
Lucas Weber
Principal Chemist
Selank
Product information
Product description
Selank is a stabilised heptapeptide analog of tuftsin, studied for anxiolytic activity reported to occur without the sedation characteristic of conventional anxiolytics. Proposed mechanisms span GABAergic modulation, serotonin metabolism and inhibition of enkephalin degradation; none is established as primary. Requires reconstitution before use.


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Selank
- Characteristics
- How does Selank work?
- Research
- Safety & Handling
- Summary
- References
- Resource
- Peptonova Labs peptides
Characteristics
Compound class | Synthetic heptapeptide, stabilised tuftsin analog |
CAS Number | 129954-34-3 |
Molecular Formula | C33H57N11O9 |
Molar Mass | 751.9 g/mol |
Sequence | Thr-Lys-Pro-Arg-Pro-Gly-Pro |
Synonyms | Selank, TP-7 |
Molecular target | No single receptor established; GABAergic and enkephalinase routes proposed |
Physical form | Lyophilized powder |
Solubility | Water-soluble |
Lot documentation | Lot-specific Certificate of Analysis recording identity and measured purity |
How does Selank work?
Selank is a synthetic heptapeptide, Thr-Lys-Pro-Arg-Pro-Gly-Pro, constructed by extending the immunomodulatory tetrapeptide tuftsin with a Pro-Gly-Pro tail. The extension is the same stabilising strategy used in Semax: proline-rich C-terminal sequences resist aminopeptidase cleavage and substantially increase half-life in biological fluids.
The pharmacology attributed to it is anxiolytic without sedation, which is the property that distinguishes it from benzodiazepines and makes it interesting as a research tool. Proposed mechanisms include modulation of GABAergic transmission, effects on serotonin metabolism, and regulation of enkephalin-degrading enzyme activity — the last of which would prolong endogenous opioid peptide signalling rather than acting on opioid receptors directly.
Reported effects on brain-derived neurotrophic factor expression in hippocampus link it to the same neurotrophic literature as Semax, with which it is often studied in parallel.
Research
Findings below are drawn from published preclinical and clinical work and are presented for research context only.
Tuftsin lineage. The peptide is a stabilised tuftsin analog; the parent tetrapeptide has its own immunomodulatory literature.
Anxiolysis without sedation. The reported separation of anxiolytic effect from sedation is the property most often cited as distinguishing this compound from conventional anxiolytics.
Enkephalin degradation. Inhibition of enkephalin-degrading enzymes is proposed as a mechanism, which would act by prolonging endogenous opioid signalling rather than by receptor agonism.
Neurotrophic signalling. Reported effects on brain-derived neurotrophic factor expression connect it to the Semax literature.
Connectomic studies. Recent functional connectomic work has examined Selank and Semax together, comparing their network-level effects directly.
Safety & Handling
This section describes laboratory handling. It is not clinical guidance, and no safety claim for human or veterinary administration is made or implied.
Supplied lyophilized. Reconstituted peptide solutions have materially shorter working stability than the dry powder — prepare working aliquots and avoid repeated freeze-thaw cycles.
Handle as a research chemical of undetermined hazard. Use gloves, eye protection and a laboratory coat.
Storage temperature and, where applicable, reconstitution conditions are stated on the item specification sheet and the lot Certificate of Analysis, which take precedence over general guidance.
Dispose of unused material and consumables in accordance with the institutional chemical waste policy.
For laboratory research use only. Not for human or veterinary use. Not a drug, food, cosmetic or dietary supplement.
Summary
Selank is a stabilised heptapeptide analog of tuftsin studied for anxiolytic activity that is reported to occur without the sedation characteristic of conventional anxiolytics.
Proposed mechanisms span GABAergic modulation, serotonin metabolism and inhibition of enkephalin degradation; none is established as primary. Much of the literature originates in Russian-language pharmacology and is often studied in parallel with Semax.
References
Resource
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