N-Acetyl-Thr-Lys-Pro-Arg-Pro-Gly-Pro-NH2 (N-acetylated, C-terminal amidated analog of Selank/TP-7)
Investigational derivative of selank. Not FDA-approved or evaluated for compounding. Available as a research chemical.
A chemically stabilized version of Selank, an anti-anxiety peptide developed in Russia, modified to last longer in the body. No human trials exist for this specific form; its expected effects on anxiety and thinking ability are based on studies of the original Selank compound.
This entry is a cited research summary, not an established treatment reference. Dosing language is included as source context, not as medical instruction.
N-Acetyl Selank Amidate is preclinical or hypothesis-only.
Investigational derivative of selank. Not FDA-approved or evaluated for compounding. Available as a research chemical.
Safety data is primarily extrapolated from the parent compound Selank, not from direct NA-Selank-Amidate studies. Published Selank clinical trials (sample sizes ~60-70 patients, durations up to ~1 month) reported no treatment-related serious adverse events and no dose-limiting toxicities (PMID 25176261, PMID 26356395). No FAERS or EudraVigilance safety signals found for NA-Selank-Amidate as of March 2026. No chronic toxicology, carcinogenicity, reproductive toxicology, or organ-impairment studies have been published. Preclinical rodent data for Selank show no tolerance, tachyphylaxis, withdrawal effects, or dependence signals (PMC5322660; PMID 24913576). The absence of long-term safety data should NOT be interpreted as evidence of absence of risk.
If real-world use or exposure is being considered, review potential interactions, contraindications, and monitoring needs with a licensed clinician rather than relying on summary copy alone.
Every claim on this page links to one of the 11 sources below. Identifiers are PubMed (PMID), ClinicalTrials.gov (NCT), or DOI; click through to the source of record before acting on a claim.