Related Experiment Video
Updated: Apr 12, 2026

Visualization of SARS-CoV-2 using Immuno RNA-Fluorescence In Situ Hybridization
Published on: December 23, 2020
Potential of 6'‑hydroxy justicidin B from Justicia procumbens as a therapeutic agent against coronavirus disease 2019
Min Heui Yoo1, Han Young Eom1, Wan-Jung Im1
1Department of Advanced Toxicology Research, Korea Institute of Toxicology, Daejeon 34114, South Korea.
Background:
Since the onset of the coronavirus disease 2019 (COVID-19) pandemic, remarkable advances have been made in vaccine development to reduce mortality. However, therapeutic interventions for COVID-19 are comparatively limited despite these intensive efforts. Furthermore, the rapid mutation capability of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a characteristic of its RNA structure, has led to the emergence of multiple variants, necessitating a shift from a predominantly vaccine-centric approach to one that encompasses therapeutic strategies. 6'-Hydroxy justicidin B (6'-HJB), an arylnaphthalene lignan isolated from Justicia procumbens, a traditional Chinese medicine, is known for its antiviral properties.
Hypothesis/Purpose:
The aim of the present study was to assess the effectiveness and safety of 6'-HJB against SARS-CoV-2 in order to determine its potential as a therapeutic agent against COVID-19.
Methods:
The efficacy of 6'-HJB was evaluated both in vitro using Vero and Calu-3 cell lines and in vivo using ferrets. The safety assessment included toxicokinetics, safety pharmacology, and Good Laboratory Practice (GLP)-compliant toxicity evaluations following single- and repeated-dose toxicity studies in dogs.
Results:
The anti-SARS-CoV-2 efficacy of 6'-HJB was evaluated through dose-response curve (DRC) analysis using immunofluorescence; 6'-HJB demonstrated superior inhibition of SARS-CoV-2 growth and lower cytotoxicity than remdesivir. In SARS-CoV-2-infected ferret, 6'-HJB showed efficacy comparable to that of the positive control, Truvada. Further GLP toxicity studies corroborated the safety profile of 6'-HJB. Single-dose and 4-week repeated oral toxicity studies in Beagle dogs demonstrated minimal harmful effects at the highest dosages. The lethal dose of 6'-HJB exceeded 2,000 mg kg-1 in Beagle dogs. Toxicokinetic and GLP safety pharmacology studies demonstrated no adverse effects of 6'-HJB on metabolic processes, respiratory or central nervous systems, or cardiac functions.
Conclusion:
This research highlights both the antiviral efficacy and safety profile of 6'-HJB, underscoring its potential as a novel COVID-19 treatment option. The potential of 6'-HJB was demonstrated using modern scientific methodologies and standards.
Insights
6'-Hydroxy justicidin B (6'-HJB) shows significant antiviral activity against SARS-CoV-2 in vitro and in vivo. This traditional Chinese medicine compound demonstrates a strong safety profile, positioning it as a promising therapeutic candidate for COVID-19 treatment.
Area of Science:
- Virology and Pharmacology
- Drug Discovery and Development
Background:
- Limited therapeutic options for COVID-19 despite advances in vaccine development.
- Emergence of SARS-CoV-2 variants necessitates development of novel therapeutic strategies.
- 6'-Hydroxy justicidin B (6'-HJB), a lignan from Justicia procumbens, possesses known antiviral properties.
Purpose of the Study:
- To evaluate the efficacy and safety of 6'-HJB as a potential therapeutic agent for COVID-19.
- To assess the antiviral potential of 6'-HJB against SARS-CoV-2.
Main Methods:
- In vitro efficacy testing using Vero and Calu-3 cell lines.
- In vivo efficacy evaluation in a ferret model of SARS-CoV-2 infection.
- Safety assessment including toxicokinetics, safety pharmacology, and GLP-compliant toxicity studies in dogs.
Main Results:
- 6'-HJB demonstrated superior inhibition of SARS-CoV-2 growth and lower cytotoxicity compared to remdesivir in vitro.
- Efficacy in SARS-CoV-2-infected ferrets was comparable to the positive control, Truvada.
- GLP toxicity studies in dogs indicated a favorable safety profile, with no adverse effects observed at high dosages and a lethal dose exceeding 2,000 mg/kg.
Conclusions:
- 6'-HJB exhibits significant antiviral efficacy against SARS-CoV-2.
- The compound possesses a robust safety profile, with minimal toxicity observed in preclinical studies.
- 6'-HJB represents a promising novel therapeutic candidate for the treatment of COVID-19.
Related Concept Videos
Upper Respiratory Drugs: Antitussives, Expectorants, and Mucolytics
Antitussives include codeine, dextromethorphan (Robitussin), and benzonatate (Tessalon). Codeine and dextromethorphan exert their effects centrally by suppressing the cough reflex center in the medulla. Benzonatate operates peripherally within the respiratory tract by...
Hypersensitivity Reactions: Cytolytic Reactions
Antimicrobial Effectiveness
Subviral Agents
Inhibitors of Bacterial DNA Synthesis
Inhibitors of Viral Protein Synthesis

