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Reference library

Educational peptide reference — research use only.

Research & educational use only

For laboratory and educational research only. Not for human or veterinary consumption. This is not medical advice. Always follow applicable laws and consult qualified professionals.

The calculator performs unit math for research reference. It must not be used to plan or guide dosing in humans or animals. Verify all figures independently in your lab protocol.

Semax

An ACTH-fragment peptide studied in neuroprotection research.

Half-life (approx.)
~minutes (approx.); NA-amidate extended
Diluent
Bacteriostatic water (0.9% benzyl alcohol)
Common vials
5, 10 mg

Half-life figures are literature approximations for educational reference — not pharmacokinetic advice.

Overview

Semax is a synthetic ACTH(4-10) analog developed for stroke and cognitive disorders in Russian clinical research. Studies examine BDNF upregulation, attention performance, and neuroprotection after ischemic injury. ACTH(4-10) analog with BDNF upregulation in stroke and cognitive rodent models.

Structure & identity

Heptapeptide Met-Glu-His-Phe-Pro-Gly-Pro (ACTH 4-10 analog)

Sequence / structure
Heptapeptide Met-Glu-His-Phe-Pro-Gly-Pro (ACTH 4-10 analog)

Mechanism

ACTH(4-10) analog upregulates BDNF and modulates dopaminergic and serotonergic systems. Melanocortin and monoaminergic modulation supplement neurotrophic mechanism literature.

Studies & clinical programs

  • Stroke neuroprotection trials

    Published research models

    • Peer-reviewed literature documents endpoints under Stroke neuroprotection trials experimental designs.
  • Attention task performance

    Published research models

    • Peer-reviewed literature documents endpoints under Attention task performance experimental designs.

Research models in literature

  • Stroke neuroprotection trials
  • Attention task performance

Literature highlights

  • ACTH(4-10) analog upregulates BDNF in stroke neuroprotection and attention-task rodent studies.
  • Dopaminergic and serotonergic modulation examined in CNS pharmacology assays.
  • Parent compound for Adamax and component of Semax+Selank research blends.

Combination research notes

Semax + Selank mix; Adamax is a modified analog.

Key targets & pathways

BDNFDopamineMelanocortinCREB/BDNF pathwayPrefrontal cortex plasticity

Research areas

NeuroprotectionBDNFStroke modelsACTH fragment

Routes in research literature

IntranasalSubcutaneous

Also known as

NA Semax AmidateNA Semax

Handling cautions

  • Intranasal and injectable forms differ

Stability & storage phases

PhaseConditionGuidance
LyophilizedRefrigerated (2–8 °C), sealedResearch peptide powder for nasal formulations should remain cold and dry until reconstitution; amidate forms may have distinct published stability guidance.
Reconstituted (nasal solution)Sterile water or bacteriostatic water, refrigeratedNasal research solutions are often prepared at lower concentrations; use within published stability windows (commonly 1–2 weeks refrigerated).
Working aliquotsSingle-use nasal sprayer fills or frozen micro-aliquotsAvoid contamination of multi-use bottles in lab settings; sterile technique and cold chain reduce protease and microbial risk.

Stability windows are formulation-dependent — verify published data and your lab SOP.

Reconstitution reference table

Vial (mg)Diluent (mL)mcg/mLUnits @ 100 mcgUnits @ 250 mcgUnits @ 500 mcg
522500.041020
1025000.02510

U-100 insulin syringe scale (100 units = 1 mL). Illustrative only — not dosing guidance.

Reconstitution steps

  1. Allow vial to reach room temperature (15–30 min)
  2. Swab rubber stopper with alcohol prep pad
  3. Draw calculated bacteriostatic water into syringe
  4. Inject diluent slowly down vial wall — do not spray directly onto cake
  5. Gently swirl until fully dissolved — do not shake vigorously
  6. Label with date, concentration, and diluent volume
  7. Refrigerate and use within your lab stability window

Reconstituted per research protocol; intranasal forms differ.

Laboratory record checklist

  • Compound identity recorded in lab notebook (name, lot, preparation date)
  • Analytical identity cross-checked against published sequence or structure
  • Potency or concentration documented from analytical certificate when available
  • Purity or HPLC data filed when provided with research material
  • Appearance noted: intact lyophilized cake or uniform powder
  • Sterility / endotoxin report archived when available
  • Storage temperature applied immediately per published stability guidance