Selank For Sale
Description
Selank Research Standard
Selank (CAS 129954-34-3) is a synthetic heptapeptide built on the endogenous immunopeptide tuftsin, supplied as a 5 mg lyophilized powder in a 3 mL vial. Its published pharmacology spans two areas that are usually studied separately: neurotrophin regulation and immune gene expression.
Mechanism of Action & Research Context
Like the other peptides in this lineage, Selank has no established receptor target and its documented effects are measured as changes in expression.
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It normalises BDNF rather than raising it. The direction matters and is easy to get backwards. In rats given 10% ethanol as their sole fluid for 30 weeks, Selank (0.3 mg/kg/day for 7 days) prevented the ethanol-induced increase in BDNF content in hippocampus and frontal cortex, while preventing memory and attention disturbances during withdrawal. It also produced a cognitive-stimulating effect in non-ethanol-exposed animals. So the compound moves BDNF toward baseline in a perturbed system rather than pushing it up unconditionally.[1]
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Immune gene expression. A single dose significantly changed expression of chemokine, cytokine and receptor genes in mouse spleen at 6 and 24 hours.[2]
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A two-residue pharmacophore. Most of those mRNA-level changes were reproduced by Gly-Pro alone, identified as the Selank pharmacophore and the minimum fragment carrying antiviral activity. A dipeptide accounting for the majority of a heptapeptide’s transcriptional signature is a genuinely useful structure-activity result, and a cheap control arm.[2]
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Built from tuftsin. The parent is an endogenous immunopeptide, which is why the immune and neuro readouts sit side by side in this literature rather than in separate fields.[1,2]
Research Applications
Primary fields of laboratory investigation include:
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BDNF quantification in hippocampus and prefrontal cortex, in perturbed and unperturbed animals.[1]
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Chemokine and cytokine gene expression panels in spleen at multiple timepoints.[2]
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Fragment structure-activity work comparing full peptide against Gly-Pro.[2]
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Object recognition and attention paradigms paired with molecular endpoints.[1]
Analytical Documentation
Purity and identity vary by manufacturing lot. Kimera Chems does not publish a single fixed purity figure for this item; refer to the batch-specific Certificate of Analysis (COA) issued for the lot received, which reflects third-party analytical testing for that lot.’
Storage & Handling
Store at controlled room temperature, sealed and protected from light.
Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.
| Compound Class | Synthetic heptapeptide / Tuftsin analog |
| 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 |




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