Evidence map›Paper›PMID 35475273›Full record

ArticleJournal of clinical and translational research2022

Lichen planus drugs re-purposing as potential anti COVID-19 therapeutics through molecular docking and molecular dynamics simulation approach.

Unnati Soni, Pratyush Singh, Om Prakash Gupta, Shalini Gupta, Saurabh Pratap Singh, Prerna Singh, Sangeeta Singh, Krishna Mishra

Open access · diamondAbstract read
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Article in Journal of clinical and translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

8 authors at 3 institutions in 1 country.

Unnati SoniDepartment of Applied Sciences, Indian Institute of Information Technology, Allahabad, Uttar Pradesh, India.
Pratyush SinghDepartment of Oral Pathology and Microbiology, MaharanaPratap Dental College, Kanpur, Uttar Pradesh, India.
Om Prakash GuptaDepartment of General Surgery, Career Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Shalini GuptaDepartment of Oral Pathology and Microbiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Saurabh Pratap SinghDepartment of Oral Pathology and Microbiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Prerna SinghDepartment of Oral Pathology and Microbiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
Sangeeta SinghDepartment of Applied Sciences, Indian Institute of Information Technology, Allahabad, Uttar Pradesh, India.
Krishna MishraDepartment of Applied Sciences, Indian Institute of Information Technology, Allahabad, Uttar Pradesh, India.
Indian Institute of Information Technology Allahabad · INKing George's Medical University · INCareer Institute Of Medical & Dental Sciences and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: The present study intends to investigate COVID-19 by targeting their main proteins with 17 selected drugs used for treating Oral Lichen Planus (OLP) which is a chronic muco-cutaneous disorder. Here, an attempt is made to gain better insight into the structure of various drugs targeting specific proteins which will be helpful in developing drugs useful for therapeutic and preventive measures. Method: Results: Epigallocatechin-3-gallate (EGCG) showed the highest docking values among the drugs selected for repurposing. Among the target proteins, EGCG has shown maximum binding affinity with ACE-2 receptor. Further, according to the molecular dynamic simulation studies, EGCG has shown the least conformational fluctuations with M Conclusion: EGCG can be a potential inhibitor drug which can bind with ACE-2 receptor thus inhibiting the interaction of mainly M Relevance for Patients: EGCG, a natural compound shows antiviral potential having considerably high affinity and stability with SARS-CoV-2. It might be further employed as a lead drug against selective inhibitors of SARS-CoV-2 for the therapeutic management of COVID-19 patients after necessary clinical trials.

Indexed as

angiotensin converting enzyme-2main-proteaseoral lichen planusSARS-CoV-2spike glycoprotein

Identifiers

PMID35475273
PMCPMC9036082
OpenAlexW4214538290

What OpenQuestion holds

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Registered trials

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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.