Semax is a performance-enhancing peptide studied for its effects on cognition, neuroprotection, mood. Semax is a synthetic ACTH(4-10) analogue used in Russia as a nootropic and neuroprotective medicine; it holds no FDA or EMA approval.
Semax, an abbreviation of "seven amino acids", is a medication which is used in Eastern Europe for the treatment of a broad range of conditions like brain trauma but predominantly for its claimed nootropic, neuroprotective, and neurorestorative effects. It is a synthetic analogue of the ACTH(4-10) fragment of adrenocorticotropic hormone, extended with a C-terminal Pro-Gly-Pro tail that slows enzymatic degradation, and it is reported to raise brain-derived neurotrophic factor (BDNF) without the corticosteroid-releasing activity of full-length ACTH. It is registered as a medicine in Russia but holds no FDA or EMA approval.
Overview
Semax is not named individually on the World Anti-Doping Agency (WADA) Prohibited List, but is treated here as prohibited under section S2.2.2, which covers corticotrophins and their releasing factors together with substances of similar chemical structure; Semax shares the ACTH sequence even though it lacks the corticotropic activity of the full hormone.
Mechanism of action
Synthetic ACTH(4-10) analogue used in Russia as a nootropic and neuroprotectant. Reported to raise BDNF without corticosteroid effects. Evidence is mostly preclinical; no FDA or EMA approval.
Reported effects
Effects reported in the literature and from preclinical models include:
- Semax is described as a neuroactive peptide that enhances brain-derived neurotrophic factor signaling in pathways central to neuroplasticity. [2] Preclinical
- Semax is grouped among peptide interventions aimed at neuroprotection in age-related decline. [1] Preclinical
- Evidence for Semax remains preclinical and clinically limited, with no long-term safety data and no established optimal dosing regimen. [1][2] Preclinical
Evidence grades: FDA approvedApproved (non-US)Phase IIIPhase IIPhase IPreclinicalAnecdotal
Dosage and administration
No FDA
- or EMA-approved dose; Russian clinical protocols are the only formal dosing reference
General
- Nootropic use commonly cited at 200-600mcg daily intranasally, using a 0.1% solution
- Typically split across both nostrils and cycled rather than taken continuously
Higher
- strength 1% solution is used in Russian stroke and brain-injury protocols under medical supervision
Doses outside the Russian indications are self
- reported and not established by controlled trials
Natty status
Semax is classified as not natty. It appears on the WADA prohibited list and is banned by major natural bodybuilding federations.[3] Use of this compound places the athlete in the enhanced category rather than the natural category in competitive contexts.
Research
The peptide has been the subject of 3 studies and reference works collected on this site. Additional bibliography is in § External links below.
Related compounds
Other peptides in this catalogue with overlapping mechanisms or status:
References
- a b Therapeutic peptides in gerontology: mechanisms and applications for healthy aging. Recent review
- a b Therapeutic Peptides in Orthopaedics: Applications, Challenges, and Future Directions. Recent review
- a b World Anti-Doping Agency. (2026). Prohibited List 2026.
External links
- Wikipedia article
- 10mg Semax — commercial
- Semax + Spray Kit — commercial
This page was last updated on August 4, 2026, at 00:42 (UTC).
Research last reviewed on August 4, 2026.
Text is available under the Creative Commons Attribution-ShareAlike License; additional terms may apply.