Evidence map›Paper›PMID 35936029›Full record

ArticleChem2022

Selective cellular probes for mammalian thioredoxin reductase TrxR1: rational design of RX1, a modular 1,2-thiaselenane redox probe.

Lukas Zeisel, Jan G Felber, Karoline C Scholzen, Lena Poczka, Dorian Cheff, Martin S Maier, Qing Cheng, Min Shen, Matthew D Hall, Elias S J Arnér and 2 more

Open access · greenAbstract read
In one paragraph

Article in Chem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Selenium Nucleophilicity and Electrophilicity in the Intra- and Intermolecular SChemistry (Weinheim an der Bergstrasse, Germany) · 2025
    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 5 institutions in 4 countries.

Lukas ZeiselDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Jan G FelberDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Karoline C ScholzenDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solnavägen 9, 17177 Stock-holm, SE.
Lena PoczkaDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Dorian CheffNational Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, Maryland 20850, USA.
Martin S MaierDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Qing ChengDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solnavägen 9, 17177 Stock-holm, SE.
Min ShenNational Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, Maryland 20850, USA.
Matthew D HallNational Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, Maryland 20850, USA.
Elias S J ArnérDivision of Biochemistry, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solnavägen 9, 17177 Stock-holm, SE.
Julia Thorn-SesholdDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Oliver Thorn-SesholdDepartment of Pharmacy, Ludwig-Maximilians University of Munich, Butenandtstr. 5-13, 81377 Munich, DE.
Ludwig-Maximilians-Universität München · DEKarolinska Institutet · SENational Institutes of Health · USNational Center for Advancing Translational Sciences · USNational Institute of Oncology · HU

Funding

Screening for novel inhibitors of Glutathione Peroxidase 1 and 4ZIATR000418 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI HALL, MATTHEW · 2020 to 2025
$1.1M
Intramural NIH HHS ZIA TR000418
6 · The paper itself

Abstract

Quantifying the activity of key cellular redox players is crucial for understanding physiological homeostasis, and for targeting their perturbed states in pathologies including cancer and inflammatory diseases. However, cellularly-selective probes for oxidoreductase turnover are sorely lacking. We rationally developed the first probes that selectively target the mammalian selenoprotein thioredoxin reductase (TrxR), using a cyclic selenenylsulfide oriented to harness TrxR's unique selenolthiol chemistry while resisting the cellular monothiol background. Lead probe

Indexed as

cellular probechemical designdichalcogenidedisulfidefluorogenic probehigh-throughput screeningredox biologyselenenyl sulfidethioredoxinthioredoxin reductase

Identifiers

PMID35936029
PMCPMC9351623
OpenAlexW4226143764

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.