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BiologicalX

Comparison

GHK-Cu vs Noopept

Side-by-side of GHK-Cu and Noopept. 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

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

Noopept

  • Russian dipeptide nootropic developed in the 1990s, registered in Russia 2002 for cognitive impairment
  • Roughly 1,000-fold higher per-mg potency than piracetam; therapeutic dose 10 to 30 mg/day
  • Active metabolite cycloprolylglycine modulates AMPA receptors and increases NGF and BDNF in rodent hippocampus
  • Russian RCTs in stroke recovery and vascular cognitive impairment show modest improvements over 4 to 8 weeks
  • Western evidence base is essentially absent; healthy-adult enhancement trials have not been published
  • Unscheduled in the US but not approved for human consumption; UK is prescription-only since 2014

Side-by-side

Attribute GHK-Cu Noopept
Category peptide nootropic
Also known as Copper Peptide, Glycyl-L-histidyl-L-lysine copper, GHK GVS-111, N-phenylacetyl-L-prolylglycine ethyl ester, Omberacetam
Half-life (hr) 0.5 0.7
Typical dose (mg) 2 20
Dosing frequency daily 2 to 3 times daily, last dose before mid-afternoon
Routes topical, subcutaneous oral, sublingual
Onset (hr) 24 0.5
Peak (hr) 168 1
Molecular weight 340.85 318.37
Molecular formula C14H24N6O4 (GHK alone); C14H22CuN6O4 with Cu(II) C17H22N2O4
Mechanism 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. Hydrolyzed to active metabolite cycloprolylglycine; AMPA receptor modulation, BDNF and NGF upregulation, antioxidant and antiexcitotoxic effects.
Legal status Topical cosmetics legal in most jurisdictions; injectable form not FDA approved for any indication; research-use-only grey market Approved in Russia and CIS states; prescription-only in UK; unscheduled and unapproved in US, EU varies
WADA status allowed unknown
DEA / Rx Topical OTC (cosmetic); injectable not FDA approved; research-chemical status Not scheduled in the US
Pregnancy Insufficient data; topical use likely low-risk; injectable not recommended Not recommended
CAS 49557-75-7 157115-85-0
PubChem CID 73587 183503
Wikidata Q3104638 Q4321022

Safety profile

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)

Noopept

Common side effects

  • headache
  • irritability
  • sleep disturbance with late-day dosing
  • occasional blood pressure elevation

Contraindications

  • pregnancy
  • lactation
  • pediatric use
  • severe hepatic impairment
  • severe renal impairment

Interactions

  • memantine and other glutamatergic agents: theoretical AMPA-pathway interaction(minor)
  • antidepressants: theoretical effect via BDNF axis, undocumented(minor)
  • antihypertensives: occasional blood pressure elevation may require monitoring(minor)

Which Should You Take?

Noopept comes out ahead for most readers on the criteria we weight: 3 catalogued goals, controlled substance, oral dosing, with a Tier-B outcome catalogued. GHK-Cu is the right call when one of the conditionals below applies.

  • If your priority is skin health, pick GHK-Cu.
  • If your priority is wound healing, pick GHK-Cu.
  • If your priority is focus or working memory, pick Noopept.
  • If your priority is memory, pick Noopept.

Edge case: If you cannot self-administer injections, Noopept is the only oral option in this pair.

Default choice: Noopept. Wider use case, 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 GHK-Cu and Noopept?

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

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

GHK-Cu half-life is 0.5 hours; Noopept half-life is 0.7 hours.

Can you stack GHK-Cu with Noopept?

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

Go deeper