GHK-Cu

A copper-carrying tripeptide that behaves more like a transcriptional signal than a nutrient.

Skin & dermal · 8 min read · updated 13 Aug 2026

Research use only. The ranges below are what published studies and community protocols report. They are reference material for laboratory research, not medical advice or a recommendation for human or veterinary use.

The compound

GHK-Cu

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Type
Copper Peptide Complex
CAS
49557-75-7
Formula
C₁₄H₂₂CuN₆O₄
Mass
401.9 g/mol

At a glance

Class
Copper(II) tripeptide complex
Sequence
Gly-His-Lys, complexed with Cu²⁺
Molecular weight
401.9 g/mol
CAS
89030-95-5
Endogenous
Yes — plasma levels fall roughly 60% between ages 20 and 60
Vial sizes stocked
50 mg, 100 mg

GHK was identified in human plasma in the early 1970s as the factor that made old liver tissue behave like young liver tissue in culture. It is a three-residue peptide — glycine, histidine, lysine — with an exceptionally high affinity for copper(II). The physiological form is the copper complex, GHK-Cu, and the copper is not incidental: the peptide is a copper transporter, delivering the ion to enzymes that need it while keeping free copper, which is pro-oxidant, out of circulation.

The reason it attracts so much research interest is that its effects are far broader than copper delivery explains. Gene-expression profiling found GHK-Cu significantly altering the expression of a very large number of human genes — resetting expression patterns in fibroblasts toward a younger profile, upregulating the DNA repair and antioxidant programmes and downregulating a number of inflammatory ones. Whether the copper or the peptide is doing the signalling is still argued.

Plasma GHK falls with age, from roughly 200 ng/ml in young adults to around 80 ng/ml by age sixty. That decline is the observation that frames most of the research narrative around it.

Mechanism in detail

  • Matrix synthesis: stimulates fibroblast production of collagen (types I and III), elastin, glycosaminoglycans and proteoglycans — the structural programme of dermal remodelling rather than a single fibre type.
  • Matrix remodelling: modulates both matrix metalloproteinases and their tissue inhibitors, so it influences the breakdown side as well as the synthesis side. Repair requires both.
  • Antioxidant: raises superoxide dismutase activity and, by chelating copper, prevents the Fenton chemistry that free copper would otherwise drive.
  • Anti-inflammatory: reduces TNF-α and IL-6 signalling; part of why it appears in inflammation-resolution blends rather than only in cosmetic contexts.
  • Angiogenesis and nerve outgrowth: promotes both in wound models, complementing the migration and vascular arms that TB-500 and BPC-157 supply.
  • Hair follicle: extends the anagen phase and enlarges follicles in culture, the basis of the topical hair research literature.

Topical versus injected

GHK-Cu has the strongest topical evidence base of anything in this catalogue. Controlled cosmetic-dermatology studies of GHK-Cu creams and serums have reported measurable changes in skin density, wrinkle depth and photodamage markers over weeks to months. Topical is also the route where the concentration is well established: cosmetic formulations sit in the 0.1–2% range depending on the vehicle.

Injected GHK-Cu is a different proposition. It delivers the complex systemically, and the reported research protocols are correspondingly cautious about total copper load. It is the route used when the question is systemic — connective tissue, wound repair at depth, or the blend work described below — rather than skin surface.

The copper ceiling

This is the one compound in the catalogue where a hard upper limit comes from something other than peptide pharmacology. Each molecule of GHK-Cu carries one copper ion, and copper accumulates. The complex is roughly 16% copper by mass, so 50 mg of GHK-Cu carries in the region of 8 mg of copper — a meaningful amount against a typical daily dietary intake of 1–2 mg.

This is why reported injectable protocols run in short blocks — commonly 2–4 weeks on followed by 2–4 weeks off — rather than continuous use, and why total monthly exposure matters more here than daily dose. Copper accumulation is also the mechanism behind the bluish-grey discolouration occasionally reported at repeatedly used injection sites.

Storage

  • Lyophilised: 2–8 °C, or −20 °C for extended storage, protected from light.
  • Reconstituted: 2–8 °C, used within about 28 days.
  • Light exposure matters more here than for most peptides — copper complexes are photo-reactive. Keep the vial in its box.

Cautions

  • Copper accumulation is the real dose-limiting factor. Wilson's disease and any condition of impaired copper handling is an absolute exclusion.
  • Injection-site discolouration is reported with repeated use at the same site; rotate.
  • Do not co-formulate with ascorbic acid, retinoids at low pH, or strong chelators.
  • Topical evidence is much stronger than injectable evidence. Systemic protocols are extrapolations from wound-healing work.

References & credit

  1. 1Pickart L, Margolina A — Int J Mol Sci 2018 — Regenerative and protective actions of GHK-Cu, including the gene-expression findings.
  2. 2Pickart L — J Biomater Sci Polym Ed 2008 — The GHK peptide in skin remodelling and wound repair.
  3. 3Maquart FX et al., FEBS Letters 1988 — Stimulation of collagen synthesis in fibroblast cultures by GHK-Cu.

This article was written in-house. Where a dose range reflects community practice rather than a published trial, the community references we consulted are credited above and the article says which is which.

In the catalogueGHK-Cu

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    GHK-Cu — A copper-carrying tripeptide that behaves more like a transcriptional signal than a nutrient.