Last updated: March 2026
Selank is a synthetic heptapeptide derived from the immunomodulatory peptide tuftsin, developed at Russia's Institute of Molecular Genetics. It modulates GABA receptor function with anxiolytic effects comparable to benzodiazepines — without the sedation, cognitive impairment, or dependence risk.
Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro) is a modified tuftsin analog with a Pro-Gly-Pro tripeptide extension that stabilizes it against enzymatic degradation. It was developed for treating generalized anxiety disorder and neurasthenia.
Allosterically modulates GABAA receptors, altering the expression of genes involved in GABAergic neurotransmission — including GABRA2, GABRA6, and GABRB2 subunit genes.
Influences serotonin, dopamine, and norepinephrine metabolism. Stabilizes enkephalin degradation, extending the activity of endogenous opioid peptides.
Derived from tuftsin, retains immunomodulatory properties. Influences IL-6 and interferon expression, bridging the neuro-immune axis.
Increases brain-derived neurotrophic factor expression, providing potential neuroprotective effects alongside its anxiolytic action.
Context: Selank was approved in Russia in 2009 for anxiety and neurasthenia. Clinical data predominantly comes from Russian institutions. The anxiolytic effects are well-documented, but Western clinical data is limited.
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Selank is NOT FDA approved in the United States. It is approved in Russia for anxiety and neurasthenia. This page is for educational purposes only. Not medical advice. Approved Russia Not Available US