Investigational — Not FDA-Approved Authoritative Evidence Reference Regional Clinical Use / Preclinical in Western Jurisdictions

Selank (TP-7)

Synthetic heptapeptide analogue of the naturally occurring immunomodulatory peptide Tuftsin (Thr-Lys-Pro-Arg) extended with a C-terminal Pro-Gly-Pro tripeptide. Developed in Russia as an anxiolytic and nootropic agent; acts via allosteric modulation of GABA-A receptors and neurotrophin upregulation without sedative or addictive properties. Not approved by US FDA, EMA, or EDA; FDA Category 2 compounding substance.

Language: English العربية (Arabic) →
Drug Class Tuftsin-Derived Anxiolytic Neuropeptide
FDA Regulatory Status Investigational — Not FDA-Approved
Clinical Stage Regional Clinical Use / Preclinical in Western Jurisdictions
Evidence Verification Active Reference Standards
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60-Second Scientific Briefing

Selank is a synthetic heptapeptide derived from the naturally occurring immunomodulatory peptide tuftsin (Thr-Lys-Pro-Arg) extended with a C-terminal Pro-Gly-Pro tripeptide. Developed in Russia as an anxiolytic and nootropic agent for generalized anxiety disorder. It is NOT FDA-approved.

What is Selank?

Pharmacological Classification & Molecular Identity

Synthetic heptapeptide composed of the natural tetrapeptide tuftsin linked to the metabolically stabilizing tripeptide Pro-Gly-Pro.

Verified Chemical & Regulatory Registry Identifiers

CAS 129954-34-3 Verified Registry
FDA_UNII XF4Z344M7P ↗ Verified Registry
PUBCHEM_CID 11765600 ↗ Verified Registry
Documented Aliases & Research Codes:
TP-7 Tuftsin-Pro-Gly-Pro Heptapeptide Selank

Mechanism of Action & Receptor Targets

Biological Pathway and Target Binding

Biological pathway and target receptor binding mechanism.

Receptor Selectivity: Modulates GABA-ergic neurotransmission, allosterically interacts with GABA-A receptors, and influences serotonin and dopamine metabolism in the brain.

Regulatory & FDA Approval Status

Legal and Regulatory Classifications
⚠️ STRICT REGULATORY NOTICE: UNAPPROVED INVESTIGATIONAL DRUG

Not approved by the US FDA or EMA for any medical condition. Holds regional regulatory registration in Russia.

Selank is not approved for commercial sale, prescription therapy, or compounded medication distribution. It exists strictly within authorized scientific and clinical research frameworks.

Human Evidence & Clinical Trials

Clinical Study Readouts and Evidence Syntheses

Regional clinical studies evaluated intranasal Selank in patients with generalized anxiety disorder (GAD) and neurasthenia compared to benzodiazepines.

Clinical Evidence

Regional clinical studies evaluated intranasal Selank in patients with generalized anxiety disorder (GAD) and neurasthenia compared to benzodiazepines.

Safety Profile & Clinical Limitations

Documented Adverse Events and Known Uncertainties

Generally reported as non-sedating without withdrawal symptoms in Russian literature. Local nasal dryness or irritation can occur.

ℹ️ Active Research Safety Surveillance

Lack of large-scale international multi-center randomized controlled trial safety data.

Dose Approval Status

Commercial Dosing Status and Policy Directives
🛑 NO APPROVED COMMERCIAL DOSING REGIMEN

NOT ESTABLISHED in FDA jurisdictions. Russian pharmaceutical labeling prescribes 0.15% intranasal drops.

Under Egypt Peptides medical governance policies, no personal dosages, titration intervals, cycles, stacking recommendations, or self-injection instructions may be provided for unapproved investigational compounds. Clinical study protocols represent controlled experimental research parameters exclusively.

Storage & Handling Status: NOT ESTABLISHED for Western retail distribution. Stored under refrigeration at 2°C to 8°C.

What is Known vs. What is Unknown

Evidence Comparison and Clinical Evidence Boundaries

✓ Confirmed Scientific Evidence

  • Synthetic heptapeptide composed of the natural tetrapeptide tuftsin linked to the metabolically stabilizing tripeptide Pro-Gly-Pro.
  • Targets & Selectivity: Modulates GABA-ergic neurotransmission, allosterically interacts with GABA-A receptors, and influences serotonin and dopamine metabolism in the brain.
  • Regional clinical studies evaluated intranasal Selank in patients with generalized anxiety disorder (GAD) and neurasthenia compared to benzodiazepines.
  • Safety considerations: Generally reported as non-sedating without withdrawal symptoms in Russian literature. Local nasal dryness or irritation can occur.

? Unknown / Under Ongoing Investigation

  • Lack of large-scale international multi-center randomized controlled trial safety data.

Verified Questions & Answers

10 Verified scientific answers with permanent anchor keys
#1

What is Selank and how is it classified?

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Direct Answer

Selank is classified as a Tuftsin-Derived Anxiolytic Neuropeptide. Molecular structure: Synthetic heptapeptide composed of the natural tetrapeptide tuftsin linked to the metabolically stabilizing tripeptide Pro-Gly-Pro..

Pharmacological classification and molecular integrity are documented in verified regulatory and scientific literature.

Authoritative Citations:
#2

What is the mechanism of action and receptor profile of Selank?

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Direct Answer

Selank exerts biological activity via Modulates GABA-ergic neurotransmission, allosterically interacts with GABA-A receptors, and influences serotonin and dopamine metabolism in the brain..

Receptor binding affinity and selectivity dictate the physiological response observed in laboratory and clinical trials.

Authoritative Citations:
#3

Is Selank approved by the US FDA or health authorities?

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Direct Answer

Regulatory status: Not approved by the US FDA or EMA for any medical condition. Holds regional regulatory registration in Russia.

Investigational and research-only compounds cannot be legally distributed or marketed as prescription drugs.

Authoritative Citations:
#4

What human clinical evidence and trials exist for Selank?

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Direct Answer

Clinical evaluation status: Regional clinical studies evaluated intranasal Selank in patients with generalized anxiety disorder (GAD) and neurasthenia compared to benzodiazepines.

Clinical trial readouts and systematic analyses establish the boundary between demonstrated findings and experimental hypotheses.

Authoritative Citations:
#5

What adverse effects and safety risks are documented for Selank?

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Direct Answer

Reported safety profile: Generally reported as non-sedating without withdrawal symptoms in Russian literature. Local nasal dryness or irritation can occur.

Adverse reaction monitoring and contraindications are critical parameters in pharmacological risk-benefit evaluation.

Authoritative Citations:
#6

What are the critical unknown safety aspects and clinical limitations of Selank?

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Direct Answer

Key scientific uncertainties: Lack of large-scale international multi-center randomized controlled trial safety data.

Egypt Peptides enforces strict transparency regarding scientific limitations and gaps in longitudinal clinical data.

Authoritative Citations:
#7

What is the approved dosing status for Selank?

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Direct Answer

NOT ESTABLISHED in FDA jurisdictions. Russian pharmaceutical labeling prescribes 0.15% intranasal drops.

Under medical governance mandates, clinical study dosages represent strictly controlled experimental parameters and must never be interpreted as individual therapeutic advice.

Authoritative Citations:
#8

What are the storage and handling requirements for Selank?

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Direct Answer

Storage status: NOT ESTABLISHED for Western retail distribution. Stored under refrigeration at 2°C to 8°C.

Peptide integrity degrades rapidly when exposed to elevated temperatures, repeated freeze-thaw cycles, or direct UV light exposure.

Authoritative Citations:
#9

Is Selank prohibited in competitive sports by WADA?

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Direct Answer

Yes. Unapproved pharmacological substances are strictly prohibited at all times in competitive sports under WADA Category S0 (Non-approved substances) or Category S2.

Athletes subject to drug testing face strict liability and multi-year competition bans upon detection of prohibited peptides or their metabolites.

Authoritative Citations:
#10

What is Egypt Peptides' official medical policy regarding Selank?

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Direct Answer

Egypt Peptides provides peer-reviewed scientific reference monographs for research documentation. We strictly prohibit individual medical consultations, reconstitution guides, stacking recipes, or off-label use instructions.

All scientific claims must link to verified authoritative sources (FDA, PubMed, ClinicalTrials.gov) with zero tolerance for ungrounded marketing claims.

Authoritative Citations:

Authoritative Sources & Literature Registry

Regulatory dossiers, clinical trial registries, and peer-reviewed studies
Source [1] Tier 2 Regulatory / Academic

Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia ↗

Publisher / Registry: Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova Publication Date: 2008-01-01 PubMed PMID: 18454096
Verified Locator: https://pubmed.ncbi.nlm.nih.gov/18454096/

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