Evidence map›Paper›PMID 36105346›Full record

ArticleACS medicinal chemistry letters2022

Stereoisomers of an Aryl Pyrazole Glucocorticoid Receptor Agonist Scaffold Elicit Differing Anti-inflammatory Responses.

Ashley M Lato, Susan J Burke, Maggie P Ducote, Brandon J Kennedy, J Jason Collier, Shawn R Campagna

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2022. 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
0.6field-weighted citation impact, top 28% 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, 3 citations in OpenAlex.

  1. Review
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

6 authors at 3 institutions in 1 country.

Ashley M LatoDepartment of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States.ORCID https://orcid.org/0000-0003-4076-9714
Susan J BurkePennington Biomedical Research Center, Baton Rouge, Louisiana 70808, United States.
Maggie P DucotePennington Biomedical Research Center, Baton Rouge, Louisiana 70808, United States.
Brandon J KennedyDepartment of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.ORCID https://orcid.org/0000-0003-1892-8926
J Jason CollierPennington Biomedical Research Center, Baton Rouge, Louisiana 70808, United States.ORCID https://orcid.org/0000-0003-2817-4152
Shawn R CampagnaDepartment of Chemistry, University of Tennessee, Knoxville, Tennessee 37996, United States.ORCID https://orcid.org/0000-0001-6809-3862
Pennington Biomedical Research Center · USUniversity of Tennessee at Knoxville · USPrinceton University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
SGK1 is a regulator of islet beta cell mass and secretory functionR01DK123183 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI COLLIER, JAMES JASON · 2020 to 2024
$1.8M
A Unique Receptor Agonist Approach for Type 1 Diabetes PreventionR21AI138136 · NIAID · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI COLLIER, JAMES JASON · 2018 to 2019
$436k
NIAID NIH HHS R21 AI138136NIDDK NIH HHS R01 DK123183NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Glucocorticoids (GCs) are heavily prescribed to control inflammation in various human diseases; however, side effects associated with GCs are well documented and lead to serious metabolic and immunological complications with long-term use. The paradigm for GC function includes two well described modes of activity: dimer formation of the glucocorticoid receptor (GR) promotes transactivation, while monomeric interaction with co-regulators promotes transrepression. Previously, a set of aryl pyrazole-derived glucocorticoid receptor agonists (APGRAs) with potency rivaling current commercially available glucocorticoids were described. In this study, a further series of existing and novel stereopure APGRAs were thoroughly examined for biological activity and evaluated for structure-activity relationships (SARs). The

Identifiers

PMID36105346
PMCPMC9465825
OpenAlexW4292615999

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.