Evidence map›Paper›PMID 31404942›Full record

ArticleBritish journal of pharmacology2019

Biological characterization of new inhibitors of microsomal PGE synthase-1 in preclinical models of inflammation and vascular tone.

Karin Larsson, Julia Steinmetz, Filip Bergqvist, Samsul Arefin, Linda Spahiu, Johan Wannberg, Sven-Christian Pawelzik, Ralf Morgenstern, Patric Stenberg, Karolina Kublickiene and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
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  8. Biosynthesis of prostaglandin 15dPGJJournal of lipid research · 2022
    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

12 authors at 4 institutions in 1 country.

Karin LarssonRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Julia SteinmetzRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Filip BergqvistRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-0075-6751
Samsul ArefinDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Linda SpahiuBiochemical Toxicology Unit, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Johan WannbergSciLifeLab Drug Discovery and Development Platform, Medicinal Chemistry-Lead Identification, Department of Medicinal Chemistry, Uppsala University, Uppsala, Sweden.
Sven-Christian PawelzikRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Ralf MorgensternBiochemical Toxicology Unit, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Patric StenbergGesynta Pharma AB, Solna, Sweden.
Karolina KublickieneDivision of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Marina KorotkovaRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Per-Johan JakobssonRheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Karolinska University Hospital · SEKarolinska Institutet · SEGesynta Pharma (Sweden) · SEUppsala University · SE

Funding

IMMUNE RESPONSES TO HPVS INVOLVED IN GENITAL NEOPLASIAK11CA001391 · NCI · UNIVERSITY OF NEW MEXICO · PI JENISON, STEVEN A · 1989 to 1993
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6 · The paper itself

Abstract

background and purposeMicrosomal PGE synthase-1 (mPGES-1), the inducible synthase that catalyses the terminal step in PGE EXPERIMENTAL APPROACH: Potency was determined based on the reduction of PGE KEY

resultsWe report five new mPGES-1 inhibitors (named 934, 117, 118, 322, and 323) that selectively inhibit recombinant human and rat mPGES-1 with IC CONCLUSION AND IMPLICATIONS: These mPGES-1 inhibitors can be used as refined tools in further investigations of the role of mPGES-1 in inflammation and microvascular disease.

Indexed as

A549 CellsAnimalsAnti-Inflammatory AgentsArteriesDinoprostoneDisease Models, AnimalDose-Response Relationship, DrugEdemaEnzyme InhibitorsEscherichia coliHumansIn Vitro TechniquesMaleMiceMice, Inbred C57BLMolecular StructureAnti-Inflammatory AgentsDinoprostoneEnzyme InhibitorsProstaglandin-E SynthasesPTGES protein, human

Identifiers

PMID31404942
PMCPMC6965680
OpenAlexW2968223365

What OpenQuestion holds

Textmetadata
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.