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    NA-Semax Amidate

    Nootropic PeptidePreclinical

    Also known as: NA-Semax Amide, N-Acetyl Semax Amide, NA-Semax-NH2, Acetyl-Semax-Amide

    NA-Semax Amidate is the C-terminally amidated NA-Semax — the carboxylic acid at the peptide's C-terminus is replaced with an amide group (-NH2), which is reported to further extend metabolic half-life by resisting carboxypeptidase cleavage in addition to the aminopeptidase resistance the N-acetyl group already provides. The practical effect is a peptide with dosing-frequency use: where standard Semax often requires 3-4 daily doses to maintain effect, NA-Semax Amidate is reported (in vendor monographs and community usage) to maintain subjective effects on a 1-2x daily schedule. Direct pharmacokinetic comparisons in peer-reviewed literature remain absent — this framing is honest about the evidence base..

    Half-Life: ~30-45 minutes (estimated, longer than standard Semax)MW: ~855.0 g/mol (C39H54N10O10S; monoisotopic ~854.4)2 PubMed Studies
    Last reviewed:

    Overview

    At A Glance

    Mechanism

    Mechanism (inherited from parent Semax - the N-acetyl / C-amidate analog itself has not been directly studied):

    Half-Life
    ~30-45 minutes (estimated, longer than standard Semax)
    Safety Notes
    Common
    Mild nasal irritation

    Mechanism of Action

    Mechanism (inherited from parent Semax - the N-acetyl / C-amidate analog itself has not been directly studied):

    • BDNF upregulation in hippocampus + cortex - a single intranasal dose of Semax raises hippocampal BDNF protein and TrkB expression in rodents, alongside improved learning ([Dolotov et al., 2006; PMID 16996037])
    • Dopaminergic + serotonergic modulation - Semax raises striatal serotonin turnover (5-HIAA) and potentiates amphetamine-evoked striatal dopamine release in rodents ([Eremin et al., 2005; PMID 16362768])
    • NE turnover modulation
    • Anti-inflammatory (IL-6, TNF- suppression)

    Pharmacokinetic improvements (theoretical, not measured for this analog):

    • N-acetyl group - intended to block aminopeptidase cleavage at the N-terminus
    • C-terminal amide - intended to block carboxypeptidase cleavage at the C-terminus
    • Net result - reportedly 2-4x longer functional duration vs. unmodified Semax (vendor + community claim, not peer-reviewed)

    Note: every mechanism above is extrapolated from published research on Semax itself. NA-Semax Amidate has no pharmacology or human clinical data of its own - the acetyl and amide modifications have not been separately characterized.

    Overview

    NA-Semax Amidate is the C-terminally amidated NA-Semax — the carboxylic acid at the peptide's C-terminus is replaced with an amide group (-NH2), which is reported to further extend metabolic half-life by resisting carboxypeptidase cleavage in addition to the aminopeptidase resistance the N-acetyl group already provides.

    The practical effect is a peptide with dosing-frequency use: where standard Semax often requires 3-4 daily doses to maintain effect, NA-Semax Amidate is reported (in vendor monographs and community usage) to maintain subjective effects on a 1-2x daily schedule. Direct pharmacokinetic comparisons in peer-reviewed literature remain absent — this framing is honest about the evidence base.

    Chemical Information

    IUPAC Name

    Not yet available

    CAS Number

    Not yet available

    Molecular Formula

    C40H57N13O10

    Molecular Mass

    ~855.0 g/mol (C39H54N10O10S; monoisotopic ~854.4)

    Amino Acid Sequence

    Ac-Met-Glu-His-Phe-Pro-Gly-Pro-NH2 (Ac-MEHFPGP-NH2)

    Dosing & Protocols

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    Research

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    Interactions

    Contraindications

    Do not use outside of a research setting. NA-Semax Amidate is not a medicine and has not been evaluated for human use; the points below are conservative precautions, not trial-derived medical contraindications for this compound.

    • Pregnancy and lactation - avoid; there are no reproductive or developmental safety data for this analog.
    • Known peptide or Semax hypersensitivity - discontinue immediately if any allergic or hypersensitivity reaction occurs.
    • Mania or bipolar-spectrum instability - caution; nootropic, dopaminergic-modulating peptides may theoretically aggravate activation, though this is not established for this compound.
    • Concurrent CNS-active medications or stimulants - no interaction data exist for this analog; combining is untested.

    These precautions are extrapolated from the parent peptide Semax and from general peptide-research safety practice, not from any published study of NA-Semax Amidate itself.

    Research Disclaimer

    This interaction data is compiled from published research and community reports. It may not be exhaustive. Always consult a healthcare professional before combining compounds.

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    Adalank

    Nootropic PeptidePreclinical / Research compound

    Adalank is a hybrid research peptide combining structural elements of Adamax (the adamantyl-modified Semax analog) and Selank (the anxiolytic Pro-Gly-Pro tuftsin analog).

    t½ The commonly cited ~72-hour "functional duration" is an unverified community/vendor claim, not a measured value - no pharmacokinetic study of Adalank has ever been run. The figure is extrapolated from parent Adamax marketing claims. Actual serum half-life is unknown; there is no published PK data. 200-1200 mcg per dose (intranasal or subcutaneous), 1-2x daily
    PreclinicalView Profile

    Adamax

    Nootropic PeptidePreclinical / Research compound

    Adamax is a synthetic nonapeptide (Ac-MEHFPGPAG-NH2) classified as a designer analog of Semax.

    t½ No pharmacokinetic data. Community reports describe a subjectively long duration of effect (~2-3 days), supporting every-other-day or 3x/week dosing; serum half-life not characterized. 500-2000 mcg subcutaneous (community research dosing)
    PreclinicalView Profile

    Cerebrolysin

    Nootropic PeptideClinical

    Cerebrolysin is a porcine brain-derived peptide complex developed by EVER Neuro Pharma (Austria) — a low-molecular-weight neurotrophic preparation containing a mixture of free amino acids and bioactive peptides extracted from purified pig brain proteins.

    t½ ~2-4 hours (multi-component peptide mix)
    85 studiesView Profile

    Cortexin

    Nootropic PeptideMarketed in Russia/CIS (Geropharm); human clinical use with limited-quality evidence (small, mostly Russian-language studies; no Western RCT; not FDA/EMA approved)

    Cortexin is a purified peptide preparation extracted from cattle and pig cerebral cortex tissue — a low-molecular-weight neuropeptide complex used clinically in Russia and Eastern Europe for cognitive impairment, post-stroke recovery, encephalopathy, attention disorders, and pediatric developmental conditions. Like Cerebrolysin, Cortexin is positioned as a broad-spectrum neurotrophic preparation supplying bioactive peptides that mimic endogenous neurotrophic factors.

    t½ ~2-3 hours (estimated from analog peptide preparations)
    18 studiesView Profile

    NA-Semax

    Nootropic PeptidePreclinical

    NA-Semax is the N-acetyl-l-aspartyl variant of Semax — the original ACTH(4-7) Pro-Gly-Pro analog developed at the Russian Academy of Sciences in the 1990s.

    t½ ~20-30 minutes (intranasal, estimated from analog data)
    3 studiesView Profile

    P-21

    Nootropic PeptidePreclinical

    P-21 is a synthetic cyclic dipeptide — Cyclo(L-prolyl-glycine) — derived from the Selank/Semax C-terminal Pro-Gly-Pro motif.

    t½ Not formally characterized in published work. P021 has only been studied in rodents (oral/dietary and subcutaneous dosing); no human pharmacokinetic data exist.
    4 studiesView Profile

    View Full Dosage Guide →

    Protocols, calculator & safety for NA-Semax Amidate

    Research Score

    60

    2 PubMed studies

    Quality Indicators

    Data Completeness

    75%
    Description
    Mechanism of Action
    Chemical Data
    Dosing Protocols
    Safety Profile
    PubMed Studies
    Interactions
    Vendor Listings

    Research Credibility

    2PubMed studies

    Limited research available

    Quick Facts

    Half-Life

    ~30-45 minutes (estimated, longer than standard Semax)

    Molecular Weight

    ~855.0 g/mol (C39H54N10O10S; monoisotopic ~854.4)

    Trial Phase

    Preclinical

    Safety Profile

    Low Risk

    Common Side Effects

    • Mild nasal irritation

    Stop Use If

    • Pregnancy/lactation
    • Mania
    • Peptide allergy

    Research Disclaimer

    This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.

    Frequently Asked Questions

    What is NA-Semax Amidate used for in research?

    NA-Semax Amidate is the C-terminally amidated NA-Semax — the carboxylic acid at the peptide's C-terminus is replaced with an amide group (-NH2), which is reported to further extend metabolic half-life by resisting carboxypeptidase cleavage in addition to the aminopeptidase resistance the N-acetyl group already provides.

    The practical effect is a peptide with dosing-frequency use: where standard Semax often requires 3-4 daily doses to maintain effect, NA-Semax Amidate is reported (in vendor monographs and community usage) to maintain subjective effects on a 1-2x daily schedule. Direct pharmacokinetic comparisons in peer-reviewed literature remain absent — this framing is honest about the evidence base.

    What forms does NA-Semax Amidate come in?

    NA-Semax Amidate is available in vials, capsules, and sprays forms.

    How much does NA-Semax Amidate cost?

    Pricing varies by vendor and form.

    How do I compare NA-Semax Amidate vendors?

    Compare prices, payment methods, shipping, and COA scores across 0 vendors.

    Research Tools

    Related Compounds

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    Adalank

    Nootropic PeptidePreclinical / Research compound

    Adalank is a hybrid research peptide combining structural elements of Adamax (the adamantyl-modified Semax analog) and Selank (the anxiolytic Pro-Gly-Pro tuftsin analog).

    t½ The commonly cited ~72-hour "functional duration" is an unverified community/vendor claim, not a measured value - no pharmacokinetic study of Adalank has ever been run. The figure is extrapolated from parent Adamax marketing claims. Actual serum half-life is unknown; there is no published PK data. 200-1200 mcg per dose (intranasal or subcutaneous), 1-2x daily
    PreclinicalView Profile

    Adamax

    Nootropic PeptidePreclinical / Research compound

    Adamax is a synthetic nonapeptide (Ac-MEHFPGPAG-NH2) classified as a designer analog of Semax.

    t½ No pharmacokinetic data. Community reports describe a subjectively long duration of effect (~2-3 days), supporting every-other-day or 3x/week dosing; serum half-life not characterized. 500-2000 mcg subcutaneous (community research dosing)
    PreclinicalView Profile

    Cerebrolysin

    Nootropic PeptideClinical

    Cerebrolysin is a porcine brain-derived peptide complex developed by EVER Neuro Pharma (Austria) — a low-molecular-weight neurotrophic preparation containing a mixture of free amino acids and bioactive peptides extracted from purified pig brain proteins.

    t½ ~2-4 hours (multi-component peptide mix)
    85 studiesView Profile

    Cortexin

    Nootropic PeptideMarketed in Russia/CIS (Geropharm); human clinical use with limited-quality evidence (small, mostly Russian-language studies; no Western RCT; not FDA/EMA approved)

    Cortexin is a purified peptide preparation extracted from cattle and pig cerebral cortex tissue — a low-molecular-weight neuropeptide complex used clinically in Russia and Eastern Europe for cognitive impairment, post-stroke recovery, encephalopathy, attention disorders, and pediatric developmental conditions. Like Cerebrolysin, Cortexin is positioned as a broad-spectrum neurotrophic preparation supplying bioactive peptides that mimic endogenous neurotrophic factors.

    t½ ~2-3 hours (estimated from analog peptide preparations)
    18 studiesView Profile

    NA-Semax

    Nootropic PeptidePreclinical

    NA-Semax is the N-acetyl-l-aspartyl variant of Semax — the original ACTH(4-7) Pro-Gly-Pro analog developed at the Russian Academy of Sciences in the 1990s.

    t½ ~20-30 minutes (intranasal, estimated from analog data)
    3 studiesView Profile

    P-21

    Nootropic PeptidePreclinical

    P-21 is a synthetic cyclic dipeptide — Cyclo(L-prolyl-glycine) — derived from the Selank/Semax C-terminal Pro-Gly-Pro motif.

    t½ Not formally characterized in published work. P021 has only been studied in rodents (oral/dietary and subcutaneous dosing); no human pharmacokinetic data exist.
    4 studiesView Profile

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