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Antiviral Drug Discovery To Address the COVID-19 Pandemic

https://doi.org/10.1128/mbio.02134-20
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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/j.cell.2020.02.052openalex-snapshot
SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor
inferredcites →https://doi.org/10.1016/j.chom.2020.05.009openalex-snapshot
The Innate Immune System: Fighting on the Front Lines or Fanning the Flames of COVID-19?
inferredcites →https://doi.org/10.1016/s0140-6736(20)31042-4openalex-snapshot
Triple combination of interferon beta-1b, lopinavir–ritonavir, and ribavirin in the treatment of patients admitted to hospital with COVID-19: an open-label, randomised, phase 2 trial
inferredcites →https://doi.org/10.1056/nejmoa2021436openalex-snapshot
Dexamethasone in Hospitalized Patients with Covid-19
inferredcites →https://doi.org/10.1073/pnas.83.6.1911openalex-snapshot
Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2',3'-dideoxynucleosides.
inferredcites →https://doi.org/10.1093/nass/nrl001openalex-snapshot
2′-Deoxy-4′-C-ethynyl-2-fluoroadenosine: A nucleoside reverse transcriptase inhibitor with highly potent activity against all HIV-1 strains, favorable toxic profiles and stability in plasma
inferredcites →https://doi.org/10.1101/2020.08.11.242834openalex-snapshot
AT-527 is a potent in vitro replication inhibitor of SARS-CoV-2, the virus responsible for the COVID-19 pandemic
inferredcites →https://doi.org/10.1126/science.abb4489openalex-snapshot
Structure-based design of antiviral drug candidates targeting the SARS-CoV-2 main protease
inferredcites →https://doi.org/10.1126/scitranslmed.abb5883openalex-snapshot
An orally bioavailable broad-spectrum antiviral inhibits SARS-CoV-2 in human airway epithelial cell cultures and multiple coronaviruses in mice
inferredcites →https://doi.org/10.1128/aac.01201-19openalex-snapshot
Safety, Pharmacokinetics, and Antiviral Activity of AT-527, a Novel Purine Nucleotide Prodrug, in Hepatitis C Virus-Infected Subjects with or without Cirrhosis
inferredcites →https://doi.org/10.1128/aac.47.10.3123-3129.2003openalex-snapshot
Novel bis -Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI) UIC-94017 (TMC114) with Potent Activity against Multi-PI-Resistant Human Immunodeficiency Virus In Vitro
inferredcites →https://doi.org/10.1128/mbio.01833-20openalex-snapshot
GRL-0920, an Indole Chloropyridinyl Ester, Completely Blocks SARS-CoV-2 Infection

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3710623openalex-extracted
inferred← citeshttps://doi.org/10.1016/j.antiviral.2026.106529openalex-snapshot
Application of emerging technologies in the antiviral field
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2021.100013openalex-snapshot
Darunavir ethanolate: Repurposing an anti-HIV drug in COVID-19 treatment
inferred← citeshttps://doi.org/10.1101/2020.10.06.20208066openalex-snapshot
Real-World Effectiveness of Hydroxychloroquine, Azithromycin, and Ivermectin Among Hospitalized COVID-19 Patients: Results of a Target Trial Emulation Using Observational Data from a Nationwide Healthcare System in Peru
inferred← citeshttps://doi.org/10.1128/jvi.01551-21openalex-snapshot
Highly Neutralizing COVID-19 Convalescent Plasmas Potently Block SARS-CoV-2 Replication and Pneumonia in Syrian Hamsters
inferred← citeshttps://doi.org/10.1186/s43141-021-00206-2openalex-snapshot
Anti-HIV reverse transcriptase plant polyphenolic natural products with in silico inhibitory properties on seven non-structural proteins vital in SARS-CoV-2 pathogenesis
inferred← citeshttps://doi.org/10.2478/abmj-2021-0005openalex-snapshot
Perspectives on Antiviral Drugs Development in the Treatment of COVID-19
inferred← citeshttps://doi.org/10.26434/chemrxiv.14125433openalex-snapshot
Repurposing Multi-Targeting Plant Natural Product Scaffolds In Silico Against SARS-CoV-2 Non-Structural Proteins Implicated in Viral Pathogenesis
inferred← citeshttps://doi.org/10.3390/ijms22115434openalex-snapshot
Existing Drugs Considered as Promising in COVID-19 Therapy
inferred← citeshttps://doi.org/10.3390/microorganisms9081731openalex-snapshot
The New Generation hDHODH Inhibitor MEDS433 Hinders the In Vitro Replication of SARS-CoV-2 and Other Human Coronaviruses
inferred← citeshttps://doi.org/10.5772/intechopen.111523openalex-snapshot
Drug Repurposing: Challenges and Successes in the Treatment of SARS-CoV-2
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