Longevity & bioregulatorsPeptideEvidence B4 cited

GHK-Cu

Copper Peptide

aka Copper Peptide GHK · GHK-Cu tripeptide · glycyl-L-histidyl-L-lysine copper

A naturally occurring copper-binding peptide research associates with collagen synthesis and tissue remodelling.

Molecular wt
401.91g/mol
Formula
C14H22CuN6O4
CAS
89030-95-5
Half-life
3 h
clinical
Tmax
1 h
Route
Topical / subcutaneous

Sequence

One-letter3 residues

GHK

Three-letter

Gly-His-Lys

Read this before quoting the sequence
Copper(II) complex of the human tripeptide glycyl-L-histidyl-L-lysine. The peptide itself is a conventional tripeptide; 'GHK-Cu' denotes the coordination complex, in which Cu(II) is chelated by the glycine amine, the peptide-bond nitrogen and the histidine imidazole. The free peptide GHK is PubChem CID 73587 (C14H24N6O4, MW 340.38, CAS 49557-75-7).
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Mechanism of action

GHK-Cu binds to copper ions, facilitating their transport into cells. It activates tissue remodeling by upregulating collagen synthesis and promoting wound healing. The peptide also modulates gene expression related to inflammation and oxidative stress, enhancing skin repair and regeneration.

What the evidence actually shows

Grade B

There are a few small human trials that suggest GHK-Cu can improve skin healing and reduce signs of aging. However, larger and more rigorous studies are needed to confirm these effects and establish optimal dosing.

Regulatory status

Status
Not approved as a medicine in any jurisdiction identified. Used as a cosmetic ingredient under the INCI name 'copper tripeptide-1'. No entry in Drugs@FDA or the EMA medicines register for a GHK-Cu drug product.
Clinical stage
No registered controlled human therapeutic trials identified. Evidence base is in vitro, animal wound-healing studies and cosmetic-science work.
WADA
Not named on the WADA 2026 Prohibited List. S0 (Non-Approved Substances) prohibits at all times any pharmacological substance with no current approval by any governmental regulatory health authority for human therapeutic use, which on its face covers injectable GHK-Cu (cosmetic-ingredient status is not therapeutic approval).
UK
research_compound

In the UK, GHK-Cu is considered a research compound and is not approved for therapeutic use by the MHRA.

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Pharmacokinetics

Half-life
3 h
Tmax
1 h
Absorption
subcutaneous
Elimination
renal
Washout
3 days
Low-confidence pharmacokinetics
These figures are recorded as clinical rather than measured in a published PK study. Treat them as an order of magnitude. Anything downstream of them — accumulation, steady state, washout — inherits that uncertainty.

Dosing — what backs each figure

GHK-Cu's human evidence base is entirely topical and cosmetic/dermatological: a 0.4% copper-tripeptide cream in a randomised venous ulcer trial (which failed to beat placebo), a randomised post-CO2-laser skincare study (also null), and ongoing cosmetic and topical wound-gel studies. Dosing is expressed as a percentage concentration in a formulation, not a milligram injection - there is no published human injectable dose for GHK-Cu, so asking 'how many mcg do I inject' has no evidence-based answer.

ClinicalApproved labelling or a published human trial
Commonly circulatedNot established by any study
Dose
Topical cosmetic use well established; injectable research dosing not standardised
Frequency
Daily
Cycle
8-12 weeks· unsourced

Why this isn't evidence
The first clause is broadly fair (topical GHK-Cu has been used in controlled human trials at defined percentage concentrations such as 0.4% cream), but 'Daily' with an '8-12 weeks' cycle is community convention rather than a trial regimen, and framing GHK-Cu as having any injectable 'dose' is a category error - no human study has ever injected it.

This figure is shown because it is what circulates and what people search for — not because it is supported. Cycle lengths in particular tend to be convention copied between compounds rather than anything derived from a compound's own pharmacokinetics.

Handling and storage

Lyophilized
No compound-specific data documented
Reconstituted
In a published preformulation study, GHK-Cu was stable in water and in buffers across pH 4.5-7.4 for at least two weeks at 60 C. It degraded with first-order kinetics under basic and oxidative stress, and to a lesser extent under acidic stress; three degradation products were identified by HPLC-MS, one of which was free histidine.
Solvent
Water or a buffer in the pH 4.5-7.4 range

This is genuine compound-specific stability data from a peer-reviewed preformulation study (Badenhorst 2016, PMID 25384620), not vendor guidance. It also found GHK-Cu compatible with Span 60 based niosomes but less stable in the presence of the negatively charged lipid dicetyl phosphate. No photostability data was found, so lightSensitive is left null. No lyophilised-powder shelf-life study was found. Practical implication: avoid alkaline and oxidising vehicles.

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Safety

Commonly reported
  • ·Mild skin irritation
Rarely reported
  • ·Allergic reactions
Contraindications
  • ·Known allergy to copper or peptide components
Drug interactions
  • ·Copper supplements may enhance effects, leading to potential toxicity

Topical: generally well tolerated; injectable data limited

Reported combinations

Reported as synergistic
  • ·Vitamin C, which supports collagen synthesis
Reported as antagonistic
  • ·High-dose zinc, which competes with copper absorption

Combination claims in this dataset are largely unsourced and should be treated as folk knowledge until a citation appears beside them.

References (4)

Data provenance

Chemistry and citations on this page were checked against primary sources on 2026-08-14. Values that could not be verified were left blank rather than filled with a plausible guess.

Research use only
This profile is educational reference material. It is not medical advice, not a prescription, and not an endorsement of self-administration. Compounds discussed here are research chemicals and most are not approved for human therapeutic use.