Evidence map›Paper›PMID 41540178›Full record

ArticleFolia microbiologica2026

Molecular docking, dynamics and experimental approach integrated identification of phytopharmaceuticals against methicillin-resistant Staphylococcus aureus (MRSA) infection.

Saima, Hitesh K Sharma, S Latha, Viney Lather, Devesh Tewari, Ruchika Sharma, Gaurav Kumar Jain, Deepti Pandita, Anoop Kumar

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In one paragraph

Article in Folia microbiologica, 2026. 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

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

1 citing paper in PubMed.

  1. Article
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

9 authors.

SaimaDepartment of Pharmacology, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India.
Hitesh K SharmaAmity Institute of Pharmacy, Amity University, Noida, India.
S LathaDepartment of Pharmacology, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India.
Viney LatherAmity Institute of Pharmacy, Amity University, Noida, India.
Devesh TewariDepartment of Pharmacognosy and Phytochemistry, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India.
Ruchika SharmaCentre for Precision Medicine and Pharmacy, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, 110017, India.
Gaurav Kumar JainDSIR-DPSRU-CRTDH, Centre of Advanced Formulation Technology, Department of Pharmaceutics, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India.
Deepti PanditaDSIR-DPSRU-CRTDH, Centre of Advanced Formulation Technology, Department of Pharmaceutics, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India.
Anoop KumarDepartment of Pharmacology, Delhi Pharmaceutical Sciences and Research University (DPSRU), New Delhi, India. anoopdpsru@dpsru.edu.in.

Funding

Defence Science and Technology Organisation DST/SRG/00011
6 · The paper itself

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is indeed a significant public health issue, affecting millions of people worldwide which can range from mild skin infections to life-threatening conditions like bloodstream infections and pneumonia. The aim of the current study is to decipher the possible mechanism of some selected natural compounds against MRSA. The natural compounds were selected based on our earlier systematic literature review. The selected compounds were screened against various targets of MRSA using molecular docking techniques. The stability of selected compounds was checked using molecular dynamics. Further, Absorption, Distribution, Metabolism and Excretion (ADME) was predicted using QikProp module. All the computational studies were conducted using the Schrodinger Maestro version 13.5.128. In-vitro assays were conducted to check the anti-bacterial effects of selected natural compounds against MRSA. Among 60 selected natural compounds, theasinensin A, xanthohumol, luteolin, oxyresveratrol, liquiritigenin and baicalin has shown the energetically favoured binding conformation in the active site of targets. Further, molecular dynamics results have shown the stable conformation of xanthohumol and theasinensin A in the active site of targets. Further, the pharmacokinetic profile of xanthohumol was found to be better among other natural compounds. The minimum inhibitory concentration (MIC) of xanthohumol was found to be 3.12 µg/mL as indicated by disk diffusion and micro broth dilution assays. Xanthohumol can be promising anti-bacterial agent against MRSA through multi modal mechanism. However, further detailed experimental studies are required to confirm its possible antibacterial mechanisms.

Indexed as

Anti-bacterial tests and activityMolecular dockingMolecular dynamicsMRSANatural compounds

Identifiers

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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.