Selank: Benefits, Dosage & FDA Status
Selank (TP-7)
A synthetic analog of tuftsin with anxiolytic and nootropic properties. Modulates GABA and serotonin systems to reduce anxiety without sedation.
FDA Status
Not FDA-approved in US — approved in Russia as anxiolytic
Typical Dose
200–400 mcg intranasal, evening
Evidence Grade
BLimited clinical + robust preclinical evidence
Half-Life
~30 minutes (effects last hours)
Routes of Administration
intranasal
First Synthesized
1995
Clinics Indexed
72 providers have offered Selank in our tracked directory.
Mechanism of Action
Tuftsin analog that enhances GABA-A signalling and modulates serotonergic and noradrenergic tone without benzodiazepine-like dependence.
Key Reported Benefits
- ✓Anxiety reduction
- ✓Stress resilience
- ✓Cognitive clarity
- ✓Immune modulation
Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade B indicates limited clinical + robust preclinical evidence.
Reported Side Effects
- •Nasal irritation
- •Drowsiness (rare)
Contraindications
- ⚠Pregnancy
- ⚠Severe psychiatric illness without supervision
Commonly Stacked With
Selank vs Other Peptides
Regulatory & Safety Context
FDA status: Not FDA-approved in US — approved in Russia as anxiolytic
This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.
See state-by-state legality: US peptide legality by state →
References
Selected primary literature on Selank. Full PubMed records linked. Additional citations are available on request.
Last reviewed: 2026-04-30
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