
Semax
Sharper focus and brain protection, built from a stress hormone with the stress removed.
- Evidence
- BHuman trials what's this?
Grade B. Russian clinical data and approval, strongest in stroke; no Western replication. - Also known as
- Met-Glu-His-Phe-Pro-Gly-Pro · ACTH(4–10) analogue
- Class
- Synthetic heptapeptide; BDNF inducer. Approved prescription drug in Russia.
What it is
Semax was developed at the same Russian institute as Selank, and the two share a stabilising Pro-Gly-Pro tail and a nasal-spray route. It has been a Russian prescription drug since the 1990s and is on the country’s essential-medicines list for stroke and cognitive disorders. That gives it real clinical history, but almost all of it is published in Russian and hasn’t been replicated in large Western trials.
How it works
Semax clears from the blood in minutes, but the BDNF effect lasts for hours to days.
What the research shows
In people: Russian trials in acute ischaemic stroke found nasal Semax gave measurable neuroprotection and better cognitive and motor recovery than standard care1. Smaller human and imaging studies cover cognitive impairment. In animals: robust BDNF/TrkB data2 and well-characterised anti-inflammatory neuroprotection in stroke models3.
Evidence at a glance
| Use | Grade | Best evidence | Main gap | Read |
|---|---|---|---|---|
| Stroke recovery | BHuman trials | Neuroprotection, better recovery1 | Russian, unreplicated | Strongest use |
| BDNF, neuroplasticity | ELab & animal | Single dose tripled BDNF2 | Animal | Striking |
| Focus and cognition | DCommunity use | Faster processing reported | Limited human data | Plausible |
Dosing: what has been reported
| Setting | Figure | Route | Grade |
|---|---|---|---|
| Approved (Russia), cognition | 600–1,200 mcg/day via 0.1% solution, split | Intranasal | B |
| Approved (Russia), acute stroke | 9,000–18,000 mcg/day via 1% solution, within 6–12 h, clinical care only | Intranasal | B |
| Community | 600–1,200 mcg/day in 5–10-day courses with breaks, often with Selank | Intranasal | D |
Nasal use is the studied route and the one to prefer. Injectable forms lack that evidence. Take it earlier in the day, because it’s stimulating.
Preparing & storing
Research Semax is reconstituted with bacteriostatic water and made into nasal drops. Refrigerate once mixed. The Pro-Gly-Pro tail gives it good stability.
Timeline: focus within 15–40 minutes, peaking at 1–2 hours and lasting 4–6 hours. BDNF effects build over a course.
Reported side effects
- Mild nasal irritation
- Overstimulation or poor sleep if dosed high or late
- Occasional mild headache
- No cortisol rise and no stimulant crash
Who should avoid it
- Pregnancy and breastfeeding
- Stimulant or psychiatric medication: get medical input (dopamine and serotonin)
- A real stroke is an emergency, not something to self-treat
Regulatory status checked Oct 2026
| Body | Status | Detail |
|---|---|---|
| FDA (US) | Not approved | Research use only. |
| EMA (EU) | Not approved | — |
| Russia | Approved | Prescription drug; essential-medicines list. |
| WADA | Not listed | Low doping relevance. |
A real neuroprotective drug, used as a nootropic
Semax has approval, a striking BDNF mechanism and a clean safety profile. Its strongest data are for stroke. Use it nasally, early in the day, and expect noticeable but modest focus.
References
- Gusev EI, Skvortsova VI, et al. Neuroprotective effects of Semax in acute ischemic stroke. Russian clinical trials.
- Dolotov OV, Karpenko EA, Inozemtseva LS, et al. Semax upregulates BDNF and TrkB expression in rat hippocampus. 2006. PMID 16996037
- Dergunova LV, et al. Semax suppresses pro-inflammatory gene expression during cerebral ischemia-reperfusion.