Skip to content
BiologicalX

Comparison

DHEA vs GHK-Cu

Side-by-side of DHEA and GHK-Cu. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

DHEA

  • Adrenal androgen precursor; serum DHEA-S declines progressively after the third decade of life
  • OTC dietary supplement in US under DSHEA 1994; prescription in EU, UK, Canada, Australia
  • FDA approved as Intrarosa (6.5 mg vaginal insert) for postmenopausal dyspareunia in 2016
  • Acts as tissue-specific prohormone converted intracrinologically to testosterone and estrogens
  • Best evidence: adrenal insufficiency replacement and vaginal atrophy; weaker on cognition and longevity
  • WADA banned in competitive sport; banned in NCAA, MLB, NFL, IOC settings

GHK-Cu

  • Endogenous tripeptide that binds copper(II); plasma levels decline ~60% from age 20 to 60
  • Topical RCTs show improvement in skin firmness, fine lines, and barrier function over 12 weeks
  • Wound-healing models report accelerated re-epithelialization in diabetic and aged skin
  • Pickart gene-expression analyses show reset of >4000 genes toward a younger expression profile in cell culture
  • Anecdotal subcutaneous longevity protocols use 1 to 3 mg daily; no human longevity RCTs exist
  • Hair-growth claims rest on small open-label trials and topical scalp formulations

Side-by-side

Attribute DHEA GHK-Cu
Category hormone peptide
Also known as dehydroepiandrosterone, prasterone, Intrarosa Copper Peptide, Glycyl-L-histidyl-L-lysine copper, GHK
Half-life (hr) 12 0.5
Typical dose (mg) 25 2
Dosing frequency daily, typically morning daily
Routes oral, vaginal, topical topical, subcutaneous
Onset (hr) 1 24
Peak (hr) 1 168
Molecular weight 288.42 340.85
Molecular formula C19H28O2 C14H24N6O4 (GHK alone); C14H22CuN6O4 with Cu(II)
Mechanism Steroid prohormone converted intracrinologically to testosterone and estrogens in target tissues; also exerts direct effects via sigma-1 receptor, GABA-A modulation, and glucocorticoid receptor interaction. Tripeptide that chelates Cu(II) and delivers it to copper-dependent enzymes (lysyl oxidase, superoxide dismutase). Modulates expression of >4000 genes toward a younger profile in fibroblast culture, including upregulation of decorin and downregulation of pro-inflammatory cytokines.
Legal status OTC supplement in US (DSHEA 1994); prescription in EU, UK, Canada, Australia Topical cosmetics legal in most jurisdictions; injectable form not FDA approved for any indication; research-use-only grey market
WADA status banned allowed
DEA / Rx OTC supplement in US (not scheduled); Rx in EU, UK, Canada, Australia Topical OTC (cosmetic); injectable not FDA approved; research-chemical status
Pregnancy Contraindicated in pregnancy Insufficient data; topical use likely low-risk; injectable not recommended
CAS 53-43-0 49557-75-7
PubChem CID 5881 73587
Wikidata Q411733 Q3104638

Safety profile

DHEA

Common side effects

  • acne
  • oily skin
  • hirsutism (women)
  • gynecomastia (men, higher doses)
  • irritability
  • insomnia

Contraindications

  • hormone-sensitive cancer (breast, ovarian, prostate)
  • active liver disease
  • uncontrolled lipid disorder
  • pregnancy and lactation

Interactions

  • warfarin: case reports of altered INR; monitor(moderate)
  • estrogens (HRT): additive estrogenic effect via conversion; monitor(moderate)
  • insulin: may improve insulin sensitivity slightly; monitor glucose(minor)
  • anastrozole: may reduce DHEA-derived estrogen; clinical relevance unclear(minor)

GHK-Cu

Common side effects

  • mild erythema at topical site
  • transient itch
  • blue-green discoloration of injection site (copper)
  • rare contact dermatitis

Contraindications

  • copper allergy
  • Wilson disease
  • open wound near injection site (caution)
  • pregnancy (no data)

Interactions

  • topical retinoids: additive irritation; alternate days or apply at different times(minor)
  • topical vitamin C (ascorbic acid): ascorbate reduces Cu(II) to Cu(I), which can destabilize the GHK-Cu complex; separate by 30 minutes(minor)

Which Should You Take?

DHEA comes out ahead for most readers on the criteria we weight: 2 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-A outcome catalogued. GHK-Cu is the right call when one of the conditionals below applies.

  • If your priority is hormonal optimization, pick DHEA.
  • If your priority is skin health, pick GHK-Cu.
  • If your priority is wound healing, pick GHK-Cu.

Edge case: If you want to avoid research-only / gray-market sourcing, DHEA is the more accessible choice.

Default choice: DHEA. Lower friction to source, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for GHK-Cu only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between DHEA and GHK-Cu?

DHEA and GHK-Cu differ in category (hormone vs peptide), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, DHEA or GHK-Cu?

DHEA half-life is 12 hours; GHK-Cu half-life is 0.5 hours.

Can you stack DHEA with GHK-Cu?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

Go deeper