Last updated: March 2026
Semax is a synthetic ACTH(4-10) analog developed at Russia's Institute of Molecular Genetics. It upregulates BDNF protein levels by 1.4-fold and is approved in Russia for acute stroke therapy, cognitive disorders, and neuroprotection with over two decades of clinical use.
Semax (Met-Glu-His-Phe-Pro-Gly-Pro) combines the active ACTH(4-7) fragment with a stabilizing Pro-Gly-Pro tripeptide. Unlike full ACTH, it does not significantly stimulate adrenal hormone production — its effects are concentrated on neurotrophin modulation and neuroprotection.
A single dose increases BDNF protein levels 1.4-fold and TrkB phosphorylation 1.6-fold. Also induces 3-fold increase in BDNF mRNA and 2-fold increase in NGF mRNA in rat hippocampus.
Modulates dopaminergic and serotonergic neurotransmission, enhancing motivation, focus, and mood without stimulant-like side effects.
Improves cerebral microcirculation — a key mechanism for its approved use in acute ischemic stroke therapy in Russia.
Activates neurotrophic factor expression after cerebral ischemia, promoting neuronal survival and recovery through BDNF/NGF and TrkB receptor pathways.
Context: Semax has been approved and used clinically in Russia since the 1990s. It has a substantial Russian literature base. The BDNF modulation data is well-replicated across multiple labs. Western clinical data remains limited.
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Semax is NOT FDA approved in the United States. It is approved in Russia for stroke and cognitive disorders. This page is for educational purposes only. Not medical advice. Approved Russia Not Available US