Evidence map›Paper›PMID 37764424›Full record

ArticleMolecules (Basel, Switzerland)2023

May 1,2-Dithiolane-4-carboxylic Acid and Its Derivatives Serve as a Specific Thioredoxin Reductase 1 Inhibitor?

Anna Nikitjuka, Kristaps Krims-Davis, Iveta Kaņepe-Lapsa, Melita Ozola, Raivis Žalubovskis

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. 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
0.2field-weighted citation impact, top 41% 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, 1 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.

Anna NikitjukaLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.ORCID 0000-0003-1622-6349
Kristaps Krims-DavisLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.
Iveta Kaņepe-LapsaLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.ORCID 0000-0002-0022-2813
Melita OzolaLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.ORCID 0000-0002-3453-0099
Raivis ŽalubovskisLatvian Institute of Organic Synthesis, Aizkraukles 21, LV-1006 Riga, Latvia.ORCID 0000-0002-9471-1342
Latvijas Organiskās Sintēzes Institūts · LVRiga Technical University · LV

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thioredoxin reductase is an essential enzyme that plays a crucial role in maintaining cellular redox homeostasis by catalyzing the reduction of thioredoxin, which is involved in several vital cellular processes. The overexpression of TrxR is often associated with cancer development. A series of 1,2-dithiolane-4-carboxylic acid analogs were obtained to verify the selectivity of 1,2-dithiolane moiety toward TrxR. Asparagusic acid analogs and their bioisoters remain inactive toward TrxR, which proves the inability of the 1,2-dithiolane moiety to serve as a pharmacophore during the interaction with TrxR. It was found that the Michael acceptor functionality-containing analogs exhibit higher inhibitory effects against TrxR compared to other compounds of the series. The most potent representatives exhibited micromolar TrxR1 inhibition activity (IC

Indexed as

Enzyme InhibitorsThioredoxin Reductase 1Antineoplastic AgentsCell Line, TumorHumansMolecular StructureStructure-Activity RelationshipAntineoplastic AgentsEnzyme InhibitorsThioredoxin Reductase 11,2-dithiolaneasaparagusic acidMichael acceptorTrxR

Identifiers

PMID37764424
PMCPMC10535816
OpenAlexW4386838672

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.