Evidence map›Paper›PMID 33467931›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2021

Pyridinium-2-carbaldoximes with quinolinium carboxamide moiety are simultaneous reactivators of acetylcholinesterase and butyrylcholinesterase inhibited by nerve agent surrogates.

Hyun Myung Lee, Rudolf Andrys, Jakub Jonczyk, Kyuneun Kim, Avinash G Vishakantegowda, David Malinak, Adam Skarka, Monika Schmidt, Michaela Vaskova, Kamil Latka and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 3 institutions in 3 countries.

Hyun Myung LeeDivision of Bio and Drug Discovery, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0003-3591-7268
Rudolf AndrysDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0003-1108-3924
Jakub JonczykDepartment of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland.ORCID https://orcid.org/0000-0002-9731-908X
Kyuneun KimDivision of Bio and Drug Discovery, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0002-8610-5414
Avinash G VishakantegowdaDivision of Bio and Drug Discovery, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0003-0712-6418
David MalinakDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0002-0665-0667
Adam SkarkaDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0002-7355-6857
Monika SchmidtDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0003-4984-9155
Michaela VaskovaDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0001-8858-5434
Kamil LatkaDepartment of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland.ORCID https://orcid.org/0000-0002-8240-592X
Marek BajdaDepartment of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland.ORCID https://orcid.org/0000-0001-6032-0354
Young-Sik JungDivision of Bio and Drug Discovery, Korea Research Institute of Chemical Technology, Daejeon, Republic of Korea.ORCID https://orcid.org/0000-0001-9492-6848
Barbara MalawskaDepartment of Physicochemical Drug Analysis, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland.ORCID https://orcid.org/0000-0003-4637-5820
Kamil MusilekDepartment of Chemistry, Faculty of Science, University of Hradec Kralove, Hradec Kralove, Czech Republic.ORCID https://orcid.org/0000-0002-7504-4062
University of Hradec Králové · CZDaejeon University · KRJagiellonian University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pyridinium-2-carbaldoximes with quinolinium carboxamide moiety were designed and synthesised as cholinesterase reactivators. The prepared compounds showed intermediate-to-high inhibition of both cholinesterases when compared to standard oximes. Their reactivation ability was evaluated

Indexed as

AcetylcholinesteraseButyrylcholinesteraseCholinesterase InhibitorsDose-Response Relationship, DrugHumansMolecular Docking SimulationMolecular StructurePyridinium CompoundsQuinolinium CompoundsRecombinant ProteinsStructure-Activity RelationshipAcetylcholinesteraseButyrylcholinesteraseCholinesterase InhibitorsPyridinium CompoundsQuinolinium CompoundsRecombinant ProteinsacetylcholinesterasebutyrylcholinesteraseOrganophosphateoximereactivator

Identifiers

PMID33467931
PMCPMC7822067
OpenAlexW3124523025

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.