Evidence map›Paper›PMID 36882080›Full record

ArticleJournal of medicinal chemistry2023

Oxadiazolopyridine Derivatives as Efficacious Mitochondrial Uncouplers in the Prevention of Diet-Induced Obesity.

Jacob H Murray, Ariel L Burgio, Martina Beretta, Stefan R Hargett, Thurl E Harris, Ellen Olzomer, R Justin Grams, Christopher J Garcia, Catherine Li, Joseph M Salamoun and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-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

9 citing papers in PubMed, 14 citations in OpenAlex.

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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 3 institutions in 2 countries.

Jacob H MurrayDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.
Ariel L BurgioDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.
Martina BerettaSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales 2033, Australia.
Stefan R HargettDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia 22908, United States.
Thurl E HarrisDepartment of Pharmacology, University of Virginia, Charlottesville, Virginia 22908, United States.ORCID 0000-0003-1742-6043
Ellen OlzomerSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales 2033, Australia.
R Justin GramsDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.ORCID 0000-0001-7306-3473
Christopher J GarciaDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.
Catherine LiSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales 2033, Australia.
Joseph M SalamounDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.
Kyle L HoehnSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, New South Wales 2033, Australia.
Webster L SantosDepartment of Chemistry and Virginia Tech Center for Drug Discovery, Virginia Tech, Blacksburg, Virginia 24061, United States.ORCID 0000-0002-4731-8548
Virginia Tech · USUNSW Sydney · AUUniversity of Virginia · US

Funding

VT Initiative for Maximizing Student DiversityR25GM072767 · NIGMS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SMITH, EDWARD J · 2007 to 2021
$6.9M
Therapeutic Mitochondrial UncouplersR01DK128612 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HOEHN, KYLE LEE, SANTOS, WEBSTER L · 2021 to 2024
$2.2M
NIDDK NIH HHS R01 DK128612NIGMS NIH HHS R25 GM072767
6 · The paper itself

Abstract

Small-molecule mitochondrial uncouplers are gaining recognition as potential therapeutics for metabolic diseases such as obesity, diabetes, and nonalcoholic steatohepatitis (NASH). Specifically, heterocycles derived from BAM15, a potent and mitochondria-selective uncoupler, have yielded promising preclinical candidates that are efficacious in animal models of obesity and NASH. In this study, we report the structure-activity relationship studies of 6-amino-[1,2,5]oxadiazolo[3,4-

Indexed as

Non-alcoholic Fatty Liver DiseaseAnimalsDietMiceMitochondriaObesityOxygen Consumption

Identifiers

PMID36882080
PMCPMC10167758
OpenAlexW4323350014

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.