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Home / Research Trials / Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro)
Human (small/observational)

Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro)

Cognitive & Nootropic

Selank is a synthetic tuftsin analogue developed in Russia and studied there as an intranasal anxiolytic. The indexed human evidence consists of Russian-language comparative clinical studies (2008-2015) in generalised anxiety disorder, neurasthenia and anxiety-phobic/somatoform disorders, benchmarked against benzodiazepines (medazepam, phenazepam) rather than placebo, plus one placebo-controlled fMRI study in healthy volunteers. Doses and routes are not reported in most English abstracts, and no Western replication has been published.

5 published trials1 reported adverse effect1 documented interaction6 references
🔬 Research use only — not for human or veterinary use. The regimens below are records of what published studies administered to their own subjects; they are not instructions and K4 Elite does not provide dosing instructions.
Published trial usage Adverse effects Interactions Contraindications References
Published trial usage

Each row records what a published study did: who it enrolled, the regimen it administered to those subjects, and what it reported. These are historical study descriptions, not protocols to follow.

StudyPopulationRegimen as reportedPrimary findings
Zozulia et al., Zh Nevrol Psikhiatr Im S S Korsakova 2008 (comparative study vs medazepam; Russian-language) 62 patients with generalised anxiety disorder or neurasthenia (Selank n=30; medazepam n=32) Patients received Selank or medazepam; dose, route and duration are not stated in the English abstract. Serum enkephalin activity was measured alongside Hamilton, Zung and CGI scales. Anxiolytic effects were reported as similar between Selank and medazepam; the authors additionally described antiasthenic and psychostimulant effects with Selank, and an increase in leu-enkephalin half-life during treatment.
Medvedev et al., Zh Nevrol Psikhiatr Im S S Korsakova 2014 (comparative study vs phenazepam; Russian-language) 60 patients with anxiety-phobic and somatoform disorders (ICD-10 F40.2-9, F41.1-9, F45.0-1) Patients received Selank or phenazepam; dose and duration are not stated in the English abstract. The authors reported an anxiolytic effect with a mild nootropic component for Selank, persisting for about a week after the last administration.
Medvedev et al., Zh Nevrol Psikhiatr Im S S Korsakova 2015 (add-on study; Russian-language) 70 patients with anxiety-phobic, hypochondriac and somatoform disorders (phenazepam alone n=30; Selank plus phenazepam n=40) Patients received phenazepam monotherapy or phenazepam plus Selank; tolerability was rated on the UKU scale and cognition with Stroop and verbal fluency tests. Selank dose is not stated in the English abstract. Combined treatment was reported to reduce phenazepam-associated side effects (attention/memory impairment, asthenia, sedation, orthostatism) during treatment and after benzodiazepine withdrawal.
Uchakina et al., Zh Nevrol Psikhiatr Im S S Korsakova 2008 (Russian-language) Patients with generalised anxiety disorder and neurasthenia Patients received Selank for 14 days; serum Th1/Th2 cytokine balance was measured before and after. Changes in serum Th1/Th2 cytokine balance were reported over 14 days of treatment; in vitro, Selank suppressed IL-6 gene expression in blood cells from depressed patients.
Panikratova et al., Dokl Biochem Biophys 2020 (placebo-controlled resting-state fMRI study) 52 healthy participants Participants received a single administration of Selank, Semax or placebo; resting-state fMRI was acquired before and 5 and 20 minutes after administration (dose not stated in the abstract). Between-group differences in functional connectivity between the right amygdala and right temporal cortex were reported after Selank or Semax compared with placebo.
Reported adverse effects

Effects recorded in the cited reports. Frequencies are those the source reported, in the population that source studied.

EffectFrequency / contextSource
Tolerability relative to benzodiazepines In Medvedev 2014 (n=60) Selank was compared with phenazepam on tolerability; the English abstract reports no specific Selank adverse-event rates. Zozulya 2001 described Selank as not causing the side effects characteristic of most anxiolytics; no quantitative safety data are given. [A comparison of the anxiolytic effect and tolerability of selank and phenazepam in the treatment of anxiety disorders] ↗
Interactions

Interactions documented in trial reports, prescribing information or pharmacology references.

AgentTypeNoteSource
Phenazepam (benzodiazepine) pharmacodynamic (studied combination) Selank was co-administered with phenazepam in 40 patients; the authors reported fewer benzodiazepine-type side effects with the combination than with phenazepam alone (Medvedev 2015). [Optimization of the treatment of anxiety disorders with selank] ↗
Contraindications noted in trials

No contraindications with a verifiable citation have been indexed for this compound.

References
  1. [Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia], Zh Nevrol Psikhiatr 2008
  2. [A comparison of the anxiolytic effect and tolerability of selank and phenazepam in the treatment of anxiety disorders], Zh Nevrol Psikhiatr 2014
  3. [Optimization of the treatment of anxiety disorders with selank], Zh Nevrol Psikhiatr 2015
  4. [Immunomodulatory effects of selank in patients with anxiety-asthenic disorders], Zh Nevrol Psikhiatr 2008
  5. The inhibitory effect of Selank on enkephalin-degrading enzymes as a possible mechanism of its anxiolytic activity, Bull Exp Biol Med 2001
  6. Functional Connectomic Approach to Studying Selank and Semax Effects, Dokl Biochem Biophys 2020
Elsewhere on K4 Elite
Selank — product pageSelank — Peptide Research LibraryAll indexed compounds — Research Trials
Research use only. This record summarises published literature for reference. It is not medical advice, not a protocol, and not a recommendation to administer this compound to any subject. Regimens are reported as the historical record of how a cited study was conducted; findings are reported without interpretation and constitute no claim of safety or efficacy. Determining any research procedure is the sole responsibility of the qualified researcher. Products referenced on this site are supplied strictly for in-vitro laboratory and research purposes, are not for diagnostic or therapeutic use, and have not been evaluated by the FDA.