Evidence map›Paper›PMID 31052551›Full record

ArticleInternational journal of molecular sciences2019

Synthesis and In Vitro Antitumor Activity of Naringenin Oxime and Oxime Ether Derivatives.

Ahmed Dhahir Latif, Tímea Gonda, Máté Vágvölgyi, Norbert Kúsz, Ágnes Kulmány, Imre Ocsovszki, Zoltán Péter Zomborszki, István Zupkó, Attila Hunyadi

Abstract 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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. A Review of Biologically Active Oxime Ethers.Molecules (Basel, Switzerland) · 2023
    Review
  5. Antiproliferative Activity and Impact on Human Gut Microbiota of NewInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Less Cytotoxic Protoflavones as Antiviral Agents: Protoapigenone 1'-International journal of molecular sciences · 2019
    Article
  18. 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

9 authors.

Ahmed Dhahir LatifInstitute of Pharmacodynamics and Biopharmacy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. latif.ahmed@pharmacognosy.hu.
Tímea GondaInstitute of Pharmacognosy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. gonda.timea@pharm.u-szeged.hu.
Máté VágvölgyiInstitute of Pharmacognosy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. vagvolgyi.mate@pharm.u-szeged.hu.
Norbert KúszInstitute of Pharmacognosy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. kusz.norbert@pharm.u-szeged.hu.
Ágnes KulmányInstitute of Pharmacodynamics and Biopharmacy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. agnes.kulmany@gmail.com.
Imre OcsovszkiDepartment of Biochemistry, University of Szeged, 6720 Szeged, Hungary. imre@biochem.szote.u-szeged.hu.
Zoltán Péter ZomborszkiInstitute of Pharmacognosy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. zombozope@pharmacognosy.hu.
István ZupkóInstitute of Pharmacodynamics and Biopharmacy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. zupko@pharm.u-szeged.hu.ORCID 0000-0003-3243-5300
Attila HunyadiInstitute of Pharmacognosy, Interdisciplinary Excellence Centre, University of Szeged, 6720 Szeged, Hungary. hunyadi.a@pharm.u-szeged.hu.

Funding

Emberi Eroforrások Minisztériuma 20391-3/2018/FEKUSTRATNemzeti Kutatási Fejlesztési és Innovációs Hivatal K119770
6 · The paper itself

Abstract

Naringenin is one of the most abundant dietary flavonoids exerting several beneficial biological activities. Synthetic modification of naringenin is of continuous interest. During this study our aim was to synthesize a compound library of oxime and oxime ether derivatives of naringenin, and to investigate their biological activities. Two oximes and five oxime ether derivatives were prepared; their structure has been elucidated by NMR and high-resolution mass spectroscopy. The antiproliferative activity of the prepared compounds was evaluated by MTT assay against human leukemia (HL-60) and gynecological cancer cell lines isolated from cervical (HeLa, Siha) and breast (MCF-7, MDA-MB-231) cancers.

Indexed as

Antineoplastic AgentsApoptosisCell CycleCell Cycle CheckpointsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorFlavanonesHeLa CellsHumansMCF-7 CellsNeoplasmsOximesStructure-Activity RelationshipAntineoplastic AgentsFlavanonesnaringeninOximesantioxidantantiproliferativecaspase activitycell cycle analysisnaringenin derivativenaringenin-oximeoxime ether

Identifiers

PMID31052551
PMCPMC6539930

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.