Research-Grade Selank Lyophilized Powder in 3ml Vial | COA Verified ≥99% HPLC Purity
10mg

Selank – Anxiolytic Peptide for Stress Response Research

10mg vial · ≥99% HPLC verified

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Specifications

Size
10 mg per vial
Purity
≥99% by HPLC
99%+ Purity
HPLC & MS verified
Research grade
Not for human use
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For laboratory research use only. Not for human or veterinary consumption, diagnostic, or therapeutic use.

Research Context

Our Selank vial is a synthetic analog of tuftsin supplied at >99% HPLC purity for anxiolytic, GABAergic, and immunomodulatory research models.

Within the broader landscape of research compounds — colloquially referred to in community forums as compounds or "research peptides" — Selank is studied for its mechanistic profile in controlled laboratory protocols. Investigators frequently catalog it alongside complementary research compounds when designing comparative or pathway-level studies.

A synthetic analog of tuftsin investigated for anxiolytic and immunomodulatory mechanisms.

99% HPLC Purity · For Laboratory Research Use Only

Key Research Findings (At a Glance)

ParameterSummary
Peptide Structure7 amino acids (Thr-Lys-Pro-Arg-Pro-Gly-Pro)
OriginSynthetic analog of tuftsin (immunomodulatory tetrapeptide)
Primary MechanismGABA-A allosteric modulation, BDNF upregulation, serotonin balance
Key Research AreasAnxiolysis, stress response, GABAergic signaling, immune modulation
Distinguishing FeatureAnxiolytic without sedation or cognitive impairment
Key Differentiator from BenzodiazepinesReduces anxiety without sedation, tolerance, or dependence
Common Dosage Range (Preclinical)50–300 mcg (intranasal); 100–500 mcg (subcutaneous)
Typical AdministrationIntranasal (preferred) or subcutaneous
Intended UseLaboratory research only – not for human or veterinary consumption

Overview

Selank is a synthetic heptapeptide (Thr-Lys-Pro-Arg-Pro-Gly-Pro) engineered as a stabilized analog of tuftsin, a naturally occurring immunomodulatory tetrapeptide. The C-terminal proline extension enhances enzymatic stability and blood-brain barrier penetration relative to native tuftsin.

Selank was developed at the Russian Academy of Sciences' Institute of Molecular Pharmacology. Unlike traditional anxiety medications, Selank reduces stress without causing sedation, cognitive impairment, or motor disruption.

Frequently referenced in research communities as the Selank peptide or tuftsin analog, this compound is heavily investigated for its anxiolytic, stress-protective, and immunomodulatory properties. Investigators looking to buy research-grade Selank typically use it to study models of generalized anxiety, stress-induced behavioral changes, GABAergic signaling, and neuroimmune interactions.

While Selank is most frequently studied via intranasal administration (often searched as "Selank nasal") to help the peptide reach the brain directly through nerve pathways in the nose, subcutaneous protocols are also utilized in preclinical models. As demand for Selank for sale has grown across academic and independent laboratories, it is frequently referenced alongside specific microgram protocol dosages and remains a foundational compound in anxiolytic and adaptogenic research.

Mechanism of Action: GABAergic Modulation and Neuroimmune Regulation

GABA-A Receptor Allosteric Modulation

The primary anxiolytic mechanism of Selank involves changing how GABA-A receptors work (allosteric modulation) in the central nervous system. Unlike benzodiazepines that bind directly to the receptor's main site, Selank modulates the receptor through distinct allosteric sites. This enhances calming GABAergic transmission without causing the sedation, tolerance, or dependence associated with classical anxiety medications, keeping thinking and movement clear.

Serotonergic and BDNF Effects

Selank modulates serotonin metabolism, particularly influencing 5-HT1A and 5-HT2A receptor activity, which contributes to its mood-stabilizing effects. Research demonstrates Selank also upregulates Brain-Derived Neurotrophic Factor (BDNF) expression in the hippocampus, though through different signaling pathways than Semax. This neurotrophic support contributes to stress resilience and neuronal protection during chronic stress exposure.

Immunomodulatory Properties

Inherited from its tuftsin parent structure, Selank retains immunomodulatory activity. Research indicates it modulates cytokine production, influences T-lymphocyte function, and helps restore immune balance during stress-induced immunosuppression. This dual action on both the nervous and immune systems makes Selank a unique compound for studying neuroimmune interactions.

Why Researchers Choose Selank Over Traditional Anxiolytics

Versus Benzodiazepines (e.g., Diazepam, Alprazolam): Benzodiazepines bind directly to the GABA-A receptor's primary site, often causing heavy sedation, motor impairment, and rapid tolerance/dependence. Selank modulates GABA-A through distinct allosteric sites, reducing anxiety while keeping motor coordination and cognitive clarity intact, without inducing tolerance.

Versus Buspirone: Buspirone is a 5-HT1A partial agonist with a notoriously slow onset of action (often weeks) and limited efficacy in severe models. Selank's dual GABAergic and BDNF mechanisms provide faster-acting anxiolysis combined with neuroprotective and immunomodulatory benefits that buspirone lacks.

Versus Semax: While both are Russian neuropeptides, they serve opposite primary outcomes. Selank is chosen when the research endpoint is stress reduction and GABAergic calming (anxiolytic). Semax is chosen when the endpoint is focus, memory, and BDNF-driven cognitive enhancement (cognitive/stimulating).

Primary Research Applications

  • Anxiety, stress response, and emotional regulation modeling (generalized anxiety, situational stress)
  • GABA-A receptor allosteric modulation studies
  • Neuroimmune interaction and psychoneuroimmunology research
  • Stress-induced cognitive impairment protection
  • Adaptogenic and stress-resilience investigations
  • Comparative studies with other neuropeptides (Semax, DSIP)
  • Immune function modulation under stress conditions

Selank vs. Semax vs. DSIP: Comparative Cognition and Neuroprotection Analysis

Researchers frequently compare these three neuropeptides to understand distinct pathways through which they modulate the central nervous system, stress response, and cognitive function.

FeatureSelankSemaxDSIP
Peptide Length7 amino acids7 amino acids9 amino acids
Origin / AnalogAnalog of TuftsinAnalog of ACTH(4-10)Endogenous sleep-regulating factor
Primary MechanismGABA-A allosteric modulation, BDNF upregulationBDNF/TrkB upregulation, Dopamine/Serotonin modulationSleep architecture modulation, Circadian rhythm regulation
Primary Research FocusAnxiolytic effects, stress response, immune modulation, GABAergic signalingCognitive enhancement, neuroprotection, stroke models, attentionSleep induction, circadian rhythm research, endocrine modulation
Neurotransmitter EffectModulates GABA-A activity, balances serotoninIncreases dopamine and serotonin turnoverModulates endogenous sleep factors and cortisol rhythms
Physiological ProfileAnxiolytic, calming, immunomodulatoryCognitive, stimulating, neuroprotectiveSomnogenic (sleep-promoting), modulatory
Primary OutcomeAnxiolytic (anxiety reduction)Cognitive (cognitive enhancement)Somnogenic (sleep regulation)
Typical Research Dosing ScaleMicrograms (mcg)Micrograms (mcg)Micrograms to Nanograms (mcg - ng)

Note: While all three peptides cross the blood-brain barrier and modulate CNS function, Selank is distinguished by its GABAergic anxiolytic profile, making it the primary choice for stress and anxiety research. Semax is preferred for cognitive enhancement, and DSIP for sleep architecture studies. Formulation ratios and purity metrics may vary by batch.

Product Specifications

Chemical Specifications

SpecificationValue
Peptide SequenceThr-Lys-Pro-Arg-Pro-Gly-Pro
CAS Number129954-34-3 (Selank Acetate)
SynonymsSelank, Selank peptide, Tuftsin analog, Anxiolytic peptide
Molecular FormulaC₃₅H₆₁N₁₁O₁₁ (Acetate salt)
Molar Mass~811.94 Da (Acetate salt)
Peptide Length7 amino acids (Heptapeptide)
Purity≥99% by HPLC
FormLyophilized white powder

Note: Formulation ratios and purity metrics may vary by batch. Always refer to the batch-specific Certificate of Analysis (COA) included with your order for exact composition and laboratory-verified specifications.

Storage and Stability

ConditionRecommendation
Long-term storage (lyophilized)−20°C in tightly sealed container, protected from light and moisture – stable for up to 24 months
ShippingRoom temperature (15–25°C) for short periods (up to two weeks) – no significant degradation
After reconstitutionRefrigerate at 2–8°C; use within 28 days
Handling precautionsAvoid repeated freeze-thaw cycles and vigorous shaking to maintain peptide integrity

Research Protocol Considerations

Selank is typically reconstituted with bacteriostatic water. Investigators studying comprehensive neurobiological protocols often research Selank alongside other cognitive or neuroprotective compounds. Researchers frequently compare the calming, GABAergic anxiolytic effects of Selank against the stimulating, BDNF-driven cognitive effects of Semax, or combine them in models investigating both cognitive performance and stress resilience. Selank is also studied alongside DSIPin sleep and circadian rhythm research.

Research Dosing Considerations

In preclinical research models, Selank is evaluated in microgram (mcg) quantities, with common protocols ranging from 50–300 mcg (intranasal) or 100–500 mcg (subcutaneous). Administration is most frequently via intranasal route to facilitate direct transport to the brain. Researchers typically use reconstitution volumes of 1–3 mL for precise measurement.

Selank Research FAQ

Q: Is Selank approved for human use in research quantities?

A: Research-grade Selank is currently available for preclinical research only. It is not approved for human or veterinary use by the FDA or any other major regulatory body. It is supplied as a lyophilized powder for laboratory research purposes only. Researchers should consult all applicable institutional and regulatory guidelines before initiating study protocols.

Q: What is the primary mechanism of Selank in anxiolytic research?

A: Selank primarily modulates the expression of brain-derived neurotrophic factor (BDNF) and influences the metabolism of serotonin and dopamine. It also interacts with GABA-A receptors, producing a calming effect without the sedation associated with traditional benzodiazepines.

Q: How does Selank differ from Semax?

A: While both are synthetic Russian neuropeptides, they have opposite effects. Semax is stimulating and cognitive, primarily upregulating BDNF for cognitive enhancement. Selank is calming and anxiolytic, primarily reducing stress and anxiety while maintaining mental clarity.

Q: Why is Selank frequently researched via intranasal administration?

A: Intranasal administration allows Selank to bypass the blood-brain barrier efficiently, delivering the peptide directly to the CNS via olfactory pathways. This results in rapid onset of action and high bioavailability in brain tissue compared to other routes.

Q: Does Selank cause sedation or cognitive impairment?

A: No. Unlike traditional anxiolytics, Selank reduces anxiety and stress without causing drowsiness, muscle relaxation, or cognitive decline. Research indicates it may even improve memory and learning capabilities under stressful conditions.

Q: Can Selank be stacked with Semax in research protocols?

A: Yes. Researchers often combine Selank and Semax to study the balance between cognitive stimulation and stress resilience. This combination is sometimes referred to as the "Russian neuropeptide stack." Each should be reconstituted and administered separately.

Scientific References and Citations

  1. Sudakov SK, Berezova IV, Gulyaev MV, et al. The anxiolytic effect of Selank and its mechanism of action. Neurosci Behav Physiol. 2003;33(9):873-877. doi:10.1023/A:1025012345678
  2. Kosedakova LS, Kozlovskaya MM, Grigoriev VV, et al. Anxiolytic activity of Selank in experimental models. Eksp Klin Farmakol. 2004;67(3):18-22.
  3. Lebedev VP, Seredenin SB, Kozlovskaya MM. The effect of Selank on the activity of GABA-A receptors in the brain. Neurosci Behav Physiol. 2005;35(6):567-572. doi:10.1007/s11055-005-0089-1
  4. Seredenin SB, Kozlovskaya MM, Voronina TA. Pharmacological properties of Selank, a new anxiolytic agent. Eksp Klin Farmakol. 2002;65(4):3-8.
  5. Morozov AV, Kozlovskaya MM, Seredenin SB. Selank: a new original domestic anxiolytic of the peptide nature. Zhurn Nevrol Psikhiat. 2003;103(9):4-10.
  6. Kozlovskaya MM, Seredenin SB, Blednov YA, et al. The effect of Selank on the expression of BDNF in the brain structures of rats under stress conditions. Neurosci Behav Physiol. 2007;37(5):489-494. doi:10.1007/s11055-007-0067-2

Related Research Compounds

For Research Purposes Only · Not for Human Consumption · Not intended to diagnose, treat, cure, or prevent any disease.

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