N-Acetyl Semax Amidate
Price range: $101.56 through $312.76
Earn 87 – 313 points upon purchasing this product.
✅ 99% Purity – Third-Party Tested
🚚 Free U.S. Shipping on Orders $100+
🇺🇸 Proudly Made in the USA
⚡ Fast & Reliable Shipping
🔒 Secure Checkout Guaranteed
Enjoy 24/7 customer support, 1st & 3rd party verified 99% purity, and free shipping on orders over $100!
Full disclaimer ↓
≥99% Purity — HPLC Verified
Dual COA — HPLC + LAL Endotoxin
Unique Lot Numbers — Full Traceability
USA Manufactured & Third-Party Tested
Ships USA in 1 Business Day
QC: 2025-09-14
≥99.2% HPLC
Buy Semax —
≥99% Purity + Dual COA
When you buy Semax from PureRawz, every vial arrives with two independent Certificates of Analysis — HPLC purity verification and an LAL endotoxin assay — traceable to a unique batch lot number. USA-manufactured, third-party tested, ships in 1 business day. No prescription required.
LAL Endotoxin Tested
Unique Lot Number
USA Manufactured
Ships in 1 Business Day
per vial · free shipping $[THRESHOLD]+
In-stock orders ship same business day — USA domestic only
Full Product Specifications
All data is verifiable via the lot-specific COA documents included with every order.
| Compound Name | Semax (ACTH 4-7 PGP) |
| Synonyms | ACTH(4-10)PGP, Pro-Gly-Pro-ACTH, HY-P1146 |
| Amino Acid Sequence | Met-Glu-His-Phe-Pro-Gly-Pro |
| Molecular Formula | C₃₇H₅₁N₉O₁₀S |
| Molecular Weight | 813.92 g/mol |
| CAS Number | 80714-61-0 |
| Purity (HPLC) | ≥99% — third-party verified per lot |
| Endotoxin (LAL) | Tested — COA included per lot |
| Physical Form | Lyophilised (freeze-dried) white powder |
| Solubility | Sterile water, PBS, or dilute acetic acid (0.1–1%) |
| Storage — Lyophilised | −20 °C, desiccated, protected from light |
| Storage — Reconstituted | 2–8 °C short-term (≤7 d); −20 °C long-term |
| Stability | 12–24 months lyophilised at −20 °C |
| Lot Traceability | Unique lot number — every vial, every batch |
| Manufacturing | USA (domestic synthesis and lyophilisation) |
| Testing | Independent third-party laboratory |
| Shipping | 1 business day · USA domestic only |
| Intended Use | In-vitro laboratory research only |
Why PureRawz Provides a Dual COA — And Why It Matters
Most peptide suppliers stop at HPLC purity. PureRawz issues two separate, lot-specific Certificates of Analysis for every batch of Semax. Here's the science behind why both are essential.
HPLC Purity Certificate
High-Performance Liquid Chromatography separates and quantifies every molecular species in the sample. Our Semax consistently measures ≥99% purity at lot release. The full chromatogram with peak integration is available in the COA PDF, confirming chemical identity and ruling out synthesis by-products or oxidation impurities. This is the industry-standard method — and where most suppliers stop.
≥99% purity confirmed per lot
LAL Endotoxin Assay Certificate
The Limulus Amebocyte Lysate (LAL) assay is the pharmacopoeial gold standard for detecting bacterial lipopolysaccharides (LPS). HPLC cannot detect endotoxins — LPS are large heteropolymers that don't resolve as chromatographic peaks. Even sub-nanogram LPS contamination activates TLR4 on macrophages, invalidating cytokine assays, cell-viability studies, and inflammatory pathway experiments. Neither of our two main competitors provides this test.
LAL endotoxin tested — per lot
Both COA documents are lot-number-specific and available for download from the product page.
What Is Semax?
Semax is a synthetic heptapeptide with the amino acid sequence Met-Glu-His-Phe-Pro-Gly-Pro, structurally derived from the 4th through 7th residues of adrenocorticotropic hormone (ACTH), extended at the C-terminus with a Pro-Gly-Pro (PGP) tripeptide motif. Semax was originally developed by the Institute of Molecular Genetics of the Russian Academy of Sciences in the 1980s and has accumulated a substantial body of peer-reviewed preclinical literature spanning neurotrophic signalling, cerebral ischaemia models, and gene expression profiling.
Unlike native ACTH, Semax does not stimulate corticosteroid secretion from the adrenal cortex. The PGP C-terminal extension is considered by researchers to enhance the compound's lipophilicity, potentially supporting passive diffusion characteristics relevant to blood–brain barrier (BBB) permeability studies. Lipid raft-mediated endocytosis and receptor-mediated transcytosis at BBB tight junctions are two proposed mechanisms examined in the literature.
The acetylated variant — N-Acetyl Semax — adds an acetyl group to the N-terminal methionine. In preclinical pharmacokinetics modelling, acetylation is associated with reduced affinity for competing metal ions at the N-terminus and improved resistance to enzymatic degradation, potentially extending measurable half-life in biological matrices [1].
In published literature, Semax has been examined in preclinical contexts relating to BDNF and NGF upregulation, cerebral ischaemia models, serotonergic and dopaminergic pathway modulation, hippocampal and cortical gene expression profiling, and default mode network fMRI imaging. All findings cited here arise from in-vitro or animal-model studies only.
Mechanism of Action — Six Research Pathways
Peer-reviewed preclinical literature has characterised at least six distinct molecular pathways. All findings are from in-vitro or animal studies only.
Transcriptomic studies in rodent models document time-dependent upregulation of BDNF and NGF gene expression in the hippocampus and frontal cortex following Semax exposure, with peak changes observed within 20 minutes of administration. BDNF signalling through TrkB receptors is the most-studied downstream target.
Agapova et al., 2008 [5]; Dolotov et al., Brain Res Bull 2011
Semax has been reported to inhibit dipeptidyl peptidase IV and related serine proteases implicated in enkephalin catabolism. Elevated enkephalin availability in preclinical models may modulate opioidergic, dopaminergic, and serotonergic pathway crosstalk — producing measurable changes in neurotransmitter metabolite levels.
Kost et al., Bioorg Khim 2001 [9]
Whole-transcriptome analyses in rodent focal ischaemia models identified Semax-associated changes across 24 genes regulating vascular biology — including smooth-muscle cell migration, erythropoiesis, and angiogenesis-related transcription factors in brain and spinal cord tissue.
Medvedeva et al., BMC Genomics 2014 [1]
Rodent studies measuring 5-HIAA (a primary serotonin metabolite) found progressive increases up to 180% over four hours following Semax exposure. Co-administration with D-amphetamine produced additive elevations in 5-HIAA, indicating monoamine pathway interaction beyond a simple direct receptor effect.
Eremin et al., Neurochem Res 2005 [8]
Functional MRI research reported Semax-associated changes in default mode network (DMN) connectivity — the resting-state brain system involved in social cognition, self-referential processing, and environmental monitoring. DMN disruption is observed in multiple neurodegenerative research models.
Lebedeva et al., Bull Exp Biol Med 2018 [3]
Post-ischaemia transcriptomics identified Semax-associated effects on microglial activation, leukocyte pathway genes, and dendritic cell populations at 3 h and 24 h time points. Immunoglobulin and chemokine gene clusters were among the most significantly modulated.
Medvedeva et al., BMC Genomics 2014 [1]
Batch Traceability — Our Public Lot Verification Portal
Neither Peptide Sciences nor Biotech Peptides offers public batch-level verification. PureRawz does — because researchers shouldn't have to take our word for it.
Every vial is traceable to a specific, independently tested batch.
Our lot numbering system encodes the compound code, synthesis batch number, and QC release date. Every lot is indexed in our public verification portal — enter the lot number printed on your vial at officialpurerawz.us/verify and retrieve:
- The HPLC purity COA PDF for your exact batch
- The LAL endotoxin COA PDF for your exact batch
- The name of the independent third-party testing laboratory
- The QC release date and synthesis batch ID
- Documentation suitable for IRB submissions and publication methodology sections
SX-2025-0941
Verify at /verify →
PureRawz vs. Competitors — Semax Side-by-Side
Based on publicly available supplier information as of April 2026.
| Feature | PureRawz ✦ | Peptide Sciences | Biotech Peptides |
|---|---|---|---|
| Purity Standard | ≥99% HPLC | 99% HPLC | 99% HPLC |
| HPLC Purity COA | ✔ Per lot | ✔ Per lot | ✔ Per lot |
| LAL Endotoxin COA | ✔ Per lot — full assay | ✗ Not provided | ✗ Not provided |
| Unique Lot Number Per Vial | ✔ Every vial | Partial | ✗ Not mentioned |
| Public Lot Verification Portal | ✔ officialpurerawz.us/verify | ✗ | ✗ |
| USA Manufactured | ✔ | ✔ | ✔ |
| Ships in 1 Business Day (USA) | ✔ | Not stated | ✔ Same-day by 12 PST |
| No Prescription Required | ✔ | ✔ | ✔ |
| Trust Badge Strip on Page | ✔ 5 badges | 3 badges | ✗ None |
| FAQ Section (Schema Rich Results) | ✔ 10 Q&As | ✗ | ✗ |
| PubMed-Linked References | ✔ 9 cited | ✔ ~8 cited | ✔ 9 cited |
| Site Operational (Apr 2026) | ✔ Active | ✗ Reports of shutdown | ✔ Active |
✦ PureRawz. Data from publicly available pages, April 2026. Subject to change.
Researchers Studying Semax Also Explore
Semax Research FAQ
For research and educational purposes only. Nothing here constitutes medical advice.
References
- Medvedeva EV et al. The peptide semax affects the expression of genes related to the immune and vascular systems in rat brain focal ischemia. BMC Genomics. 2014;15:228. doi:10.1186/1471-2164-15-228
- Gusev EI et al. The efficacy of semax in the treatment of patients at different stages of ischemic stroke. Zh Nevrol Psikhiatr Im S S Korsakova. 2018;118(3):61–68. doi:10.17116/jnevro20181183261-68
- Lebedeva IS et al. Effects of Semax on the Default Mode Network of the Brain. Bull Exp Biol Med. 2018;165(5):653–656. doi:10.1007/s10517-018-4234-3
- Mars RB et al. On the relationship between the "default mode network" and the "social brain". Front Hum Neurosci. 2012;6:189. doi:10.3389/fnhum.2012.00189
- Agapova TIu et al. Mol Gen Mikrobiol Virusol. 2008;(3):28–32. PMID: 18756811
- Scantlebury MH et al. ACTH protects learning and memory function in epileptic Kcna1-null mice. Neurosci Lett. 2017;645:14–18. doi:10.1016/j.neulet.2017.02.069
- Glazova NY et al. Semax attenuates behavioural and neurochemical alterations following early-life fluvoxamine exposure. Neuropeptides. 2021;86:102114. doi:10.1016/j.npep.2020.102114
- Eremin KO et al. Semax activates dopaminergic and serotoninergic brain systems in rodents. Neurochem Res. 2005;30(12):1493–1500. doi:10.1007/s11064-005-8826-8
- Kost NV et al. Semax and selank inhibit the enkephalin-degrading enzymes from human serum. Bioorg Khim. 2001;27(3):180–183. PMID: 11443939
N-Acetyl Semax Amidate
N-Acetyl Semax Amidate is a premium nootropic research peptide commonly explored for cognitive studies, focus support, memory research, and advanced laboratory applications.
Browse related Purerawz products and trusted scientific references below.
Related Products
- Buy Semax – cognitive and focus research peptide
- Buy Selank – mood and nootropic support studies
- Buy NSI-189 – neurogenesis and cognitive research
- Buy Bromantane – advanced nootropic performance support
- Buy MK-677 – growth and recovery research
- Buy Epithalon – longevity and peptide research
Research References
-
PubMed Research Database
– scientific studies and published research -
National Center for Biotechnology Information (NCBI)
– biomedical and research resources -
U.S. Food and Drug Administration
– regulatory and compliance reference
Additional information
| Attribute | Nasal Spray 30mg/300mcg per spray, Nasal Spray 60mg/600mcg per spray, Nasal Spray 120mg/1200mcg per spray |
|---|






Reviews
There are no reviews yet.