Component

ortho-Hydroxyphenylacetic acid

ortho-Hydroxyphenylacetic acid. Species, exposure and limitations are retained in each linked claim.

2 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. Pooled human liver cytosols oxidized o-HPA to o-HPAA, with intrinsic clearance over 50-fold greater than rat cytosols.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/coumarin-research/15141102.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5", "start_char": 0, "end_char": 2618, "text_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5"}
    experimental_model
    Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols
    exposure
    Controlled epoxide generation with cofactors supplied
    limitations
    Cell-free species comparison does not quantify human dietary injury risk or supplement benefit.
    nutrient_topic
    Coumarin research collection; topical membership is not evidence of a direct dietary effect. · Coumarin
    organism
    Human pooled cytosols, F344 rat and B6C3F1 mouse
    plain_language
    Human and rat preparations cleared the aldehyde at very different rates.
    primary_references
    [coumarin-p15141102] Metabolic detoxification determines species differences in coumarin-induced hepatotoxicity. (2004). https://pubmed.ncbi.nlm.nih.gov/15141102/ DOI: 10.1093/toxsci/kfh162
    tissue_or_cell_type
    Liver cytosolic detoxification system

    Coumarin: metabolism, signaling and nutrient connections (2026-09-17) · lines 501–512

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols · source_derived_draft · unverified_draft

    ### coumarin-human-aldehyde-oxidation Pooled human liver cytosols oxidized o-HPA to o-HPAA, with intrinsic clearance over 50-fold greater than rat cytosols. Condition category: normal nutrient_topic: Coumarin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Human and rat preparations cleared the aldehyde at very different rates. organism: Human pooled cytosols, F344 rat and B6C3F1 mouse tissue_or_cell_type: Liver cytosolic detoxification system experimental_model: Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols limitations: Cell-free species comparison does not quantify human dietary injury risk or supplement benefit. exposure: Controlled epoxide generation with cofactors supplied evidence_span: {"source_cache": "artifacts/coumarin-research/15141102.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5", "start_char": 0, "end_char": 2618, "text_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5"} [coumarin-p15141102] Metabolic detoxification determines species differences in coumarin-induced hepatotoxicity. (2004). https://pubmed.ncbi.nlm.nih.gov/15141102/ DOI: 10.1093/toxsci/kfh162
    Complete structured claim and evidence
  2. With cofactors supplied, human cytosolic products were approximately 90% o-HPAA and 10% glutathione conjugate.

    Coumarin 3,4-epoxide → ortho-Hydroxyphenylacetic acid source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/coumarin-research/15141102.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5", "start_char": 0, "end_char": 2618, "text_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5"}
    experimental_model
    Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols
    exposure
    Controlled epoxide generation with cofactors supplied
    limitations
    Cell-free species comparison does not quantify human dietary injury risk or supplement benefit.
    nutrient_topic
    Coumarin research collection; topical membership is not evidence of a direct dietary effect. · Coumarin
    organism
    Human pooled cytosols, F344 rat and B6C3F1 mouse
    plain_language
    Glutathione capture was not the dominant measured human route.
    primary_references
    [coumarin-p15141102] Metabolic detoxification determines species differences in coumarin-induced hepatotoxicity. (2004). https://pubmed.ncbi.nlm.nih.gov/15141102/ DOI: 10.1093/toxsci/kfh162
    tissue_or_cell_type
    Liver cytosolic detoxification system

    Coumarin: metabolism, signaling and nutrient connections (2026-09-17) · lines 514–525

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols · source_derived_draft · unverified_draft

    ### coumarin-human-route-partition With cofactors supplied, human cytosolic products were approximately 90% o-HPAA and 10% glutathione conjugate. Condition category: normal nutrient_topic: Coumarin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Glutathione capture was not the dominant measured human route. organism: Human pooled cytosols, F344 rat and B6C3F1 mouse tissue_or_cell_type: Liver cytosolic detoxification system experimental_model: Coumarin epoxide generated with mouse microsomes plus species-specific liver cytosols limitations: Cell-free species comparison does not quantify human dietary injury risk or supplement benefit. exposure: Controlled epoxide generation with cofactors supplied evidence_span: {"source_cache": "artifacts/coumarin-research/15141102.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5", "start_char": 0, "end_char": 2618, "text_sha256": "2ddbcb7b41520d3405b9abe3ed8b492c5a6063e88d52c549481d444dcd541dc5"} [coumarin-p15141102] Metabolic detoxification determines species differences in coumarin-induced hepatotoxicity. (2004). https://pubmed.ncbi.nlm.nih.gov/15141102/ DOI: 10.1093/toxsci/kfh162
    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