Evidence map›Paper›PMID 30934674›Full record

ArticleInternational journal of molecular sciences2019

Novel Benzene-Based Carbamates for AChE/BChE Inhibition: Synthesis and Ligand/Structure-Oriented SAR Study.

Andrzej Bak, Violetta Kozik, Dariusz Kozakiewicz, Kamila Gajcy, Daniel Jan Strub, Aleksandra Swietlicka, Sarka Stepankova, Ales Imramovsky, Jaroslaw Polanski, Adam Smolinski and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Chemistry towards Biology-Instruct: Snapshot.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Novel Sulfonamide-Based Carbamates as Selective Inhibitors of BChE.International journal of molecular sciences · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. 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

11 authors at 5 institutions in 3 countries.

Andrzej BakInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. andrzej.bak@us.edu.pl.ORCID 0000-0002-9842-1289
Violetta KozikInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. violetta.kozik@us.edu.pl.
Dariusz KozakiewiczInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. dkozakiewicz@us.edu.pl.
Kamila GajcyInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. kamila.gajcy@us.edu.pl.
Daniel Jan StrubDepartment of Bioorganic Chemistry, Faculty of Chemistry, Wrocław University of Science and Technology, Wyb. Wyspiańskiego 27, 50-370 Wrocław, Poland. daniel.strub@pwr.edu.pl.ORCID 0000-0003-0858-463X
Aleksandra SwietlickaInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. aswietlicka@us.edu.pl.
Sarka StepankovaDepartment of Biological and Biochemical Sciences, Faculty of Chemical Technology, University of Pardubice, Studentska 573, 532 10 Pardubice, Czech Republic. sarka.stepankova@upce.cz.ORCID 0000-0002-1969-5258
Ales ImramovskyInstitute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studentska 573, 532 10 Pardubice, Czech Republic. ales.imramovsky@upce.cz.ORCID 0000-0001-9476-9627
Jaroslaw PolanskiInstitute of Chemistry, University of Silesia, Szkolna 9, 40 007 Katowice, Poland. jaroslaw.polanski@us.edu.pl.
Adam SmolinskiDepartment of Energy Saving and Air Protection, Central Mining Institute, Plac Gwarkow 1, 40 166 Katowice, Poland. smolin@gig.katowice.pl.ORCID 0000-0002-4901-7546
Josef JampilekDivision of Biologically Active Complexes and Molecular Magnets, Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacky University, Slechtitelu 27, 78371 Olomouc, Czech Republic. josef.jampilek@gmail.com.ORCID 0000-0003-2003-9052
University of Silesia in Katowice · PLUniversity of Pardubice · CZCentral Mining Institute · PLSlovak Academy of Sciences · SKWrocław University of Science and Technology · PL

Funding

Ministry of Education of the Czech Republic LO1305Slovak Research and Development Agency APVV-17-0373 and APVV-14-0547
6 · The paper itself

Abstract

A series of new benzene-based derivatives was designed, synthesized and comprehensively characterized. All of the tested compounds were evaluated for their in vitro ability to potentially inhibit the acetyl- and butyrylcholinesterase enzymes. The selectivity index of individual molecules to cholinesterases was also determined. Generally, the inhibitory potency was stronger against butyryl- compared to acetylcholinesterase; however, some of the compounds showed a promising inhibition of both enzymes. In fact, two compounds (23, benzyl ethyl(1-oxo-1-phenylpropan-2-yl)carbamate and 28, benzyl (1-(3-chlorophenyl)-1-oxopropan-2-yl) (methyl)carbamate) had a very high selectivity index, while the second one (28) reached the lowest inhibitory concentration IC

Indexed as

AcetylcholinesteraseAnimalsBenzeneButyrylcholinesteraseCarbamatesCholinesterase InhibitorsDrug DesignElectrophorusHorsesInhibitory Concentration 50LigandsMolecular Docking SimulationPrincipal Component AnalysisProbabilityStructure-Activity RelationshipAcetylcholinesteraseBenzeneButyrylcholinesteraseCarbamatesCholinesterase InhibitorsLigandsbenzene-based carbamatesCoMSAin vitro cholinesterase inhibitionIVE-PLSmolecular docking study

Identifiers

PMID30934674
PMCPMC6479915
OpenAlexW2924348321

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.