Evidence map›Paper›PMID 25010466›Full record

ArticleMolecules (Basel, Switzerland)2014

1,4-Disubstituted thiosemicarbazide derivatives are potent inhibitors of Toxoplasma gondii proliferation.

Katarzyna Dzitko, Agata Paneth, Tomasz Plech, Jakub Pawełczyk, Paweł Stączek, Joanna Stefańska, Piotr Paneth

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Transient Adaptation ofInternational journal of molecular sciences · 2024
    Article
  3. 4-Arylthiosemicarbazide derivatives as a new class of tyrosinase inhibitors and anti-Journal of enzyme inhibition and medicinal chemistry · 2021
    Article
  4. Article
  5. Synthesis and In Vitro Anti-Molecules (Basel, Switzerland) · 2019
    Article
  6. Article
  7. Article
  8. Article
  9. Anti-International journal of nanomedicine · 2018
    Article
  10. Thiazoles with cyclopropyl fragment as antifungal, anticonvulsant, and anti-Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2018
    Article
  11. Article
  12. Review
  13. A Systematic Review ofFrontiers in microbiology · 2017
    Review
  14. Article
  15. Article
  16. Synthesis, molecular docking, ctDNA interaction, DFT calculation and evaluation of antiproliferative and anti-Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents
    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

7 authors.

Katarzyna DzitkoDepartment of Immunoparasitology, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland. dzika@biol.uni.lodz.pl.
Agata PanethDepartment of Organic Chemistry, Medical University, Chodźki 4a, 20-093 Lublin, Poland. piotr.paneth@p.lodz.pl.
Tomasz PlechDepartment of Organic Chemistry, Medical University, Chodźki 4a, 20-093 Lublin, Poland. tomasz.plech@umlub.pl.
Jakub PawełczykInstitute for Medical Biology of the Polish Academy of Sciences, Lodowa 106, 93-232 Łódź, Poland. jpawelczyk@cbm.pan.pl.
Paweł StączekDepartment of Genetics of Microorganisms, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland. pstaczek@biol.uni.lodz.pl.
Joanna StefańskaDepartment of Pharmaceutical Microbiology, Medical University of Warsaw, Oczki 3, 02-007 Warszawa, Poland. jstefanska@wum.edu.pl.
Piotr PanethInstitute of Applied Radiation Chemistry, Technical University of Lodz, Zeromskiego 116, 90-924 Lodz, Poland. piotr.paneth@p.lodz.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 4-arylthiosemicarbazides substituted at the N1 position with a 5-membered heteroaryl ring was synthesized and evaluated in vitro for T. gondii inhibition proliferation and host cell cytotoxicity. At non-toxic concentrations for the host cells all studied compounds displayed excellent anti-parasitic effects when compared to sulfadiazine, indicating a high selectivity of their anti-T. gondii activity. The differences in bioactivity investigated by DFT calculations suggest that the inhibitory activity of 4-aryl-thiosemicarbazides towards T. gondii proliferation is connected with the electronic structure of the molecule. Further, these compounds were tested as potential antibacterial agents. No growth-inhibiting effect on any of the test microorganisms was observed for all the compounds, even at high concentrations.

Indexed as

AnimalsAnti-Bacterial AgentsAntiprotozoal AgentsCell LineFemaleInhibitory Concentration 50MiceMolecular StructureParasitic Sensitivity TestsSemicarbazidesStaphylococcus aureusTopoisomerase II InhibitorsToxoplasmaAnti-Bacterial AgentsAntiprotozoal AgentsSemicarbazidesthiosemicarbazideTopoisomerase II Inhibitors

Identifiers

PMID25010466
PMCPMC6290556

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.