Evidence map›Paper›PMID 39250602›Full record

ReviewJournal of medicinal chemistry2024

The "Doorstop Pocket" In Thioredoxin Reductases─An Unexpected Druggable Regulator of the Catalytic Machinery.

Matteo Ardini, Sammy Y Aboagye, Valentina Z Petukhova, Irida Kastrati, Rodolfo Ippoliti, Gregory R J Thatcher, Pavel A Petukhov, David L Williams, Francesco Angelucci

Abstract readReview
In one paragraph

Review in Journal of medicinal chemistry, 2024. 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
–field-weighted citation impact
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.

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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

9 authors.

Matteo ArdiniDepartment of Life, Health and Environmental Sciences, University of L'Aquila, 67100 L'Aquila, Italy.
Sammy Y AboagyeDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, Illinois 60612, United States.
Valentina Z PetukhovaDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Illinois Chicago, Chicago, Illinois 60612, United States.
Irida KastratiDepartment of Cancer Biology, Loyola University Chicago, 60153 Maywood, Illinois 60153, United States.
Rodolfo IppolitiDepartment of Life, Health and Environmental Sciences, University of L'Aquila, 67100 L'Aquila, Italy.
Gregory R J ThatcherDepartment of Pharmacology & Toxicology, R. Ken Coit College of Pharmacy, University of Arizona, Tucson, Arizona 85721, United States.ORCID 0000-0002-7757-1739
Pavel A PetukhovDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Illinois Chicago, Chicago, Illinois 60612, United States.ORCID 0000-0003-1554-242X
David L WilliamsDepartment of Microbial Pathogens and Immunity, Rush University Medical Center, Chicago, Illinois 60612, United States.ORCID 0000-0002-6815-4909
Francesco AngelucciDepartment of Life, Health and Environmental Sciences, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0001-7305-7903

Funding

The Institute for Translational MedicineUL1TR002389 · NCATS · UNIVERSITY OF CHICAGO · PI Joshua J Jacobs, DAVID O MELTZER · 2017 to 2026
$71.6M
Development of novel TGR inhibitors for the treatment of schistosomiasisR01AI177493 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Pavel A Petukhov, DAVID LEE WILLIAMS · 2024 to 2026
$2.3M
Identification of preclinical drug candidates for the treatment of schistosomiasisR33AI127635 · NIAID · RUSH UNIVERSITY MEDICAL CENTER · PI PETUKHOV, PAVEL A, THATCHER, GREGORY R. J · 2019 to 2021
$1.3M
Identification of preclinical drug candidates for the treatment of schistosomiasisR21AI127635 · NIAID · RUSH UNIVERSITY MEDICAL CENTER · PI PETUKHOV, PAVEL A, THATCHER, GREGORY R. J · 2017 to 2018
$392k
NCATS NIH HHS UL1 TR002389NIAID NIH HHS R01 AI177493NIAID NIH HHS R21 AI127635NIAID NIH HHS R33 AI127635
6 · The paper itself

Abstract

Pyridine nucleotide-disulfide oxidoreductases are underexplored as drug targets, and thioredoxin reductases (TrxRs) stand out as compelling pharmacological targets. Selective TrxR inhibition is challenging primarily due to the reliance on covalent inhibition strategies. Recent studies identified a regulatory and druggable pocket in

Indexed as

Enzyme InhibitorsSchistosoma mansoniThioredoxin-Disulfide ReductaseAnimalsHumansMultienzyme ComplexesNADH, NADPH OxidoreductasesNADPEnzyme InhibitorsMultienzyme ComplexesNADH, NADPH OxidoreductasesNADPThioredoxin-Disulfide Reductasethioredoxin glutathione reductase

Identifiers

PMID39250602
PMCPMC12013724

What OpenQuestion holds

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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.