Component
Carbohydrate-derived fulvic acid / CHD-FA (preparation class)
Context-specific entity; species, compartment and exposure are stated on each claim.
9 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 it acts on
CHD-FA did not produce a clear reproducible mutagenic response in the reported Ames tests.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- Salmonella and E. coli assays with/without S9, up to 5000 micrograms/plate.
- limitations
- The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. High-dose toxicity and a doubtful TA1537 response were reported.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- Bacterial mutation testing was interpreted as negative.
- primary_references
- Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 284–290
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Salmonella and E. coli assays with/without S9, up to 5000 micrograms/plate. · source_derived_draft · unverified_draft
## fulvic-acid-ames Bacterial mutation testing was interpreted as negative. CHD-FA did not produce a clear reproducible mutagenic response in the reported Ames tests. Model: Salmonella and E. coli assays with/without S9, up to 5000 micrograms/plate. Limitations: The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. High-dose toxicity and a doubtful TA1537 response were reported. Evidence access: Primary full text Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Complete structured claim and evidenceInvestigator global response favored topical CHD-FA over vehicle; several other measures improved in both groups.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- 36 volunteers aged at least two years; twice-daily topical treatment for four weeks; randomized blinded study.
- limitations
- Small exploratory trial; do not convert within-group improvement into a between-group benefit. Transient burning occurred; topical results do not prove oral efficacy.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- One overall score favored the active topical preparation.
- primary_references
- Randomized, parallel-group, double-blind, controlled study to evaluate the efficacy and safety of carbohydrate-derived fulvic acid in topical treatment of eczema. · 2011 · https://pubmed.ncbi.nlm.nih.gov/21931500/ · DOI 10.2147/CCID.S23110
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 276–282
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · 36 volunteers aged at least two years; twice-daily topical treatment for four weeks; randomized blinded study. · source_derived_draft · unverified_draft
## fulvic-acid-eczema One overall score favored the active topical preparation. Investigator global response favored topical CHD-FA over vehicle; several other measures improved in both groups. Model: 36 volunteers aged at least two years; twice-daily topical treatment for four weeks; randomized blinded study. Limitations: Small exploratory trial; do not convert within-group improvement into a between-group benefit. Transient burning occurred; topical results do not prove oral efficacy. Evidence access: Primary abstract Randomized, parallel-group, double-blind, controlled study to evaluate the efficacy and safety of carbohydrate-derived fulvic acid in topical treatment of eczema. · 2011 · https://pubmed.ncbi.nlm.nih.gov/21931500/ · DOI 10.2147/CCID.S23110
Complete structured claim and evidenceCHD-FA exposure caused extracellular ATP leakage from Candida cells.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- Candida membrane-permeability assay; ATP release followed over time.
- limitations
- ATP leakage indicates microbial membrane damage, not increased host ATP production.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- Cell contents escaped after membrane injury.
- primary_references
- Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 132–138
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Candida membrane-permeability assay; ATP release followed over time. · source_derived_draft · unverified_draft
## fulvic-acid-fungal-atp Cell contents escaped after membrane injury. CHD-FA exposure caused extracellular ATP leakage from Candida cells. Model: Candida membrane-permeability assay; ATP release followed over time. Limitations: ATP leakage indicates microbial membrane damage, not increased host ATP production. Evidence access: Primary full text Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
Complete structured claim and evidenceCHD-FA exposure increased membrane permeability in Candida albicans assays.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- Clinical Candida isolate panel; planktonic and biofilm growth; inhibitory concentrations reported as 0.125% and 0.25%.
- limitations
- An in-vitro antiseptic concentration is not a systemic supplement exposure or demonstrated infection treatment.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- The tested antifungal action involved a leaky membrane.
- primary_references
- Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 124–130
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Clinical Candida isolate panel; planktonic and biofilm growth; inhibitory concentrations reported as 0.125% and 0.25%. · source_derived_draft · unverified_draft
## fulvic-acid-fungal-membrane The tested antifungal action involved a leaky membrane. CHD-FA exposure increased membrane permeability in Candida albicans assays. Model: Clinical Candida isolate panel; planktonic and biofilm growth; inhibitory concentrations reported as 0.125% and 0.25%. Limitations: An in-vitro antiseptic concentration is not a systemic supplement exposure or demonstrated infection treatment. Evidence access: Primary full text Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
Complete structured claim and evidenceThe small oral CHD-FA trial reported reduced skin-prick responses.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- 30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week.
- limitations
- Short duration and a surrogate endpoint do not establish treatment of allergic disease or effects of other preparations.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- An allergy-test response changed in a short trial.
- primary_references
- Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 260–266
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · 30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week. · source_derived_draft · unverified_draft
## fulvic-acid-human-atopy An allergy-test response changed in a short trial. The small oral CHD-FA trial reported reduced skin-prick responses. Model: 30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week. Limitations: Short duration and a surrogate endpoint do not establish treatment of allergic disease or effects of other preparations. Evidence access: Primary abstract Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784
Complete structured claim and evidenceNo severe adverse events were reported and measured safety parameters remained stable during the trial.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- 30 atopic male volunteers; acute/subacute escalating exposures and one-week crossover treatment.
- limitations
- Cannot establish chronic safety, pregnancy safety, safety in children, or equivalence of contaminated/environmental extracts.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- This specified preparation was monitored for a short period.
- primary_references
- Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 268–274
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · 30 atopic male volunteers; acute/subacute escalating exposures and one-week crossover treatment. · source_derived_draft · unverified_draft
## fulvic-acid-human-short-safety This specified preparation was monitored for a short period. No severe adverse events were reported and measured safety parameters remained stable during the trial. Model: 30 atopic male volunteers; acute/subacute escalating exposures and one-week crossover treatment. Limitations: Cannot establish chronic safety, pregnancy safety, safety in children, or equivalence of contaminated/environmental extracts. Evidence access: Primary abstract Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784
Complete structured claim and evidenceCHD-FA increased micronucleus frequency in human lymphocyte testing under growth-inhibiting conditions.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- In-vitro lymphocyte assay with/without metabolic activation; acidic high-dose conditions.
- limitations
- The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. Acidity is a proposed explanation, not a demonstrated causal resolution; no mechanistic follow-up isolated it.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- One mammalian-cell test gave a positive signal.
- primary_references
- Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 292–298
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · In-vitro lymphocyte assay with/without metabolic activation; acidic high-dose conditions. · source_derived_draft · unverified_draft
## fulvic-acid-lymphocyte-micronuclei One mammalian-cell test gave a positive signal. CHD-FA increased micronucleus frequency in human lymphocyte testing under growth-inhibiting conditions. Model: In-vitro lymphocyte assay with/without metabolic activation; acidic high-dose conditions. Limitations: The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. Acidity is a proposed explanation, not a demonstrated causal resolution; no mechanistic follow-up isolated it. Evidence access: Primary full text Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Complete structured claim and evidenceCHD-FA did not significantly increase micronucleated polychromatic erythrocytes in tested mice.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- Male mouse micronucleus assay; reported doses up to 100 mg/kg, sampling at 24/48 hours.
- limitations
- The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. Full results report reduced PCE/NCE at 100 mg/kg after 48 hours despite the abstract summary; retain this marrow-response finding.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- The mouse chromosomal-damage endpoint was negative.
- primary_references
- Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 300–306
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Male mouse micronucleus assay; reported doses up to 100 mg/kg, sampling at 24/48 hours. · source_derived_draft · unverified_draft
## fulvic-acid-mouse-micronuclei The mouse chromosomal-damage endpoint was negative. CHD-FA did not significantly increase micronucleated polychromatic erythrocytes in tested mice. Model: Male mouse micronucleus assay; reported doses up to 100 mg/kg, sampling at 24/48 hours. Limitations: The 2026 study was electronically published June 21, with a December issue date. Negative results in one assay do not erase positive or uncertain findings in another; chronic exposure remains unresolved. Full results report reduced PCE/NCE at 100 mg/kg after 48 hours despite the abstract summary; retain this marrow-response finding. Evidence access: Primary full text Genotoxicity of Carbohydrate Derived Fulvic Acid. · 2026 · https://pubmed.ncbi.nlm.nih.gov/42383226/ · DOI 10.1016/j.toxrep.2026.102298
Complete structured claim and evidence
Where it participates (unsigned role)
Chitin-synthesis inhibition with nikkomycin Z increased Candida susceptibility to CHD-FA.
Experimental context and source evidence
- evidence_access
- Primary full text
- experimental_model
- Candida planktonic and biofilm combination experiments.
- limitations
- This supports a cell-envelope mechanism; it is not a clinically established combination.
- nutrient_topic
- Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
- plain_language
- Weakening the wall made the tested membrane-active exposure more effective.
- primary_references
- Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 140–146
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Candida planktonic and biofilm combination experiments. · source_derived_draft · unverified_draft
## fulvic-acid-fungal-chitin Weakening the wall made the tested membrane-active exposure more effective. Chitin-synthesis inhibition with nikkomycin Z increased Candida susceptibility to CHD-FA. Model: Candida planktonic and biofilm combination experiments. Limitations: This supports a cell-envelope mechanism; it is not a clinically established combination. Evidence access: Primary full text Carbohydrate Derived Fulvic Acid: An in vitro Investigation of a Novel Membrane Active Antiseptic Agent Against Candida albicans Biofilms. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22479260/ · DOI 10.3389/fmicb.2012.00116
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.