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Adamax: Adamantane-Modified Semax-Family Analog Research Overview

Adamax is a synthetic nine-amino-acid peptide from the Semax family of ACTH(4-10) analogs, carrying an N-terminal acetyl group and a C-terminal adamantane moiety (sequence Ac-MEHFPGPAG-NH2). It is studied in preclinical neuropeptide research, where its structural modifications are of interest for peptide stability and central-nervous-system signaling models.

Last reviewed: 2026-07-18·Reviewed by Chris Doty, Founder, Instant Peptides

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Research-use reference only. The content below summarizes published preclinical and in vitro research. Not for human or animal consumption, diagnostic, or therapeutic use. Information is provided as an educational resource for qualified research professionals.

What is Adamax?

Adamax belongs to the Semax family — synthetic analogs derived from the ACTH(4-10) fragment of adrenocorticotropic hormone. Where Semax itself is a heptapeptide, Adamax carries additional structural features: an N-acetyl group and a C-terminal adamantane cage. The adamantane modification is a lipophilic, metabolically stable structure used in medicinal chemistry to increase resistance to enzymatic degradation and to influence membrane interaction, giving Adamax a longer characterized stability profile than unmodified Semax.

It is produced to research-grade purity for controlled laboratory investigation. For the parent-compound detail, see the NA-Semax research overview.

Semax-family signaling background

The Semax family is studied in preclinical models of neuropeptide signaling. Semax, the reference compound of the family, has been reported to bind specifically in rat basal forebrain tissue and to increase levels of brain-derived neurotrophic factor (BDNF) protein — a neurotrophin central to neuroplasticity research.[1] The family is also examined in relation to melanocortin-associated and neurotrophic expression pathways.

As an adamantane-modified member of this family, Adamax is studied for how its structural stabilization affects peptide behavior across experimental conditions relative to the shorter, unmodified Semax sequence. Direct Adamax-specific literature is limited; researchers typically interpret it against the broader Semax-family record.

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Structure and characterization

Adamax's defined nine-residue sequence, N-acetyl cap, and adamantane cage give it a specific, reproducible analytical signature. Researchers characterize it by amino-acid sequence stability, solubility, and consistent behavior across experimental conditions, which support reproducible preclinical work.

Analytical testing

Each Adamax batch undergoes the 7-round independent analytical program: reversed-phase HPLC for purity, mass spectrometry for identity confirmation, endotoxin screening, and sterility verification, with additional conformity vials. Independent testing is performed by third-party laboratories Kovera Labs and Freedom Diagnostics, and a full Certificate of Analysis is available for each production lot. For research use only. Not for human or veterinary use; not approved by the FDA for any human therapeutic, diagnostic, or medical purpose.

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Common Questions

What is Adamax?

Adamax is a synthetic nine-amino-acid peptide from the Semax family of ACTH(4-10) analogs, carrying an N-acetyl group and a C-terminal adamantane modification for enhanced stability. It is produced to research-grade purity for controlled laboratory applications.

How does Adamax differ from Semax?

Adamax builds on the Semax sequence with an adamantane modification designed to increase metabolic stability and extend the compound's activity window relative to unmodified Semax, making it a useful tool for studying stabilized peptide behavior in preclinical models.

What research areas involve Adamax?

Adamax is examined in preclinical models studying neuropeptide signaling, neurotrophic factor expression pathways, and peptide-mediated regulatory mechanisms in controlled laboratory settings.

How is product quality verified?

Every batch undergoes 7 rounds of independent analytical testing including HPLC purity analysis, mass spectrometry identity confirmation, endotoxin screening, and sterility verification. Full Certificates of Analysis documenting all results are available for each production lot.

References

  1. 1.Dolotov OV, Karpenko EA, Inozemtseva LS, et al. Semax, an analog of adrenocorticotropin (4-10), binds specifically and increases levels of brain-derived neurotrophic factor protein in rat basal forebrain. Journal of Neurochemistry. 2006. PMID: 16981885

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