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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What acts on it
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 evidenceWith cofactors supplied, human cytosolic products were approximately 90% o-HPAA and 10% glutathione conjugate.
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
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.