Component

Human cytochrome P450 2A13 / CYP2A13

Human cytochrome P450 2A13 / CYP2A13

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 it acts on

  1. Recombinant human CYP2A13 converted apigenin to luteolin, with reported substrate S50 of 14 micromolar.

    Experimental context and source evidence
    evidence_access
    Indexed primary abstract and publisher-indexed Results; recombinant-enzyme selectivity, not complete human metabolic mass balance.
    experimental_model
    Recombinant human enzyme; not whole-body metabolic flux.
    interpretation_status
    Recorded from source with stated access limits; ungraded, not independent replication.
    limitations
    Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation.
    nutrient_topic
    Apigenin collection; exact intervention and molecular form govern interpretation. · Apigenin
    plain_language
    Recombinant human CYP2A13 converted apigenin to luteolin, with reported substrate S50 of 14 micromolar.
    primary_references
    Oxidation of Naringenin, Apigenin, and Genistein by Human Family 1 Cytochrome P450 Enzymes and Comparison of Interaction of Apigenin with Human P450 1B1.1 and Scutellaria P450 82D.1. | https://pubmed.ncbi.nlm.nih.gov/37783573/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC11497155/ | https://doi.org/10.1021/acs.chemrestox.3c00229
    source_locator
    Reviewed reference api-cyp2a13-luteolin;

    Apigenin: detailed mechanisms of action (reviewed 10 October 2026) · lines 106–112

    AI-assisted original curation of primary studies; claim-local access and experimental limitations stated. Includes original-draft correction history. No independent replication claimed. · supports · Recombinant human enzyme; not whole-body metabolic flux. · Recorded from source · Recorded from source

    ### api-cyp2a13-luteolin Recombinant human CYP2A13 converted apigenin to luteolin, with reported substrate S50 of 14 micromolar. Model and exposure: Recombinant human enzyme; not whole-body metabolic flux. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Oxidation of Naringenin, Apigenin, and Genistein by Human Family 1 Cytochrome P450 Enzymes and Comparison of Interaction of Apigenin with Human P450 1B1.1 and Scutellaria P450 82D.1. | 2023 | https://pubmed.ncbi.nlm.nih.gov/37783573/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC11497155/ | https://doi.org/10.1021/acs.chemrestox.3c00229 | Access: Indexed primary abstract and publisher-indexed Results; recombinant-enzyme selectivity, not complete human metabolic mass balance.
    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.