Evidence map›Paper›PMID 31312406›Full record

ArticleACS medicinal chemistry letters2019

High Affinity Fluorescent Probe for Proteinase-Activated Receptor 2 (PAR2).

Jordan C LeSarge, Pierre Thibeault, Mark Milne, Rithwik Ramachandran, Leonard G Luyt

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ACS medicinal chemistry letters, 2019. 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
0.8field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  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

5 authors at 2 institutions in 1 country.

Jordan C LeSargeDepartment of Chemistry, Department of Physiology and Pharmacology, Department of Oncology, and Department of Medical Imaging, University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 3K7, Canada.
Pierre ThibeaultDepartment of Chemistry, Department of Physiology and Pharmacology, Department of Oncology, and Department of Medical Imaging, University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 3K7, Canada.
Mark MilneLondon Regional Cancer Program, Lawson Health Research Institute, 800 Commissioners Road East, London, Ontario N6A 5W9, Canada.
Rithwik RamachandranDepartment of Chemistry, Department of Physiology and Pharmacology, Department of Oncology, and Department of Medical Imaging, University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 3K7, Canada.
Leonard G LuytDepartment of Chemistry, Department of Physiology and Pharmacology, Department of Oncology, and Department of Medical Imaging, University of Western Ontario, 1151 Richmond Street, London, Ontario N6A 3K7, Canada.
Western University · CALawson Health Research Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PAR2 is a proteolytically activated G protein-coupled receptor (GPCR) that is implicated in various cancers and inflammatory diseases. Ligands with low nanomolar affinity for PAR2 have been developed, but there is a paucity of research on the development of PAR2-targeting imaging probes. Here, we report the development of seven novel PAR2-targeting compounds. Four of these compounds are highly potent and selective PAR2-targeting peptides (EC

Identifiers

PMID31312406
PMCPMC6627725
OpenAlexW2951699133

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.