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Selank: Research Overview & Current Status

Approved (non-drug / other indication)

Selank is a Synthetic heptapeptide (tuftsin analog) / anxiolytic neuropeptide. Current research status: approved (non-drug / other indication). Selank is approved as a prescription anxiolytic in the Russian Federation and marketed there in intranasal form. It has no FDA or EMA approval and is not a legally marketed drug in the U.S. or EU.

Overview

Selank is a synthetic heptapeptide analog of tuftsin, incorporating a fragment of the human immunoglobulin G heavy chain (Thr-Lys-Pro-Arg) extended with additional amino acids (Pro-Gly-Pro) for metabolic stability. It is studied primarily in Russia as an anxiolytic, with a proposed mechanism involving enkephalinase inhibition and GABAergic modulation.

Synthetic heptapeptide (tuftsin analog) / anxiolytic neuropeptide

Research timeline

  1. 1990s

    Selank developed in Russia as a synthetic tuftsin analog engineered for anxiolytic activity via enkephalinase inhibition.

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  2. Late 1990s-2010s

    Regulatory approval granted in the Russian Federation for prescription anxiolytic use, marketed in intranasal formulation.

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  3. 2000s

    Comparative clinical study of 62 patients with generalized anxiety disorder and neurasthenia found Selank's anxiolytic effect comparable to the benzodiazepine medazepam, with additional antiasthenic and psychostimulant effects reported for Selank.

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  4. 2010s

    Study using pharmaco-EEG and clinical scales reported response-pattern subgroups (rapid vs. gradual responders) to intranasal Selank (2700 mcg/day) in anxiety patients.

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  5. 2017

    Frontiers in Pharmacology study examined Selank's effects on GABAergic gene expression in IMR-32 neuroblastoma cells, finding no significant transcriptional changes and suggesting a non-transcriptional mechanism.

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  6. 2017

    Rat study reported Selank enhanced the anxiolytic effect of diazepam under chronic mild stress conditions.

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Active & recent research

Clinical trial, 62 patients (GAD/neurasthenia)

Selank vs. benzodiazepine in generalized anxiety disorder

Comparative anxiolytic efficacy and enkephalin serum activity versus medazepam

Clinical study with pharmaco-EEG

Response-pattern and EEG correlates of intranasal Selank

Characterizing rapid vs. gradual anxiolytic responders and associated EEG rhythm changes

In vitro, IMR-32 neuroblastoma cells

Selank and GABAergic gene expression

Testing whether Selank's anxiolytic effect involves transcriptional changes in GABAergic pathway genes

Rat chronic mild stress model

Selank combined with diazepam under chronic stress

Potential synergistic anxiolytic effect between Selank and benzodiazepine treatment

Key findings

  • A comparative clinical study of 62 patients reported Selank's anxiolytic effect was similar in magnitude to the benzodiazepine medazepam, with additional antiasthenic and psychostimulant effects noted specifically for Selank.
  • A clinical study using intranasal Selank (2700 mcg/day) reported roughly 40% of patients showed rapid symptom reduction within 1-3 days, with Hamilton Anxiety Rating Scale scores dropping from a mean of 20.3 to 7.0 by day 3 in that subgroup.
  • A 2017 in vitro study found no significant changes in GABAergic gene transcription in neuroblastoma cells treated with Selank, suggesting its mechanism may not be primarily transcriptional despite behavioral GABA-pathway associations reported elsewhere.
  • As with Semax, the bulk of Selank's clinical evidence comes from Russian-language trials conducted from the late 1990s through the 2010s and has not been independently replicated in large Western randomized trials.

Safety & regulatory notes

Selank holds prescription drug approval in Russia only; it has no FDA or EMA approval and is not legally marketed as a drug in the U.S. or EU. Reported Russian trial data describe a favorable side-effect profile relative to benzodiazepines, but this has not been verified through independent Western regulatory review.

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Selank FAQ

Is Selank FDA-approved?+

No. Selank is approved as a prescription anxiolytic in Russia only; it has no FDA or EMA approval.

How does Selank's anxiolytic effect compare to benzodiazepines in studies?+

A Russian comparative trial reported Selank produced anxiolytic effects similar to the benzodiazepine medazepam in patients with generalized anxiety disorder, with researchers also noting antiasthenic and psychostimulant effects specific to Selank.

What is Selank's proposed mechanism of action?+

Selank is proposed to inhibit enkephalinase (slowing breakdown of endogenous enkephalins) and to interact with GABAergic signaling, though a 2017 cell study found no significant GABA-related gene transcription changes, indicating the mechanism is not fully resolved.

Has Selank been studied outside Russia?+

The large majority of clinical evidence for Selank comes from Russian clinical research; independent replication in Western randomized controlled trials is limited.

Sources for this page (6)

  1. 1 https://www.researchgate.net/publication/299052506_Efficacy_and_possible_mechanisms_of_action_of_a_new_peptide_anxiolytic_selank_in_the_therapy_of_generalized_anxiety_disorders_and_neurasthenia
  2. 2 https://www.sciencedirect.com/science/article/abs/pii/S0924933812752811
  3. 3 https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00089/full
  4. 4 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322660/
  5. 5 https://www.regeneristherapy.com/en/blog/selank-nootropic-peptide
  6. 6 https://peptideslabuk.com/selank-anxiety-research-what-studies-show/

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