Evidence map›Paper›PMID 30018949›Full record

ArticleFrontiers in chemistry2018

Selenazolyl-hydrazones as Novel Selective MAO Inhibitors With Antiproliferative and Antioxidant Activities: Experimental and

Hana Elshaflu, Tamara R Todorović, Milan Nikolić, Aleksandar Lolić, Aleksandar Višnjevac, Stefanie Hagenow, José M Padrón, Alfonso T García-Sosa, Ivana S Djordjević, Sonja Grubišić and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in chemistry, 2018. 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
1.9field-weighted citation impact, top 15% 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, 44 citations in OpenAlex.

  1. Article
  2. Novel Pyridine-Based Thiazolyl-Hydrazone as a Promising Attenuator ofInternational journal of molecular sciences · 2026
    Article
  3. Harnessing coumarin-thio(seleno)cyanate conjugates: potentJournal of enzyme inhibition and medicinal chemistry · 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 6 institutions in 5 countries.

Hana ElshafluFaculty of Technology and Metallurgy, University of Belgrade, Belgrade, Serbia.
Tamara R TodorovićDepartment of General and Inorganic Chemistry, University of Belgrade - Faculty of Chemistry, Belgrade, Serbia.
Milan NikolićDepartment of General and Inorganic Chemistry, University of Belgrade - Faculty of Chemistry, Belgrade, Serbia.
Aleksandar LolićDepartment of General and Inorganic Chemistry, University of Belgrade - Faculty of Chemistry, Belgrade, Serbia.
Aleksandar VišnjevacDivision of Physical Chemistry, Ruder Bošković Institute, Zagreb, Croatia.
Stefanie HagenowInstitute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
José M PadrónInstituto Universitario de Bio-Orgánica "Antonio González", Universidad de La Laguna, Tenerife, Spain.
Alfonso T García-SosaInstitute of Chemistry, University of Tartu, Tartu, Estonia.
Ivana S DjordjevićInstitute of Chemistry, Technology and Metallurgy, University of Belgrade, Belgrade, Serbia.
Sonja GrubišićInstitute of Chemistry, Technology and Metallurgy, University of Belgrade, Belgrade, Serbia.
Holger StarkInstitute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Nenad R FilipovićDepartment of Chemistry and Biochemistry, Faculty of Agriculture, University of Belgrade, Belgrade, Serbia.
University of Belgrade · RSHeinrich Heine University Düsseldorf · DEUniversity of Belgrade – Faculty of ChemistryRudjer Boskovic Institute · HRUniversidad de La Laguna · ESUniversity of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The novel approach in the treatment of complex multifactorial diseases, such as neurodegenerative disorders and cancer, requires a development of efficient multi-targeting oriented drugs. Since oxidative stress significantly contributes to the pathogenesis of cancer and neurodegenerative disorders, potential drug candidates should possess good antioxidant properties. Due to promising biological activities shown for structurally related (1,3-thiazol-2-yl)hydrazones, a focused library of 12 structurally related benzylidene-based (1,3-selenazol-2-yl)hydrazones was designed as potential multi-targeting compounds. Monoamine oxidases (MAO) A/B inhibition properties of this class of compounds have been investigated. Surprisingly, the

Indexed as

Anticancer activityAntioxidant agentsDockingMAO Bselenazoles

Identifiers

PMID30018949
PMCPMC6037691
OpenAlexW2808261736

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.