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For research purposes onlyThese compounds aren't FDA approved. All data presented is from clinical trials for educational reference.

Semax

4.9 (84)

Cognitive & Neuroprotective Peptide

Dosage

Quantity

1

Price

$26.99

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Made in the USA

Certificate of Analysis

Batch verified lab data

Latest

99.93%

Purity

Variant
Semax 10mg
Lot #
A0112
Labeled
20mg
Actual
22.56mg
Tested
Feb 4, 2026

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Research Purposes Snapshot

Semax is a synthetic heptapeptide (ACTH4–7 analog extended with Pro-Gly-Pro) developed in Russia with decades of intranasal clinical use for neurologic indications. Summaries below are educational—this listing is not an FDA-approved drug claim in the United States.

~1.4×

BDNF increase

Hippocampal BDNF protein elevations reported after intranasal exposure in rodent pharmacology.

~3×

Gene expression

Exon III BDNF mRNA upregulation after single-dose protocols in published IMG work.

24h+

Duration cue

Pro-Gly-Pro tail extends plasma stability versus shorter ACTH fragments in PK discussions.

~1.6×

TrkB activation

Increased TrkB phosphorylation readouts alongside BDNF axis engagement in model systems.

7 aa

Heptapeptide

Sequence Met-Glu-His-Phe-Pro-Gly-Pro (MEHFPGP).

Development status

Regulatory information

Developed at the Institute of Molecular Genetics, Russian Academy of Sciences. Marketed as prescription nasal sprays in Russia for selected neurologic indications—not cleared by FDA for any use in the US.

Developer
Russian Academy of Sciences (IMG)
Approval
Russia (1990s onward)
Indications (national labels)
Stroke recovery, cognitive impairment (context-dependent)
Formulations
0.1% and 1% intranasal spray
US status
Not FDA-approved
Related peptide
Selank (separate tuftsin-family analog)
Wikipedia overview (verify against primaries)

What research has shown

Russian preclinical/clinical literature and review summaries

Molecular readouts (rodent models)

~3× BDNF mRNA after single dose

BDNF / TrkB axis (bars scaled to max ~300% for comparison)

BDNF mRNA (exon III)~300%
TrkB mRNA~200%
BDNF protein~140%
TrkB phosphorylation~160%

Intranasal Semax (~50 mcg/kg in cited rat work) at IMG was associated with rapid neurotrophin expression changes and improved conditioned avoidance performance—species- and dose-specific.

Trace statistics to Russian primary pharmacology papers.

Research outcomes

Key findings from studies

Treated animals — BDNF axis response (narrative)100%
Conditioned avoidance / learning improvement (models)100%
Extended duration vs short ACTH fragments (PK narrative)25%
Clinical use (Russia): 0.1% and 1% nasal products are prescribed for stroke, traumatic brain injury, and cognitive impairment in national practice; rehabilitation cohorts sometimes show higher plasma BDNF—outcomes are indication- and protocol-specific.

Beyond cognitive enhancement

Multi-system motifs in reviews

BDNF

Neuroprotection

Plasticity and repair signaling in hippocampal circuits.

Stroke

Neuroprotection

Licensed clinical niche in Russia; motor recovery narratives.

VEGF

Vascular support

Angiogenesis-associated gene programs after CNS injury models.

No ACTH

Safety profile

ACTH analog without systemic corticotropic activity in standard doses.

Cognitive enhancement

Nootropic effects

Learning, memory, and attention improvements are attributed to BDNF–TrkB engagement in hippocampal summaries.

  • Memory↑ enhanced
  • Learning↑ improved
  • Attention↑ sharpened
  • Focus↑ sustained

Conditioned avoidance improvements are a recurring behavioral endpoint in rodent Semax papers.

Neuroprotection

Stroke recovery support

Russian clinical experience emphasizes motor and functional gains during early rehabilitation—figures below are illustrative review scales, not universal effect sizes.

BDNF increase (review scale)100%
Motor recovery (review scale)85%
Functional recovery (review scale)80%

Vascular health

Angiogenesis support

Gene-expression reviews cite VEGF-family upregulation and improved perfusion metrics after experimental brain injury.

  • VEGF genes↑ upregulated
  • Angiogenesis↑ promoted
  • Blood flow↑ improved
  • Neurovascular unit✓ supported

Stress response

Adaptive regulation

As an ACTH4–7-derived peptide, Semax is discussed in melanocortin / stress-adaptation frameworks without the adrenal steroid surge associated with full ACTH.

MC — melanocortin pathway modulation

Key advantage: retains cognitive and neurotrophic narratives linked to ACTH fragments while lacking systemic hormonal activity at therapeutic exposures in summarized data.

Safety profile from research

Russian clinical experience since the 1990s (summaries)

Reviews describe favorable tolerability with mostly mild, route-related complaints. Unlike ACTH, Semax does not meaningfully stimulate cortisol release or disrupt HPA homeostasis in cited dose ranges.

Frequently reported mild events

10%

Nasal irritation

Mild
8%

Mild headache

Mild
5%

Dizziness

Mild
3%

Taste disturbance

Mild
Safety advantage

No hormonal ACTH effects

Comparative safety text contrasts Semax with systemic ACTH on adrenal stimulation and steroid-related adverse profiles.

  • No cortisol excursions in standard summarized doses
  • No adrenal cortex stimulation narrative like injectable ACTH
  • No HPA-axis suppression / rebound patterns attributed to Semax monotherapy
  • No steroid-type adverse-effect bundle in registry reviews
Tolerability in clinical use

Formulation experience

  • 0.1% nasal solutionWell tolerated
  • 1% nasal solutionGood tolerability
  • Long-term exposureNo major red flags in reviews
  • No dependence pattern described in Russian clinical summaries.
  • No withdrawal syndrome on cessation in those narratives.
  • Hydrolysis to natural amino acids often cited for metabolic safety.
Research considerations

Planning flags

Limited Western RCT corpus vs Russian dataPregnancy / lactation not characterizedSeizure history — use caution (theoretical excitability)Psychotropic interactions under-mapped
Regulatory snapshot
  • Approved in Russia since the 1990s for stroke and cognitive impairment per national labeling.
  • 0.1% and 1% nasal sprays are Rx products where legally marketed—not equivalent to research-grade vials.
  • Not FDA-approved; most Western jurisdictions treat non-registered material as unapproved for human therapy.

Storage handling reference

Peptide handling

Cold

Lyophilized: store per COA / SOP.

Reconstitution

Sterile technique if non-intranasal prep.

Light

Protect during aliquoting.

Documentation

Log batch, route, and concentration.

Researcher notes

  • Decades of Russian post-market exposure informs tolerability, yet Western regulatory files remain thin.
  • Absence of ACTH-like hormonal effects is a recurring differentiator in safety reviews.
  • Most AEs are mild, local (nasal), and transient.
  • Stroke-rehab populations dominate clinical narratives—do not generalize to healthy volunteer data.

Important Research Notice

Not for human consumption. This product and all products are sold exclusively for research and educational purposes. It is not intended to diagnose, treat, cure, or prevent any disease.

All clinical trial data and research findings presented on this page are sourced from journals and official publications but should be fact checked. They are provided for educational reference only and should not be interpreted as medical advice or product claims.

By purchasing this product, you confirm that you are a qualified researcher and will use it in accordance with all applicable laws and regulations and you do not intend to use it for human consumption.