Selank is available from Kimerachems for controlled laboratory and analytical research. Review the product-specific information, available formats and documentation below before ordering.
Selank (Tuftsin Analog) Research Standard
Selank (Thr–Lys–Pro–Arg–Pro–Gly–Pro) is a synthetic heptapeptide developed as an analog of the endogenous tetrapeptide tuftsin. It is widely utilized in laboratory research as a multimodal neuromodulator. Distinct from traditional benzodiazepines, Selank is investigated for its non-sedative anxiolytic properties and its unique capacity to influence cognitive and neuroimmune signaling pathways. Its structural design, derived from the tuftsin motif, provides a stable framework for probing stress-response mechanisms and the regulation of neurotransmitter systems in in vitro and in vivo research models.
Technical Specifications
| Property | Specification |
| Product Name | Selank |
| Peptide Sequence | Thr–Lys–Pro–Arg–Pro–Gly–Pro |
| CAS Number | 129954-34-3 |
| Chemical Formula | C33H57N11O9 |
| Molecular Weight | 751.86 g/mol |
| Chemical Class | Synthetic heptapeptide (Tuftsin analog) |
| Physical Appearance | White to off-white lyophilized powder |
| Solubility | Soluble in water and buffered aqueous solutions |
Mechanism of Action & Research Context
Selank is investigated as a complex neuromodulator that influences multiple signaling cascades without the classic profile of GABA-A receptor agonists.
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Neuromodulatory Activity: Research suggests Selank acts as an indirect modulator of GABAergic signaling. It is studied for its ability to affect serotonergic and dopaminergic pathways, which are critical in stress-related neural models.
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Neuroimmune Modulation: The compound’s interaction with neuroimmune pathways, particularly regarding cytokine signaling, makes it a valuable tool for studying the intersection between the immune system and neuronal health.
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Cognitive & Memory Support: In experimental systems, Selank is utilized to observe how peptides can support cognitive and memory-related signaling, especially under conditions of metabolic or psychological stress.
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Structural Stability: Its linear heptapeptide design is optimized for resilience, allowing for precise tracking of peptide-signaling interactions in laboratory environments.
Research Applications
Selank is a specialized reagent essential for neuropharmacological studies.
Primary fields of laboratory investigation include:
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Stress-Response Modeling: Analyzing the anxiolytic mechanisms of non-sedative peptides in isolated neural tissue.
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Cognitive & Memory Research: Investigating the modulation of neural pathways involved in information retention and recall.
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Neuroimmune Studies: Mapping the interaction between peptide regulators and cytokine-mediated immune signaling.
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Peptide-Based Neuromodulation: Utilizing Selank as a benchmark for researching synthetic peptides that bypass standard GABA-benzodiazepine receptor sites.
Storage & Handling Guidelines
To maintain the chemical stability and experimental viability of the peptide:
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Lyophilized State: Store in a cold, dry place. Maintain at temperatures below 0°C (typically -20°C) for long-term stability.
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Environmental Control: Protect from light and moisture to prevent the degradation of the peptide sequence.
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Reconstitution: Use sterile, buffered aqueous solutions. Once reconstituted, aliquot the solution to minimize freeze-thaw cycles and maintain the integrity of the peptide.
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Aseptic Technique: Handle with clean, sterile laboratory equipment in a controlled environment to ensure experimental accuracy and prevent contamination.
Research Use Disclaimer
Research Use Only Disclaimer: This product is developed and distributed strictly as a Research Use Only (RUO) laboratory reference chemical intended exclusively for non-clinical analytical and scientific investigation. It is not an FDA-approved drug, medical treatment, dietary supplement, or food ingredient, and is strictly prohibited for human or animal consumption. Kimera Chems supplies this high-purity research material solely to qualified institutions and professional investigators for authorized laboratory research.
| CAS Number | 129954-34-3 |
| Other Names | Selanc, TP-7, Thr-Lys-Pro-Arg-Pro-Gly-Pro, TP 7, UNII-TS9JR8EP1G, TS9JR8EP1G |
| IUPAC Name | (2S)-1-[2-[[(2S)-1-[(2S)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-5-(diaminomethylideneamino)pentanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid |
| Molecular Formula | C₃₃H₅₇N₁₁O₉ |
| Molecular Weight | 751.9 |
Product FAQs
What is Selank supplied for?
This material is supplied strictly for controlled, non-clinical laboratory and analytical research. It is not intended for human or animal consumption.
Which formats are available for Selank?
Available formats or options are shown in the product selector above. Current availability can change.
Where can I review product documentation?
Where available, batch documentation can be reviewed in the Certificate of Analysis library before ordering.



