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Product Overview

Selank

Selank is a synthetic heptapeptide nootropic and anxiolytic that reduces anxiety, improves mood, and supports cognition without the sedation, memory impairment, or dependence risks typical of benzodiazepines.[1–3]

Mechanism of Action

  • GABAA positive allosteric modulator: Subtype-selective, concentration-dependent modulation of GABAergic neurotransmission; distinct from but partially overlapping benzodiazepines. Supported by radioligand binding and cortical gene-expression studies.[1–3]
  • Network effects: Context-dependent interaction with other GABAergic agents (e.g., diazepam, olanzapine); possible ancillary influence on serotonergic pathways implicated in mood and anxiety.[1,3–6]

Efficacy & Cognition

  • Anxiolytic efficacy comparable to classical benzodiazepines without sedation or cognitive impairment; anti-amnesic properties reported.[1–3][8]
  • Improvements in memory, focus, and learning via modulation of neurotransmitter and neuropeptide signaling.[1–3][7]

Immunomodulatory Profile

  • Modulates inflammation/immune-response genes (e.g., downregulates complement C3; affects cytokine-related genes), suggesting support of immune homeostasis and reduced inflammation.[9]

Dosing & Safety (Research)

  • Typical ranges: 0.15–0.3 mg per administration intranasally or subcutaneously; 10 mg reflects a higher research dose—long-term safety at this dose not fully established in literature.[1–3]
  • Generally well tolerated in preclinical/clinical settings; no dependence, withdrawal, or benzodiazepine-like cognitive adverse effects observed.[1–3]

References

  1. Vyunova TV, Andreeva L, Shevchenko K, Myasoedov N. Protein Pept Lett. 2018;25(10):914-923.
  2. Volkova A, Shadrina M, Kolomin T, et al. Front Pharmacol. 2016;7:31.
  3. Filatova E, Kasian A, Kolomin T, et al. Front Pharmacol. 2017;8:89.
  4. Santarelli L, Gobbi G, Debs PC, et al. PNAS. 2001;98(4):1912-1917.
  5. Lin EJ. Curr Pharm Des. 2012;18(35):5709-5727.
  6. Kormos V, Gaszner B. Neuropeptides. 2013;47(6):401-419.
  7. Khan H, Khattak S, Mubarak MS, et al. CNS Neurol Disord Drug Targets. 2018;17(1):9-13.
  8. Wilhelm EA, Torres MLCP, Pereira CF, et al. Can J Physiol Pharmacol. 2020;98(5):304-313.
  9. Kolomin T, Morozova M, Volkova A, et al. Mol Immunol. 2014;58(1):50-55.

All information provided is for research purposes only.

ALL ARTICLES AND PRODUCT INFORMATION PROVIDED ON THIS WEBSITE ARE FOR INFORMATIONAL AND EDUCATIONAL PURPOSES ONLY. The products offered on this website are furnished for in-vitro studies only. In-vitro studies (Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.