Evidence map›Paper›PMID 39494867›Full record

ArticleJournal of agricultural and food chemistry2024

Reactivity of the 2-Methylfuran Phase I Metabolite 3-Acetylacrolein Toward DNA.

Verena Schäfer, Simone Stegmüller, Hanna Becker, Elke Richling

Abstract read
In one paragraph

Article in Journal of agricultural and food chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Verena SchäferDepartment of Chemistry, Division of Food Chemistry and Toxicology, University of Kaiserslautern-Landau, Kaiserslautern D-67663, Germany.
Simone StegmüllerDepartment of Chemistry, Division of Food Chemistry and Toxicology, University of Kaiserslautern-Landau, Kaiserslautern D-67663, Germany.
Hanna BeckerDepartment of Chemistry, Division of Food Chemistry and Toxicology, University of Kaiserslautern-Landau, Kaiserslautern D-67663, Germany.
Elke RichlingDepartment of Chemistry, Division of Food Chemistry and Toxicology, University of Kaiserslautern-Landau, Kaiserslautern D-67663, Germany.ORCID 0000-0001-5746-8032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

2-Methylfuran (2-MF) is a well-known industrial chemical and also formed via thermal treatment of food. One main source of 2-MF in the human diet is coffee. 2-MF is known to form 3-acetylacrolein (AcA, 4-oxopent-2-enal) via cytochrome P 450 metabolism and further reacts with amino acids in vivo. Still the reactivity toward other biomolecules is rather scarce. Therefore, AcA was synthesized, and its reaction with 2'-deoxyadenosine (dA), 2'deoxyguanosine (dG), 2'deoxycytosine (dC), and 2'-deoxythymidine (dT) was tested. For this purpose, adduct formation was performed by acid hydrolysis of 2,5-dihydro-2,5-dimethoxy-2-methylfuran (DHDMMF) as well as pure AcA. The structures of these adducts were confirmed by UPLC-ESI

Indexed as

DNAFuransAnimalsChromatography, High Pressure LiquidDNA AdductsHepatocytesHumansMaleRatsRats, WistarTandem Mass Spectrometry2-methylfuranDNADNA AdductsFurans2-methylfuran3-acetylacroleinDNA adductshuman liverprimary rat hepatocytes

Identifiers

PMID39494867
PMCPMC11565790

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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.