Selank
Selank is a synthetic heptapeptide (Thr-Lys-Pro-Arg-Pro-Gly-Pro) developed at the Institute of Molecular Genetics of the Russian Academy of Sciences in collaboration with the V.V. Zakusov Research Institute of Pharmacology. It is derived from the naturally occurring immunomodulatory peptide tuftsin, with additional stabilizing amino acids that extend its biological activity. Selank is approved in Russia as a prescription anxiolytic and nootropic medication, though it has no regulatory approval in the United States or Europe.
Selank's mechanism of action involves modulation of multiple neurotransmitter systems including GABAergic, dopaminergic, and serotonergic pathways. It acts as a subtype-selective, concentration-dependent allosteric modulator of GABA-A receptors, which underlies its anxiolytic effects. Additionally, it rapidly elevates brain-derived neurotrophic factor (BDNF) expression in the hippocampus, supporting its nootropic (cognitive-enhancing) properties. Clinical studies in 62 patients with generalized anxiety disorder and neurasthenia[1] demonstrated that Selank's anxiolytic effect was comparable to the benzodiazepine medazepam, with the added benefits of psychostimulant and antiasthenic effects, and without the sedation, dependence, or withdrawal symptoms associated with benzodiazepines.
The peptide is typically administered intranasally, which allows it to bypass the blood-brain barrier more efficiently. Research also indicates immunomodulatory properties inherited from its parent peptide tuftsin, giving Selank a unique dual anxiolytic-immunomodulatory profile. The evidence base remains predominantly from Russian research institutions, and broader international clinical validation is still needed. No human safety concerns have been identified in published research, though long-term data remains limited.
Key Details
| Category | Nootropic/Anxiolytic |
| Primary Uses | Anxiety reduction, Cognitive enhancement, Stress resilience, Immune modulation, Mood stabilization |
| Mechanism of Action | Allosteric modulation of GABA-A receptors; increases hippocampal BDNF expression; modulates serotonergic and dopaminergic systems; immunomodulatory effects via tuftsin derivative activity |
| Administration Route | Intranasal (primary), Subcutaneous injection |
| Typical Research Dosage | 250-500mcg intranasally 2-3x daily; research protocols vary |
| Protocol Duration | 2-4 weeks, can be cycled |
| Half-Life | ~1-3 minutes (rapidly metabolized; effects persist due to downstream signaling) |
| Legal Status | Approved as prescription medication in Russia; not FDA-approved; available as research chemical in the US and Europe |
| FDA Status | Not approved by the FDA. No US clinical trials registered. Approved in Russia for anxiety and cognitive disorders. |
| Notable Studies | Clinical study (62 patients): Anxiolytic effect comparable to benzodiazepine medazepam in generalized anxiety disorder, Research showing Selank enhances BDNF expression in hippocampal neurons, GABAergic research: Demonstrated subtype-selective allosteric modulation of GABA-A receptors, Preclinical studies showing enhanced effect when combined with diazepam under chronic mild stress conditions, Immunomodulatory research demonstrating tuftsin-related immune system effects |
| Safety Profile | Well-tolerated in clinical studies with no reported serious adverse events. No sedation, dependence, or withdrawal symptoms (unlike benzodiazepines). Minimal side effects reported. Long-term safety data limited to Russian clinical experience. |
| Typical Price Range | $30-55 per 5mg vial; $35-60 for intranasal preparation |
| Molecular Weight | 751.88 Da |
References
- Selank Anxiolytic Effect Comparable to Medazepam in Generalized Anxiety Disorder (2008)
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