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Cognitive & Neuropeptides · Source-reviewed dossier

Semax

Source-Reviewed Research Dossier

Semax is an ACTH(4-10)-derived heptapeptide analogue studied in ischemia, neuroprotection and gene-expression models. Recent public records remain predominantly preclinical and do not establish broad human cognitive or recovery claims.

Research use only Lot documents on request
Semax research product family with 2 catalog variants
AI-generated packaging mockup for catalog navigation. It is not a photograph of an actual supplied lot; container, label and presentation may vary.

Product family

Compound overview

Shared values below are consolidated from the current catalog record. They are not independent verification or lot results; the current product specification and lot COA control.

Product identity

Product type
Peptide research compound
Catalog family
Semax
Research category
Cognitive & Neuropeptides
Catalog CAS RN
80714-61-0
Catalog molecular formula
C37H51N9O10S
Catalog molecular weight
813.92 g/mol
Catalog sequence
Met-Glu-His-Phe-Pro-Gly-Pro
Evidence status
Predominantly rodent and molecular evidence; limited independently accessible clinical evidence
Intended use
Research, development and manufacturing use only

Literature reference parameters

Compound or material class
ACTH(4-10)-derived heptapeptide analogueCatalog-family identity
Evidence scope
Predominantly rodent and molecular evidence; limited independently accessible clinical evidenceDo not generalize beyond the cited model
Source review
Primary or authoritative records linked belowChecked 2026-09-01

Identity safeguard Reference identifiers above describe the literature compound record. The supplied form, formula, molecular weight, purity and storage conditions must be verified against the product-specific specification and lot COA.

Mechanism of action

How Semax is studied

A target-to-pathway view grounded in the linked research records.

ACTH(4-10)-derived heptapeptide analogue research basis

Semax research examines neurotrophin, inflammatory, transcriptional and injury-response pathways rather than one universally accepted target.

Evidence and material boundary

Rodent stroke or spinal-cord-injury outcomes cannot establish human effectiveness, dosing or route.

Reported research findings

What published studies report about Semax

Reported outcomes are paired with their experimental model and evidence boundary.

Mouse spinal-cord model

Functional-recovery mechanisms were preclinical

A 2025 mouse study linked Semax with Oprm1-related deubiquitination and functional-recovery outcomes after spinal-cord injury.

The result is sex-, species- and injury-model-specific.

Read the primary study
Rat ischemia model

Brain gene-expression profiles were examined after experimental stroke

A 2024 study reported partial compensation of ischemia-disrupted brain gene expression after ACTH-like peptide exposure.

Gene-expression normalization in rats is not a clinical outcome.

Read the primary study
Translation boundary: findings are limited to the evidence level stated on each card. Experimental protocol quantities are research details, not usage instructions.

Catalog options

Variant specifications

Pack-level catalog data; lot-level controls remain document-specific.

Catalog no.XA5
Pack size5 mg × 10 vials
Specification & documents for XA5

Product specification

Single-component peptide · 5 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Request by lot: CoA, HPLC purity and MS identity

Catalog no.XA10
Pack size10 mg × 10 vials
Specification & documents for XA10

Product specification

Single-component peptide · 10 mg/vial nominal · 10-vial pack · supplied form and release limits controlled by lot specification.

Lot documentation

Request by lot: CoA, HPLC purity and MS identity

Quality system

Quality documentation

Document availability is stated honestly and can vary by catalog variant or lot.

Lot-specific Certificate of AnalysisAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Product Specification SheetAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request
Analytical Method SummaryAvailability and scope must be confirmed for the selected catalog variant and lot
Confirm before ordering Request

Analytical interpretation

Interpret the documents, not just the headline number.

Use the source-reviewed guide to separate chromatographic area purity, quantitative assay, LC-MS identity, composition and stability evidence before comparing variants or requesting a lot record.

Open the Quality & Documentation Hub

HPLC area ≠ assayA dominant peak does not establish target mass fraction.

Intact mass ≠ full sequenceIdentity strength depends on resolution and orthogonal evidence.

Counterions affect contentWater, salt form and solvents change the as-is composition.

Storage needs a data basisShipping practice is not the same as stability evidence.

Evidence map

Research context

Published studies and regulatory records, not customer testimonials or usage guidance.

Mouse spinal-cord model

Functional-recovery mechanisms were preclinical

The result is sex-, species- and injury-model-specific.

View primary record
Rat ischemia model

Brain gene-expression profiles were examined after experimental stroke

Gene-expression normalization in rats is not a clinical outcome.

View primary record
Evidence boundary: each card states its evidence type. Human trials and regulatory records describe the studied or regulated intervention; preclinical records remain model-specific. None verifies the identity, quality, safety or efficacy of this catalog lot or provides usage instructions.

Literature basis

Curated references

Third-party publications selected for direct relevance.

  1. 01

    Semax targets Oprm1 in a spinal-cord-injury mouse model

    Preclinical study. 2025. PMID 40692165.

    Mouse spinal-cord model
  2. 02 Rat ischemia model

Research FAQ

Semax questions

Concise answers for researchers comparing identity, evidence and catalog variants.

What is Semax?

Semax is an ACTH(4-10)-derived heptapeptide analogue studied in ischemia, neuroprotection and gene-expression models. Recent public records remain predominantly preclinical and do not establish broad human cognitive or recovery claims.

What evidence is available for Semax?

The accessible evidence is mainly animal and molecular research, with limited controlled human replication.

Does the cited research validate this catalog material?

No. The cited records describe their own intervention, formulation, model and controls. They do not verify the identity, purity, sterility, safety or efficacy of a catalog lot.

Which quality documents can be requested?

A lot-specific COA, product specification sheet and analytical method summary can be requested where applicable.

How should Semax be stored?

Store at -20 °C, protected from light and moisture. After reconstitution, aliquot and avoid repeated freeze-thaw cycles. Confirm the applicable storage statement on the product-specific specification and lot documentation.

Knowledge center

Related insights

Owned educational content connected to this family.

AI-generated illustration: Peptide laboratory visualization of the seven-residue Semax sequence and LC-MS

Semax Identity Guide: ACTH(4–7)-Pro-Gly-Pro Sequence and Testing

Semax is the synthetic heptapeptide Met-Glu-His-Phe-Pro-Gly-Pro, also written ACTH(4–7)-Pro-Gly-Pro. It should not be confused with semaxanib, an unrelated small molecule with a similar name.

Updated September 1, 2026

Knowledge tools

Continue with structured evidence

Move from this dossier into canonical evidence maps, verified status records, analytical interpretation and laboratory calculations.

Internal technical source review

Claims were checked against the linked primary publication, regulatory label or authoritative compound record. Published findings stay attached to their study model, formulation and route. Catalog identity and lot quality remain controlled by the applicable specification and lot-specific documents.

Editorial status: NHD evidence editorial workflow · 2026-09-01 · Not independent medical review · Review policy

Technical procurement

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Selected: XA10 · 10 mg × 10 vials