Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Cognitive
Also known as: ACTH(4-7) analogue
A peptide discussed for cognitive and neuroprotective effects. Approved in some jurisdictions but not others.
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Semax is a synthetic peptide derived from an ACTH fragment, studied for nootropic and neuroprotective effects.
Some human studies exist in the countries where it is used clinically; broader independent replication is limited.
Where used clinically it is intranasal and prescribed; research-market use is unverified.
Approved/used as a medicine in some countries (e.g. Russia); not approved in the EU/US.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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Semax is a synthetic peptide derived from an ACTH fragment, studied for nootropic and neuroprotective effects.
Semax is a synthetic peptide derived from a fragment of adrenocorticotropic hormone (ACTH), specifically the ACTH(4-7) sequence modified to improve stability. It is most often discussed as a nootropic and neuroprotective compound, and it occupies an unusual position in the peptide landscape: it is approved and prescribed as a medicine in a small number of countries, most notably Russia, while remaining unapproved in the European Union and the United States. On peptides.cx it is categorized as a cognitive peptide, and the honest evidence picture is best described as regionally established but not yet broadly validated outside its areas of clinical use.
Semax is researched primarily for its proposed effects on attention, learning, mood, and the protection of neural tissue under stress or ischemic conditions. The mechanisms most frequently cited in the literature include modulation of brain-derived neurotrophic factor (BDNF) and related neurotrophic signalling, alongside broader neuroprotective pathways. It is important to distinguish the strength of the evidence behind these ideas. Much of the neuroprotective and cognitive-enhancement data comes from preclinical animal studies, while human data exists mainly within the countries where Semax is used clinically as an intranasal formulation. Independent replication of those human findings in large Western trials remains limited, which is why Semax carries a mid-tier evidence grade rather than a strong one.
Anyone researching Semax should treat it as an educational and scientific subject rather than a validated over-the-counter supplement. Where it is used clinically, it is a prescribed, intranasally administered medicine; material sold on the research-chemical market is not quality-controlled, and its purity and identity are unverified. It is frequently compared and discussed alongside Selank, a related peptide studied for anxiolytic rather than cognitive effects. This page summarizes what Semax is, why it is studied, and what the current evidence does and does not support, without offering medical advice, dosing guidance, or purchasing recommendations.
Evidence grade: C
Some human studies exist in the countries where it is used clinically; broader independent replication is limited. Preclinical work reports neuroprotective and cognitive effects.
Some human studies exist in the countries where it is used clinically; broader independent replication is limited.
Preclinical work reports neuroprotective and cognitive effects.
Where used clinically it is intranasal and prescribed; research-market use is unverified.
Approved/used as a medicine in some countries (e.g. Russia); not approved in the EU/US.
1980s
Semax is developed in Russia at the Institute of Molecular Genetics and Moscow State University as a synthetic analogue of the ACTH(4-10) fragment, designed to keep behavioural/neurotropic activity while removing the hormone's classic corticotropic effects.
1990s
Preclinical work in Russia describes neuroprotective and cognition-related effects and reports that the peptide is resistant to rapid breakdown, and it moves toward domestic clinical use as an intranasal formulation.
Late 1990s to 2000s
Semax is registered and used as a medicine within Russia for indications discussed in the local literature (such as stroke recovery and cognitive complaints); it does not gain approval in the EU or US.
2000s to 2010s
Mechanistic studies, largely from the originating research groups, explore proposed effects on BDNF and other neurotrophic signalling, though broad independent replication outside these groups remains limited.
Early 2020s
Semax and its N-acetyl variant become widely discussed in international nootropic communities and sold on the research-chemical market, well outside any clinical approval and without verified purity.