Component

DNA adducts from peroxidase-activated eugenol

Species, preparation, dose and limitations are retained on linked claims.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Ascorbic acid and glutathione reduced DNA-adduct formation during in-vitro peroxidase activation of eugenol by about 66% and 90%, respectively.

    Experimental context and source evidence
    dose
    Eugenol with peroxidase/hydrogen peroxide plus ascorbate or glutathione
    duration
    Acute
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    evidence_scope
    literature_reviewed; model-specific source-derived curation
    experimental_model
    Cell-free peroxidase systems and human HL-60 cells
    limitations
    Cell-free protection does not prove that vitamin supplementation prevents toxicity in exposed humans.
    nutrient_topic
    Eugenol chapter; interacting nutrients, drugs, peptides and proteins retain their experimental settings. · Eugenol
    organism
    Cell-free peroxidase systems and human HL-60 cells
    plain_language
    Ascorbic acid and glutathione reduced DNA-adduct formation during in-vitro peroxidase activation of eugenol by about 66% and 90%, respectively.
    primary_references
    Oxidation of eugenol to form DNA adducts and 8-hydroxy-2'-deoxyguanosine: role of quinone methide derivative in DNA adduct formation. (1998). https://pubmed.ncbi.nlm.nih.gov/9525278/ DOI: 10.1093/carcin/19.3.437
    route
    In vitro
    tissue
    DNA adducts and oxidative base damage

    Eugenol: mechanism of action and interactions (2026-09-20) · lines 121–130

    Original AI-assisted source-specific curation with primary-study citations, model, exposure, route, duration, negative findings and limitations preserved. Not publisher full text. · supports · Cell-free peroxidase systems and human HL-60 cells · source_derived_draft · unverified_draft

    ## eugenol-ascorbate-gsh-adduct-protection Ascorbic acid and glutathione reduced DNA-adduct formation during in-vitro peroxidase activation of eugenol by about 66% and 90%, respectively. Model/species: Cell-free peroxidase systems and human HL-60 cells Tissue/system: DNA adducts and oxidative base damage Exposure: Eugenol with peroxidase/hydrogen peroxide plus ascorbate or glutathione Route: In vitro Duration: Acute Limits: Cell-free protection does not prove that vitamin supplementation prevents toxicity in exposed humans. Primary reference: Oxidation of eugenol to form DNA adducts and 8-hydroxy-2'-deoxyguanosine: role of quinone methide derivative in DNA adduct formation. (1998). https://pubmed.ncbi.nlm.nih.gov/9525278/ DOI: 10.1093/carcin/19.3.437 Access: Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards