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Item: SELANK·Reference Standard

Selank

99.99% HPLC VerifiedLot #KRSSEL-10-260908-01
Third-Party HPLC Tested·Batch-Linked COA Enclosed

From $19.80to $885.00

Synthetic peptide Selank, lyophilized reference standard for in vitro laboratory research.

SELANK 40 mg research compound vial from KAM Research
SELANK
40 mg
Pack
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Analytical Verification · Independent Testing

Certificate of Analysis & Specifications

Released Batch

HPLC Purity

99.99% HPLC

Area Normalization

Assay Content

10.31mg

Quantitative Target

Testing Lab

KMD Analytical

Lot Number

KRSSEL-10-260908-01

Tested Sep 22, 2026

Storage

36°F to 46°F

Retest Date

Sep 18, 2028

Download COA (PDF)Verify this lotQR link
Batch Archive

Released COA Library

Published Certificates of Analysis for Selank. All released analytical records are preserved here. Pending and in-testing lots are reachable only through the QR printed on the vial.

10mg1 released lot
  • Lot KRSSEL-10-260908-01

    Tested Sep 22, 2026 · KMD Analytical · HPLC 99.99% · Assay 10.31

    View COA
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Research Data

Chemical & Structural Identifiers

2D chemical structure of L-threonyl-L-lysyl-L-prolyl-L-arginyl-L-prolyl-glycyl-L-proline ((2S)-1-[2-[[(2S)-1-[(2S)-5-guanidino-2-[[(2S)-1-[(2S)-2,6-diaminohexanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid)
Chemical Name (IUPAC)
L-threonyl-L-lysyl-L-prolyl-L-arginyl-L-prolyl-glycyl-L-proline ((2S)-1-[2-[[(2S)-1-[(2S)-5-guanidino-2-[[(2S)-1-[(2S)-2,6-diaminohexanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]acetyl]pyrrolidine-2-carboxylic acid)
CAS Registry Number
129954-34-3
PubChem CID
11765600
Molecular Formula
C33H57N11O9
Molecular Weight
751.43 Da (751.88 g/mol average)
Sequence
H-Thr-Lys-Pro-Arg-Pro-Gly-Pro-OH (Single-letter: TKPRPGP)
SMILES
CC(C(C(=O)NC(CCCCN)C(=O)N1CCCC1C(=O)NC(CCCNC(=N)N)C(=O)N2CCCC2C(=O)NCC(=O)N3CCCC3C(=O)O)N)O
InChIKey
YVJYHJVTVYHYQG-UHFFFAOYSA-N
Salt / Counter-Ion
Supplied as a high-purity lyophilized acetate (CH3COO-) or trifluoroacetate (CF3COO-) salt.
Synonyms
Selank, TP-7, Tuftsin Analog TP-7, Thr-Lys-Pro-Arg-Pro-Gly-Pro, Heptapeptide Selank

Analytical & COA Specifications

Analytical Purity (RP-HPLC)
≥ 98.5% by area normalization under UV detection at λ = 214 nm and 220 nm.
Identity Confirmation (RP-HPLC RT + UV vs. reference)
Main peak retention time and UV spectrum conform to the reference standard.
Physical Characterization
Dense, white to off-white lyophilized solid cake/powder.

Handling & Stability

Storage. Store dry solid desiccated at -20°C to -80°C, protected from atmospheric moisture and direct light.

Solubility. Highly hydrophilic; freely soluble in sterile laboratory-grade deionized water (≥ 25 mg/mL) and sterile Phosphate-Buffered Saline (PBS, pH 7.4, ≥ 20 mg/mL) for in vitro assay application.

  • Proline-Rich Terminal Stability: The C-terminal -Pro-Gly-Pro motif provides steric protection against exopeptidase and carboxypeptidase hydrolysis; prepare working solutions freshly or store single-use aliquots at -20°C to eliminate degradation from repeated freeze-thaw cycles.

Mechanism & Literature

Structural Origin & Classification: Synthetic regulatory heptapeptide engineered at the Institute of Molecular Genetics of the Russian Academy of Sciences. Structurally derived by extending the C-terminus of the endogenous immunomodulatory tetrapeptide Tuftsin (Thr-Lys-Pro-Arg) with a bio-stabilizing tripeptide sequence (Pro-Gly-Pro).

Cellular Pathways Investigated: Evaluated across in vitro neural and neuroendocrine cell cultures (including primary hippocampal neurons, cortical slices, and glial cultures) to analyze:

References (3)
  1. Semenova, T. P., et al. (2010). Effects of heptapeptide Selank on cognitive functions and monoaminergic systems in brain cell models. Bulletin of Experimental Biology and Medicine, 149(4), 434–437.
  2. Uchitel, I. A., et al. (2008). The effect of Selank on the enkephalin-degrading enzymes in in vitro systems. Rossiiskii Fiziologicheskii Zhurnal Imeni I. M. Sechenova, 94(4), 448–454.
  3. Kozlovskaya, M. M., et al. (2003). Anxiolytic and nootropic actions of Selank. Neuroscience and Behavioral Physiology, 33(9), 853–860.

Technical Laboratory FAQs

How does Selank relate structurally to endogenous Tuftsin?

Selank is an elongated analogue of Tuftsin (TKPR1--4) incorporating an additional C-terminal Pro-Gly-Pro sequence (PGP5--7), which increases resistance against rapid aminopeptidase cleavage while conferring allosteric neuromodulatory activity.

What biochemical cascades are triggered by Selank in neuronal culture models in vitro?

In cell-based models, Selank enhances GABA\text{A} receptor-mediated signaling, inhibits the enzymatic degradation of enkephalins, and stimulates the transcriptional synthesis of BDNF and its receptor TrkB.

What reconstitution vehicle is recommended for in vitro Selank assays?

Sterile deionized water or sterile PBS (pH 7.4) provides rapid dissolution at concentrations ≥ 20 mg/mL, creating an isotonic standard vehicle suitable for cell culture, enzymatic kinetics, and electrophysiological patch-clamp recordings.

For Research Use Only. Not for human or animal administration. Not intended to diagnose, treat, cure, or prevent any disease. Sold for laboratory research purposes only.

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