Digitoxin

A plasma membrane sodium-potassium ATPase inhibitor.

Phase of research

Potential treatment - pre-clinical evidence

How it helps

Antiviral

Drug status

Used to treat other disease

6
Supporting references
0
Contradictory references
5
AI-suggested references
0
Clinical trials

General information

Digitoxin is a cardiac glycoside. It inhibits the plasma membrane sodium/potassium ATPase, which results in decreased intracellular potassium levels and increased intracellular sodium and calcium levels. Its activity leads to caspase activation and DNA fragmentation, causing apoptosis. Digitoxin was shown to inhibit cancer cell growth (NCIt).

Digitoxin on DrugBank
Digitoxin on PubChem
Digitoxin on Wikipedia

 

Structure image - Digitoxin

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Supporting references

Link Tested on Impact factor Notes Publication date
Screening of FDA-approved drugs using a MERS-CoV clinical isolate from South Korea identifies potential therapeutic options for COVID-19
Preprint Screening
VERO cells Mar/19/2020
Identification of Potent and Safe Antiviral Therapeutic Candidates Against SARS-CoV-2
Small molecule In vitro Screening
Vero cells 5.09 Nov/25/2020
In Silico Screening of Potential Spike Glycoprotein Inhibitors of SARS-CoV-2 with Drug Repurposing Strategy
in silico 1.55

In silico screening of potential virus spike protein inhibitors within a set of molecules including FDA aproved drugs and traditional chinese medicine compounds.

Aug/01/2020
Comparative analysis of antiviral efficacy of FDA-approved drugs against SARS-CoV-2 in human lung cells: Nafamostat is the most potent antiviral drug candidate
Preprint
Calu-3 human airway epithelial cells

lower IC50 value in Calu-3 cells than VERO E6 cells

May/12/2020
Classical Drug Digitoxin Inhibits Influenza Cytokine Storm, With Implications for Covid-19 Therapy
Cytokine storm Small molecule Animal model
cotton rats (influenza model only); influenza strain A/Wuhan/H3N2/359/95 1.54

Digitoxin suppresed cytokine storm in a rat influenza model, which according to the authors has implications for COVID-19 induced cytokine storm management.

Nov/01/2020
Repurposing of the approved small molecule drugs in order to inhibit SARS-CoV-2 S protein and human ACE2 interaction through virtual screening approaches
Spike protein Small molecule In silico
in silico 3.22

Predicted to inhibit the SARS-CoV-2 spike protein binding to the host's ACE2 receptor.

Sep/24/2020

AI-suggested references