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GHK-cu Copper Tripeptide

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GHK-Cu Copper Tripeptide is a biological signal for tissue remodelling, repair coordination, and extracellular matrix maintenance.

$58.00

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Form
Lyophilized
Molecular Formula
See COA
Molecular Weight
See COA
CAS Number
See COA
PubChem CID
See COA
Research Data
Primary Effect Over Time
Literature
Cellular Ratio
Comparative Metric
Activity Profile
Activity Profile
Mechanism
Cellular Pathway
01
Collagen Synthesis Stimulation
02
Balanced ECM Remodeling via MMP-TIMP
03
Genomic Modulation & Repair Cell Signaling
Metabolic Network
Biosynthesis Map
Collagen Synthesis Stimulation
Balanced ECM Remodeling via MMP-TIMP
Genomic Modulation & Repair Cell Signaling
Signal Output
Response
Repair Systems
Stress
Mitochondria
Energy
GHK-cu Copper Tripeptide CENTRAL HUB
Sequence Analysis
Amino Acid Sequence
Single-letter residue map colored by physicochemical property class. Hover any residue for full name and position.
G L Y H I S L Y S
9Residues
See COAMol. Weight
+1Net Charge
1Basic
0Acidic
■ Hydrophobic ■ Polar ■ Positively Charged ■ Negatively Charged ■ Glycine
Research Focus
Research Coverage
Product Data
Compound Identity
Product NameGHK-Cu Copper Tripeptide-1 (Oral Encapsulated)
Functional ClassPeptidics
FormLyophilized
Purity99%+
Content5mg
Count1 capsule
Research UseResearch Grade
Specifications
Technical Specs
CAS NumberSee COA
Molecular WeightSee COA
Molecular FormulaSee COA
PubChem CIDSee COA
AppearanceWhite to off-white powder
Storage2-8C preferred
Formulation Reference
Anatomy of a Peptide
A reference guide to the components of a lyophilized research peptide — from the active sequence to the excipients, solvents, buffers, and stabilizers used in formulation.
Active Peptide 2 items
Synthetic Amino Acid Sequence
The primary chain of amino acids synthesized via solid-phase peptide synthesis (SPPS). Defined by sequence length and molecular weight.
Peptide Modifications
Acetylation (N-terminus), amidation (C-terminus), PEGylation, or cyclization applied to improve stability, receptor binding, or half-life.
Excipients 4 items
Mannitol
Sugar alcohol bulking agent that forms an elegant lyophilized cake, aids reconstitution, and provides structural matrix during freeze-drying.
Trehalose
Non-reducing disaccharide that stabilizes peptide secondary structure by replacing water molecules through hydrogen bonding during dehydration.
Sucrose
Disaccharide used as a lyoprotectant and tonicity agent. Forms an amorphous glassy matrix that immobilizes the peptide and prevents aggregation.
Glycine
Amino acid bulking agent used in lyophilization. Crystallizes to provide mechanical strength to the freeze-dried cake structure.
Reconstitution Solvents 4 items
Bacteriostatic Water (BAC Water)
Sterile water containing 0.9% benzyl alcohol as a preservative. Preferred for multi-dose vials — inhibits microbial growth after initial puncture.
Sterile Water for Injection
USP-grade water, pyrogen-free, without preservatives. Used for single-dose preparations or when benzyl alcohol sensitivity is a concern.
Acetic Acid Solution (0.1–1%)
Dilute acid used for peptides with poor aqueous solubility at neutral pH. Protonates basic residues to improve dissolution.
Sodium Chloride 0.9%
Isotonic saline diluent. Provides physiological osmolality (~308 mOsm/L) and can improve stability of certain charged peptides.
Buffer Systems 4 items
Phosphate Buffered Saline (PBS)
Maintains pH 7.2–7.4. Composed of sodium phosphate dibasic, potassium phosphate monobasic, NaCl, and KCl. Mimics physiological ionic strength.
Acetate Buffer
Effective pH range 3.7–5.6. Composed of acetic acid and sodium acetate. Ideal for acidic peptides and those requiring lower pH for solubility.
Citrate Buffer
Effective pH range 3.0–6.2. Offers strong buffering capacity and metal-chelating properties. Used when oxidation-sensitive residues (Met, Cys) are present.
Histidine Buffer
Effective pH range 5.5–7.0. Low ionic strength, minimal interaction with peptides. Increasingly preferred in modern biopharmaceutical formulations.
Lyoprotectants & Cryoprotectants 3 items
Trehalose / Sucrose (Lyoprotectant)
Protect peptide conformation during the drying phase of lyophilization by forming hydrogen bonds that substitute for water molecules around the peptide.
Glycerol (Cryoprotectant)
Polyol that depresses the freezing point and reduces ice crystal formation, preventing mechanical damage to peptide structure during freezing steps.
Polyethylene Glycol (PEG)
Hydrophilic polymer that provides steric stabilization, reduces aggregation, and can serve as both cryoprotectant and solubility enhancer.
Preservatives & Antimicrobials 3 items
Benzyl Alcohol (0.9%)
Aromatic alcohol preservative in bacteriostatic water. Acts as antimicrobial agent by disrupting microbial cell membranes. Standard for multi-use vials.
Methyl / Propyl Parabens
Broad-spectrum antimicrobial preservatives effective against fungi and bacteria. Used in some peptide formulations where benzyl alcohol is incompatible.
Phenol (0.5%)
Bacteriostatic preservative used in certain injectable peptide formulations. Also acts as a conformational stabilizer for some peptide structures.
Counter Ions & Salt Forms 3 items
Trifluoroacetate (TFA)
Most common counter ion from RP-HPLC purification. Forms TFA salt with basic residues (Lys, Arg, His). May affect bioassay results and cell toxicity.
Acetate
Milder alternative to TFA obtained via ion exchange. Lower cytotoxicity, preferred for cell-based research assays and in vivo studies.
Hydrochloride (HCl)
Chloride salt form, sometimes used for improved stability or specific solubility profiles. Common in pharmaceutical-grade peptide preparations.
Chelating Agents 2 items
EDTA (Disodium)
Chelates divalent metal ions (Cu²⁺, Fe²⁺, Zn²⁺) that catalyze oxidative degradation of methionine and cysteine residues in peptides.
Citric Acid
Natural chelator with moderate metal-binding capacity. Dual function as buffer component and oxidation inhibitor in peptide formulations.
Antioxidants & Stabilizers 3 items
L-Methionine
Free methionine added as a sacrificial antioxidant. Preferentially oxidizes before methionine residues within the peptide chain.
Ascorbic Acid
Water-soluble antioxidant that scavenges reactive oxygen species. Used at low concentrations to prevent oxidative peptide degradation.
Polysorbate 20 / 80
Non-ionic surfactants that prevent surface adsorption and aggregation of peptides at air-liquid and container-liquid interfaces.
Preparation Tool
Reconstitution Calculator
Enter your target working concentration to calculate the exact solvent volume needed for this vial.
mg
Recommended solvents
Bacteriostatic Water Sterile Water for Injection Acetic Acid 0.1% Sodium Chloride 0.9%
Product Specs
Solubility Profile
WaterHighly soluble
Acidified WaterHighly soluble
DMSOHighly soluble
EthanolModerate
Lipid solventsPoor compatibility
Product Specs
Storage Specs
Lyophilized2–8°C preferred
Long-term−20°C recommended
Light SensitivityModerate
MoistureHigh sensitivity
StabilityStable when dry
ContainerSterile sealed vial
Literature
Research Citations
Catalogue Pathway
Related Systems
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Important Notice
Research Use Only

AminoBox products are supplied for research, analytical, and laboratory use only. Product information is provided for educational and technical reference and does not constitute medical advice. Products are not intended to diagnose, treat, cure, or prevent any disease.

Product Composition

Property Specification
Product Name GHK-Cu (Copper Tripeptide)
Alternate Names Glycyl-L-histidyl-L-lysine copper complex, Copper peptide
Capsule Content 2 mg
Package Size 60 Capsules
Compound Class Endogenous tripeptide–metal complex
Physical Form Encapsulated powder
Appearance Blue to blue-green powder (copper-bound peptide)
Purity Typically ≥98% (research grade, supplier dependent)
Research Category Skin repair / collagen signaling / regenerative biology compound

Molecular Information

Property Specification
Molecular Formula C14H24CuN6O4
Molecular Weight ~403.9 g/mol
CAS Number 89030-95-5
PubChem CID 3084370
Compound Type Copper-bound tripeptide complex
Stereochemistry All-L amino acid peptide backbone

Structural Classification

Category Description
Compound Type Copper chelated tripeptide
Functional Class Tissue remodeling and wound-healing signaling peptide
Biological Focus Skin regeneration and extracellular matrix repair
Mechanistic Focus Copper-dependent enzymatic activation (collagen, elastin synthesis pathways)
Chemical Family Endogenous bioactive peptide-metal complex

Mechanism Research Profile

Research Focus Description
Collagen Synthesis Stimulates collagen and glycosaminoglycan production in fibroblasts
Skin Remodeling Enhances extracellular matrix repair and dermal restructuring
Wound Healing Promotes tissue regeneration and repair signaling cascades
Antioxidant Activity Copper-mediated reduction of oxidative stress in tissue environments
Hair Follicle Research Studied for follicular signaling and growth-phase support

Research Areas Commonly Associated

Research Area Focus
Dermatological Biology Skin regeneration and anti-aging pathways
Wound Healing Science Tissue repair and recovery mechanisms
Cosmetic Biochemistry Collagen and elastin remodeling
Cellular Aging Research Extracellular matrix degradation and repair
Connective Tissue Biology Fibroblast and structural protein synthesis

Solubility Profile

Solvent Solubility
Sterile Water Highly soluble
Bacteriostatic Water Compatible
Saline Soluble
DMSO Limited compatibility
Organic solvents Not soluble

Storage Specifications

Parameter Recommendation
Capsule Storage 2–8°C preferred
Long-term Storage -20°C recommended
Light Sensitivity Moderate
Moisture Sensitivity High
Stability Stable in dry encapsulated form
Container Type Sealed opaque capsule bottle

Technical Characteristics

Feature Notes
Delivery Format Encapsulated powder (2 mg per capsule, 60-count bottle)
Structural Advantage Copper chelation enhances bioactivity in collagen-related pathways
Bioactivity Profile Endogenous repair peptide signaling molecule
Configuration Linear tripeptide complexed with Cu²⁺ ion
Stability Profile High stability in dry form; sensitive when in solution
Research Use Laboratory research only

GHK-cu Copper Tripeptide | 2mg

Within advanced biochemical and dermatological research, GHK-Cu is widely investigated for its ability to influence gene expression patterns associated with skin regeneration, wound repair, inflammation modulation, and structural protein synthesis. Its unique ability to bind copper ions (Cu²⁺) gives it a dual function: peptide signaling combined with trace mineral delivery, both of which are essential to enzymatic and structural processes in connective tissue biology.

What is GHK-cu Copper Tripeptide?

GHK-Cu is a naturally occurring tripeptide composed of:

Glycyl–L-Histidyl–L-Lysine + Copper (Cu²⁺)

This simple structure belies a highly complex biological role. Discovered in the 1970s, GHK-Cu was originally isolated from human plasma and later identified as a molecule that significantly decreases in concentration with age. This decline has led researchers to investigate its relationship to aging phenotypes, including reduced tissue repair capacity, collagen fragmentation, and diminished skin elasticity.

The peptide is now widely studied in the fields of:

  • Dermatological regeneration science
  • Wound healing biology
  • Extracellular matrix remodeling
  • Anti-inflammatory signaling pathways
  • Oxidative stress modulation
  • Stem cell activation environments

Mechanism of Action: Why GHK-cu Copper Tripeptide is Biologically Unique

GHK-cu Copper Tripeptide operates through multiple interconnected biological mechanisms rather than a single linear pathway. This pleiotropic activity is one of the reasons it has remained a major focus in regenerative science.

1. Gene Expression Modulation

One of the most well-documented properties of GHK-cu Copper Tripeptide is its ability to influence gene expression. Research indicates it may modulate hundreds of genes associated with tissue repair and regeneration, including:

  • Upregulation of collagen-related genes (COL1A1, COL3A1)
  • Increased expression of elastin and dermal matrix proteins
  • Activation of wound healing and repair signaling pathways
  • Modulation of growth factor-related gene networks

At the same time, GHK-cu Copper Tripeptide has been observed in experimental models to downregulate genes associated with inflammation and tissue degradation.


2. Collagen, Elastin & Extracellular Matrix Remodeling

The extracellular matrix (ECM) is the structural scaffold of the skin and connective tissue. With aging, ECM integrity declines due to reduced fibroblast activity and increased enzymatic breakdown (matrix metalloproteinases, or MMPs).

GHK-cu Copper Tripeptide is studied for its ability to:

  • Support fibroblast activity
  • Promote collagen synthesis and organization
  • Improve elastin fiber structure
  • Reduce excessive ECM degradation signaling
  • Enhance dermal structural density

This makes it a key molecule in research involving visible aging, skin firmness, and connective tissue integrity.


3. Copper-Dependent Enzymatic Support

Copper is an essential cofactor for several enzymes involved in tissue stability and antioxidant defense. GHK-cu Copper Tripeptide acts as a biologically safe transport system for copper ions, supporting:

  • Lysyl oxidase activity (collagen cross-linking enzyme)
  • Superoxide dismutase (SOD) antioxidant defense
  • Cellular respiration pathways
  • Connective tissue maturation processes

This copper-delivery mechanism is tightly regulated, allowing biological systems to utilize copper without triggering oxidative toxicity.


4. Anti-Inflammatory and Antioxidant Signaling

Chronic low-grade inflammation and oxidative stress are key contributors to visible and structural aging. GHK-cu Copper Tripeptide has been observed in research models to help regulate inflammatory mediators and oxidative stress markers.

Proposed mechanisms include:

  • Reduction of pro-inflammatory cytokine signaling
  • Modulation of oxidative stress response pathways
  • Support of cellular detoxification systems
  • Protection of dermal structural proteins from degradation

This positions GHK-cu Copper Tripeptide as both a regenerative and protective signaling molecule.


5. Angiogenesis and Tissue Oxygenation

Another important area of research involves GHK-cu Copper Tripeptide’s influence on angiogenesis — the formation of new microvasculature.

Experimental findings suggest potential involvement in:

  • Vascular endothelial growth signaling
  • Capillary network support
  • Tissue oxygenation improvement pathways
  • Nutrient delivery to regenerating tissue

These effects are particularly relevant in wound healing and tissue repair models.


Age-Related Decline of GHK-Cu

Scientific literature suggests that endogenous GHK-cu Copper Tripeptide levels decline significantly with age. This decline correlates with several observable biological changes:

  • Reduced skin elasticity
  • Slower wound healing response
  • Increased collagen fragmentation
  • Higher oxidative stress burden
  • Decreased dermal regeneration efficiency

Because of this, GHK-cu Copper Tripeptide is widely studied as a “youth-associated regulatory peptide” within regenerative biology research.


Cosmetic & Research Applications

GHK-Cu is extensively used in advanced cosmetic and experimental research contexts involving:

  • Skin rejuvenation systems
  • Fine line and wrinkle appearance studies
  • Dermal thickness and firmness research
  • Hair follicle stimulation models
  • Post-injury tissue recovery research
  • Anti-aging peptide formulations
  • Extracellular matrix repair systems
  • Oxidative stress reduction studies

Its broad biological footprint makes it one of the most multifunctional peptides in regenerative science.


Stability & Formulation Considerations

GHK-Cu is a water-soluble peptide complex that integrates effectively into aqueous systems such as serums, gels, and oral capsule formats.

However, its stability is influenced by:

  • pH conditions
  • Light exposure
  • Oxidation state of copper ions
  • Chelation balance
  • Storage temperature

Proper formulation is essential to maintain copper-peptide integrity and ensure biological activity in research settings.


Important Disclaimer

This product is supplied strictly for laboratory, analytical, and research purposes only. It is not intended to diagnose, treat, cure, or prevent any disease. Not approved for human consumption. GHK-Cu remains an investigational compound within scientific and cosmetic research environments, with most findings derived from preclinical and experimental studies.

GHK-Cu Research References Table

Category Study / Paper Focus Link
Core Review GHK-Cu Mechanisms & Applications (Peptide Breakdown Review) Collagen synthesis, wound healing, gene expression modulation https://peptidebreakdown.com/peptides/ghk-cu/
Comprehensive Database Review GHK-Cu Research Profile (Peptide Research Guide) Gene regulation, ECM remodeling, anti-inflammatory activity https://peptideresearchguide.org/ghk-cu/
Scientific Summary GHK-Cu Research Review (BioTech Pharma Literature Review) Tissue regeneration, aging biology, copper signaling https://biotechpharma.org/ghk-cu-research
Physicochemical Study Stability & formulation characteristics of GHK-Cu Stability, solubility, dermal delivery properties https://www.allofpeptides.com/peptides/ghk-cu/studies/1328
Clinical Evidence Summary Post-procedure & skin regeneration clinical review Skin density, wrinkle reduction, cosmetic outcomes https://www.peptidejournal.org/skincare/ghk-cu-post-procedure-recovery-clinical-evidence
Cosmetic Evidence Review Copper Peptides in Dermatology (Vogue summary of clinical data) Collagen production, skin elasticity, anti-aging outcomes https://www.vogue.com/article/copper-peptides
Research Aggregation Database GHK-Cu Evidence Overview (PeptideTrace) Human/animal/in-vitro study breakdown https://www.peptidetrace.com/compounds/ghk