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GHK-Cu – 100mg

$70.00

GHK-Cu is the copper(II) complex of glycyl-L-histidyl-L-lysine. It is widely used in vitro to study copper transport, redox balance, extracellular matrix regulation, and gene expression signatures related to tissue remodeling and cellular stress responses.

329 in stock

SKU: NUV-GHKCU-100MG Category: Tags: , , Product ID: 6231

Description

Research Overview

GHK is an endogenous tripeptide that forms a stable high-affinity complex with Cu(II), yielding GHK-Cu, a well-characterized ligand-metal pair.[1,2] In research settings, GHK-Cu serves as a model for copper delivery and signaling, enabling investigation of matrix protein synthesis, metalloproteinase regulation, antioxidant responses, and transcriptional reprogramming under standardized conditions.[3,4] Its versatility has made it a reference tool in dermatologic, regenerative, and oxidative stress research.

Molecular Structure & Copper Coordination

GHK (C₁₄H₂₄N₆O₄) coordinates Cu(II) through the histidine imidazole, terminal amine, and amide nitrogens to form a compact complex with defined geometry.[1] This allows precise analysis of binding constants, redox cycling, and competition with other copper ligands in biochemical systems.

Extracellular Matrix & Dermal Research

In skin- and fibroblast-derived models, GHK-Cu is used to assess effects on collagen, elastin, proteoglycans, and matrix metalloproteinases, as well as integrin and TGF-β associated pathways.[3] These experiments map gene and protein expression patterns associated with matrix maintenance and controlled remodeling.

Oxidative Stress & Gene Expression Studies

Studies utilizing GHK-Cu report modulation of antioxidant defenses, DNA repair-related transcripts, and cell viability under toxic or oxidative challenge.[4] These data are interpreted as mechanistic evidence for copper-peptide–dependent signaling, not as clinical outcomes.

Referenced Citations

  1. PubChem: Glycyl-L-histidyl-L-lysine
  2. PubChem: GHK-Cu
  3. J Biomater Sci Polym Ed. 2008; Pickart L et al. PubMed
  4. Int J Mol Sci. 2018; Pickart L et al. PubMed

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