Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Semax (ACTH(4-10) analog, Met-Glu-His-Phe-Pro-Gly-Pro)
Semax is a synthetic heptapeptide derived from ACTH(4-10). It is registered as a drug in Russia (1994) for acute ischemic stroke, asthenic states, and optic nerve disease; it is not FDA-approved.
Semax upregulates BDNF and NGF expression and activates the BDNF/TrkB pathway in the hippocampus, cortex, and basal forebrain. It retains melanocortin-receptor activity from its ACTH(4-10) core but lacks the steroidogenic C-terminus, so it does not stimulate cortisol release. Additional reported mechanisms include inhibition of enkephalin-degrading enzymes and modulation of dopaminergic and serotonergic tone.
Registered in Russia (1994) as intranasal drops in 0.1% (cognitive/asthenic indications) and 1% (acute ischemic stroke and optic nerve disease) formulations. Russian clinical trials (Gusev, Skvortsova and colleagues) reported improved neurological recovery when started early in acute ischemic stroke. Primary evidence base is Russian-language literature; no Western regulatory approvals and no pivotal Western trials exist.
Typical Dose
600mcg
Range
200-2000mcg/day
Frequency
2-3x/day (intranasal)
Route
Nasal
Duration
2-4 weeks (cognitive use); 10-day hospital courses (stroke)
Reconstitution
5mg vial + 2mL bacteriostatic water = 2,500mcg/mL
Notes
Russian clinical dosing uses 0.1% drops for cognitive/asthenic use (~200–600 mcg/day) and 1% drops for acute stroke (up to ~6000 mcg/day in hospital protocols). Grey-market subcutaneous dosing (250–1000 mcg/day) is not clinically validated.
Aggregated from 67 lab-verified Certificates of Analysis uploaded directly by 1 verified lab. Purity averages exclude values outside [50%, 100%] to filter unit-misreads.
COAs
67
Verified labs
1
Avg purity
99.43%
±0.54%
Endotoxin tested
45%
Tested by
These biomarkers are commonly tracked to assess response and safety. Run baseline labs before starting, mid-cycle labs halfway through, and post-cycle labs 1–2 weeks after the final dose.
This platform provides informational tools only, not medical advice. This information is for educational purposes only. Consult a licensed provider.