Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
Cognitive / Mood
Also known as: TP-7 analogue
An anxiolytic-discussed peptide analogue. Approved in some jurisdictions, limited independent evidence elsewhere.
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Selank is a synthetic analogue of the endogenous peptide tuftsin, studied for anxiolytic effects.
Some regional clinical use; limited independent replication.
Research-market purity is unverified; not a validated treatment outside its regional approvals.
Used as a medicine in some countries; not approved in the EU/US.
Vendor comparison
The table lists only product-specific offers that were checked and for which a real destination exists. Missing prices, quantities, stock and laboratory details are not inferred.
Documentation
Vendor-supplied data
COA stated as available
Not independently documented
Checked
Jul 18, 2026
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Selank is a synthetic analogue of the endogenous peptide tuftsin, studied for anxiolytic effects.
Selank is a synthetic peptide developed as a stabilized analogue of tuftsin, a naturally occurring immunomodulatory fragment of the immunoglobulin G molecule. Sometimes referenced in research literature in connection with the designation TP-7, it was designed to resist rapid enzymatic breakdown in the body, giving it a longer window of activity than the parent peptide. It is most often categorized as a cognitive and mood-focused compound and is studied primarily for potential anxiolytic (anxiety-reducing) properties, which places it alongside peptides like Semax in discussions of so-called nootropic or neuropeptide research.
The scientific interest in Selank centers on how it may interact with the brain's signaling systems. Preclinical and mechanistic work has discussed possible effects on GABAergic and monoamine (serotonin and dopamine) pathways, as well as on the expression of factors related to stress and immune signaling. Animal studies have reported anxiolytic-like effects, and Selank has seen regional clinical use as an intranasally administered medicine in a small number of countries, notably within Russian pharmacology. However, independent, large-scale human replication outside those jurisdictions remains limited, which is why its overall evidence rating is best described as modest rather than well-established. Claims about memory, focus, or generalized well-being should be read against this backdrop of preliminary and geographically concentrated data.
From a regulatory and safety standpoint, the picture is nuanced. Selank is used as an approved medicine in some countries but is not approved by the EU or US regulators, and material sold on the research-chemical market has unverified purity and identity. Reported side effects are limited but include nasal irritation associated with intranasal use, and its long-term safety profile in the general population is not fully characterized. This page is an educational reference intended to summarize what the research literature does and does not show; it is not medical advice, and it does not provide dosing, protocols, or sourcing guidance. Anyone considering peptide-related decisions for health reasons should consult a qualified, licensed clinician.
Evidence grade: C
Some regional clinical use; limited independent replication. Preclinical anxiolytic effects reported.
Some regional clinical use; limited independent replication.
Preclinical anxiolytic effects reported.
Research-market purity is unverified; not a validated treatment outside its regional approvals.
Used as a medicine in some countries; not approved in the EU/US.
1980sβ1990s
Selank is designed at the Institute of Molecular Genetics of the Russian Academy of Sciences as a synthetic analogue of the endogenous immunopeptide tuftsin, a heptapeptide fragment, aimed at more stable anxiolytic activity.
1990s
Early preclinical work in rodents reports anxiolytic-like and behavioral effects, and researchers describe proposed interactions with GABA and monoamine systems as a rationale for further study.
2000s
Small clinical studies, largely conducted by Russian research groups, explore intranasal use for generalized anxiety; the peptide is registered and marketed as a medicine within Russia.
2010s
Additional regional publications examine mechanisms and effects on gene expression and BDNF-related pathways, while independent replication outside the originating groups remains limited.
early 2020s
Selank remains unapproved in the EU and US and circulates internationally through the research-chemical market, where product identity and purity are not independently guaranteed.