Evidence map›Paper›PMID 37042673›Full record

ArticleChemical research in toxicology2023

Chemistry of Isoeugenol and Its Oxidation Products: Mechanism and Kinetics of Isoeugenol as a Skin Sensitizer.

Jongmin Ahn, Cristina Avonto, Pankaj Pandey, Shabana I Khan, Ikhlas A Khan, David W Roberts, Amar G Chittiboyina

Open access · greenAbstract read
In one paragraph

Article in Chemical research in toxicology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Intranasal Administration of Isoeugenol Improves Memory Deficits in APP/PS1 Old Mice-A Role Beyond Nrf2 Activation?FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Article
  4. 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 2 institutions in 3 countries.

Jongmin AhnNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.ORCID 0000-0002-9362-7384
Cristina AvontoNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.ORCID 0000-0002-8209-6813
Pankaj PandeyNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.ORCID 0000-0001-9128-8254
Shabana I KhanNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.ORCID 0000-0001-6429-7219
Ikhlas A KhanNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.
David W RobertsSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool L3 3AF, England, U.K.ORCID 0000-0001-6112-5868
Amar G ChittiboyinaNational Center for Natural Products Research, Research Institute of Pharmaceutical Science, School of Pharmacy, The University of Mississippi, University, Mississippi 38677, United States.ORCID 0000-0002-7047-5373
University of Mississippi · USLiverpool John Moores University · GB

Funding

Science based authentication, validation & safety of botanical ingredientsU01FD004246 · FDA · UNIVERSITY OF MISSISSIPPI · PI Amar G. Chittiboyina, Ikhlas Ahmad Khan · 2011 to 2026
$38.2M
FDA HHS U01 FD004246
6 · The paper itself

Abstract

Structurally similar phytochemical compounds may elicit markedly different skin sensitization responses. Eugenol and isoeugenol are natural phenylpropanoids found in various essential oils are frequently used as fragrance ingredients in consumer products due to their pleasing aromatic properties. Both compounds are also skin sensitizers with isoeugenol being a stronger sensitizer than eugenol. The most commonly accepted mechanisms for haptenation by eugenol involve formation of a quinone methide or an

Indexed as

EugenolIndolequinonesSkinEugenolIndolequinonesisoeugenolquinone methide

Identifiers

PMID37042673
PMCPMC12083750
OpenAlexW4365135764

What OpenQuestion holds

Textmetadata
LicenceTDM
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.