FOR LABORATORY RESEARCH USE ONLY. Not for human or veterinary use, not for consumption, not medicines. Research use policy
UK only · Prepared to order · approx. 7 days + Royal Mail Tracked 24 · No international shipping
Peptide blend · Lyophilised vial

Semax / Selank blend

Neuropeptide research peptides

Pre-mixed lyophilised combination of Semax and Selank (10 mg + 10 mg per vial), for comparative neuropeptide research.

£39.49 ex. VAT · per vial
Available

Prepared to order · approx. 7 days + Royal Mail Tracked 24

SKU BP-SXSK-20 · ≥99% (see COA) · Lyophilised powder

For laboratory research use only. Not for human or veterinary use. Not a medicine, food supplement or cosmetic. Purchasers confirm research use, age 18+ and institutional/professional status at checkout. UK delivery only.
Data pending verification. Identity data in the specification below has been compiled for pre-launch and is awaiting verification against supplier documentation and batch COAs. Highlighted fields are unconfirmed.
Note: Component ratio taken from the supplier list ("Semax 10mg+Selank 10mg"). Confirm the per-component content from the batch COA.

Semax / Selank blend overview

Each vial contains Semax 10 mg and Selank 10 mg (20 mg total peptide), co-lyophilised, per the supplier specification. See the individual Semax and Selank pages for component data. Supplied for in-vitro laboratory research only.

Sequence
Mixture. Semax: MEHFPGP; Selank: TKPRPGP
Molecular formula
Mixture. Semax C₃₇H₅₁N₉O₁₀S; Selank C₃₃H₅₇N₁₁O₉
Molecular weight
Mixture. Semax ≈813.9 g/mol; Selank ≈751.9 g/mol
Purity
≥99% (see COA)
Form
Lyophilised powder
Vial sizes & prices
20 mg – £39.49 (ex. VAT)
Delivery
UK only · prepared to order (approx. 7 days) then Royal Mail Tracked 24, £5.95

Semax / Selank blend research background

Blend – components only

Evidence status: This combination has not been studied as a blend; findings summarised here relate to the individual components, much of it preclinical (cell or animal) or small-scale. They are not established effects in humans, have not been evaluated by the MHRA, and are provided for scientific context only. This product is supplied strictly for laboratory research and is not for human or veterinary use.

Semax

Semax (Met-Glu-His-Phe-Pro-Gly-Pro) is a synthetic heptapeptide. It joins the ACTH(4–7) fragment to a C-terminal Pro-Gly-Pro sequence for stability, and is described as an ACTH(4–10) analogue. It was developed in Russia, and most of the literature comes from Russian institutions [1][2].

Selank

Selank (Thr-Lys-Pro-Arg-Pro-Gly-Pro) is a synthetic heptapeptide analogue of the immunomodulatory tetrapeptide tuftsin, extended with Pro-Gly-Pro. It was developed in Russia [3][4].

Established research

Peer-reviewed published findings, with references
Overview & discovery history
  • This research blend combines 2 separately characterised compounds. The combination itself has not been studied in peer-reviewed research; the summaries below relate to each component individually. See each component's own product page for its full research background.
Chemical identity
Sequence
Mixture. Semax: MEHFPGP; Selank: TKPRPGP
Molecular formula
Mixture. Semax C₃₇H₅₁N₉O₁₀S; Selank C₃₃H₅₇N₁₁O₉
Molecular weight
Mixture. Semax ≈813.9 g/mol; Selank ≈751.9 g/mol
CAS number
Not applicable (mixture). Components: 80714-61-0 / 129954-34-3 [TO VERIFY against supplier COA]
Form
Lyophilised powder
Purity
≥99% (see COA)
Format
Lyophilised vial
Vial sizes
20 mg

Identity values are confirmed per lot on the certificate of analysis. Salt/counter-ion form (e.g. acetate or TFA) is stated on the COA where applicable.

Mechanisms investigated
  • Semax: BDNF: specific Semax binding sites were reported in rat basal forebrain, with increased BDNF levels [1].
  • Selank: GABAergic system: changes in expression of genes involved in GABAergic neurotransmission were reported, and allosteric modulation of GABA-A receptors was proposed [5][3].
Research areas & model types
Research areaModel typeSummary
Semax – Cerebral ischaemia modelsRat[9][10][11]
Semax – Neurotransmitter systemsRodent[2]
Selank – Gene expressionRat; in vitro (IMR-32)[5][12]
Selank – Behavioural modelsRat[13]
Human clinical research status
  • No studies of this combination were identified. Clinical-status notes for individual components are summarised below; they do not apply to the blend.
  • Semax: Clinical studies of Semax in ischaemic stroke have been published in Russian journals [6][7]. Semax is not authorised as a medicine in the UK, the EU or the US.
  • Selank: A Russian clinical study compared Selank with medazepam [8]. Selank is not authorised as a medicine in the UK, the EU or the US.
Safety observations reported in studies
  • No safety data exist for the combination. Interactions between components have not been studied.
Known limitations
  • The combination has not been studied; whether the components interact chemically or biologically in solution is unknown.
Storage & handling for laboratory use

Store at −20 °C. Protect from light.

Store lyophilised material sealed at −20 °C or below, protected from light and moisture. Allow the vial to equilibrate to room temperature before opening to limit condensation.

  • Allow the sealed vial to reach room temperature before opening to limit condensation.
  • Any solutions should be prepared only for in-vitro laboratory work under your own validated protocol; aliquoting limits repeated freeze–thaw cycles.
  • Handle with standard laboratory PPE in line with your risk assessment and the Safety Data Sheet (SDS). Britpep does not provide preparation or administration guidance.

Emerging & theoretical

Unconfirmed — hypotheses & ongoing research

These are unconfirmed hypotheses and early-stage lines of enquiry, not established effects. Not evaluated by the MHRA. Not for human or veterinary use.

Hypotheses proposed by researchers

  • Semax: Researchers have proposed that Semax's effects are mediated in part by modulating neurotrophin (BDNF/TrkB) expression [1][9].
  • Selank: Researchers have proposed that Selank acts as a positive allosteric modulator of GABA-A receptors [3].

Open scientific questions

  • Whether the components are chemically compatible and stable when combined has not been reported.

Preprints: none included (no relevant preprint could be verified). Anecdotal, user-reported or social-media material is deliberately excluded.

References

  1. Dolotov OV, Karpenko EA, Seredenina TS et al.. Semax, an analogue of adrenocorticotropin (4-10), binds specifically and increases levels of brain-derived neurotrophic factor protein in rat basal forebrain. J Neurochem. 2006. PubMed 16635254 · doi:10.1111/j.1471-4159.2006.03658.x
  2. Eremin KO, Kudrin VS, Saransaari P et al.. Semax, an ACTH(4-10) analogue with nootropic properties, activates dopaminergic and serotoninergic brain systems in rodents. Neurochem Res. 2005. PubMed 16362768 · doi:10.1007/s11064-005-8826-8
  3. Vyunova TV, Andreeva L, Shevchenko K et al.. Peptide-based Anxiolytics: The Molecular Aspects of Heptapeptide Selank Biological Activity. Protein Pept Lett. 2018. PubMed 30255741 · doi:10.2174/0929866525666180925144642
  4. Kozlovskaya MM, Kozlovskii II, Val'dman EA et al.. Selank and short peptides of the tuftsin family in the regulation of adaptive behavior in stress. Neurosci Behav Physiol. 2003. PubMed 14969422 · doi:10.1023/a:1025988519919
  5. Volkova A, Shadrina M, Kolomin T et al.. Selank Administration Affects the Expression of Some Genes Involved in GABAergic Neurotransmission. Front Pharmacol. 2016. PubMed 26924987 · doi:10.3389/fphar.2016.00031
  6. Gusev EI, Martynov MY, Kostenko EV et al.. [The efficacy of semax in the tretament of patients at different stages of ischemic stroke]. Zh Nevrol Psikhiatr Im S S Korsakova. 2018. PubMed 29798983 · doi:10.17116/jnevro20181183261-68
  7. Gusev EI, Skvortsova VI, Miasoedov NF et al.. [Effectiveness of semax in acute period of hemispheric ischemic stroke (a clinical and electrophysiological study)]. Zh Nevrol Psikhiatr Im S S Korsakova. 1997. PubMed 11517472
  8. Zozulia AA, Neznamov GG, Siuniakov TS et al.. [Efficacy and possible mechanisms of action of a new peptide anxiolytic selank in the therapy of generalized anxiety disorders and neurasthenia]. Zh Nevrol Psikhiatr Im S S Korsakova. 2008. PubMed 18454096
  9. Dmitrieva VG, Povarova OV, Skvortsova VI et al.. Semax and Pro-Gly-Pro activate the transcription of neurotrophins and their receptor genes after cerebral ischemia. Cell Mol Neurobiol. 2010. PubMed 19633950 · doi:10.1007/s10571-009-9432-0
  10. Medvedeva EV, Dmitrieva VG, Povarova OV et al.. The peptide semax affects the expression of genes related to the immune and vascular systems in rat brain focal ischemia: genome-wide transcriptional analysis. BMC Genomics. 2014. PubMed 24661604 · doi:10.1186/1471-2164-15-228
  11. Sudarkina OY, Filippenkov IB, Stavchansky VV et al.. Brain Protein Expression Profile Confirms the Protective Effect of the ACTH((4-7))PGP Peptide (Semax) in a Rat Model of Cerebral Ischemia-Reperfusion. Int J Mol Sci. 2021. PubMed 34201112 · doi:10.3390/ijms22126179
  12. Filatova E, Kasian A, Kolomin T et al.. GABA, Selank, and Olanzapine Affect the Expression of Genes Involved in GABAergic Neurotransmission in IMR-32 Cells. Front Pharmacol. 2017. PubMed 28293190 · doi:10.3389/fphar.2017.00089
  13. Kasian A, Kolomin T, Andreeva L et al.. Peptide Selank Enhances the Effect of Diazepam in Reducing Anxiety in Unpredictable Chronic Mild Stress Conditions in Rats. Behav Neurol. 2017. PubMed 28280289 · doi:10.1155/2017/5091027

Every reference was checked against PubMed (NCBI) before publication. Summaries describe published research only and are not claims of any effect in humans or animals.

Certificates of analysis

[No batch COA published yet. The certificate for each lot will be listed here and in the COA checker before release.]

Open the COA checker