N-Acetyl Semax Amidate – Spray
From €34.80
N-Acetyl Semax Amidate is a double-modified synthetic derivative of Semax (ACTH 4-10). Featuring both N-terminal acetylation and C-terminal amidation, this peptide exhibits superior metabolic stability against enzymatic breakdown, optimized lipophilicity, and enhanced blood-brain barrier permeability compared to standard Semax. Highly valued in research for investigating neuroprotective mechanisms, BDNF upregulation, and synaptic plasticity. Fully batch-tested via HPLC/MS.
For a more detailed description and lab analysis, please see the sections below.
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N-Acetyl Semax Amidate, Spray
1. Overview & Origins
N-Acetyl Semax Acetate is a synthetic peptide — a short chain of amino acids (the building blocks of proteins) — engineered as a further-stabilized, doubly-modified version of a compound called Semax.
Semax itself was developed in Russia in the 1980s by the Institute of Molecular Genetics, in collaboration with the Russian Academy of Medical Sciences. It’s derived from a fragment of ACTH (adrenocorticotropic hormone), specifically the piece known as ACTH(4-7), fused with a short additional tripeptide tail (Pro-Gly-Pro). ACTH is a hormone your body naturally makes to regulate the stress response — but the fragment used in Semax has been stripped of ACTH’s hormonal (cortisol-stimulating) activity. What’s left is a small peptide fragment that appears to act primarily on the brain rather than the endocrine (hormone) system.
💡 Analogy: Think of ACTH as a long sentence, and Semax as just one meaningful phrase clipped out of it — a phrase that happens to talk to your neurons, not your adrenal glands.
N-Acetyl Semax Amidate is a chemically modified version of this original molecule, carrying two separate protective modifications designed to address Semax’s biggest practical weakness: how quickly it breaks down in the body.
2. Structural Upgrades (The “Why”)
The “Straw” Analogy: To understand why this modified version exists, picture a peptide as a paper drinking straw. It works, but the open ends get soggy and fall apart quickly once exposed to liquid (in this case, your body’s enzymes). Chemists can “cap” each end of the straw with a small protective seal to slow down that breakdown. That’s essentially what’s happening here — and N-Acetyl Semax Amidate is the version with both ends capped.
N-terminal acetylation (the “N-Acetyl” part of the name) means a small chemical group called an acetyl group is attached to one end of the peptide (the “N-terminus,” or amino end). This acts like a plastic cap on that end of the straw — it makes the peptide more resistant to certain enzymes in the blood and gut that would otherwise chew through it starting from that end.
C-terminal amidation (the “Amidate” part) does something similar to the other end of the peptide (the “C-terminus”). Instead of leaving that end as an exposed, chemically “raw” carboxylic acid group — which is a magnet for degrading enzymes — an amide group is attached instead. This is like sealing the second end of the straw. Amidation is actually something the body does naturally to many of its own signaling peptides (like oxytocin and vasopressin) because it tends to improve stability and, in some cases, receptor binding.
Why does stability matter so much for a brain-targeting molecule? To have any effect on brain tissue, a peptide first has to survive long enough to reach the brain, and then get across the blood-brain barrier (BBB) — a tightly regulated cellular checkpoint that keeps most large or foreign molecules out of brain tissue. A peptide that’s degraded in seconds never gets a real chance to cross that barrier in meaningful amounts. Capping both ends is thought to extend the peptide’s functional half-life further than capping just one, giving it the best theoretical shot among the Semax variants of reaching its target intact.
Quick Comparison
| Version | Modification | Practical Implication |
|---|---|---|
| Standard Semax | Unmodified peptide | Well-studied (particularly in Russian clinical literature), but breaks down quickly once in solution or in the body |
| N-Acetyl Semax | Acetyl cap on N-terminus only | Improved resistance to enzymatic breakdown from one end |
| N-Acetyl Semax Amidate | Acetyl cap (N-terminus) + amide cap (C-terminus) | Both ends protected; considered the most stable and bioavailable variant of the three, at least in theory and in early research |
It’s worth being honest here: most of the comparative stability and bioavailability claims for N-Acetyl Semax Amidate come from peptide chemistry principles and preliminary/anecdotal reports rather than large head-to-head human trials. The core Semax pharmacology research base is much larger than the research base specific to this doubly-modified analog.
3. Mechanism of Action (How It Works in the Brain)
N-Acetyl Semax Amidate is generally described as working through three overlapping pathways, inherited from and studied alongside its parent compound, Semax.
Neurotrophin Boost (BDNF & NGF) — “Fertilizer for Brain Connections”
BDNF (brain-derived neurotrophic factor) and NGF (nerve growth factor) are proteins your brain produces that support the growth, survival, and connectivity of neurons. If neurons are like a garden of trees and shrubs, BDNF and NGF act like fertilizer — they don’t create new soil out of nothing, but they encourage existing branches (dendrites) to grow, strengthen connections between neurons (synapses), and help neurons survive stress that might otherwise damage them.
Research on the Semax family has repeatedly linked it to increased expression of BDNF in brain regions like the hippocampus and cortex — areas heavily involved in memory and higher-order thinking. The proposed mechanism involves activation of intracellular signaling cascades (such as the MAPK/ERK pathway) that ultimately switch on genes responsible for producing these growth factors.
Neurotransmitter Balancing — Dopamine & Serotonin
Semax-derived peptides have been studied for effects on the dopaminergic (dopamine) and serotonergic (serotonin) systems — the two neurotransmitter networks most closely tied to attention, motivation, mood regulation, and reward.
Dopamine is often loosely described as your brain’s “motivation and focus” signal — it helps you sustain attention on a task and feel driven to pursue a goal. Serotonin is more associated with mood stability and emotional regulation. Some research suggests Semax-family peptides modulate the turnover (production and breakdown cycle) of these neurotransmitters, particularly in the frontal cortex, which could plausibly explain reported subjective effects on focus and mood in existing literature — though the exact receptor-level mechanisms are still not fully mapped out.
Cell Protection & Anti-Hypoxia
A separate and well-documented line of Semax research focuses on neuroprotection — the ability to shield brain cells from damage. Three overlapping protective mechanisms show up in the literature:
- Antioxidant activity: helping neutralize reactive oxygen species (unstable molecules that damage cell structures — essentially chemical “sparks” that can char cellular machinery if left unchecked).
- Anti-inflammatory effects: dampening excessive immune/inflammatory signaling in brain tissue, which can otherwise contribute to neuronal injury.
- Anti-hypoxic effects: the Semax family has been studied extensively in Russian stroke and ischemia (restricted blood flow) research for its apparent ability to help neurons tolerate low-oxygen conditions better and recover more effectively afterward.
4. Primary Reported Effects
Based on the existing (largely preclinical and Russian-sourced clinical) research literature, the most commonly reported areas of interest for N-Acetyl Semax Amidate are:
- Focus and sustained attention — often the most frequently cited subjective effect
- Executive function — planning, task-switching, and working-memory-dependent decision-making
- Working memory — short-term retention and manipulation of information
- Neuroprotection — resilience of neurons against oxidative stress, inflammation, and hypoxic (low-oxygen) conditions
- Mood stabilization — reported in some literature, generally considered secondary to the cognitive effects
⚠️ Research Context: It’s important to flag that a meaningful portion of this evidence base comes from animal studies and Russian-language clinical research on Semax generally, some of which hasn’t been replicated in large, independent, peer-reviewed Western trials, and even less of which is specific to this doubly-modified analog. Treat these as research findings and hypotheses under active investigation — not settled clinical facts.
5. Storage, Handling & Bioavailability Context
Peptides are structurally fragile compared to small-molecule drugs — think of the difference between a strand of cooked spaghetti (the peptide) and a marble (a small molecule like aspirin). Heat, moisture, light, and time all threaten peptide structural integrity. Some general, widely-cited principles for peptide research materials:
- Lyophilized (freeze-dried) powder is the most stable form. Properly stored, unreconstituted lyophilized peptide is generally far more shelf-stable than peptide that has been dissolved.
- Cold storage matters. Lyophilized powder is typically kept in a freezer (around -20°C) for long-term storage, or a standard refrigerator (2-8°C) for shorter-term storage, away from light.
- Once reconstituted (dissolved in a solvent, typically sterile or bacteriostatic water), stability drops substantially. Reconstituted peptide solution is generally stored refrigerated and used within a limited window, as enzymatic and hydrolytic (water-driven) degradation accelerates once in liquid form.
- Avoid freeze-thaw cycling of reconstituted solution — repeatedly freezing and thawing a liquid peptide solution can physically damage the peptide structure.
- Light and agitation are also degradation stressors; amber vials and gentle handling (avoiding vigorous shaking) are standard practice in peptide research.
- Route and bioavailability context: the dual capping discussed in Section 2 is specifically aimed at improving the molecule’s odds of surviving long enough — chemically and enzymatically — to exert central (brain-level) effects, which is a core focus of ongoing peptide-delivery research generally.
For detailed lab analysis and product specifications, please refer to the next tabs.
Lab analysis — Certificates of Analysis
Every batch is independently tested by HPLC/LC-MS. Purity for current lots: ≥98%. Select a lot to view the full report.
Chemical Informations
| Application | Antagonist of melanocortin receptor full agonist α-melanocyte-stimulating hormone (α-MSH) at the MC4 and MC5 receptors. |
| CAS | 80714-61-0 |
| Molar Mass | 813.9 g/mol |
| Chemical Formula | C37H51N9O10S |
| IUPAC Name | (2S)-1-[2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-4-carboxybutanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-3-phenylpropanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid |
| Synonyms | Semax, UNII-I5FAL2585H, I5FAL2585H, Met-Glu-His-Phe-Pro-Gly-Pro, ACTH (4-7), Pro-Gly-Pro-, 80714-61-0, Pro-gly-pro-acth (4-7), ACTH (4-7), prolyl-glycyl-proline- |
| Storage | Store in refrigerator at 4ºC, tightly sealed, away from heat, light and moisture |
| Solubility | Soluble in Water |
| Organoleptic Profile | Clear, colorless liquid |
| Physical Form | Liquid, solved in Deionized Water (Type II), contains Acetate, BKC for stability purposes. |
| Specification | Concentration for each variant (per vial): 20mg (2mg/mL) ±10% |
N-Acetyl Semax Amidate, Spray
1. Overview & Origins
N-Acetyl Semax Acetate is a synthetic peptide — a short chain of amino acids (the building blocks of proteins) — engineered as a further-stabilized, doubly-modified version of a compound called Semax.
Semax itself was developed in Russia in the 1980s by the Institute of Molecular Genetics, in collaboration with the Russian Academy of Medical Sciences. It’s derived from a fragment of ACTH (adrenocorticotropic hormone), specifically the piece known as ACTH(4-7), fused with a short additional tripeptide tail (Pro-Gly-Pro). ACTH is a hormone your body naturally makes to regulate the stress response — but the fragment used in Semax has been stripped of ACTH’s hormonal (cortisol-stimulating) activity. What’s left is a small peptide fragment that appears to act primarily on the brain rather than the endocrine (hormone) system.
💡 Analogy: Think of ACTH as a long sentence, and Semax as just one meaningful phrase clipped out of it — a phrase that happens to talk to your neurons, not your adrenal glands.
N-Acetyl Semax Amidate is a chemically modified version of this original molecule, carrying two separate protective modifications designed to address Semax’s biggest practical weakness: how quickly it breaks down in the body.
2. Structural Upgrades (The “Why”)
The “Straw” Analogy: To understand why this modified version exists, picture a peptide as a paper drinking straw. It works, but the open ends get soggy and fall apart quickly once exposed to liquid (in this case, your body’s enzymes). Chemists can “cap” each end of the straw with a small protective seal to slow down that breakdown. That’s essentially what’s happening here — and N-Acetyl Semax Amidate is the version with both ends capped.
N-terminal acetylation (the “N-Acetyl” part of the name) means a small chemical group called an acetyl group is attached to one end of the peptide (the “N-terminus,” or amino end). This acts like a plastic cap on that end of the straw — it makes the peptide more resistant to certain enzymes in the blood and gut that would otherwise chew through it starting from that end.
C-terminal amidation (the “Amidate” part) does something similar to the other end of the peptide (the “C-terminus”). Instead of leaving that end as an exposed, chemically “raw” carboxylic acid group — which is a magnet for degrading enzymes — an amide group is attached instead. This is like sealing the second end of the straw. Amidation is actually something the body does naturally to many of its own signaling peptides (like oxytocin and vasopressin) because it tends to improve stability and, in some cases, receptor binding.
Why does stability matter so much for a brain-targeting molecule? To have any effect on brain tissue, a peptide first has to survive long enough to reach the brain, and then get across the blood-brain barrier (BBB) — a tightly regulated cellular checkpoint that keeps most large or foreign molecules out of brain tissue. A peptide that’s degraded in seconds never gets a real chance to cross that barrier in meaningful amounts. Capping both ends is thought to extend the peptide’s functional half-life further than capping just one, giving it the best theoretical shot among the Semax variants of reaching its target intact.
Quick Comparison
| Version | Modification | Practical Implication |
|---|---|---|
| Standard Semax | Unmodified peptide | Well-studied (particularly in Russian clinical literature), but breaks down quickly once in solution or in the body |
| N-Acetyl Semax | Acetyl cap on N-terminus only | Improved resistance to enzymatic breakdown from one end |
| N-Acetyl Semax Amidate | Acetyl cap (N-terminus) + amide cap (C-terminus) | Both ends protected; considered the most stable and bioavailable variant of the three, at least in theory and in early research |
It’s worth being honest here: most of the comparative stability and bioavailability claims for N-Acetyl Semax Amidate come from peptide chemistry principles and preliminary/anecdotal reports rather than large head-to-head human trials. The core Semax pharmacology research base is much larger than the research base specific to this doubly-modified analog.
3. Mechanism of Action (How It Works in the Brain)
N-Acetyl Semax Amidate is generally described as working through three overlapping pathways, inherited from and studied alongside its parent compound, Semax.
Neurotrophin Boost (BDNF & NGF) — “Fertilizer for Brain Connections”
BDNF (brain-derived neurotrophic factor) and NGF (nerve growth factor) are proteins your brain produces that support the growth, survival, and connectivity of neurons. If neurons are like a garden of trees and shrubs, BDNF and NGF act like fertilizer — they don’t create new soil out of nothing, but they encourage existing branches (dendrites) to grow, strengthen connections between neurons (synapses), and help neurons survive stress that might otherwise damage them.
Research on the Semax family has repeatedly linked it to increased expression of BDNF in brain regions like the hippocampus and cortex — areas heavily involved in memory and higher-order thinking. The proposed mechanism involves activation of intracellular signaling cascades (such as the MAPK/ERK pathway) that ultimately switch on genes responsible for producing these growth factors.
Neurotransmitter Balancing — Dopamine & Serotonin
Semax-derived peptides have been studied for effects on the dopaminergic (dopamine) and serotonergic (serotonin) systems — the two neurotransmitter networks most closely tied to attention, motivation, mood regulation, and reward.
Dopamine is often loosely described as your brain’s “motivation and focus” signal — it helps you sustain attention on a task and feel driven to pursue a goal. Serotonin is more associated with mood stability and emotional regulation. Some research suggests Semax-family peptides modulate the turnover (production and breakdown cycle) of these neurotransmitters, particularly in the frontal cortex, which could plausibly explain reported subjective effects on focus and mood in existing literature — though the exact receptor-level mechanisms are still not fully mapped out.
Cell Protection & Anti-Hypoxia
A separate and well-documented line of Semax research focuses on neuroprotection — the ability to shield brain cells from damage. Three overlapping protective mechanisms show up in the literature:
- Antioxidant activity: helping neutralize reactive oxygen species (unstable molecules that damage cell structures — essentially chemical “sparks” that can char cellular machinery if left unchecked).
- Anti-inflammatory effects: dampening excessive immune/inflammatory signaling in brain tissue, which can otherwise contribute to neuronal injury.
- Anti-hypoxic effects: the Semax family has been studied extensively in Russian stroke and ischemia (restricted blood flow) research for its apparent ability to help neurons tolerate low-oxygen conditions better and recover more effectively afterward.
4. Primary Reported Effects
Based on the existing (largely preclinical and Russian-sourced clinical) research literature, the most commonly reported areas of interest for N-Acetyl Semax Amidate are:
- Focus and sustained attention — often the most frequently cited subjective effect
- Executive function — planning, task-switching, and working-memory-dependent decision-making
- Working memory — short-term retention and manipulation of information
- Neuroprotection — resilience of neurons against oxidative stress, inflammation, and hypoxic (low-oxygen) conditions
- Mood stabilization — reported in some literature, generally considered secondary to the cognitive effects
⚠️ Research Context: It’s important to flag that a meaningful portion of this evidence base comes from animal studies and Russian-language clinical research on Semax generally, some of which hasn’t been replicated in large, independent, peer-reviewed Western trials, and even less of which is specific to this doubly-modified analog. Treat these as research findings and hypotheses under active investigation — not settled clinical facts.
5. Storage, Handling & Bioavailability Context
Peptides are structurally fragile compared to small-molecule drugs — think of the difference between a strand of cooked spaghetti (the peptide) and a marble (a small molecule like aspirin). Heat, moisture, light, and time all threaten peptide structural integrity. Some general, widely-cited principles for peptide research materials:
- Lyophilized (freeze-dried) powder is the most stable form. Properly stored, unreconstituted lyophilized peptide is generally far more shelf-stable than peptide that has been dissolved.
- Cold storage matters. Lyophilized powder is typically kept in a freezer (around -20°C) for long-term storage, or a standard refrigerator (2-8°C) for shorter-term storage, away from light.
- Once reconstituted (dissolved in a solvent, typically sterile or bacteriostatic water), stability drops substantially. Reconstituted peptide solution is generally stored refrigerated and used within a limited window, as enzymatic and hydrolytic (water-driven) degradation accelerates once in liquid form.
- Avoid freeze-thaw cycling of reconstituted solution — repeatedly freezing and thawing a liquid peptide solution can physically damage the peptide structure.
- Light and agitation are also degradation stressors; amber vials and gentle handling (avoiding vigorous shaking) are standard practice in peptide research.
- Route and bioavailability context: the dual capping discussed in Section 2 is specifically aimed at improving the molecule’s odds of surviving long enough — chemically and enzymatically — to exert central (brain-level) effects, which is a core focus of ongoing peptide-delivery research generally.
For detailed lab analysis and product specifications, please refer to the next tabs.
Lab analysis — Certificates of Analysis
Every batch is independently tested by HPLC/LC-MS. Purity for current lots: ≥98%. Select a lot to view the full report.
Chemical Informations
| Application | Antagonist of melanocortin receptor full agonist α-melanocyte-stimulating hormone (α-MSH) at the MC4 and MC5 receptors. |
| CAS | 80714-61-0 |
| Molar Mass | 813.9 g/mol |
| Chemical Formula | C37H51N9O10S |
| IUPAC Name | (2S)-1-[2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-4-carboxybutanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-3-phenylpropanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid |
| Synonyms | Semax, UNII-I5FAL2585H, I5FAL2585H, Met-Glu-His-Phe-Pro-Gly-Pro, ACTH (4-7), Pro-Gly-Pro-, 80714-61-0, Pro-gly-pro-acth (4-7), ACTH (4-7), prolyl-glycyl-proline- |
| Storage | Store in refrigerator at 4ºC, tightly sealed, away from heat, light and moisture |
| Solubility | Soluble in Water |
| Organoleptic Profile | Clear, colorless liquid |
| Physical Form | Liquid, solved in Deionized Water (Type II), contains Acetate, BKC for stability purposes. |
| Specification | Concentration for each variant (per vial): 20mg (2mg/mL) ±10% |
