Evidence map›Paper›PMID 38446233›Full record

ArticleArchives of toxicology2024

A-series agent A-234: initial in vitro and in vivo characterization.

Martina Hrabinova, Jaroslav Pejchal, Vendula Hepnarova, Lubica Muckova, Lucie Junova, Jakub Opravil, Jana Zdarova Karasova, Tomas Rozsypal, Alzbeta Dlabkova, Helena Rehulkova and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Archives of toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
10.7field-weighted citation impact, top 1% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Accelerating countermeasure candidate discovery for A-series chemical warfare agent exposure.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Undescribed Amaryllidaceae Alkaloids fromJournal of natural products · 2024
    Article
  10. Review
  11. 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

16 authors at 3 institutions in 2 countries.

Martina Hrabinova *University of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Jaroslav Pejchal *University of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Vendula HepnarovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic. vendula.hepnarova@unob.cz.ORCID 0000-0002-6445-2669
Lubica MuckovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Lucie JunovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Jakub OpravilUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Jana Zdarova KarasovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Tomas RozsypalUniversity of Defence, Nuclear, Biological, and Chemical Defence Institute, Vita Nejedleho 1, 68203, Vyskov, Czech Republic.
Alzbeta DlabkovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Helena RehulkovaUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Tomas KuceraUniversity of Defence, Military Faculty of Medicine, Department of Military Medical Service Organization and Management, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Zbyněk VeceraUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic.
Filip CaisbergerUniversity Hospital Hradec Kralove, Department of Neurology, Sokolska 581, 500 05, Hradec Králové, Czech Republic.
Monika SchmidtUniversity Hospital Hradec Kralove, Biomedical Research Centre, Sokolska 581, 500 05, Hradec Králové, Czech Republic.
Ondrej SoukupUniversity Hospital Hradec Kralove, Biomedical Research Centre, Sokolska 581, 500 05, Hradec Králové, Czech Republic.
Daniel JunUniversity of Defence, Military Faculty of Medicine, Department of Toxicology and Military Pharmacy, Trebesska 1575, 500 01, Hradec Králové, Czech Republic. daniel.jun@unob.cz.ORCID 0000-0002-0882-6304
University of Defence · CZUniversity Hospital Hradec Králové · CZUniversity of Defence · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A-series agent A-234 belongs to a new generation of nerve agents. The poisoning of a former Russian spy Sergei Skripal and his daughter in Salisbury, England, in March 2018 led to the inclusion of A-234 and other A-series agents into the Chemical Weapons Convention. Even though five years have already passed, there is still very little information on its chemical properties, biological activities, and treatment options with established antidotes. In this article, we first assessed A-234 stability in neutral pH for subsequent experiments. Then, we determined its inhibitory potential towards human recombinant acetylcholinesterase (HssAChE; EC 3.1.1.7) and butyrylcholinesterase (HssBChE; EC 3.1.1.8), the ability of HI-6, obidoxime, pralidoxime, methoxime, and trimedoxime to reactivate inhibited cholinesterases (ChEs), its toxicity in rats and therapeutic effects of different antidotal approaches. Finally, we utilized molecular dynamics to explain our findings. The results of spontaneous A-234 hydrolysis showed a slow process with a reaction rate displaying a triphasic course during the first 72 h (the residual concentration 86.2%). A-234 was found to be a potent inhibitor of both human ChEs (HssAChE IC

Indexed as

Cholinesterase ReactivatorsPralidoxime CompoundsAcetylcholinesteraseAnimalsAntidotesButyrylcholinesteraseCholinesterase InhibitorsHumansOximesOxygenPhosphorusPyridinium CompoundsRatsTaurineTrimedoxime2-(N-cyclohexylamino)ethanesulfonic acidAcetylcholinesteraseAntidotesasoxime chlorideButyrylcholinesteraseCholinesterase InhibitorsCholinesterase ReactivatorsN,N'-monomethylenebis(pyridiniumaldoxime)OximesOxygenPhosphoruspralidoximePralidoxime CompoundsPyridinium CompoundsTaurineTrimedoximeAcute toxicityHydrolysisNerve agent A-234ReactivationTherapy

Identifiers

PMID38446233
PMCPMC10944400
OpenAlexW4392512570

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.