Selank

Tuftsin analogue heptapeptide (peptide anxiolytic)

Status

Approved elsewhere

Registered as a peptide anxiolytic in Russia, where it is one of a small group of domestically developed peptide drugs, but not approved by the FDA or the EMA; FDA lists selank acetate (TP-7) among bulk substances whose compounding nomination was withdrawn, it is not on the 503A Bulks List, and it was not among the seven peptides reviewed at the July 2026 advisory committee meeting.

Evidence

Preliminary

Human data come from small Russian trials in anxiety and neurasthenia, several published only in Russian, with no independent replication outside Russia.

A seven-amino-acid tuftsin derivative developed in Russia and registered there as a nasal anxiolytic. Outside Russia it is an unapproved research chemical marketed for anxiety and focus.

Structure

7 residues

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Sequence as text
H-T-K-P-R-P-G-P-OH

What it is used for

  • Anxiety disorders and neurasthenia, as a registered product in Russia (approved)
  • Generalised anxiety disorder compared with benzodiazepines in small Russian trials (studied)
  • Attention, memory and stress resilience (claimed, unproven)

How it works

Selank is a synthetic analogue of tuftsin, a fragment of an antibody that acts on immune cells. Laboratory work from its developers describes it as a positive allosteric modulator of GABA-A receptor binding, which would give a benzodiazepine-like calming effect without acting at the benzodiazepine site itself, alongside effects on monoamine turnover and on enkephalin breakdown in rodents. The human mechanism has not been confirmed with imaging or receptor studies in people.

How strong the evidence is

PreliminarySmall human studies, pilots or observational data.

Radioligand studies by Vyunova and colleagues (2018) support allosteric modulation of GABA binding. Rodent studies report anxiolytic and antidepressant-like effects and interaction with diazepam. Human evidence rests on small Russian trials: a comparison in 60 patients with phobic-anxiety and somatoform disorders reported anxiolytic effects comparable with phenazepam and a persisting effect after dosing stopped, and earlier trials reported benefit in generalised anxiety disorder and neurasthenia. These studies are small, mostly open or single-centre, and published in Russian, so the effect size is not independently established.

Risks and side effects

  • Not assessed by the FDA or the EMA; the supporting trials are small, Russian and not independently replicated
  • FDA notes a risk of immune reactions from peptide aggregation and impurities, particularly for injected forms
  • Research-chemical supply is unregulated, so identity, purity and sterility are unverified
  • Interactions with benzodiazepines and antipsychotics have been described in laboratory work and are not characterised clinically
  • No long-term human safety data, and none in children, pregnancy or breastfeeding

Regulatory status

Registered outside the US and EU. We could not verify the registration details from a primary source, so none are listed; the status note above says what is known.

Status by country

JurisdictionStatusSource
USUnited StatesNo authorised medicineSource 4
EUEuropean UnionNo authorised medicineSource 6
UKUnited KingdomNo authorised medicineSource 7
AUAustraliaNo authorised medicineSource 8
CACanadaNo authorised medicineSource 9
Whether a medicine containing it is authorised, checked in each regulator’s records on Oct 1, 2026.

Status of every peptide by country

Sources

  1. 01Peptide-based Anxiolytics: The Molecular Aspects of Heptapeptide Selank Biological Activity(opens the source in a new tab) Protein and Peptide Letters (PubMed), 2018
  2. 02A comparison of the anxiolytic effect and tolerability of selank and phenazepam in the treatment of anxiety disorders(opens the source in a new tab) Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova (PubMed), 2014
  3. 03Development of Peptide Biopharmaceuticals in Russia(opens the source in a new tab) Pharmaceutics (PubMed Central), 2022
  4. 04Certain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks(opens the source in a new tab) US Food and Drug Administration, 2026
  5. 05Selank, CID 11765600(opens the source in a new tab) PubChem, National Library of Medicine, 2026
  6. 06Find medicine: centrally authorised medicines(opens the source in a new tab) European Medicines Agency, 2026
  7. 07MHRA Products: active substances beginning with S(opens the source in a new tab) Medicines and Healthcare products Regulatory Agency, 2026
  8. 08Australian Register of Therapeutic Goods (ARTG)(opens the source in a new tab) Therapeutic Goods Administration
  9. 09Unauthorized injectable peptide drugs seized and sold by Canada Peptide may pose serious health risks(opens the source in a new tab) Health Canada, 2025
  1. Approved elsewhereCerebrolysinMixture of low molecular weight peptides and free amino acids derived from porcine brainNo single sequence·
  2. Not approvedDelta sleep-inducing peptideNonapeptide of uncertain physiological role, first described as a sleep factor9 WADA banned
  3. Not approvedDihexaAngiotensin IV derived dipeptide mimetic, described as a hepatocyte growth factor (HGF) and c-Met potentiator2 WADA banned
  4. Approved elsewhereSemaxACTH(4-10) fragment analogue (melanocortin-derived neuropeptide)7
  5. ApprovedOxytocinOxytocin receptor agonist (posterior pituitary hormone)9

Educational information, not medical advice. Talk to a licensed clinician before starting, stopping or changing any medicine.