Component

Hippuric acid / benzoylglycine

Hippuric acid / benzoylglycine. 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. Hippuric acid was the major urinary metabolite after radiolabeled trans-cinnamaldehyde administration in rats and mice.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/ceylon-research/7959441.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "5bab6bd0ad082e4064c601368d147bfcd87566a98ba749a37974fb1057e8c1be", "start_char": 0, "end_char": 1564, "text_sha256": "5bab6bd0ad082e4064c601368d147bfcd87566a98ba749a37974fb1057e8c1be"}
    experimental_model
    Radiolabeled disposition experiment
    exposure
    2 or 250 mg/kg intraperitoneal, with an additional 250 mg/kg oral arm
    limitations
    High experimental exposures and rodent species; metabolite recovery does not quantify human nutrient demand or identify every enzyme.
    nutrient_topic
    Ceylon cinnamon research collection; topical membership is not evidence of a direct dietary effect. · Ceylon cinnamon / Cinnamomum verum bark preparations
    organism
    Rats and mice
    plain_language
    Much of the measured rodent dose left as hippurate, a benzoate-glycine conjugate.
    primary_references
    [ceylon-p7959441] Studies on trans-cinnamaldehyde. 1. The influence of dose size and sex on its disposition in the rat and mouse. (1994). https://pubmed.ncbi.nlm.nih.gov/7959441/ DOI: 10.1016/0278-6915(94)90084-1
    tissue_or_cell_type
    Urine and excreta

    Ceylon cinnamon: metabolism, signaling and nutrient connections (2026-09-17) · lines 194–205

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Radiolabeled disposition experiment · source_derived_draft · unverified_draft

    ### ceylon-hippurate Hippuric acid was the major urinary metabolite after radiolabeled trans-cinnamaldehyde administration in rats and mice. Condition category: normal nutrient_topic: Ceylon cinnamon research collection; topical membership is not evidence of a direct dietary effect. plain_language: Much of the measured rodent dose left as hippurate, a benzoate-glycine conjugate. organism: Rats and mice tissue_or_cell_type: Urine and excreta experimental_model: Radiolabeled disposition experiment limitations: High experimental exposures and rodent species; metabolite recovery does not quantify human nutrient demand or identify every enzyme. exposure: 2 or 250 mg/kg intraperitoneal, with an additional 250 mg/kg oral arm evidence_span: {"source_cache": "artifacts/ceylon-research/7959441.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "5bab6bd0ad082e4064c601368d147bfcd87566a98ba749a37974fb1057e8c1be", "start_char": 0, "end_char": 1564, "text_sha256": "5bab6bd0ad082e4064c601368d147bfcd87566a98ba749a37974fb1057e8c1be"} [ceylon-p7959441] Studies on trans-cinnamaldehyde. 1. The influence of dose size and sex on its disposition in the rat and mouse. (1994). https://pubmed.ncbi.nlm.nih.gov/7959441/ DOI: 10.1016/0278-6915(94)90084-1
    Complete structured claim and evidence
  2. Recombinant human GLYAT variants conjugated glycine to benzoyl-CoA in kinetic assays, forming the glycine-conjugation product hippurate.

    Experimental context and source evidence
    evidence_access
    Primary full text
    experimental_model
    Purified human GLYAT haplotypes, two-substrate kinetic analysis.
    limitations
    Reaction uses an activated acyl-CoA, not free benzoate; pathway activation and CoA release remain separate steps.
    nutrient_topic
    Glycine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Glycine
    plain_language
    Activated acyl groups can be transferred onto glycine for disposal.
    primary_references
    Functional Characterisation of Three Glycine N-Acyltransferase Variants and the Effect on Glycine Conjugation to Benzoyl-CoA. · 2021 · https://pubmed.ncbi.nlm.nih.gov/33803916/ · DOI 10.3390/ijms22063129

    Glycine: supply, one-carbon allocation, receptors and cross-nutrient mechanisms (2026-09-19) · lines 274–280

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Purified human GLYAT haplotypes, two-substrate kinetic analysis. · source_derived_draft · unverified_draft

    ## glycine-glyat-benzoyl Activated acyl groups can be transferred onto glycine for disposal. Recombinant human GLYAT variants conjugated glycine to benzoyl-CoA in kinetic assays, forming the glycine-conjugation product hippurate. Model: Purified human GLYAT haplotypes, two-substrate kinetic analysis. Limitations: Reaction uses an activated acyl-CoA, not free benzoate; pathway activation and CoA release remain separate steps. Evidence access: Primary full text Functional Characterisation of Three Glycine N-Acyltransferase Variants and the Effect on Glycine Conjugation to Benzoyl-CoA. · 2021 · https://pubmed.ncbi.nlm.nih.gov/33803916/ · DOI 10.3390/ijms22063129
    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