Public educational draft · 04 November 2026Clinical review pending →
AXON Glutathione card with verified molecular model and 2D structure, exact GPx/GR redox cycle, cell-study diagram of SLC25A39 mitochondrial GSH import, and two separate human biomarker-trial panels with qualified outcomes and participant counts.

Visual summary only. The research findings, limitations and references accompany the card on this page.

The molecular view uses a source-provided computational conformer, not an experimental or unique bioactive geometry. The biological setting is an illustration. Original study diagrams summarize cited research without reproducing publication artwork or inventing quantitative results.

PubChem computational conformer (3D SDF) · Download visual source SDF

Read the research ↓ · View all references ↓

Mitochondrial / longevity

Glutathione

Three amino acids. One redox-active thiol.

Reduced L-glutathione, neutral parent structure
Molecular formula
C10H17N3O6S
Molecular weight
307.33 g/mol
Class
Tripeptide
Identity
γ-L-glutamyl-L-cysteinylglycine

Research snapshot

A naturally occurring tripeptide involved in cellular redox regulation and antioxidant defense.

Established biochemistry; selected placebo-controlled human biomarker trials with mixed results

Identity & representation

The card describes the reduced neutral parent molecule, not a particular salt, formulation, or batch. PubChem depicts glutamate and cysteine stereochemistry.

Educational reference only. Not a dosing guide, treatment recommendation or product endorsement.

Reduced L-form · GSH[2]

View the chemical structure →

Sources checked: 2026-11-06. Identity and evidence limits are stated above. Independent specialist review is pending.

ClassTripeptide

3 amino acid residues[2]

Biological roleCellular redox balance

Enzyme co-substrate[1]

Evidence contextEstablished biochemistry

Mixed human biomarker results[1][3][4]

U.S. statusNo FDA-approved

glutathione products[6]

As of 2026-11-06

What researchers study

GSH is made in cells from glutamate, cysteine and glycine. Its sulfur-containing thiol participates in redox reactions and conjugation chemistry.

  • Oxidative stress

    Peroxide metabolism and GSH/GSSG balance.[1]

  • Cell signaling

    Redox-sensitive proteins and cellular responses.[1]

  • Chemical metabolism

    Conjugation of electrophilic compounds.[1]

How the redox cycle works[1][8][9][10]

  1. 2 GSHReducedGlutathione peroxidases (GPx) ↓
  2. GSSGOxidizedGlutathione reductase (GR) ↓
  3. 2 GSHRegenerated

Glutathione peroxidases use GSH to reduce peroxides. Glutathione reductase recycles GSSG to GSH.

Cellular chemistry does not establish that supplementation improves health outcomes.

Original publication-grounded biochemical schematic; enzyme reactions are stoichiometrically balanced.

Human evidence

54 analyzed | 6 months[3]

Richie et al., 2015 · Randomized, double-blind, placebo-controlled trial

Healthy non-smoking adults; 61 enrolled, 60 received intervention, 54 completed at least six months and entered analyses. Oral glutathione supplementation; no dosing guidance provided.

Observed: GSH increased in several measured compartments; the reported increases used in the visual are versus baseline.

Limit: Biomarker findings in healthy adults do not establish disease prevention or treatment. The two selected trials were not a head-to-head comparison.

Endpoint: Biomarker

40 enrolled | 39 completed | 4 weeks[4]

Allen and Bradley, 2011 · Randomized, double-blind, placebo-controlled trial

Adults without acute or chronic disease; 40 enrolled and 39 completed per protocol. Oral glutathione supplementation; no dosing guidance provided.

Observed: No significant between-group changes in erythrocyte GSH indices or measured urinary oxidative-stress biomarkers.

Limit: A small, short study; nonsignificance is not proof of zero effect or equivalence. Findings cannot establish treatment benefit or injectable safety.

Endpoint: Biomarker

Measured endpoints: Erythrocyte glutathione indices; Urinary F2-isoprostanes; Urinary 8-OHdG

Safety & evidence limits

  • Biomarkers are not clinical outcomes[3][4]

    Small healthy-adult studies cannot establish disease treatment, longevity or broad benefit.

  • Preparation and route matter[3][4][5]

    Oral trial results do not establish injectable safety or the quality of a different product.

  • Contamination can cause serious harm[5]

    FDA warns against using dietary supplement-grade glutathione to make injectable drugs.

Practical identity notes

  • GSH is the reduced form; GSSG is the disulfide.
  • This structure is the neutral parent, not a salt, mixture or formulation.
  • Chemical identity does not certify product purity, sterility or suitability for human use.

The 10-second takeaway

Essential endogenous redox chemistry. Mixed supplementation biomarker results. The two trials summarized here do not establish treatment benefit.

Enzyme reactions

  • Glutathione peroxidase (GPx)[1][8][10]

    2 GSH + H2O2 → GSSG + 2 H2O

  • Glutathione reductase (GR)[1][9][10]

    GSSG + NADPH + H+ → 2 GSH + NADP+

Biochemical reactions describe cellular chemistry, not treatment outcomes.

What the visual panels show

Original diagrams summarize the cited research or documented evidence search. They are not copied publication figures or claims of treatment benefit.

  • Enzyme redox cycle[1][8][9][10]

    Established biochemistry · Original biochemical cycle schematic

    2 GSH · GSSG · GPx · peroxide reduction · H2O2 → 2 H2O · GR · regeneration · NADPH + H+ → NADP+

    Interpretation: Cell mechanisms do not establish clinical benefit from supplementation.

  • Cell study: mitochondrial GSH[7]

    Cell and biochemical study · Original cytosol-to-mitochondrion transport diagram

    Cytosol · SLC25A39 · Cytosol → mitochondria · Transport mechanism in cells

    Interpretation: SLC25A39 is placed at the schematic inner membrane. This is cellular biology, not a treatment-target map or a solved protein structure.

    Source context: Figure 2. See the linked references.

  • Human trial: Richie et al.[3]

    Randomized placebo-controlled human biomarker trial · Original blood, plasma and cell specimen icons; no quantitative chart

    54 analyzed · 6 months · Measured compartments · Blood · Plasma · Cells · Several GSH measures increased vs baseline

    Interpretation: The icon strip depicts measured compartments, not a claim that every compartment improved at every tested dose.

    Source context: Figure 2, Figure 3. See the linked references.

  • Human trial: Allen and Bradley[4]

    Randomized placebo-controlled human biomarker trial · Original erythrocyte and urinary-specimen icons; no quantitative chart

    40 enrolled · 4 weeks · 39 completed · Erythrocyte GSH · Urine markers · No significant between-group changes

    Interpretation: Nonsignificance is not proof of zero effect or equivalence. The selected trials have different designs and are not a head-to-head comparison.

    Source context: Figure 1, Figure 2, Figure 3. See the linked references.

Follow the evidence

Sources & what they support

  1. Glutathione and glutathione-dependent enzymes: From biochemistry to gerontology and successful aging

    Lapenna D · Ageing Res Rev. · 2023;92:102066 · PMID: 37683986 · DOI: 10.1016/j.arr.2023.102066

    Supports: Overview; redox homeostasis; peroxidase/reductase mechanism; conjugation; research areas

  2. Glutathione, PubChem CID 124886

    Supports: Chemical identity, connectivity, stereochemistry, molecular formula, molecular weight

    Original structure record · Download depicted structure SDF

    Generated 2D layout from the verified reference graph; not an original 2D source-record download.

  3. Randomized controlled trial of oral glutathione supplementation on body stores of glutathione

    Richie JP Jr et al. · Eur J Nutr. · 2015;54(2):251–263 · PMID: 24791752 · DOI: 10.1007/s00394-014-0706-z

    Supports: Healthy-adult biomarker study: 61 enrolled, 60 received intervention, 54 completed at least six months and entered analyses; increases described in the visual are versus baseline; scope limits

  4. Effects of oral glutathione supplementation on systemic oxidative stress biomarkers in human volunteers

    Allen J, Bradley RD · J Altern Complement Med. · 2011;17(9):827–833 · PMID: 21875351 · DOI: 10.1089/acm.2010.0716

    Supports: Healthy-adult biomarker study: 40 enrolled, 39 completed, four weeks; no significant between-group changes in measured erythrocyte GSH and urinary oxidative-stress biomarkers; scope limits

  5. FDA reminds compounders not to use dietary supplement grade glutathione for injectables

    FDA · 2026 · Published 2026-08-27

    Supports: Route/formulation-specific contamination safety; supplement-grade ingredients unsuitable for injection

  6. Adverse Events Linked to Injectable Glutathione Compounded with Dietary Supplement Grade Ingredient: Current Situation

    CDC · 2026 · Published 2026-09-15

    Supports: No FDA-approved glutathione products in the United States as stated by current CDC advisory; safety context

  7. SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells

    Read full text

    Wang Y et al. · Nature · 2021;599(7883):136–140 · PMID: 34707288 · DOI: 10.1038/s41586-021-04025-w

    Supports: Cytosolic GSH and mitochondrial import with SLC25A39 involvement; source Figure 2. The card uses an original schematic, not copied figure artwork.

  8. Glutathione peroxidase, EC 1.11.1.9

    Supports: 2 GSH + H2O2 → GSSG + 2 H2O.

  9. Glutathione-disulfide reductase, EC 1.8.1.7

    Supports: GSSG + NADPH + H+ → 2 GSH + NADP+.

  10. Glutathione and mitochondria

    Read full text

    Ribas V, García-Ruiz C, Fernández-Checa JC · Front Pharmacol. · 2014;5:151 · PMID: 25024695 · DOI: 10.3389/fphar.2014.00151

    Supports: Figure 2 provides publication grounding for GSH/GPx/GR mitochondrial peroxide metabolism. The card uses an original diagram rather than reproducing the figure.

Source-linked educational drafts. Scientific and clinical review is pending. These cards describe molecules and study context, not product quality, approval or treatment recommendations.

← Explore the Molecular Atlas Continue to the research library →

Advertisement · AXON network

More of AXON.
One place to explore.

These promotional links lead to affiliated AXON websites. Their placement is separate from the educational content and does not validate any product, service or scientific claim.

You will leave this educational preview. Each destination has its own content, access requirements and privacy practices. No advertising tracker or referral parameter is added to these links.