Cognitive

NA-Semax Amidate

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

Clinical Trials
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Key Facts: NA-Semax Amidate

Category
Cognitive
FDA Status
Not FDA Approved
Clinical Status
Not approved in the US or EU. Parent compound Semax is a registered medicine in Russia. The amidate variant is sold as a research chemical. Parent compound is FDA Category 2, pending reclassification review.
Administration
Intranasal is the standard and best-supported route, since it was developed as a nasal formulation
Typical Dose
300-600 mcg daily (intranasal)
Frequency
Once or twice daily, morning and early afternoon
Duration
Community protocols commonly report 2-4 week blocks
Also Known As
N-Acetyl Semax Amidate, NA-Semax, Semax Amidate

Mechanism of Action

Semax is a synthetic analog of ACTH (4-10), a fragment of adrenocorticotropic hormone that has been stripped of hormonal activity while retaining effects on the brain. Its best-characterized action is a marked increase in BDNF and NGF expression in the hippocampus, which is the mechanistic basis for the memory and neuroprotection claims. It also modulates dopaminergic and serotonergic transmission, and affects the melanocortin system, which is thought to contribute to its effects on attention and motivation. Notably it does this without the HPA axis activation you would expect from something derived from ACTH, because the fragment lacks the region responsible for that. The acetylation and amidation slow degradation by peptidases, so more of the dose survives to act.

Research Summary

Semax has a genuine and reasonably large research base, concentrated in Russia, where it is a registered medicine used for ischemic stroke, cognitive impairment and optic nerve disorders. Animal work consistently supports the BDNF and NGF upregulation, and there is human clinical work in stroke recovery. The important caveat is the same as for Selank: this literature is largely Russian, much of it predates modern trial standards, replication in large Western randomized trials has not happened, and neither the FDA nor the EMA has assessed it. For the amidate variant specifically there is no independent published pharmacology comparing it to standard Semax in humans. The stability modification is chemically sound and widely used, and the assumption that it improves real-world effect is reasonable but unproven.

Trial Progress:Preclinical
Pre
I
II
III
IV
FDA

Dosing Information

Human Trials·Parent compound Semax has Russian clinical data including stroke trials. This variant does not.

Typical Dosing

Community experience

Common Dose

300-600 mcg daily (intranasal)

Range

300-600 mcg daily (community reported)

Frequency

Once or twice daily, morning and early afternoon

The clinical evidence belongs to Semax, not to this variant. Disturbed sleep is the most consistently reported downside in user accounts, and those accounts associate it with evening dosing.

Research Dosing

Scientific studies

Community-reported, informed by Semax clinical use

Duration

Community protocols commonly report 2-4 week blocks

Administration

Intranasal is the standard and best-supported route, since it was developed as a nasal formulation

Timing & Administration

Best Time to Take

Morning, or morning and early afternoon if split

Once or twice daily, not in the evening

Food Recommendation

With or without food

Why This Timing?

Overstimulation and disrupted sleep with evening dosing is the single most consistent complaint in user reports.

Possible Side Effects

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

  • Headache, the most commonly reported effect
  • Irritability or overstimulation, particularly with late dosing
  • Nasal irritation with intranasal use
  • Disturbed sleep if dosed in the evening
  • Flat mood reported after stopping in some accounts
  • No characterized long-term safety data for the amidate variant

References

Research This Peptide Further

Frequently Asked Questions

What does NA-Semax Amidate do?

NA-Semax Amidate is the stabilized form of Semax, the Russian nootropic peptide derived from a fragment of ACTH. Same modification logic as the Selank variant: acetyl group at one end, amide at the other, both there to stop enzymes chewing it up before it does anything. It is the most widely used Semax variant in Western nootropic circles, largely on the strength of that stability argument.

How does NA-Semax Amidate work?

Semax is a synthetic analog of ACTH (4-10), a fragment of adrenocorticotropic hormone that has been stripped of hormonal activity while retaining effects on the brain. Its best-characterized action is a marked increase in BDNF and NGF expression in the hippocampus, which is the mechanistic basis for the memory and neuroprotection claims. It also modulates dopaminergic and serotonergic transmission, and affects the melanocortin system, which is thought to contribute to its effects on attention and motivation. Notably it does this without the HPA axis activation you would expect from something derived from ACTH, because the fragment lacks the region responsible for that. The acetylation and amidation slow degradation by peptidases, so more of the dose survives to act.

Is NA-Semax Amidate FDA approved?

No, NA-Semax Amidate is not currently FDA approved. Current status: Not approved in the US or EU. Parent compound Semax is a registered medicine in Russia. 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-Semax Amidate?

Reported side effects include: Headache, the most commonly reported effect, Irritability or overstimulation, particularly with late dosing, Nasal irritation with intranasal use, Disturbed sleep if dosed in the evening, Flat mood reported after stopping in some accounts. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of NA-Semax Amidate?

Community-reported common dose: 300-600 mcg daily (intranasal) (Once or twice daily, morning and early afternoon). Range: 300-600 mcg daily (community reported). Administration: Intranasal is the standard and best-supported route, since it was developed as a nasal formulation. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with NA-Semax 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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