps in our approach to drug discovery.


Subject(s)
Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Betacoronavirus/drug effects , Coronavirus Infections/drug therapy , Drug Discovery , Pneumonia, Viral/drug therapy , Angiotensin-Converting Enzyme 2 , Animals , Betacoronavirus/metabolism , COVID-19 , Chlorocebus aethiops , Computer Simulation , Drug Repositioning , Hemorrhagic Fever, Ebola/drug therapy , Humans , In Vitro Techniques , Middle East Respiratory Syndrome Coronavirus , Molecular Docking Simulation , Pandemics , Peptidyl-Dipeptidase A/metabolism , Severe acute respiratory syndrome-related coronavirus , SARS-CoV-2 , Severe Acute Respiratory Syndrome/drug therapy , Spike Glycoprotein, Coronavirus/metabolism , Vero Cells , Zika Virus Infection/drug therapy , COVID-19 Drug Treatment
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