Evidence map›Paper›PMID 32645868›Full record

ArticleMolecules (Basel, Switzerland)2020

Antioxidant Activity of Selected Phenolic Acids-Ferric Reducing Antioxidant Power Assay and QSAR Analysis of the Structural Features.

Maciej Spiegel, Karina Kapusta, Wojciech Kołodziejczyk, Julia Saloni, Beata Żbikowska, Glake A Hill, Zbigniew Sroka

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
–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

85 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Seasonal Variation in WildMolecules (Basel, Switzerland) · 2026
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  12. Polyphenols fromMembranes · 2025
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  14. Antibiotics (Basel, Switzerland) · 2025
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  20. Sustainable Meat Alternatives: Incorporation ofFoods (Basel, Switzerland) · 2025
    Article

25 more citing papers are in PubMed but not listed here.

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.

Maciej SpiegelDepartment of Pharmacognosy, Wroclaw Medical University, Borowska 211, 50-556 Wroclaw, Poland.ORCID 0000-0002-8012-1026
Karina KapustaInterdisciplinary Center for Nanotoxicity, Department of Chemistry, Physics and Atmospheric Sciences, Jackson State University, 1400 J. R. Lynch str., Jackson, MS 39217, USA.
Wojciech KołodziejczykInterdisciplinary Center for Nanotoxicity, Department of Chemistry, Physics and Atmospheric Sciences, Jackson State University, 1400 J. R. Lynch str., Jackson, MS 39217, USA.ORCID 0000-0002-7754-8969
Julia SaloniInterdisciplinary Center for Nanotoxicity, Department of Chemistry, Physics and Atmospheric Sciences, Jackson State University, 1400 J. R. Lynch str., Jackson, MS 39217, USA.
Beata ŻbikowskaDepartment of Pharmacognosy, Wroclaw Medical University, Borowska 211, 50-556 Wroclaw, Poland.
Glake A HillInterdisciplinary Center for Nanotoxicity, Department of Chemistry, Physics and Atmospheric Sciences, Jackson State University, 1400 J. R. Lynch str., Jackson, MS 39217, USA.
Zbigniew SrokaDepartment of Pharmacognosy, Wroclaw Medical University, Borowska 211, 50-556 Wroclaw, Poland.ORCID 0000-0001-6618-017X

Funding

National Science Foundation HRD-1547754Wroclaw Medical University Foundation SUB.D110.19.005
6 · The paper itself

Abstract

Phenolic acids are naturally occurring compounds that are known for their antioxidant and antiradical activity. We present experimental and theoretical studies on the antioxidant potential of the set of 22 phenolic acids with different models of hydroxylation and methoxylation of aromatic rings. Ferric reducing antioxidant power assay was used to evaluate this property. 2,3-dihydroxybenzoic acid was found to be the strongest antioxidant, while mono hydroxylated and methoxylated structures had the lowest activities. A comprehensive structure-activity investigation with density functional theory methods elucidated the influence of compounds topology, resonance stabilization, and intramolecular hydrogen bonding on the exhibited activity. The key factor was found to be a presence of two or more hydroxyl groups being located in

Indexed as

AntioxidantsHydroxybenzoatesIronOxidation-ReductionQuantitative Structure-Activity RelationshipAntioxidantsHydroxybenzoatesIronphenolic acidantioxidantsdensity functional theory (DFT)ferric reducing antioxidant power (FRAP) assaymultiple linear regression (MLR)phenolic acidspolyphenolsquantitative structure–activity relationship (QSAR)

Identifiers

PMID32645868
PMCPMC7412039

What OpenQuestion holds

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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.