Skip to content
BiologicalX

Comparison

Noopept vs Sermorelin

Side-by-side of Noopept and Sermorelin. 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

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

Sermorelin

  • Synthetic 29-amino-acid GHRH fragment; FDA approved 1997 for pediatric GH deficiency as Geref
  • Voluntarily discontinued by Serono in 2008 for commercial reasons; not safety-related
  • Compounded by 503A/503B pharmacies for off-label adult anti-aging and body-composition use
  • Produces physiologic pulsatile GH release; ~10 to 20 minute plasma half-life
  • Standard anti-aging clinic protocol: 200 to 500 mcg subcutaneously pre-bed, often with ipamorelin
  • Banned by WADA under S2 (peptide hormones, growth factors)

Side-by-side

Attribute Noopept Sermorelin
Category nootropic peptide
Also known as GVS-111, N-phenylacetyl-L-prolylglycine ethyl ester, Omberacetam Sermorelin acetate, GRF 1-29, Geref, GHRH (1-29) NH2
Half-life (hr) 0.7 0.25
Typical dose (mg) 20 0.3
Dosing frequency 2 to 3 times daily, last dose before mid-afternoon 1-2x daily
Routes oral, sublingual subcutaneous
Onset (hr) 0.5 0.25
Peak (hr) 1 0.5
Molecular weight 318.37 3357.88
Molecular formula C17H22N2O4 C149H246N44O42S
Mechanism Hydrolyzed to active metabolite cycloprolylglycine; AMPA receptor modulation, BDNF and NGF upregulation, antioxidant and antiexcitotoxic effects. Synthetic 29-amino-acid GHRH fragment that binds the GHRH receptor on pituitary somatotrophs to stimulate endogenous pulsatile GH synthesis and release while preserving the GH-IGF-1 negative feedback loop.
Legal status Approved in Russia and CIS states; prescription-only in UK; unscheduled and unapproved in US, EU varies FDA approved 1997 (Geref, pediatric GHD); voluntarily discontinued by Serono 2008; compounded by 503A/503B pharmacies for off-label adult use; banned by WADA
WADA status unknown banned
DEA / Rx Not scheduled in the US Rx only via compounding (no controlled-substance schedule)
Pregnancy Not recommended Category C (historical labeling); not recommended in pregnancy
CAS 157115-85-0 86168-78-7
PubChem CID 183503 16129617
Wikidata Q4321022 Q416620

Safety profile

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)

Sermorelin

Common side effects

  • injection-site pain or irritation
  • transient flushing
  • headache
  • vivid dreams (pre-bed dosing)

Contraindications

  • pregnancy
  • active malignancy
  • history of pituitary tumor
  • diabetic retinopathy (theoretical)
  • untreated hypothyroidism

Interactions

  • ipamorelin: synergistic GH release via parallel GHRH and ghrelin pathways; standard anti-aging clinic pairing(minor)
  • CJC-1295: pharmacologically redundant (both GHRH-pathway); typically not stacked(minor)
  • insulin: sustained GH can blunt insulin sensitivity over weeks(moderate)
  • corticosteroids: blunt GH response; reduce expected efficacy(moderate)
  • levothyroxine (untreated hypothyroidism): untreated hypothyroidism blunts GH response; correct thyroid first(moderate)

Which Should You Take?

Sermorelin comes out ahead for most readers on the criteria we weight: 3 catalogued goals, FDA approved 1997 (Geref, pediatric GHD); voluntarily discontinued by Serono 2008; compounded by 503A/503B pharmacies for off-label adult use; banned by WADA, with a Tier-A outcome catalogued. Noopept is the right call when one of the conditionals below applies.

  • If your priority is focus or working memory, pick Noopept.
  • If your priority is memory, pick Noopept.
  • If your priority is growth-hormone axis, pick Sermorelin.
  • If your priority is healthspan extension, pick Sermorelin.

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

Default choice: Sermorelin. Wider use case, a Tier-A evidence outcome catalogued, and broader goal coverage. Reach for Noopept 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 Noopept and Sermorelin?

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

Which has a longer half-life, Noopept or Sermorelin?

Noopept half-life is 0.7 hours; Sermorelin half-life is 0.25 hours.

Can you stack Noopept with Sermorelin?

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

Go deeper