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Cosmetic / research peptide

GHK-Cu

GHK-Cu is the copper(II) complex of glycyl-L-histidyl-L-lysine, a tripeptide found in human plasma at about 200 ng/mL at age 20 and 80 ng/mL by 60.

By The Peptides Codex Editorial TeamReviewed September 8, 2026

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
3 aa
Class
Cosmetic / research peptide
Function
Copper-binding tripeptide studied in skin biology
Context
Permitted cosmetic ingredient for topical use; not an approved drug by any route; injected GHK-Cu has no human data

A genuine human plasma peptide with strong cell data, a huge cosmetic market, and almost no controlled clinical studies.

Also known as: copper peptide · GHK copper

Part of the Cosmetic & skin peptides cluster

Evidence brief

GHK-Cu — evidence brief

An ulcer-gel report favored area closure, while a small post-laser trial found no significant objective difference. A cell study compared bound/free forms. These selected studies leave systemic/injectable efficacy and safety unestablished; missing clinical methods limit confidence.

Version
2026-10-05.1
Snapshot updated

Prepared by Peptides Codex. Independent review by a qualified subject specialist is pending.

Scope of this brief

Selected older reports concerning copper-bound Gly-His-Lys, copper-free GHK and specific topical formulations. These materials are not interchangeable. This is not an exhaustive or systematic review, a dosing guide or batch authentication; qualified scientific review remains pending.

  1. Mulder et al., 1994 · PMID 17147644
    Material tested
    Authors' topical GHK–Cu gel versus vehicle; exact formulation unavailable in the abstract.
    Model or population
    People with diabetic neuropathic ulcers.
    Study design
    Multicenter randomized, evaluator-blinded comparison; standardized wound care in both groups.
    Sample and comparison
    Randomized/analyzed counts and follow-up timepoint not reported in the retrieved abstract.
    Reported finding
    Plantar-ulcer median area closure: 98.5% versus 60.8% with vehicle (p<0.05). These are area changes, not percentages of patients completely healed.
    Limits of this evidence
    Abstract-only subgroup result with unknown denominators and precision; no systemic or injectable inference.

    Source access: Primary PubMed and publisher abstracts inspected; full text and funding disclosures unavailable.

    Primary source ↗: Mulder et al., 1994 · PMID 17147644

  2. Miller et al., 2006 · PMID 16847171
    Material tested
    Topical regimens with or without GHK–Cu; concentration and complete product composition unavailable.
    Model or population
    Patients after circumoral CO₂ laser resurfacing.
    Study design
    Randomized comparison; blinded/image-based erythema assessment and 12-week skin assessments.
    Sample and comparison
    13 completed; randomized total and arm counts unavailable in the abstract.
    Reported finding
    No significant between-group difference in erythema, wrinkles or objective skin quality; questionnaire-reported skin improvement favored GHK–Cu (p=0.04).
    Limits of this evidence
    Small completer sample; subjective improvement does not establish objective benefit or equivalence. Topical post-laser findings cannot validate injections.

    Source access: Primary PubMed and publisher abstracts inspected; full text and funding disclosures unavailable. A linked correction could not be retrieved.

    Primary source ↗: Miller et al., 2006 · PMID 16847171

  3. Gruchlik et al., 2014 · PMID 25745767
    Material tested
    Reported equimolar GHK–Cu(II) preparation; copper-free GHK and CuCl₂ comparators.
    Model or population
    Commercial normal human dermal fibroblast cultures.
    Study design
    24-hour cell-culture comparison; IGF-2-stimulated total TGF-β1 measured by ELISA.
    Sample and comparison
    Key comparison: n=4 experiments, not patients; donor count unspecified.
    Reported finding
    GHK–Cu and CuCl₂ reduced stimulated secretion more than GHK alone; no change was detected in unstimulated secretion in the tested low-serum condition.
    Limits of this evidence
    Cell marker, not clinical scar or wound outcomes; no systemic efficacy/safety evidence.

    Source access: Primary full text inspected; Medical University of Silesia funding reported.

    Primary source ↗: Gruchlik et al., 2014 · PMID 25745767

A finding applies to the material, model and conditions studied. It does not establish safety or effectiveness in other settings.

Read the full, printable brief →

Overview

GHK-Cu is the copper(II) complex of glycyl-L-histidyl-L-lysine, a tripeptide found in human plasma at about 200 ng/mL at age 20 and 80 ng/mL by 60. It has a wide cell and animal literature on collagen synthesis, wound repair and anti-inflammatory signalling, a cosmetic market built on it, and — as a 2025 review notes — a surprising absence of clinical studies. Topical use is permitted as a cosmetic; it is not an approved drug.

Source & context

Biological / chemical source: Endogenous tripeptide complexed with copper(II)

Primary research or clinical context: Permitted cosmetic ingredient for topical use; not an approved drug by any route; injected GHK-Cu has no human data

What GHK-Cu is

GHK is the tripeptide glycine–histidine–lysine, a normal constituent of human plasma, saliva and urine. It binds copper(II) with very high affinity to form the chelate GHK-Cu (Dou et al., Aging Pathobiology and Therapeutics 2020). Plasma GHK averages about 200 ng/mL at age 20 and declines to about 80 ng/mL by age 60, a fall that underlies much of the “anti-ageing” framing. The peptide and its copper complex are studied for tissue remodelling, wound healing and anti-inflammatory effects, and GHK-Cu and its palmitoylated derivative Pal-GHK are among the most widely used peptides in anti-wrinkle products (Mortazavi et al., BioImpacts 2025).

Proposed mechanisms

In cell and animal systems GHK stimulates blood-vessel and nerve outgrowth, increases synthesis of collagen, elastin and glycosaminoglycans, supports dermal fibroblast function, and has been reported to improve repair in skin, lung connective tissue, bone, liver and stomach lining, alongside anti-inflammatory actions and suppression of NF-κB (Pickart and Margolina, International Journal of Molecular Sciences 2018). Gene-expression data are invoked to explain this breadth. Readers should note that the 2018 review's authors are the peptide's discoverer and a commercial affiliate; the claims are extensive and the independent replication is uneven.

Recent animal studies from independent groups

Independent preclinical work in the last few years is more specific. GHK-Cu rescued cigarette-smoke-induced skeletal muscle dysfunction in mice via a sirtuin pathway, in a study that also measured lower plasma GHK in COPD patients than in healthy controls (Deng et al., Journal of Cachexia, Sarcopenia and Muscle 2023). It attenuated lung inflammation and fibrosis in a silicosis model by targeting peroxiredoxin 6 (Bian et al., Redox Biology 2024), and reduced dextran-sulfate colitis in mice with effects on SIRT1/STAT3 signalling and tight-junction proteins (Mao et al., Frontiers in Pharmacology 2025). An injectable hydroxyapatite microsphere filler loaded with GHK-Cu showed anti-inflammatory and antioxidant properties in a materials study (Hu et al., Colloids and Surfaces B 2025).

Human evidence: what exists and what does not

For the topical market the striking fact is how little controlled human data there are. A 2025 review of GHK as an anti-wrinkle ingredient concluded that cellular studies support the concept, that GHK-Cu and Pal-GHK are widely used, and that there is “a surprising absence of clinical studies using them,” with insufficient published data on skin permeability, effectiveness and physicochemical properties (Mortazavi et al., 2025). The trial registry shows a completed phase 4 study of facial skin quality and hydration, a recruiting phase 2 trial of a topical GHK-Cu gel for acute wound healing, and a two-part study of circulating GHK. For injected or systemic GHK-Cu there are no human trials in the sources reviewed.

GHK-Cu evidence by route
RouteEvidenceStatus
Topical (cosmetic)Cell studies strong; clinical studies scarce (Mortazavi et al., 2025); one phase 4 skin-quality trial completedPermitted cosmetic ingredient
Topical (wound healing)Phase 2 gel trial recruiting (NCT07437586)Investigational
Injected / systemicMouse models only (muscle, lung, colon)No human data; not approved

Pharmacokinetics and skin permeation

Endogenous GHK circulates at nanogram-per-millilitre levels and declines with age (Dou et al., 2020). Whether topically applied GHK-Cu or Pal-GHK penetrates skin in amounts sufficient to act is unresolved; the 2025 review identifies skin permeability as an open question and reviews the enhancement methods tried (Mortazavi et al., 2025). No human pharmacokinetic study of injected GHK-Cu — half-life, copper distribution, or clearance — appears in the literature reviewed.

Regulatory status as of September 2026

GHK-Cu is permitted as a cosmetic ingredient for topical use in most markets. It is not an approved drug by any route in the United States, Canada or the European Union. Injectable “GHK-Cu” vials are sold in the grey market, alone and in the GLOW and KLOW blends; these are unlicensed products of unverified content, and the copper they carry raises an additional, unstudied question about oxidative interactions with co-formulated peptides.

GHK-Cu in the blends

GHK-Cu is the “G” in GLOW (with BPC-157 and TB-500) and in KLOW (with KPV added). It is the only component of either blend with any human data — and those data are topical, cosmetic and thin. Combining it by injection with peptides that have no human data does not borrow credibility from the skin literature. The copper-peptides guide covers the topical evidence in detail; the GLOW and KLOW guides cover the blends.

Reading the claims responsibly

GHK-Cu sits in an unusual position: a real human peptide, a coherent cell biology, a large commercial footprint, and a clinical evidence base that a sympathetic review still calls surprisingly absent. This profile describes that gap; it is not guidance on obtaining or using any product and it is not medical advice.

Sequence

One-letter sequence commonly cited for GHK-Cu (educational; isoforms and modifications may differ):

GHK

GHK

GHK-Cu3 aa · C14H21CuN6O4- · ≈ 400.9 DaPEPTIDESCODEX.COMN-terminus →→ C-terminusG1H2K+3nonpolarpolaracidicbasicGly / Pronon-canonical (X)Hydropathy (Kyte–Doolittle): ▮ hydrophobic (cyan) / ▮ hydrophilic (rose) · Side-chain charge at pH 7: + / −
GHK-Cu — Structure cardDownload SVG
G1H2K3
Helical wheel projection

Residues plotted ~100° apart around an α-helix — clustering of one color reveals an amphipathic face.

Analyze sequences in the playground →

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
Tripeptide Gly-His-Lys (GHK) chelating one copper(II) ion; the copper binds through the glycine amine, the histidine imidazole and backbone nitrogens
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Molecular formula
C14H21CuN6O4-
Average reference mass
≈ 400.9
Backbone
Tripeptide Gly-His-Lys (GHK) chelating one copper(II) ion; the copper binds through the glycine amine, the histidine imidazole and backbone nitrogens
Status
Cosmetic ingredient (topical) in most markets; not an approved drug. Registry: a phase 2 topical wound-healing gel trial recruiting and a phase 4 facial-skin study completed (snapshot September 2026)
Identifiers

Chemistry values: curated profile, PubChem · fetched 2026-10-01.

Clinical development snapshot

ClinicalTrials.gov lists 3 registered studies with “GHK-Cu” as an intervention (snapshot 2026-09-06). A registry footprint is not evidence of efficacy or approval.

Registered studies
3
Highest phase reached
Phase 4
Active in latest 100
2
Most recent update
2026-07-15
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT07706361Two-Part Study of the Effects of the X39 Patch on Circulating GHK and GHK-Cu Levels in Healthy AdultsNot applicablenot yet recruiting2026-07-15
NCT07437586Topical GHK-Cu Gel for Acute Skin Wound HealingPhase 2recruiting2026-02-27
NCT05932732Trial Assessing the Impact on Facial Skin Quality, Hydration, and Skin Barrier of Three (3) Hydrafacial TreatmPhase 4completed2024-10-24
See all on ClinicalTrials.gov →
Concentration math

GHK-Cu — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Tripeptide Gly-His-Lys (GHK) chelating one copper(II) ion; the copper binds through the glycine amine, the histidine imidazole and backbone nitrogensAverage reference mass: 400.9 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the GHK-Cu calculator on its own page →

Change log

Dated observations from the data pipeline (registry flags, trial footprints, identifiers) and editorial reviews of this profile.

  1. EditorialProfile content reviewed and updated by the editorial team.

FAQ about GHK-Cu

What is GHK-Cu?+

GHK-Cu is the copper(II) complex of glycyl-L-histidyl-L-lysine, a tripeptide found in human plasma at about 200 ng/mL at age 20 and 80 ng/mL by 60. It has a wide cell and animal literature on collagen synthesis, wound repair and anti-inflammatory signalling, a cosmetic market built on it, and — as a 2025 review notes — a surprising absence of clinical studies. Topical use is permitted as a cosmetic; it is not an approved drug.

What Canadian product status is recorded for GHK-Cu?+

Canadian product status for GHK-Cu has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of GHK-Cu?+

GHK-Cu is commonly described as approximately 3 amino acids (Cosmetic / research peptide).

What is GHK-Cu?+

The copper(II) complex of the tripeptide glycyl-L-histidyl-L-lysine, a natural component of human plasma that declines with age. It is studied for collagen synthesis, wound repair and anti-inflammatory effects.

Does GHK-Cu work on skin?+

Cell studies support collagen and glycosaminoglycan stimulation, but a 2025 review found a surprising absence of clinical studies of GHK-Cu products and unresolved questions about skin penetration.

Is GHK-Cu approved?+

As a topical cosmetic ingredient, yes in most markets. As a drug by any route, no.

Is injected GHK-Cu safe or effective?+

There are no human trials of injected GHK-Cu. Systemic data are from mouse models only.

How much GHK is in the blood?+

About 200 ng/mL at age 20, falling to about 80 ng/mL by age 60 (Dou et al., 2020).

What is the difference between GHK-Cu and GLOW?+

GLOW is a vendor blend of GHK-Cu with BPC-157 and TB-500. GHK-Cu alone has topical cosmetic data; the blend has none.

Further reading

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References & further reading

  1. 1.Pickart (2008). The human tri-peptide GHK and tissue remodeling. J Biomater Sci Polym Ed
  2. 2.Pickart et al. (2018). Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data. Int J Mol Sci
  3. 3.Maquart et al. (1988). Stimulation of collagen synthesis in fibroblast cultures by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+. FEBS Lett
  4. 4.Maquart et al. (1993). In vivo stimulation of connective tissue accumulation by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+ in rat experimental wounds. J Clin Invest
  5. 5.Fu et al. (2015). Tripeptide-copper complex GHK-Cu (II) transiently improved healing outcome in a rat model of ACL reconstruction. J Orthop Res
  6. 6.Jiang et al. (2023). Synergy of GHK-Cu and hyaluronic acid on collagen IV upregulation via fibroblast and ex-vivo skin tests. J Cosmet Dermatol
  7. 7.Pickart et al. (2014). GHK and DNA: resetting the human genome to health. Biomed Res Int
  8. 8.Dou et al. (2020). The potential of GHK as an anti-aging peptide. Aging Pathobiol Ther
  9. 9.Beretta et al. (2008). Acrolein sequestering ability of the endogenous tripeptide glycyl-histidyl-lysine (GHK): characterization of conjugation products by ESI-MSn and theoretical calculations. J Pharm Biomed Anal
  10. 10.Pickart et al. (2015). GHK Peptide as a Natural Modulator of Multiple Cellular Pathways in Skin Regeneration. Biomed Res Int
  11. 11.Pickart et al. (2017). The Effect of the Human Peptide GHK on Gene Expression Relevant to Nervous System Function and Cognitive Decline. Brain Sci
  12. 12.Pickart et al. (2012). The human tripeptide GHK-Cu in prevention of oxidative stress and degenerative conditions of aging: implications for cognitive health. Oxid Med Cell Longev
  13. 13.Pyo et al. (2007). The effect of tripeptide-copper complex on human hair growth in vitro. Arch Pharm Res
  14. 14.Conato et al. (2001). Copper complexes of glycyl-histidyl-lysine and two of its synthetic analogues: chemical behaviour and biological activity. Biochim Biophys Acta
  15. 15.Wegrowski et al. (1992). Stimulation of sulfated glycosaminoglycan synthesis by the tripeptide-copper complex glycyl-L-histidyl-L-lysine-Cu2+. Life Sci
  16. 16.Mortazavi et al. (2025). Topically applied GHK as an anti-wrinkle peptide: Advantages, problems and prospective. Bioimpacts
  17. 17.Deng et al. (2023). Glycyl-L-histidyl-L-lysine-Cu2+ rescues cigarette smoking-induced skeletal muscle dysfunction via a sirtuin 1-dependent pathway. Journal of Cachexia, Sarcopenia and Muscle
  18. 18.Bian et al. (2024). The glycyl-L-histidyl-L-lysine-Cu2+ tripeptide complex attenuates lung inflammation and fibrosis in silicosis by targeting peroxiredoxin 6. Redox Biology
  19. 19.Mao et al. (2025). Exploring the beneficial effects of GHK-Cu on an experimental model of colitis and the underlying mechanisms. Frontiers in Pharmacology
  20. 20.Mendias & Awan (2026). Safety and efficacy of approved and unapproved peptide therapies for musculoskeletal injuries and athletic performance. Sports Medicine
  21. 21.PubChem — Copper tripeptide GHK-Cu, CID 139035031
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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