Component

Coumarin-derived covalent binding to human liver microsomal proteins

Coumarin-derived covalent binding to human liver microsomal proteins. 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. Coumarin-derived material bound covalently to human microsomal proteins, averaging 4.8 pmol/min/mg.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/coumarin-research/7839702.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ca24fcb6d3561aa6605b2a53ff463aa6e2ca085d785d1f77615498580d84e909", "start_char": 0, "end_char": 1457, "text_sha256": "ca24fcb6d3561aa6605b2a53ff463aa6e2ca085d785d1f77615498580d84e909"}
    experimental_model
    Radiolabeled substrate metabolism in 12 human liver microsomal samples
    exposure
    50 micromolar [3-14C]coumarin
    limitations
    Donor-panel correlations do not assign enzyme causality; older grouping of 3-hydroxylation products is not adopted as an epoxide mechanism.
    nutrient_topic
    Coumarin research collection; topical membership is not evidence of a direct dietary effect. · Coumarin
    organism
    Human
    plain_language
    A small measured fraction became attached to proteins.
    primary_references
    [coumarin-p7839702] Metabolism of [3-14C] coumarin by human liver microsomes. (1994). https://pubmed.ncbi.nlm.nih.gov/7839702/ DOI: 10.3109/00498259409043279
    tissue_or_cell_type
    Liver microsomes

    Coumarin: metabolism, signaling and nutrient connections (2026-09-17) · lines 202–213

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Radiolabeled substrate metabolism in 12 human liver microsomal samples · source_derived_draft · unverified_draft

    ### coumarin-microsomal-binding Coumarin-derived material bound covalently to human microsomal proteins, averaging 4.8 pmol/min/mg. Condition category: normal nutrient_topic: Coumarin research collection; topical membership is not evidence of a direct dietary effect. plain_language: A small measured fraction became attached to proteins. organism: Human tissue_or_cell_type: Liver microsomes experimental_model: Radiolabeled substrate metabolism in 12 human liver microsomal samples limitations: Donor-panel correlations do not assign enzyme causality; older grouping of 3-hydroxylation products is not adopted as an epoxide mechanism. exposure: 50 micromolar [3-14C]coumarin evidence_span: {"source_cache": "artifacts/coumarin-research/7839702.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ca24fcb6d3561aa6605b2a53ff463aa6e2ca085d785d1f77615498580d84e909", "start_char": 0, "end_char": 1457, "text_sha256": "ca24fcb6d3561aa6605b2a53ff463aa6e2ca085d785d1f77615498580d84e909"} [coumarin-p7839702] Metabolism of [3-14C] coumarin by human liver microsomes. (1994). https://pubmed.ncbi.nlm.nih.gov/7839702/ DOI: 10.3109/00498259409043279
    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