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Mitochondrial · Research Compound

Glutathione

GSH; reduced glutathione

The endogenous tripeptide master antioxidant studied for redox and detoxification research.

Glutathione research peptide vial — Ethos Bio

01At a Glance

CompoundGlutathione
Also known asGSH; reduced glutathione
CAS Number70-18-8
Molecular Weight307.32 g/mol
Sequence / Formγ-Glu-Cys-Gly
ClassificationMitochondrial research compound
AppearanceLyophilized powder
Purity≥99% (HPLC · MS-verified)
Storage2–8°C; -20°C for long-term
Intended UseResearch Use Only

02Mechanism of Action

Glutathione (GSH) is an endogenous tripeptide (γ-glutamyl-cysteinyl-glycine) and the cell's principal thiol antioxidant. Its reactive cysteine thiol neutralizes reactive oxygen species and serves as a substrate for glutathione peroxidase in redox-balance research.

It also participates in phase-II detoxification via glutathione-S-transferase conjugation, making it a core tool in oxidative-stress and detoxification studies.

Research framing only · No therapeutic, dosing, or human-use claims

03Research Applications

04Purity & Verification

Every Ethos Bio lot of Glutathione is analyzed by reverse-phase HPLC and independently confirmed by mass spectrometry through our third-party testing partner, Janoshik Analytical. A signed Certificate of Analysis documenting identity and ≥99% purity is provided for every lot.

View the Glutathione Certificate of Analysis

Independent third-party HPLC & mass-spec verification. The COA shipped with your order reflects your specific lot.

View COA →

05Frequently Asked Questions

What is glutathione used for in research?

Glutathione is the endogenous tripeptide master antioxidant studied for redox balance, ROS scavenging, and phase-II detoxification in research models. It is sold for research use only.

What is the structure of glutathione?

Glutathione is a tripeptide with the sequence γ-Glu-Cys-Gly, molecular weight approximately 307.32 g/mol, and CAS number 70-18-8.

Why is the cysteine residue important?

The cysteine thiol (-SH) group is the reactive center responsible for glutathione's antioxidant and conjugation chemistry studied in redox research.

06Related Mitochondrial Compounds