Peptide Registry

CUPRA (AHK-Cu/GHK-Cu)

$51.00

  • Contents: CUPRA (AHK-Cu 30% / GHK-Cu 70% copper peptide blend)
  • Form: Lyophilized powder
  • Purity: >99%
Quantity Discount Price
1 - 3 - $51.00
4 - 7 10% $45.90
8 + 18% $41.82
SKU: N/A Category: Brand:

Description

CUPRA is a defined research blend combining two structurally related copper-binding tripeptides: AHK-Cu (Ala-His-Lys copper complex) at 30% and GHK-Cu (Gly-His-Lys copper complex) at 70%. The two compounds share the His-Lys C-terminal dipeptide and a copper coordination mechanism, but differ at the N-terminal residue. GHK-Cu uses glycine; AHK-Cu substitutes alanine. This single amino acid difference produces distinct receptor interaction profiles and tissue research applications. GHK-Cu has an extensive published research base covering extracellular matrix remodeling, collagen synthesis regulation, and TIMP-mediated MMP inhibition. AHK-Cu has a more focused research profile centered on perifollicular vascular biology and VEGF-mediated signaling in dermal papilla cell models. The blend addresses both mechanistic dimensions simultaneously, making it a tool for specialty research peptide studies where copper peptide vascular and ECM signaling are studied in the same experimental model.

Chemical Information

AHK-Cu Component (30%):

  • Chemical Name: Ala-His-Lys copper complex
  • Sequence: Ala-His-Lys
  • Molecular Weight: ~415 Da (copper complex)

GHK-Cu Component (70%):

  • Chemical Name: Gly-His-Lys copper complex (Copper Tripeptide-1)
  • Sequence: Gly-His-Lys
  • Molecular Formula: C14H24N6O4Cu
  • Molecular Weight: 401.9 g/mol
  • Appearance: Blue powder (characteristic of copper coordination)

Blend:

  • Ratio: AHK-Cu 30% / GHK-Cu 70%
  • Production: Solid-phase peptide synthesis (SPPS); copper coordination post-synthesis

Applications

  • Comparative copper peptide signaling research. AHK-Cu and GHK-Cu engage overlapping but distinct signaling profiles; the blend enables simultaneous study of both in a single experimental condition, while single-compound controls isolate each compound’s individual contribution
  • Extracellular matrix biology. GHK-Cu component drives collagen synthesis regulation, decorin upregulation, and TIMP-1/TIMP-2 induction, which inhibit MMP-mediated ECM degradation; relevant in wound biology and connective tissue remodeling research models
  • Perifollicular vascular signaling. AHK-Cu component is studied for VEGF production stimulation and perifollicular microvascular density in dermal papilla cell models; at picomolar to nanomolar concentrations, AHK-Cu has demonstrated dermal papilla cell proliferation effects in ex vivo hair follicle models
  • TGF-beta1 pathway research. Both components have been associated with TGF-beta1 modulation in dermal fibroblast models; TGF-beta1 suppression is studied in the context of fibrosis regulation and follicular biology
  • Copper transport and coordination chemistry. Both peptides coordinate Cu2+ through the His imidazole nitrogen; researchers studying copper transport mechanisms and peptide-metal coordination use these compounds as defined model systems
  • Dose-response characterization. AHK-Cu exhibits biphasic dose-response behavior in ex vivo models, with stimulatory effects at picomolar to nanomolar concentrations and inhibitory effects at higher concentrations; researchers designing protocols with this blend need to account for this concentration sensitivity

Storage and Handling

Store as lyophilized powder at -20C for long-term stability, or at 2-8C for short-term use. Protect from light; copper peptide complexes are light-sensitive. The characteristic blue color of the lyophilized powder confirms copper coordination and does not indicate contamination. Reconstitute in sterile water or bacteriostatic water immediately before use. Avoid repeated freeze-thaw cycles and prolonged exposure to high pH conditions, which can disrupt copper coordination.

Compliance Notice

CUPRA is for laboratory research use only. It is not for human or veterinary use and carries no therapeutic, diagnostic, or clinical indication. This product has not been evaluated by the FDA. By purchasing this product, the buyer confirms that they will follow appropriate institutional safety procedures and use it exclusively for controlled research.

Frequently Asked Questions

What is CUPRA and why combine AHK-Cu with GHK-Cu?

CUPRA is a copper peptide research blend combining AHK-Cu (30%) and GHK-Cu (70%). The two compounds are structurally related but mechanistically distinct: GHK-Cu is studied for extracellular matrix remodeling and collagen regulation through TIMP/MMP pathway modulation, while AHK-Cu is studied for perifollicular vascular signaling through VEGF stimulation and dermal papilla cell biology. The blend enables researchers to study both mechanistic dimensions in the same experimental model rather than designing separate single-compound protocols for each pathway.

How does AHK-Cu differ from GHK-Cu structurally and mechanistically?

Both are copper-binding tripeptides sharing the His-Lys C-terminal dipeptide and the same Cu2+ coordination mechanism through the histidine imidazole nitrogen. The structural difference is a single N-terminal amino acid substitution: glycine in GHK-Cu versus alanine in AHK-Cu. This substitution shifts the compound's research profile from GHK-Cu's broad ECM and collagen biology toward AHK-Cu's more specific perifollicular vascular and VEGF signaling focus. GHK-Cu has a significantly larger published research base; AHK-Cu research is more recent and more narrowly focused.

Why is the 30/70 ratio significant in the CUPRA blend?

The 70% GHK-Cu weighting reflects the more extensive research base and broader mechanistic profile of GHK-Cu relative to AHK-Cu. Researchers using this blend should account for the asymmetric concentration when interpreting results: observed effects attributable to ECM signaling pathways are more likely driven by the GHK-Cu component, while effects on perifollicular vascular markers are more likely attributable to AHK-Cu. Single-compound control arms using each peptide independently are recommended for mechanistic attribution in research designs using this blend.