Evidence map›Paper›PMID 26382576›Full record

ReviewInternational immunopharmacology2016

Antagonism of human formyl peptide receptor 1 with natural compounds and their synthetic derivatives.

Igor A Schepetkin, Andrei I Khlebnikov, Liliya N Kirpotina, Mark T Quinn

Abstract readReview
In one paragraph

Review in International immunopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Turn-Adopting Peptidomimetic as a Formyl Peptide Receptor-1 Antagonist.ACS pharmacology & translational science · 2024
    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

4 authors at 2 institutions in 2 countries.

Igor A SchepetkinDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, United States.
Andrei I KhlebnikovDepartment of Biotechnology and Organic Chemistry, Tomsk Polytechnic University, Tomsk 634050, Russia; Department of Chemistry, Altai State Technical University, Barnaul, Russia.
Liliya N KirpotinaDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, United States.
Mark T QuinnDepartment of Microbiology and Immunology, Montana State University, Bozeman, MT 59717, United States. Electronic address: mquinn@montana.edu.
Montana State University · USAltai State Technical University · RU

Funding

Pilot Grants ProgramP30GM110732 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI QUINN, MARK T · 2014 to 2018
$5.4M
NIGMS NIH HHS P30 GM110732
6 · The paper itself

Abstract

Formyl peptide receptor 1 (FPR1) regulates a wide variety of neutrophil functional responses and plays an important role in inflammation and the pathogenesis of various diseases. To date, a variety of natural and synthetic molecules have been identified as FPR1 ligands. Here, we review current knowledge on natural products and natural product-inspired small molecules reported to antagonize and/or inhibit the FPR1-mediated responses. Based on this literature, additional screening of selected commercially available natural compounds for their ability to inhibit fMLF-induced Ca(2+) mobilization in human neutrophils and FPR1 transfected HL-60 cells, and pharmacophore modeling, natural products with potential as FPR1 antagonists are considered and discussed in this review. The identification and characterization of natural products that antagonize FPR1 activity may have potential for the development of novel therapeutics to limit or alter the outcome of inflammatory processes.

Indexed as

Molecular Docking SimulationBiological ProductsDrug DiscoveryHumansImmune System DiseasesInflammationLigandsMolecular Targeted TherapyNeutrophilsPeptidesReceptors, Formyl PeptideBiological ProductsFPR1 protein, humanLigandsPeptidesReceptors, Formyl PeptideCa(2+) fluxFormyl peptide receptor 1Molecular modelingNatural compoundNeutrophilNeutrophil elastaseReceptor antagonistSuperoxide anion radical

Identifiers

PMID26382576
PMCPMC4791210
OpenAlexW1628780871

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.