Evidence map›Paper›PMID 39598448›Full record

ArticlePharmaceuticals (Basel, Switzerland)2024

Exploring the Antiviral Potential of

Mebarka Ouassaf, Lotfi Bourougaa, Farial Bahaz, Bader Y Alhatlani

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. 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

4 authors.

Mebarka OuassafGroup of Computational and Medicinal Chemistry, LMCE Laboratory, University of Biskra, BP 145, Biskra 07000, Algeria.ORCID 0000-0002-0292-0949
Lotfi BourougaaGroup of Computational and Medicinal Chemistry, LMCE Laboratory, University of Biskra, BP 145, Biskra 07000, Algeria.ORCID 0009-0005-4235-6077
Farial BahazLaboratory of Organic Materials and Heterochemistry, Echahid Cheikh Larbi Tebessi University, Tebessa 12000, Algeria.
Bader Y AlhatlaniUnit of Scientific Research, Applied College, Qassim University, Buraydah 52571, Saudi Arabia.ORCID 0000-0003-0871-6313

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

methodsFrom the TCMSP database, we identified eight active compounds and 335 drug targets for

resultsPPI analysis identified JAK2, MAPK3, MAPK1, JAK1, PTPN1, HSPA8, TYK2, RAF1, MAPT, and HMOX1 as key hub genes, with JAK2 emerging as a critical regulator of immune and antiviral pathways. ADMET analysis confirmed Patuletin's favorable pharmacokinetic properties, and molecular dynamics simulations showed a stable Patuletin-JAK2 complex, with FEL analysis indicating minimal disruption to JAK2's intrinsic flexibility.

conclusionsThese findings highlight JAK2 as a promising target in the antiviral activity of

Indexed as

A. annuaantiviralFELJAK-STATmolecular dynamics simulationsnetwork pharmacology

Identifiers

PMID39598448
PMCPMC11597232

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.