Select Strength — 50mg
For in vitro laboratory research use only. Not for human consumption, diagnostic, or therapeutic use.
Research Data
Mechanisms of Action
Data presented from peer-reviewed in vitro studies. All findings are laboratory observations only.
In vitro fibroblast cultures treated with GHK-Cu demonstrate significantly elevated collagen I and III production, glycosaminoglycan synthesis, and extracellular matrix remodelling activity.
GHK-Cu activates multiple wound-healing pathways simultaneously — promoting angiogenesis, reducing inflammation, and accelerating keratinocyte migration in in vitro models.
In vitro and ex vivo models show GHK-Cu enlarges follicle size and stimulates proliferative activity of dermal papilla cells, key drivers of hair growth cycling.
In vitro fibroblast cultures treated with GHK-Cu (1 µM) demonstrated significantly elevated collagen production compared to Vitamin C and untreated controls.
Analytical Data
| Specification | Value |
|---|---|
| CAS Number | 89030-95-5 |
| Molecular Formula | C₁₄H₂₃CuN₆O₄ |
| Molecular Weight | 403.91 g/mol |
| Purity (HPLC) | 99.1% |
| Appearance | Light blue lyophilised powder |
| Solubility | Soluble in water (1 mg/mL) |
| Storage | −20°C long-term / 2–8°C short-term |
| Shelf Life | 24 months from production date |
| Research Grade | Yes — For In Vitro Use Only |
What Research Has Shown
In Vitro Fibroblast Study — Accredited Laboratory
Collagen Volume Increase vs. Untreated Control
Comparative Activity Profile
In Vitro Safety Data
GHK-Cu demonstrates an excellent safety profile across in vitro and ex vivo models. No cytotoxicity observed at standard research concentrations (0.1–10 µM).
Observed Adverse Indicators
Cytotoxicity at 1 µM
NoneCell membrane disruption
MinimalOxidative stress markers
MinimalMetabolic inhibition
None⚠️ Theoretical Concern
Copper toxicity is theoretically possible at excessive concentrations but has not been observed at standard research doses (0.1–10 µM) in published literature.
Researcher Reference
GHK-Cu is a naturally occurring tripeptide (Gly-His-Lys) that chelates copper(II). First isolated from human plasma in 1973 by Loren Pickart. Plasma levels decline from ~200 ng/mL at age 20 to ~80 ng/mL at age 60, correlating with reduced tissue regenerative capacity.
Peer-reviewed studies show GHK-Cu modulates expression of 31.2% of human genes (4,000+ genes), stimulates collagen I and III synthesis by up to 70% vs. controls, accelerates fibroblast migration 3.2×, and upregulates antioxidant enzymes including superoxide dismutase and catalase.
Standard in vitro research uses concentrations between 0.1–10 µM. The most commonly cited effective concentration is 1 µM. Stock solutions are typically prepared in sterile water or DMSO (≤0.1%) and diluted into culture media immediately prior to use.
Cell viability remains above 95% as measured by MTT assay at concentrations up to 10 µM. No cytotoxic, genotoxic, or mutagenic effects observed in published in vitro literature.
Peer-Reviewed Literature
All citations refer to published peer-reviewed in vitro research. Data presented for scientific reference only. No claims made regarding human therapeutic use.
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