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Glutathione vs PNC-27

Glutathione and PNC-27 are studied in overlapping research areas, which is why they are frequently compared. This is a neutral side-by-side reference drawn from published preclinical literature and laboratory handling data.

Shared research areas:Cellular Longevity
ClassEndogenous thiol tripeptide (γ-L-glutamyl-L-cysteinyl-glycine), reduced formMembranolytic fusion peptide (32 residues): p53-derived domain + membrane-penetrating leader
Molecular weight307.3 g/molNot specified
CAS number70-18-8Not assigned / not specified
Purity spec≥99%≥99%
Research areasCellular Longevity, MetabolicCellular Longevity
Primary diluentSterile water (USP grade)Sterile water for a stock, then dilution into assay buffer
Working windowCommonly worked with for about 1 week at 2-8 °C; frozen aliquots keep longer.Short — prepare working solutions close to use.
Lead degradation routeOxidation of the cysteine thiol to glutathione disulfide (GSSG, about 612.6 Da), catalysed by trace Cu²⁺/Fe³⁺ and faster at neutral-to-alkaline pH.Aggregation of the amphipathic chain at the air-liquid interface or high concentration.
Freeze–thawTolerates a few freeze-thaw cycles, but each thaw exposes the thiol to dissolved oxygen. Aliquot once and thaw each portion only once.Aliquot on first reconstitution; the amphipathic sequence is best not repeatedly frozen and thawed.
Light sensitivityNot strongly light-sensitive, but oxygen-sensitive: minimise headspace and avoid metal spatulas or metal-contaminated buffers.No specific light requirement beyond normal practice.

How they actually differ

Comparing the two: Glutathione is endogenous thiol tripeptide (γ-l-glutamyl-l-cysteinyl-glycine), reduced form, while PNC-27 is membranolytic fusion peptide (32 residues): p53-derived domain + membrane-penetrating leader — different molecular classes with different handling consequences; they call for different primary diluents (sterile water (usp grade) versus sterile water for a stock, then dilution into assay buffer); their leading degradation routes differ (oxidation of the cysteine thiol to glutathione disulfide (gssg, about 612.6 da), catalysed by trace cu²⁺/fe³⁺ and faster at neutral-to-alkaline ph. for Glutathione, aggregation of the amphipathic chain at the air-liquid interface or high concentration. for PNC-27), so the storage precautions that matter are not the same; their practical working windows differ once reconstituted. The sections below set out each in full.

Glutathione — origin

Glutathione is the tripeptide γ-glutamyl-cysteinyl-glycine. The glutamate is joined through its side-chain (γ) carboxyl rather than the usual α link, which protects it from most peptidases. It was named by Frederick Gowland Hopkins in 1921, and its role in cellular redox chemistry was mapped out through the 20th century, most influentially in Alton Meister's work on the γ-glutamyl cycle.

PNC-27 — origin

PNC-27 is a designed 32-residue peptide fusing a p53-derived region that binds HDM-2 with a membrane-penetrating leader sequence. It is studied strictly in vitro for a reported ability to form pores in the membranes of cancer cells that display HDM-2 at their surface, while reportedly sparing normal cells.

Glutathione research themes

Cellular redox buffering (GSH/GSSG ratio)

Glutathione is the most abundant low-molecular-weight thiol in most cells, and the ratio of reduced to oxidised glutathione is widely used as a read-out of oxidative stress in cell-culture and tissue studies.

The γ-glutamyl cycle

Meister and Anderson (Annu Rev Biochem 1983) reviewed glutathione synthesis by γ-glutamylcysteine synthetase and glutathione synthetase, and its breakdown by γ-glutamyl transpeptidase — the framework most synthesis and turnover studies still use.

Detoxification by glutathione S-transferases

GSTs conjugate glutathione to electrophilic compounds, and this conjugation step is a standard model in xenobiotic-metabolism research.

The glutathione peroxidase system

Glutathione peroxidases use GSH to reduce hydrogen peroxide and lipid hydroperoxides, with glutathione reductase recycling GSSG back to GSH using NADPH — a common model for studying peroxide handling in vitro.

PNC-27 research themes

HDM-2 cell-surface targeting

Studied for binding HDM-2 displayed on the surface of certain cancer cells in vitro.

Membrane pore formation

Examined for forming transmembrane pores that lead to lysis of targeted cells in culture.

Selectivity in vitro

Investigated for a reported preference for tumour cells over normal cells in preclinical cell-culture models.

Glutathione handling

  • Let the vial reach room temperature before opening to stop condensation getting in.
  • Use degassed diluent where possible and cap promptly after drawing.
  • Avoid metal tools and buffers with trace copper or iron; plastic or glass only.
  • Label aliquots with reconstitution date and diluent.

PNC-27 handling

  • For laboratory in-vitro use only — this compound is studied strictly in cell-culture research.
  • Prepare a stock and dilute into the assay system rather than dissolving at high concentration.
  • Aliquot and refrigerate; prepare fresh working dilutions.

Both third-party tested

Every Popular Peptides batch of Glutathione and PNC-27 is independently tested by HPLC and LC-MS with a published Certificate of Analysis. Enter a lot number to pull the COA for a specific vial.

Glutathione reference

PNC-27 reference

Related comparisons

Glutathione and PNC-27 are supplied strictly as research chemicals for in-vitro laboratory and research use only. They are not intended for human or animal consumption, diagnostic, or therapeutic use. This comparison summarizes published preclinical literature and laboratory handling data; it is not medical advice, not a claim of efficacy, and not usage guidance.