Component

Measured human letrozole plasma exposure AUC

Measured human letrozole plasma exposure AUC. Species, exposure and limitations are retained in each linked claim.

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. The clinical trial found no significant letrozole AUC change with the characterized C. verum regimen; the geometric mean exposure ratio was 1.11.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/ceylon-research/41622703.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "0d12141499aba319f8c7513f708889a4dc40fae628e26600f780be2323fe0db3", "start_char": 0, "end_char": 1643, "text_sha256": "0d12141499aba319f8c7513f708889a4dc40fae628e26600f780be2323fe0db3"}
    experimental_model
    Within-person clinical pharmacokinetic comparison
    exposure
    Characterized C. verum 2 g three times daily for five days, with day-six drug coadministration and two further cinnamon doses; nicotine gum 2 mg or letrozole 2.5 mg
    limitations
    Product- and regimen-specific short-term result, not proof of no interaction with all drugs, oils or extracts. CYP2A6 model predictions did not translate into large AUC changes here.
    nutrient_topic
    Ceylon cinnamon research collection; topical membership is not evidence of a direct dietary effect. · Ceylon cinnamon / Cinnamomum verum bark preparations
    organism
    Human
    plain_language
    The large interaction predicted from enzyme models was not seen for letrozole in this human study.
    primary_references
    [ceylon-p41622703] Pharmacokinetic Evaluation of a Cinnamon Product on CYP2A6 Substrate Drugs: Application of a Novel Tool Involving the Nicotine Metabolite Ratio. (2026). https://pubmed.ncbi.nlm.nih.gov/41622703/ DOI: 10.1002/cpt.70218
    tissue_or_cell_type
    16 healthy non-nicotine-using adults; plasma drug profiles

    Ceylon cinnamon: metabolism, signaling and nutrient connections (2026-09-17) · lines 1208–1219

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Within-person clinical pharmacokinetic comparison · source_derived_draft · unverified_draft

    ### ceylon-letrozole-clinical The clinical trial found no significant letrozole AUC change with the characterized C. verum regimen; the geometric mean exposure ratio was 1.11. Condition category: normal nutrient_topic: Ceylon cinnamon research collection; topical membership is not evidence of a direct dietary effect. plain_language: The large interaction predicted from enzyme models was not seen for letrozole in this human study. organism: Human tissue_or_cell_type: 16 healthy non-nicotine-using adults; plasma drug profiles experimental_model: Within-person clinical pharmacokinetic comparison limitations: Product- and regimen-specific short-term result, not proof of no interaction with all drugs, oils or extracts. CYP2A6 model predictions did not translate into large AUC changes here. exposure: Characterized C. verum 2 g three times daily for five days, with day-six drug coadministration and two further cinnamon doses; nicotine gum 2 mg or letrozole 2.5 mg evidence_span: {"source_cache": "artifacts/ceylon-research/41622703.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "0d12141499aba319f8c7513f708889a4dc40fae628e26600f780be2323fe0db3", "start_char": 0, "end_char": 1643, "text_sha256": "0d12141499aba319f8c7513f708889a4dc40fae628e26600f780be2323fe0db3"} [ceylon-p41622703] Pharmacokinetic Evaluation of a Cinnamon Product on CYP2A6 Substrate Drugs: Application of a Novel Tool Involving the Nicotine Metabolite Ratio. (2026). https://pubmed.ncbi.nlm.nih.gov/41622703/ DOI: 10.1002/cpt.70218
    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