ID: selank
Aliases: Thr-Lys-Pro-Arg-Pro-Gly-Pro, tuftsin analog, SELANK
Type: compound
Route/form: intranasal in regional clinical/research literature; formulation varies by study and region
Status: regional_or_research
Evidence level: early human
Best data tier: human controlled/review
Support scope: human, non-human/mechanistic
Source types: human_rct, preclinical
Linked sources: 3
Broad outcomes: Brain / mood / sleep, Gut / immune / inflammation
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- tuftsin-derived immunopeptide signaling
- GABAergic/monoaminergic modulation hypotheses
- anxiolytic pathway hypotheses
Optimization domains
- anxiety
- cognition
- immune
- nootropic
- CNS
Research basis
- Mechanism and human-optimization relevance are retained only where backed by scientific sources.
Limits, risks, and missing evidence
- Evidence quality and generalizability are weaker than for standard anxiolytics, and much of the literature is regional/older or preclinical.
Risk flags
- regional evidence
- limited human data
- CNS
- intranasal delivery uncertainty
- unapproved context
Linked papers, labels, and reviews
- Efficacy and possible mechanisms of action of a new peptide anxiolytic Selank in generalized anxiety disorders and neurasthenia
human_rct / pubmed_selank_gad_2008
Russian comparative clinical study in GAD/neurasthenia; regional evidence and translation caveats apply. - Expression of inflammation-related genes in mouse spleen under tuftsin analog Selank
preclinical / pubmed_selank_immune_gene_expression_2011
Mouse spleen inflammatory-gene-expression study for Selank and fragments. - Transcriptome alteration in hippocampus under the treatment of tuftsin analog Selank
preclinical / pubmed_selank_transcriptome_2013
Rat hippocampus transcriptome study after intranasal Selank exposure.