NA-Semax Amidate
Also known as: N-Acetyl Semax Amidate, NA-Semax, Semax Amidate
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
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.
Dosing Information
Typical Dosingⓘ
Community experience
300-600 mcg daily (intranasal)
300-600 mcg daily (community reported)
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
Doses from Studies
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
- https://pubmed.ncbi.nlm.nih.gov/?term=Semax+ACTH+4-10+BDNF+hippocampus
- https://pubmed.ncbi.nlm.nih.gov/?term=Semax+ischemic+stroke+clinical
- https://pubmed.ncbi.nlm.nih.gov/?term=Semax+neuroprotection+nerve+growth+factor
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 TrialsSelank 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.
CognitiveSemax
Clinical TrialsSemax 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.
CognitiveCerebrolysin
Clinical TrialsCerebrolysin 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.
CognitiveDihexa
PreclinicalDihexa (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.
CognitiveP21
PreclinicalP21 (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.
CognitiveGB-115
Clinical TrialsGB-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.
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