Evidence map›Paper›PMID 38871595›Full record

ArticleJournal of Ayurveda and integrative medicine

Quest for Anti-SARS-CoV-2 antiviral therapeutics: in-silico and in-vitro analysis of edible mushroom- Cordyceps militaris.

Pradeep Gandhale, Rupesh Chikhale, Pukar Khanal, Vashkar Biswa, Raju Ali, Mohd Shahnawaz Khan, Nilambari Gurav, Muniappan Ayyanar, Sandeep Das, Shailendra Gurav

Abstract read
In one paragraph

Article in Journal of Ayurveda and integrative medicine. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Pradeep GandhaleICAR-National Institute of High-Security Animal Diseases, Bhopal, Madhya Pradesh- 462 021, India.
Rupesh ChikhaleUCL School of Pharmacy, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Pukar KhanalDepartment of Pharmacology, KLE College of Pharmacy Belagavi, KLE Academy of Higher Education and Research (KAHER) Belagavi- 590010, India.
Vashkar BiswaDepartment of Biotechnology, Bodoland University, Assam, 783 370, India.
Raju AliDepartment of Biotechnology, Bodoland University, Assam, 783 370, India.
Mohd Shahnawaz KhanDepartment of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Nilambari GuravDepartment of Pharmacognosy, PES's Rajaram and Tarabai Bandekar College of Pharmacy, Ponda, Goa-403 401, India.
Muniappan AyyanarDepartment of Botany, A.V.V.M. Sri Pushpam College (Autonomous), Poondi (Affiliated to Bharathidasan University), Thanjavur, Tamil Nadu, India.
Sandeep DasDepartment of Biotechnology, Bodoland University, Assam, 783 370, India.
Shailendra GuravDepartment of Pharmacognosy, Goa College of Pharmacy, Goa University, Goa- 403 001, India. Electronic address: shailendra.gurav@nic.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe emergence and evolution of SARS-CoV-2 resulted a severe threat to public health globally. Due to the lack of an effective vaccine with durable immunity, the disease transited into the endemic phase, necessitating potent antiviral therapy including a scientific basis for current traditional herbal medicine.

objectiveThis study aimed to conduct a pharmacoinformatic analysis of selected chemical ingredients and in-vitro evaluation of Cordyceps militaris extract against SARS-CoV-2. MATERIALS AND

methodsC. militaris, the widely used fungus in conventional herbal medicine, was subjected to computational investigation using molecular docking, molecular dynamic simulation and network pharmacology analysis followed by the in-vitro assay for evaluating its anti-SARS-CoV-2 potential.

resultsThe molecular docking analysis of C. militaris revealed the Cordycepin's highest affinity (-9.71 kcal/mol) than other molecules, i.e., Cicadapeptin-I, Cicadapeptin-II, Cordycerebroside-B, and N-Acetyl galactosamine to the receptor binding domain of the SARS-CoV-2 spike protein. C. militaris aqueous extract could reduce the SARS-CoV-2 viral copy numbers by 50.24% using crude extract at 100 μg/mL concentration.

conclusionThese findings suggest that C. militaris has promising anti-SARS-CoV-2 activity and may be explored as traditional medicine for managing the COVID-19 surge in the endemic phase.

Indexed as

Covid-19Edible mushroomMolecular dockingMolecular dynamicsNetwork pharmacology

Identifiers

PMID38871595
PMCPMC11282376

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.