Cognitive

NA-Selank Amidate

Also known as: N-Acetyl Selank Amidate, NA-Selank, Selank Amidate

Clinical Trials
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Key Facts: NA-Selank Amidate

Category
Cognitive
FDA Status
Not FDA Approved
Clinical Status
Not approved in the US or EU. Parent compound Selank is a registered medicine in Russia for anxiety disorders. The amidate variant is sold as a research chemical. Parent compound is FDA Category 2, pending reclassification review.
Administration
Intranasal is the standard route. Subcutaneous is reported but less common.
Typical Dose
250-500 mcg daily (intranasal)
Frequency
Once or twice daily
Duration
Community protocols commonly report 2-4 weeks, though Selank's clinical use does not indicate a dependence risk requiring cycling
Also Known As
N-Acetyl Selank Amidate, NA-Selank, Selank Amidate

Mechanism of Action

Selank is a synthetic analog of tuftsin, a naturally occurring immunomodulatory peptide fragment. Its reported mechanism has two strands. The first is modulation of GABAergic signalling, which is the basis of its anxiolytic reputation, achieved without the sedation, tolerance or dependence associated with benzodiazepines. The second is an effect on the balance of monoamines and on BDNF expression, which is where the cognitive and mood claims come from. It also retains some of tuftsin's immunomodulatory activity, including effects on interleukin expression. The N-acetylation and C-terminal amidation in this version block the exopeptidases that would otherwise clip the peptide quickly, extending how long it survives after administration. That is a pharmacokinetic change, not a new mechanism.

Research Summary

Selank itself has a real research base, almost all of it Russian, including clinical work in generalised anxiety disorder where it performed comparably to benzodiazepines without the sedation and withdrawal profile, plus animal work supporting the BDNF and monoamine effects. That literature is genuine but it is largely published in Russian journals, has not been replicated in large Western trials, and has not been through FDA or EMA assessment. The amidate variant specifically has essentially no independent published pharmacology. The stability argument is chemically sound and is the same modification used across many research peptides, but nobody has published a human comparison showing it outperforms standard Selank at equivalent doses. Treat the parent compound's evidence as real but geographically narrow, and the variant's advantage as plausible rather than demonstrated.

Trial Progress:Preclinical
Pre
I
II
III
IV
FDA

Dosing Information

Human Trials·Parent compound Selank has Russian clinical trial data. This specific variant does not.

Typical Dosing

Community experience

Common Dose

250-500 mcg daily (intranasal)

Range

250-500 mcg daily (community reported)

Frequency

Once or twice daily

The evidence you are relying on belongs to Selank, not to the amidate variant. The stability modification is chemically real, but no published human comparison shows it works better at the same dose.

Research Dosing

Scientific studies

Community-reported, informed by Selank clinical dosing

Duration

Community protocols commonly report 2-4 weeks, though Selank's clinical use does not indicate a dependence risk requiring cycling

Administration

Intranasal is the standard route. Subcutaneous is reported but less common.

Timing & Administration

Best Time to Take

Morning or split across the day

Once or twice daily

Food Recommendation

With or without food

Why This Timing?

Selank is anxiolytic without being sedating, so it does not need to be avoided in the daytime and is commonly split to keep the effect level.

Possible Side Effects

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • Generally reported as well tolerated
  • Nasal irritation or dryness with intranasal use
  • Mild fatigue or flat affect at higher doses
  • Headache
  • No dependence or withdrawal syndrome reported, unlike benzodiazepines
  • Long-term safety data for the amidate variant does not exist

References

Research This Peptide Further

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Frequently Asked Questions

What does NA-Selank Amidate do?

NA-Selank Amidate is a chemically stabilized version of Selank, a Russian anxiolytic peptide derived from the immune fragment tuftsin. The acetyl group on one end and the amide on the other are there to slow enzymatic breakdown, which is a real and sensible modification. What has not been established is whether that translates into a meaningfully better result than plain Selank in humans.

How does NA-Selank Amidate work?

Selank is a synthetic analog of tuftsin, a naturally occurring immunomodulatory peptide fragment. Its reported mechanism has two strands. The first is modulation of GABAergic signalling, which is the basis of its anxiolytic reputation, achieved without the sedation, tolerance or dependence associated with benzodiazepines. The second is an effect on the balance of monoamines and on BDNF expression, which is where the cognitive and mood claims come from. It also retains some of tuftsin's immunomodulatory activity, including effects on interleukin expression. The N-acetylation and C-terminal amidation in this version block the exopeptidases that would otherwise clip the peptide quickly, extending how long it survives after administration. That is a pharmacokinetic change, not a new mechanism.

Is NA-Selank Amidate FDA approved?

No, NA-Selank Amidate is not currently FDA approved. Current status: Not approved in the US or EU. Parent compound Selank is a registered medicine in Russia for anxiety disorders. The amidate variant is sold as a research chemical. Parent compound is FDA Category 2, pending reclassification review.

What are the side effects of NA-Selank Amidate?

Reported side effects include: Generally reported as well tolerated, Nasal irritation or dryness with intranasal use, Mild fatigue or flat affect at higher doses, Headache, No dependence or withdrawal syndrome reported, unlike benzodiazepines. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of NA-Selank Amidate?

Community-reported common dose: 250-500 mcg daily (intranasal) (Once or twice daily). Range: 250-500 mcg daily (community reported). Administration: Intranasal is the standard route. Subcutaneous is reported but less common.. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with NA-Selank Amidate or used in similar applications.

Selank

Clinical Trials

Selank is a synthetic seven-amino-acid peptide (Thr-Lys-Pro-Arg-Pro-Gly-Pro) built from the natural immune peptide tuftsin, with a small chemical tweak to make it last longer in the body. It was developed in Russia as an anti-anxiety and nootropic agent and is approved there for generalized anxiety disorder, but it has no FDA or EMA approval and almost no Western clinical data. The pitch is calm and focus without the sedation, dependence, or withdrawal that come with benzodiazepines.

Cognitive

Semax

Clinical Trials

Semax is a synthetic heptapeptide (Met-Glu-His-Phe-Pro-Gly-Pro) developed in Russia in the 1980s as an analog of the ACTH(4-10) fragment, with a Pro-Gly-Pro tail added to resist breakdown. It is researched and used as a neuroprotective and nootropic agent, typically intranasally, and keeps the cognitive and neurotrophic effects of the ACTH fragment without the parent hormone's cortisol-raising activity. It is used clinically and registered in Russia (including for ischemic stroke and cognitive disorders) but is not approved by the FDA or EMA, and Western evidence is limited.

Cognitive

Cerebrolysin

Clinical Trials

Cerebrolysin is not a single peptide but a mixture: a preparation of small peptides and free amino acids made by enzymatically breaking down purified porcine (pig) brain protein, manufactured by EVER Neuro Pharma in Austria. It is given by injection and is approved as a prescription drug in dozens of countries for stroke, traumatic brain injury, and dementia, but it is not FDA-approved in the United States. Despite decades of use abroad, the human evidence remains genuinely contested.

Cognitive

Dihexa

Preclinical

Dihexa (N-hexanoic-Tyr-Ile-(6) aminohexanoic amide) is a small synthetic peptide built from angiotensin IV, engineered at Washington State University to be orally active and to cross into the brain. The pitch is bold: it is studied as a procognitive compound that may rebuild synaptic connections, and lab claims of extreme potency made it a darling of the nootropic underground. The reality check: every supporting study is in cells or rodents, there are zero human clinical trials, and a foundational 2012 biochemistry paper describing its target was later retracted.

Cognitive

P21

Preclinical

P21 (also written P021) is a small synthetic peptide reverse-engineered from the most active region of ciliary neurotrophic factor (CNTF), with an adamantane group bolted on to help it survive in the body and reach the brain. It is studied as a neurogenic and neurotrophic compound for Alzheimer's disease and other memory disorders, with the appeal of getting CNTF-like benefits in a small, orally available molecule. The honest status: it looks genuinely promising in mouse models, but the entire evidence base comes from a single research group and there are no human trials.

Cognitive

GB-115

Clinical Trials

GB-115 is a synthetic dipeptide anxiolytic developed in Russia, chemically the amide of N-phenylhexanoyl-glycyl-L-tryptophan and described as a retro-analogue of cholecystokinin-4. Rather than acting like a benzodiazepine, it blocks cholecystokinin receptors, a different anti-anxiety route. It has been studied in animals and in a small pilot human study, but it is not an approved or widely available medication.

Cognitive

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