Synthetic heptapeptide / tuftsin analog (cognitive & anxiolytic)

Selank

Selank is a synthetic tuftsin analog developed and registered as a medicine in Russia. Its evidence base is dominated by Russian-language preclinical research and a small number of regional clinical publications. Independent replication is limited, and Selank is not FDA-approved.

Research watch: preclinical and limited Russian clinical use Last reviewed Jul 1, 2026 Next review Jul 29, 2026
Unbranded Selank nasal-drop bottle beside a folded tissue on a clinical counter

Evidence snapshot

Selank is a tuftsin analog developed at the Institute of Molecular Genetics (Russian Academy of Sciences, Moscow) and registered in Russia as an anxiolytic; it is not FDA-approved.

PubMed-indexed studies are predominantly Russian-language preclinical research in animal models (rats), with limited Russian clinical literature; independent Western clinical trials have not been published.

A 2022 study in Bulletin of Experimental Biology and Medicine found that Selank attenuated aversive signs of morphine withdrawal in rats (PMID 36322304): a preclinical finding with no human replication.

A 2021 review in the Journal of Clinical Pharmacology grouped Selank with other GABAergic sedative-hypnotic agents (flunitrazepam, GHB, phenibut), noting its pharmacological profile but not clinical efficacy data (PMID 34396551).

Research record

What the evidence record says

Selank is a synthetic tuftsin analog developed and registered as a medicine in Russia. Its evidence base is dominated by Russian-language preclinical research and a small number of regional clinical publications. Independent replication is limited, and Selank is not FDA-approved.

Evidence grade
Not Graded
Regulatory status
Selank regulatory status has not been fully reviewed by Peptide Report editorial team. See company profiles and regulatory watch for current status.

Evidence records

Studies, registries, reviews, and regulatory records

Evidence timeline

What changed, and when

Direct answers

Frequently asked questions

What is Selank?

Selank is a synthetic heptapeptide / tuftsin analog (cognitive & anxiolytic) tracked by Peptide Report. See the full profile for current editorial assessment.

Open research questions

What is still unknown

  • What is the complete human evidence base for Selank?
  • What are the long-term safety considerations for Selank?

Tracked claims

Selank is an effective anxiolytic with no sedative side effects, as claimed in online peptide communities.

Evidence level: Community discussion

Sources: Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats., Sedative-Hypnotic Agents That Impact Gamma-Aminobutyric Acid Receptors: Focus on Flunitrazepam, Gamma-Hydroxybutyric Acid, Phenibut, and Selank.

How to read this: The anxiolytic claim originates from Russian preclinical and clinical literature that has not been independently replicated in Western trials. Online discussions extrapolate animal data and Russian clinical registration to general use. Do not convert these claims into treatment guidance.

Selank is structurally derived from tuftsin and modulates the immune system.

Evidence level: Peer reviewed: preclinical

Sources: Selank, a Peptide Analog of Tuftsin, Attenuates Aversive Signs of Morphine Withdrawal in Rats., Functional Connectomic Approach to Studying Selank and Semax Effects.

How to read this: The tuftsin analog structure is well-established in the peer-reviewed literature. Immunomodulatory effects have been studied in animal models. The functional connectomics study (PMID 32342318) examined brain connectivity changes from Selank/Semax in rats.

Selank is a registered pharmaceutical in Russia for anxiety treatment.

Evidence level: Primary regulatory: Russia only

Sources: Sedative-Hypnotic Agents That Impact Gamma-Aminobutyric Acid Receptors: Focus on Flunitrazepam, Gamma-Hydroxybutyric Acid, Phenibut, and Selank.

How to read this: Selank's Russian regulatory registration does not constitute FDA, EMA, or other Western regulatory approval. The 2021 J Clin Pharmacol review (PMID 34396551) references Selank's pharmacological classification but does not provide clinical efficacy data.

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