Component
Singlet molecular oxygen
Singlet molecular oxygen. Species, exposure and limitations are retained in each linked claim.
12 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
At pH 7.4, ergothioneine and hercynine generated different products after chemically generated singlet oxygen exposure.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- LC-MS analysis with a thermal singlet-oxygen donor.
- limitations
- Product-based reaction model; not proof that this is its exclusive physiological function.
- nutrient_topic
- Ergothioneine collection; molecular form, preparation, species, exposure and manipulation remain explicit. · L-Ergothioneine
- plain_language
- The sulfur atom changes the reaction route.
- primary_references
- Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity. · 2017 · https://pubmed.ncbi.nlm.nih.gov/29074402/ · DOI 10.1016/j.freeradbiomed.2017.10.372
Ergothioneine: transport, redox chemistry and cross-nutrient mechanisms (2026-09-19) · lines 136–142
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · LC-MS analysis with a thermal singlet-oxygen donor. · source_derived_draft · unverified_draft
## ergothioneine-singlet-oxygen The sulfur atom changes the reaction route. At pH 7.4, ergothioneine and hercynine generated different products after chemically generated singlet oxygen exposure. Model: LC-MS analysis with a thermal singlet-oxygen donor. Limitations: Product-based reaction model; not proof that this is its exclusive physiological function. Evidence access: Primary abstract Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity. · 2017 · https://pubmed.ncbi.nlm.nih.gov/29074402/ · DOI 10.1016/j.freeradbiomed.2017.10.372
Complete structured claim and evidenceKI shortened singlet-oxygen lifetime; derived quenching rate was 1.1 × 10^6 M−1 s−1.
Experimental context and source evidence
- experimental_model
- Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model.
- exposure_category
- Study-specific exposure, including pharmacological and in-vitro conditions; normal is the schema fallback outside the three availability categories.
- limitations
- Local photochemical system, not an effect of oral KI alone. Peroxyiodide intermediates were proposed, not directly established.
- nutrient_topic
- Potassium iodide research collection; shared-anion and comparator studies are not all KI interventions. · Potassium iodide
- plain_language
- Iodide intercepted singlet oxygen in the photochemical system.
- primary_references
- Potassium Iodide Potentiates Antimicrobial Photodynamic Inactivation Mediated by Rose Bengal in In Vitro and In Vivo Studies. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28438946/ · DOI 10.1128/aac.00467-17
Potassium iodide: thyroid and non-thyroid mechanisms, interactions and discovery questions (2026-09-18) · lines 336–342
AI-assisted research curation; primary-study references, chemical references and label statements individually identified. Not publisher full text. · supports · Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model. · source_derived_draft · unverified_draft
## ki-pdt-singlet Iodide intercepted singlet oxygen in the photochemical system. KI shortened singlet-oxygen lifetime; derived quenching rate was 1.1 × 10^6 M−1 s−1. Model: Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model. Limitations: Local photochemical system, not an effect of oral KI alone. Peroxyiodide intermediates were proposed, not directly established. Evidence location: Full-text Figure 5 Potassium Iodide Potentiates Antimicrobial Photodynamic Inactivation Mediated by Rose Bengal in In Vitro and In Vivo Studies. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28438946/ · DOI 10.1128/aac.00467-17
Complete structured claim and evidenceLiposomes containing astaxanthin plus alpha- or gamma-tocotrienol showed radical-scavenging activity greater than the calculated additive activity in the reported singlet-oxygen/hydroxyl-radical assays.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- Cell-free co-encapsulated liposomes; matched single-agent comparisons.
- limitations
- Measured assay synergy is not demonstrated oral or clinical synergy.
- nutrient_topic
- Astaxanthin collection; molecular form, preparation, species, exposure and manipulation remain explicit. · Astaxanthin
- plain_language
- Some vitamin E forms worked together with astaxanthin in this test system.
- primary_references
- Synergistic antioxidative effect of astaxanthin and tocotrienol by co-encapsulated in liposomes. · 2016 · https://pubmed.ncbi.nlm.nih.gov/27698536/ · DOI 10.3164/jcbn.15-153
Astaxanthin: transport, membrane chemistry, signaling and nutrient interactions (2026-09-19) · lines 190–196
AI-assisted research curation; primary-abstract references and experimental limitations individually identified. Not publisher full text. · supports · Cell-free co-encapsulated liposomes; matched single-agent comparisons. · source_derived_draft · unverified_draft
## astaxanthin-tocotrienol-synergy Some vitamin E forms worked together with astaxanthin in this test system. Liposomes containing astaxanthin plus alpha- or gamma-tocotrienol showed radical-scavenging activity greater than the calculated additive activity in the reported singlet-oxygen/hydroxyl-radical assays. Model: Cell-free co-encapsulated liposomes; matched single-agent comparisons. Limitations: Measured assay synergy is not demonstrated oral or clinical synergy. Evidence access: Primary abstract Synergistic antioxidative effect of astaxanthin and tocotrienol by co-encapsulated in liposomes. · 2016 · https://pubmed.ncbi.nlm.nih.gov/27698536/ · DOI 10.3164/jcbn.15-153
Complete structured claim and evidenceLycopene had a reported singlet-oxygen quenching constant of 31 billion per molar per second in the assay.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"}
- experimental_model
- Cell-free singlet-oxygen quenching comparison
- exposure
- Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin
- limitations
- Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements.
- nutrient_topic
- Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
- organism
- Chemical assay and plasma-concentration comparison
- plain_language
- It can remove excitation energy from this reactive oxygen species.
- primary_references
- [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
- tissue_or_cell_type
- Solution kinetics
Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 416–427
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Cell-free singlet-oxygen quenching comparison · source_derived_draft · unverified_draft
### lycopene-singlet-quenching Lycopene had a reported singlet-oxygen quenching constant of 31 billion per molar per second in the assay. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: It can remove excitation energy from this reactive oxygen species. organism: Chemical assay and plasma-concentration comparison tissue_or_cell_type: Solution kinetics experimental_model: Cell-free singlet-oxygen quenching comparison limitations: Rate constants are solvent/assay-dependent, not a clinical ranking of antioxidant supplements. exposure: Lycopene, beta-carotene, alpha-tocopherol and albumin-bound bilirubin evidence_span: {"source_cache": "artifacts/lycopene-research/2802626.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521", "start_char": 0, "end_char": 1046, "text_sha256": "91ad9c300da17ee4e4c78a9ba980a7a4f05eef2328a64b5a9f75d4023abdc521"} [lycopene-p2802626] Lycopene as the most efficient biological carotenoid singlet oxygen quencher. (1989). https://pubmed.ncbi.nlm.nih.gov/2802626/ DOI: 10.1016/0003-9861(89)90467-0
Complete structured claim and evidenceThe equal-ratio meso-zeaxanthin, zeaxanthin and lutein mixture quenched more singlet oxygen than each individual pigment at the same total concentration.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"}
- experimental_model
- EPR of donor eye tissue and solution quenching assays
- exposure
- White-light challenge and equal-total-concentration carotenoid comparisons
- limitations
- Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Postmortem human tissue and cell-free systems
- plain_language
- The three pigments worked better together in this solution experiment.
- primary_references
- [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
- tissue_or_cell_type
- Macula, RPE/choroid and carotenoid solutions
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 229–240
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · EPR of donor eye tissue and solution quenching assays · source_derived_draft · unverified_draft
### lutein-mixture-quenching The equal-ratio meso-zeaxanthin, zeaxanthin and lutein mixture quenched more singlet oxygen than each individual pigment at the same total concentration. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: The three pigments worked better together in this solution experiment. organism: Postmortem human tissue and cell-free systems tissue_or_cell_type: Macula, RPE/choroid and carotenoid solutions experimental_model: EPR of donor eye tissue and solution quenching assays limitations: Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye. exposure: White-light challenge and equal-total-concentration carotenoid comparisons evidence_span: {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"} [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
Complete structured claim and evidenceLutein quenched singlet oxygen in the solution assay comparing individual macular carotenoids and mixtures.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"}
- experimental_model
- EPR of donor eye tissue and solution quenching assays
- exposure
- White-light challenge and equal-total-concentration carotenoid comparisons
- limitations
- Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye.
- nutrient_topic
- Lutein research collection; topical membership is not evidence of a direct dietary effect. · Lutein
- organism
- Postmortem human tissue and cell-free systems
- plain_language
- Lutein can reduce excited oxygen in a chemical experiment.
- primary_references
- [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
- tissue_or_cell_type
- Macula, RPE/choroid and carotenoid solutions
Lutein: metabolism, signaling and nutrient connections (2026-09-17) · lines 216–227
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · EPR of donor eye tissue and solution quenching assays · source_derived_draft · unverified_draft
### lutein-singlet-quenching Lutein quenched singlet oxygen in the solution assay comparing individual macular carotenoids and mixtures. Condition category: normal nutrient_topic: Lutein research collection; topical membership is not evidence of a direct dietary effect. plain_language: Lutein can reduce excited oxygen in a chemical experiment. organism: Postmortem human tissue and cell-free systems tissue_or_cell_type: Macula, RPE/choroid and carotenoid solutions experimental_model: EPR of donor eye tissue and solution quenching assays limitations: Solution mixture effects do not establish an optimal oral ratio or clinical benefit; exogenous pigment addition differs from delivery in a living eye. exposure: White-light challenge and equal-total-concentration carotenoid comparisons evidence_span: {"source_cache": "artifacts/lutein-research/20678467.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01", "start_char": 0, "end_char": 989, "text_sha256": "aaf88f567941ed16adb101981a218960bbd8ae3cfe0919868de63462e7c7be01"} [lutein-p20678467] Studies on the singlet oxygen scavenging mechanism of human macular pigment. (2010). https://pubmed.ncbi.nlm.nih.gov/20678467/ DOI: 10.1016/j.abb.2010.07.024
Complete structured claim and evidenceThe same experiment did not detect the carotenoid-dependent decrease in saturated DMPC liposomes.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/zeaxanthin-research/30689980.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743", "start_char": 0, "end_char": 1545, "text_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743"}
- experimental_model
- Photosensitized liposome experiment
- exposure
- Carotenoids at 0.15 mol%; toluidine-blue photosensitization
- limitations
- Measured effects depended on membrane composition; do not generalize the saturated-membrane null to all antioxidant chemistry.
- nutrient_topic
- Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
- organism
- Cell-free lipid systems
- plain_language
- A different membrane gave a different result.
- primary_references
- [zeaxanthin-p30689980] The effect of carotenoids on the concentration of singlet oxygen in lipid membranes. (2019). https://pubmed.ncbi.nlm.nih.gov/30689980/ DOI: 10.1016/j.bbamem.2019.01.012
- tissue_or_cell_type
- Saturated versus unsaturated lipid bilayers
Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 340–351
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Photosensitized liposome experiment · source_derived_draft · unverified_draft
### zeaxanthin-saturated-null The same experiment did not detect the carotenoid-dependent decrease in saturated DMPC liposomes. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: A different membrane gave a different result. organism: Cell-free lipid systems tissue_or_cell_type: Saturated versus unsaturated lipid bilayers experimental_model: Photosensitized liposome experiment limitations: Measured effects depended on membrane composition; do not generalize the saturated-membrane null to all antioxidant chemistry. exposure: Carotenoids at 0.15 mol%; toluidine-blue photosensitization evidence_span: {"source_cache": "artifacts/zeaxanthin-research/30689980.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743", "start_char": 0, "end_char": 1545, "text_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743"} [zeaxanthin-p30689980] The effect of carotenoids on the concentration of singlet oxygen in lipid membranes. (2019). https://pubmed.ncbi.nlm.nih.gov/30689980/ DOI: 10.1016/j.bbamem.2019.01.012
Complete structured claim and evidenceZeaxanthin decreased the detected singlet-oxygen concentration in unsaturated-lipid liposomes.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/zeaxanthin-research/30689980.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743", "start_char": 0, "end_char": 1545, "text_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743"}
- experimental_model
- Photosensitized liposome experiment
- exposure
- Carotenoids at 0.15 mol%; toluidine-blue photosensitization
- limitations
- Measured effects depended on membrane composition; do not generalize the saturated-membrane null to all antioxidant chemistry.
- nutrient_topic
- Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. · Dietary (3R,3-prime-R)-zeaxanthin
- organism
- Cell-free lipid systems
- plain_language
- Protection depended on the surrounding membrane.
- primary_references
- [zeaxanthin-p30689980] The effect of carotenoids on the concentration of singlet oxygen in lipid membranes. (2019). https://pubmed.ncbi.nlm.nih.gov/30689980/ DOI: 10.1016/j.bbamem.2019.01.012
- tissue_or_cell_type
- Saturated versus unsaturated lipid bilayers
Zeaxanthin: metabolism, signaling and nutrient connections (2026-09-17) · lines 327–338
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Photosensitized liposome experiment · source_derived_draft · unverified_draft
### zeaxanthin-unsaturated-quenching Zeaxanthin decreased the detected singlet-oxygen concentration in unsaturated-lipid liposomes. Condition category: normal nutrient_topic: Zeaxanthin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Protection depended on the surrounding membrane. organism: Cell-free lipid systems tissue_or_cell_type: Saturated versus unsaturated lipid bilayers experimental_model: Photosensitized liposome experiment limitations: Measured effects depended on membrane composition; do not generalize the saturated-membrane null to all antioxidant chemistry. exposure: Carotenoids at 0.15 mol%; toluidine-blue photosensitization evidence_span: {"source_cache": "artifacts/zeaxanthin-research/30689980.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743", "start_char": 0, "end_char": 1545, "text_sha256": "94c10c1ffd51016a2038f725e1e38457c47b5c929bd89f7222d8bc84a7f76743"} [zeaxanthin-p30689980] The effect of carotenoids on the concentration of singlet oxygen in lipid membranes. (2019). https://pubmed.ncbi.nlm.nih.gov/30689980/ DOI: 10.1016/j.bbamem.2019.01.012
Complete structured claim and evidenceSAC scavenged singlet molecular oxygen in the tested chemical system; IC50 was 1.93 mM.
Experimental context and source evidence
- acting_entity
- s-allylcysteine
- dose
- Assay-specific millimolar IC50 values
- duration
- Not specified in accessed abstract
- evidence_access
- Primary abstract
- experimental_comparison
- SAC concentration series versus corresponding reference scavengers
- experimental_model
- Reactive-species scavenging systems
- interpretation_status
- Source-derived research curation; not independent primary verification
- limitations
- Assay potency is not an achieved human tissue concentration.
- nutrient_topic
- S-allylcysteine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · S-allyl-L-cysteine / SAC
- organism
- Cell-free chemical assays
- plain_language
- Direct chemistry has a measured concentration requirement.
- primary_references
- [17576034] S-allylcysteine scavenges singlet oxygen and hypochlorous acid and protects LLC-PK(1) cells of potassium dichromate-induced toxicity. · 2007 · https://pubmed.ncbi.nlm.nih.gov/17576034/ · DOI 10.1016/j.fct.2007.05.002
- route
- In vitro
- tissue_or_cell_type
- Reactive-species scavenging systems
S-allylcysteine: sulfur signaling, redox responses and cross-nutrient mechanisms (2026-09-20) · lines 86–93
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Reactive-species scavenging systems · source_derived_draft · unverified_draft
## s-allylcysteine-scavenging-singlet Direct chemistry has a measured concentration requirement. SAC scavenged singlet molecular oxygen in the tested chemical system; IC50 was 1.93 mM. Model: Reactive-species scavenging systems Limitations: Assay potency is not an achieved human tissue concentration. Evidence access: Primary abstract [17576034] S-allylcysteine scavenges singlet oxygen and hypochlorous acid and protects LLC-PK(1) cells of potassium dichromate-induced toxicity. · 2007 · https://pubmed.ncbi.nlm.nih.gov/17576034/ · DOI 10.1016/j.fct.2007.05.002 Structured context: {"organism": "Cell-free chemical assays", "tissue_or_cell_type": "Reactive-species scavenging systems", "dose": "Assay-specific millimolar IC50 values", "duration": "Not specified in accessed abstract", "route": "In vitro", "experimental_comparison": "SAC concentration series versus corresponding reference scavengers", "acting_entity": "s-allylcysteine", "interpretation_status": "Source-derived research curation; not independent primary verification"}
Complete structured claim and evidence
Where it participates (unsigned role)
Oxidation of melatonin by singlet oxygen produced AFMK, verified by chemical and spectroscopic analyses.
Experimental context and source evidence
- evidence_span
- {"source_cache": "artifacts/melatonin-research/12887657.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3d221b752cc6b59d719b21fd8ec2236bd75232ff34789f544a88e37bc270e8a5", "start_char": 0, "end_char": 1108, "text_sha256": "3d221b752cc6b59d719b21fd8ec2236bd75232ff34789f544a88e37bc270e8a5"}
- experimental_model
- Isotope-labeled chemical oxidation and product identification
- exposure
- Photosensitized or chemically generated singlet oxygen
- limitations
- Chemical scavenging/product formation is not proof that normal blood melatonin provides a clinically meaningful antioxidant flux or replaces vitamin C, E or selenium enzymes.
- nutrient_topic
- Melatonin research collection; topical membership is not evidence of a direct dietary effect. · Melatonin
- organism
- Cell-free chemical systems
- plain_language
- An antioxidant reaction changes melatonin into another molecule that is recorded separately.
- primary_references
- [melatonin-p12887657] Oxidation of melatonin by singlet molecular oxygen (O2(1deltag)) produces N1-acetyl-N2-formyl-5-methoxykynurenine. (2003). https://pubmed.ncbi.nlm.nih.gov/12887657/ DOI: 10.1034/j.1600-079x.2003.00066.x
- tissue_or_cell_type
- Melatonin oxidation chemistry
Melatonin: synthesis, receptors, circadian timing and nutrient interactions (2026-09-17) · lines 513–524
AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Isotope-labeled chemical oxidation and product identification · source_derived_draft · unverified_draft
### melatonin-singlet-oxygen-afmk Oxidation of melatonin by singlet oxygen produced AFMK, verified by chemical and spectroscopic analyses. Condition category: normal nutrient_topic: Melatonin research collection; topical membership is not evidence of a direct dietary effect. plain_language: An antioxidant reaction changes melatonin into another molecule that is recorded separately. organism: Cell-free chemical systems tissue_or_cell_type: Melatonin oxidation chemistry experimental_model: Isotope-labeled chemical oxidation and product identification limitations: Chemical scavenging/product formation is not proof that normal blood melatonin provides a clinically meaningful antioxidant flux or replaces vitamin C, E or selenium enzymes. exposure: Photosensitized or chemically generated singlet oxygen evidence_span: {"source_cache": "artifacts/melatonin-research/12887657.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3d221b752cc6b59d719b21fd8ec2236bd75232ff34789f544a88e37bc270e8a5", "start_char": 0, "end_char": 1108, "text_sha256": "3d221b752cc6b59d719b21fd8ec2236bd75232ff34789f544a88e37bc270e8a5"} [melatonin-p12887657] Oxidation of melatonin by singlet molecular oxygen (O2(1deltag)) produces N1-acetyl-N2-formyl-5-methoxykynurenine. (2003). https://pubmed.ncbi.nlm.nih.gov/12887657/ DOI: 10.1034/j.1600-079x.2003.00066.x
Complete structured claim and evidenceIn the singlet-oxygen assay, 5 mM glutathione almost abolished net ergothioneine loss even though formation of selected products persisted.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- Cell-free singlet-oxygen chemistry.
- limitations
- Regeneration was proposed; its complete cellular enzymatic cycle was not established.
- nutrient_topic
- Ergothioneine collection; molecular form, preparation, species, exposure and manipulation remain explicit. · L-Ergothioneine
- plain_language
- Glutathione changes the fate of oxidized ergothioneine.
- primary_references
- Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity. · 2017 · https://pubmed.ncbi.nlm.nih.gov/29074402/ · DOI 10.1016/j.freeradbiomed.2017.10.372
Ergothioneine: transport, redox chemistry and cross-nutrient mechanisms (2026-09-19) · lines 144–150
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Cell-free singlet-oxygen chemistry. · source_derived_draft · unverified_draft
## ergothioneine-glutathione-preservation Glutathione changes the fate of oxidized ergothioneine. In the singlet-oxygen assay, 5 mM glutathione almost abolished net ergothioneine loss even though formation of selected products persisted. Model: Cell-free singlet-oxygen chemistry. Limitations: Regeneration was proposed; its complete cellular enzymatic cycle was not established. Evidence access: Primary abstract Ergothioneine stands out from hercynine in the reaction with singlet oxygen: Resistance to glutathione and TRIS in the generation of specific products indicates high reactivity. · 2017 · https://pubmed.ncbi.nlm.nih.gov/29074402/ · DOI 10.1016/j.freeradbiomed.2017.10.372
Complete structured claim and evidenceKI increased light/Rose-bengal killing by up to six logs in the tested bacterial and Candida systems.
Experimental context and source evidence
- experimental_model
- Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model.
- exposure_category
- Study-specific exposure, including pharmacological and in-vitro conditions; normal is the schema fallback outside the three availability categories.
- limitations
- Local photochemical system, not an effect of oral KI alone. Peroxyiodide intermediates were proposed, not directly established.
- nutrient_topic
- Potassium iodide research collection; shared-anion and comparator studies are not all KI interventions. · Potassium iodide
- plain_language
- KI amplified an externally activated antimicrobial reaction.
- primary_references
- Potassium Iodide Potentiates Antimicrobial Photodynamic Inactivation Mediated by Rose Bengal in In Vitro and In Vivo Studies. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28438946/ · DOI 10.1128/aac.00467-17
Potassium iodide: thyroid and non-thyroid mechanisms, interactions and discovery questions (2026-09-18) · lines 312–318
AI-assisted research curation; primary-study references, chemical references and label statements individually identified. Not publisher full text. · supports · Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model. · source_derived_draft · unverified_draft
## ki-pdt-killing KI amplified an externally activated antimicrobial reaction. KI increased light/Rose-bengal killing by up to six logs in the tested bacterial and Candida systems. Model: Rose bengal plus 540-nm light; up to 100 mM KI; microbial assays and a mouse skin-abrasion model. Limitations: Local photochemical system, not an effect of oral KI alone. Peroxyiodide intermediates were proposed, not directly established. Evidence location: Primary abstract Potassium Iodide Potentiates Antimicrobial Photodynamic Inactivation Mediated by Rose Bengal in In Vitro and In Vivo Studies. · 2017 · https://pubmed.ncbi.nlm.nih.gov/28438946/ · DOI 10.1128/aac.00467-17
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.