NA-Selank-Amidate
Nootropic- Molecular Formula
- C37H61N11O10
- Molar Mass
- 807.95 g/mol
- CAS Number
- N/A
- Purity Standard
- 99%+ (HPLC Verified)
- Amino Acid Sequence
- Ac-Thr-Lys-Pro-Arg-Pro-Gly-Pro-NH2 (N-acetyl, C-terminal amide modification of Selank)
Overview
NA-Selank-Amidate is a stability-enhanced variant of the anxiolytic-nootropic peptide Selank, featuring both N-terminal acetylation and C-terminal amidation modifications. These dual modifications protect against exopeptidase degradation, potentially resulting in extended duration of action and improved bioavailability.
The parent compound Selank is a tuftsin-derived heptapeptide with well-documented anxiolytic and cognitive-enhancing properties. It modulates GABA signaling to produce benzodiazepine-like anxiety reduction without sedation or dependence, while simultaneously enhancing memory and attention through separate neurotrophic mechanisms.
By increasing metabolic stability, NA-Selank-Amidate may achieve more sustained anxiolytic and cognitive effects, particularly relevant for applications requiring extended duration of action. The modifications are positioned to protect the most vulnerable sites for enzymatic attack while preserving the core sequence responsible for biological activity.
This modified form is of particular interest for research into stress resilience, where prolonged anxiolytic support combined with cognitive enhancement may provide comprehensive benefits. The combination of Selank's unique dual mechanism (anxiolytic plus nootropic) with enhanced stability creates a valuable research tool for psychoneuroimmunology and cognitive neuroscience applications.
Synthesis Overview
NA-Selank-Amidate is synthesized via Fmoc solid-phase peptide synthesis on amide-generating resin. The heptapeptide sequence is assembled with standard coupling protocols, followed by on-resin N-terminal acetylation using acetic anhydride. TFA cleavage with appropriate scavengers yields the doubly-modified peptide containing both the N-acetyl group and C-terminal amide. Purification via preparative HPLC separates the product from incompletely modified species. Characterization includes mass spectrometry to confirm both terminal modifications and HPLC purity analysis.
Research Applications
- Enhanced anxiolytic duration and efficacy research
- GABA system modulation with improved stability studies
- Cognitive enhancement with anxiolytic combination research
- Intranasal peptide stability and CNS delivery optimization
- Immunomodulatory activity with tuftsin-derived core investigation
- Stress resilience and adaptogenic mechanism studies
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