Evidence map›Paper›PMID 31754915›Full record

ArticleMolecular diversity2020

Discovery and evaluation of inhibitory activity and mechanism of arylcoumarin derivatives on Theileria annulata enolase by in vitro and molecular docking studies.

Sinem Yakarsonmez, Ozkan Danis, Ozal Mutlu, Murat Topuzogullari, Emrah Sariyer, Basak Yuce-Dursun, Dilek Turgut-Balik

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular diversity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Rapid and sensitive detection of bovineFrontiers in microbiology · 2025
    Article
  3. Natural source, bioactivity and synthesis of 3-Arylcoumarin derivatives.Journal of enzyme inhibition and medicinal chemistry · 2022
    Review
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

7 authors at 4 institutions in 1 country.

Sinem YakarsonmezDepartment of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Yıldız Technical University, Davutpasa Campus, 34210, Istanbul, Turkey.
Ozkan DanisDepartment of Chemistry, Faculty of Arts and Sciences, Marmara University, 34722, Istanbul, Turkey.
Ozal MutluDepartment of Biology, Faculty of Arts and Sciences, Marmara University, 34722, Istanbul, Turkey.
Murat TopuzogullariDepartment of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Yıldız Technical University, Davutpasa Campus, 34210, Istanbul, Turkey.
Emrah SariyerDepartment of Genetics and Bioengineering, Faculty of Engineering and Natural Sciences, Gumushane University, 29100, Gumushane, Turkey.
Basak Yuce-DursunDepartment of Chemistry, Faculty of Arts and Sciences, Marmara University, 34722, Istanbul, Turkey.
Dilek Turgut-BalikDepartment of Bioengineering, Faculty of Chemical and Metallurgical Engineering, Yıldız Technical University, Davutpasa Campus, 34210, Istanbul, Turkey. dilekbalik@gmail.com.ORCID http://orcid.org/0000-0003-2417-4104
Marmara University · TRYıldız Technical University · TRGümüşhane University · TRIstanbul Yeni Yüzyıl University · TR

Funding

General Directorate of Agricultural Research and Policies of Republic of Turkey Ministry of Food, Agriculture and Livestock TAGEM-14/AR-GE/17TUBITAK-BIDEB 2211-A National Scholarship Programme for PhD Students. TUBITAK BIDEB 2211-A
6 · The paper itself

Abstract

In this study, the inhibition potential of 3- and 4-arylcoumarin derivatives on Theileria annulata enolase (TaENO) was assessed for the first time in the literature. Firstly, protein stabilization analyses of TaENO were performed and it was found that the enzyme remains stable with the addition of 6 M ethylene glycol at + 4 °C. Inhibitor screening analyses were carried out using 25 coumarin derivatives on highly purified TaENO (> 95%), and four coumarin derivatives [4-(3,4-dimethoxyphenyl)-6,7-dihydroxy-2H-chromen-2-one (C8); 4-(3,4-dihydroxyphenyl)-7,8 dihydroxy-2H-chromen-2-one (C9); 4-(3,4-dihydroxyphenyl)-6,7-dihydroxy-2H-chromen-2 one (C21); and 3-(3,4-dihydroxyphenyl)-7,8-dihydroxy-2H-chromen-2-one (C23)] showed the highest inhibitory effects with the IC

Indexed as

Catalytic DomainCoumarinsDrug DesignKineticsMolecular Docking SimulationPhosphopyruvate HydrataseStructure-Activity RelationshipTheileria annulata2H-chromen-2-onecoumarinCoumarinsPhosphopyruvate HydrataseCoumarinDrug resistanceEnolaseEnzyme inhibitionStructure-based drug designTheileriosis

Identifiers

PMID31754915
OpenAlexW2990973954

What OpenQuestion holds

Textmetadata
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.