SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesCognitiveSemax

Semax

/ Synthetic heptapeptide Met-Glu-His-Phe-Pro-Gly-Pro (stabilized ACTH(4-10) fragment analog)
TIER 3 · PreclinicalN = 0 · TESTING PENDINGLAST REVIEW 2026·04·20
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Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

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§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Synthetic heptapeptide Met-Glu-His-Phe-Pro-Gly-Pro (stabilized ACTH(4-10) fragment analog)CATEGORY · Cognitive

Registered clinically in Russia for ischemic stroke, TIA, and cognitive disorders. No Western RCTs. Russian-origin literature dominates and has not been independently replicated.

§ B · Mechanism of action

Semax is a synthetic heptapeptide (Met-Glu-His-Phe-Pro-Gly-Pro) — a fragment analog of ACTH(4-10) with a C-terminal Pro-Gly-Pro extension for enzymatic stability. Proposed mechanisms include upregulation of BDNF and NGF expression in the hippocampus, modulation of the melanocortin system (MC3/MC4), inhibition of enkephalin-degrading enzymes, and anti-inflammatory effects. Mechanism work is largely from Russian institutes (Institute of Molecular Genetics, Moscow).

§ C · Human clinical evidence

Limited and largely Russian. Semax is registered in Russia for ischemic stroke, transient ischemic attack, and cognitive disorders. Multiple Russian clinical publications exist but are poorly indexed and rarely translated in full. No Western RCTs. No ClinicalTrials.gov entries from Western centers.

§ D · Primary literature
PubMed16805787Dolotov OV et al.Semax, an analog of adrenocorticotropin (4-10), binds specifically and increases levels of brain-derived neurotrophic factor protein in rat basal forebrain · Journal of Neurochemistry · rodentSemax increased BDNF protein levels in rat basal forebrain and bound specific brain sites.Limitations: Rodent only; BDNF-mediated clinical efficacy in humans not established by this work.2006
§ F · Safety signal

Russian reports describe favorable tolerability with no significant adverse events. Independent safety data from Western populations are not available.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

Strong reliance on Russian-language literature that is difficult to critically appraise from English-language abstracts alone. Neurotrophic-factor upregulation claims are largely preclinical. Independent Western replication of stroke findings is absent. Sold in the US as "research chemical" only.