Research Compound Reference

Selank Research Peptide

Selank is a synthetic heptapeptide, Thr-Lys-Pro-Arg-Pro-Gly-Pro, formed by extending the natural tetrapeptide tuftsin with a C-terminal Pro-Gly-Pro sequence. This reference covers its chemical identity, documented research history and analytical characterisation.

For research use only. Not for human consumption.

Chemical identity reference

Compound name
Selank
Common synonyms
Selanc, tuftsin-PGP analogue
Peptide sequence
TKPRPGPThr-Lys-Pro-Arg-Pro-Gly-Pro
Residue count
7 amino acids
Molecular formula
C33H57N11O9
Average molecular weight
≈ 751.9 g/mol
CAS number
129954-34-3
UNII
TS9JR8EP1G
Structural origin
Tuftsin (Thr-Lys-Pro-Arg) extended at the C-terminus with Pro-Gly-Pro
Research classification
Synthetic regulatory peptide (tuftsin analogue)
Vial Drop research format
Supplied as the Selank 10 mg component of the Semax / Selank 10 mg / 10 mg research blend

Chemical identity

Selank is a seven-residue synthetic peptide, TKPRPGP. Its first four residues are tuftsin — Thr-Lys-Pro-Arg — a naturally occurring tetrapeptide fragment derived from immunoglobulin G. The final three residues, Pro-Gly-Pro, are a synthetic extension.

The design logic parallels Semax: the same C-terminal Pro-Gly-Pro motif is appended to a short natural fragment, and it is reported to slow enzymatic degradation relative to the unmodified parent peptide. Selank and tuftsin are nonetheless separate chemical entities, and Selank carries its own CAS registry number, 129954-34-3.

The sequence is strongly basic — it contains both lysine and arginine — which influences chromatographic retention and ionisation, and distinguishes it clearly from Semax in a chromatogram.

Documented research history

Selank emerged from the same Russian institutional lineage as Semax, developed jointly by the Institute of Molecular Genetics of the Russian Academy of Sciences and the Institute of Pharmacology of the Russian Academy of Medical Sciences, from earlier tuftsin-family peptide research.

Published work includes behavioural and mechanistic studies in animal models, a small Russian comparative clinical study in anxiety-spectrum conditions involving 62 participants, and more recent in-vitro work examining effects on gene expression in cultured neuronal cell lines.

The same evidence-base caveats apply as for Semax, and they are substantial: clinical work is small in scale, not consistently blinded or placebo-controlled by contemporary standards, published predominantly in Russian venues, and largely unreplicated by independent groups. This page describes what has been studied, not what any material does in a person.

Analytical methodology

At approximately 752 g/mol, Selank is characterised the same way as the other peptides documented here: an HPLC-DAD run reporting the area-percent share of the principal component and its content against label claim, with identity reported as conforming against a reference standard.

Independent analytical documentation for Vial Drop Labs Selank 10 mg is available in the Research Documentation library. A separate report covers the Semax / Selank 10mg / 10mg blend, and each report applies only to the material and tested sample it was issued for.

Because the sequence carries multiple basic residues, it typically elutes differently from a neutral or acidic peptide of similar size — the practical reason Semax and Selank can be resolved and quantified individually within a combined preparation.

Reading the analytical documentation

A Certificate of Analysis links a submitted sample to the analytical work performed on it. Current Vial Drop Labs reports are produced by validated HPLC-DAD methodology and answer two separate questions — what the material is, and how much of it is present.

  • Identity — on current Vial Drop Labs reports, identity is reported as conforming on the basis of retention time and UV/DAD spectral comparison against a reference standard. Current reports do not include mass-spectrometry results.
  • Purity — HPLC separates the dissolved sample across a column; the target peak's share of total integrated peak area is reported as an area-percent purity figure.
  • Content — peptide and compound reports separately state the content per vial in mg against the stated label claim. Chromatographic purity and content per vial are two different measurements and should not be read as one.
  • Sample scope — the report identifiers and test date describe the randomized sample the laboratory received and the batch it was drawn from as supplied to the laboratory. Recording the certificate ID alongside your own experimental records keeps the analytical record resolvable.
  • Scope — a report describes only the specific sample submitted. Unless a report expressly states otherwise, it does not assess sterility, endotoxin, microbial content, heavy metals or residual solvents, and it is not a safety or fitness-for-use determination.

How Vial Drop publishes analytical documentation

Vial Drop Labs publishes independent analytical reports for tested research materials, with available reports accessible through the Research Documentation portal against the research material and the sample identified on each report. Each analytical report applies only to the sample submitted for analysis and should not be interpreted as testing of every vial or production unit.

Not every report is publicly listed. Where no report has been published for a material, the portal shows none rather than substituting another material's, strength's or batch's results. Documentation is never averaged, combined, or extrapolated between lots.

Current reports are issued by an independent third-party analytical laboratory using validated HPLC-DAD methodology. They report chromatographic purity as area %, content per vial against label claim, and identity as conforming by retention-time and UV/DAD comparison against a reference standard. Current reports do not include mass-spectrometry results.

Vial Drop Labs makes no representation that material is pharmaceutical grade, clinical grade, sterile, safe, or approved by any regulatory authority. Published documentation states exactly what was tested, by which method, and on which date — nothing further should be inferred from it.

Laboratory storage and handling

Material is supplied lyophilised in a sealed glass vial. General laboratory practice for lyophilised peptides applies: store sealed at -20 °C for long-term storage, protect from light, and minimise exposure to atmospheric moisture.

Allow a cold sealed vial to equilibrate to ambient temperature before opening so that atmospheric moisture does not condense onto the dry cake. Lyophilised peptide material is hygroscopic, and repeated warm/cold cycling of an opened vial is the most common cause of avoidable degradation in a laboratory setting.

Handle as an uncharacterised laboratory chemical using standard laboratory protective equipment and institutional handling procedures.

Research use only

This material is supplied strictly as a laboratory research chemical. It is not a drug, supplement, cosmetic, food or medical device, and it is not manufactured, labelled or sold for human or animal use of any kind.

Vial Drop Labs does not provide, and cannot provide, dosing, administration, preparation-for-use, therapeutic or clinical guidance. Published information is limited to chemical identity, laboratory handling and analytical documentation.

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FOR RESEARCH USE ONLY. NOT FOR HUMAN CONSUMPTION.