NA-Selank Amidate
An enhanced Selank derivative — N-terminal acetylation and C-terminal amidation improve protease resistance and nasal absorption, extending the anxiolytic and nootropic profile.
A chemically modified version of Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro) with N-acetyl and C-amide terminal modifications conferring greater enzymatic stability and enhanced CNS penetration via intranasal delivery.
Mechanism of action
Same as Selank: modulates GABA-A receptor allosteric sites, increases BDNF expression, and influences IL-6 and enkephalin metabolism. The N-acetyl modification blocks aminopeptidase degradation; the C-amide blocks carboxypeptidase attack. Net result is longer residence time at target receptors and improved intranasal-to-CNS delivery.
Primary uses
- Anxiolytic nootropic (research/community use)
- Enhanced Selank analog research
- BDNF modulation studies
Typical dosing
Community-reported dosing. No clinical trials for this specific derivative.
Regulatory status
Not approved by any regulatory body. Available through research peptide vendors. Parent compound Selank is approved in Russia.
References
- [pubmed] Derived from Selank literature. No independent publications on the acetylated/amidated form.
Related peptides
This entry is for educational purposes only and does not constitute medical advice. Dosing information reflects published regulatory or research data and is not a recommendation. Many compounds described here are not approved for human use in the United States. Consult a licensed medical professional before considering any peptide therapy.