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Selank

Neuropeptide

Also known as: TP-7, Thr-Lys-Pro-Arg-Pro-Gly-Pro, TKPRPGP, tuftsin analog

Tier 3, Preclinical only

Evidence is limited to animal or in-vitro work. No human pharmacokinetics. Any human dose in circulation is extrapolated, and extrapolation across species routinely fails.

Half-life
Not established

No reliable primary plasma-PK figure. Vendor sources give mutually contradictory values (2-3 min, 2-10 min, and 20-30 min), none traceable to a primary source, so all are flagged unverified. Wikipedia's Selank entry reports NO PK parameters. Mechanistic primary work (PubMed 11550013, 12432865) shows Selank inhibits enkephalin-degrading enzymes in mouse plasma, which is a mechanism note, not a half-life.

Dosing
No established dose

No primary-sourced microgram dose obtained. Russian registered product is a 0.15% intranasal solution; circulating per-dose microgram figures are vendor/community-derived. Route is intranasal in registered use.

Regulatory status
Registered/approved in the Russian Federation (and available in Ukraine) as an anxiolytic (intranasal), reportedly after Phase 3 Russian trials. NOT approved by FDA, EMA, or other Western regulators.
Evidence base
mixed · confidence: medium

Registered in Russia with some clinical trial history, but Western peer-reviewed evidence is limited and much of it traces to the same Institute of Molecular Genetics (RAS) lineage as Semax. Limited independent replication and few blinded Western trials.

Storage

Lyophilised: General peptide convention: -20 C lyophilized (no compound-specific data).

Reconstituted: General convention: 2-8 C refrigerated (no compound-specific data).

Safety

Human safety data derives from Russian use; not Western-reviewed. Intranasal route in registered use. GABAergic/immunomodulatory activity reported.