RESEARCH MONOGRAPH · KDC-MN-010
Selank
Selank is a synthetic seven-amino-acid peptide developed in Russia as an analog of the immune peptide tuftsin. It has anxiolytic and immunomodulating effects in research and is approved as a prescription anxiolytic in Russia. It does not produce sedation or dependence. Stocked in the Kodiac catalog as a research-only powder for laboratory work; not a medicine, not for human consumption.
Intrigue 0–100 blends mechanism novelty, evidence strength, and translational potential. Kodiac editorial, not peer-reviewed.
Synthetic heptapeptide anxiolytic, tuftsin analog
A 7-residue peptide developed at the Russian Academy of Sciences as a stable analog of tuftsin, characterized for anxiolytic, immunomodulatory, and cognitive endpoints in a substantial Russian-language literature.
Abstract
Selank (sequence Thr-Lys-Pro-Arg-Pro-Gly-Pro; CAS 129954-34-3; molecular formula C33H57N11O9; molecular weight 751.85) is a synthetic heptapeptide developed in the early 1990s at the Institute of Molecular Genetics of the Russian Academy of Sciences in collaboration with the Zakusov Research Institute of Pharmacology. The peptide is a stabilized analog of tuftsin, a naturally occurring tetrapeptide (Thr-Lys-Pro-Arg) derived from immunoglobulin G that has documented immunomodulatory effects but a very short half-life. Selank extends the tuftsin sequence with the C-terminal tripeptide Pro-Gly-Pro to confer protection against rapid peptidase degradation. The compound has been studied principally in the Russian clinical and preclinical literature, with the largest body of work on anxiolytic effects in generalized anxiety disorder, immunomodulatory effects in viral and bacterial infection models, and cognitive effects in attention and memory tasks. Selank is registered as a prescription medicine in the Russian Federation for the treatment of generalized anxiety disorder under the trade name Selank Bioregulator. The compound is not approved by any regulatory authority outside the Russian Federation; clinical use in the United States, the European Union, and Japan is off-label and outside the scope of regulatory oversight. The principal limitations on the strength of the evidence are the dominance of the Russian-language literature, limited Western independent replication of the most-cited findings, and the relatively small clinical sample sizes in the published trials.
Read the full monograph
The full reference document covers compound identification, discovery and developmental history, mechanism of action, pharmacokinetics, reported research dose ranges, sourcing and quality verification, reconstitution and handling, stack interaction considerations, and a curated reference list. Available as a research-use-only PDF download.
The full reference document is provided strictly for research use only. It reports research dose ranges from the published literature, not instructions for use in humans or animals.
Acquire Selank from the catalog
View Selank →FOR RESEARCH USE ONLY. Not for medical, diagnostic, or therapeutic purposes. Not for human consumption. All information is provided for research and educational purposes only.