Evidence map›Paper›PMID 40419556›Full record

ArticleScientific reports2025

Combining kinetics and in silico approaches to evaluate bromhexine as an anti-pancreatic lipase agent for obesity management.

Asma Gholami, Dariush Minai-Tehrani, Leif A Eriksson

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Asma GholamiDepartment of Chemistry and Molecular Biology, University of Gothenburg, 405 30, Göteborg, Sweden.ORCID https://orcid.org/0000-0002-8477-3929
Dariush Minai-TehraniBioresearch Lab, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University, Tehran, Iran. d_mtehrani@sbu.ac.ir.ORCID https://orcid.org/0000-0003-3589-7324
Leif A ErikssonDepartment of Chemistry and Molecular Biology, University of Gothenburg, 405 30, Göteborg, Sweden. leif.eriksson@chem.gu.se.ORCID https://orcid.org/0000-0001-5654-3109

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Industrialization, fast food intake and reduced physical activity, mainly in developed countries, exacerbate obesity and make it a major lifestyle disorder. A promising strategy for developing effective anti-obesity agents is to inhibit pancreatic lipase, thereby reducing lipid absorption. Currently, the only clinically approved pharmacological agent for pancreatic lipase inhibition is Orlistat. However, its undesirable gastrointestinal side effects have prompted the search for more effective and potent drugs. This study investigates the inhibitory mechanism of Bromhexine, a mucolytic drug, on pancreatic lipase using Lineweaver-Burk plot analysis and molecular docking, along with simulations, and compares its efficacy to that of the Food and Drug Administration (FDA) approved drug Orlistat. Kinetic analysis indicates that Bromhexine exhibits mixed inhibition of pancreatic lipase, with IC

Indexed as

Anti-Obesity AgentsEnzyme InhibitorsLipaseObesityPancreasCatalytic DomainComputer SimulationHumansKineticsMolecular Docking SimulationOrlistatAnti-Obesity AgentsEnzyme InhibitorsLipaseOrlistatPNLIP protein, humanBromhexineInhibition mechanismLipaseMolecular dockingObesity

Identifiers

PMID40419556
PMCPMC12106798

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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.