Comparison · Updated

DSIP VS Selank

Short answer

DSIP and Selank have the same evidence tier: both are tier A (Controlled human trials).

Neither DSIP nor Selank is FDA-approved.

Neither DSIP nor Selank is on the WADA Prohibited List.

01

Side by side

Field DSIP
PubChem CID 68816
Selank
PubChem CID 11765600
Evidence tier A Tier A · Controlled human trials A Tier A · Controlled human trials
Tier rationale Small double-blind, placebo-controlled trials in chronic insomnia (e.g. Bes et al. 1992, n=16) found weak or no meaningful benefit; registered as a medicine in Russia but not FDA/EMA-approved. One small randomized trial (62 patients with anxiety disorders, selank vs medazepam, 2008; indexed in PubMed as an RCT), otherwise small Russian clinical studies; registered in Russia but not FDA/EMA-approved.
FDA status Not approved Not approved
Other approvals
  • Russia — Deltaran® intranasal (registered 2016) for stress-related states and alcohol withdrawal
  • Russia — Selank nasal drops 0.15% (Peptogen), registration ЛСР-003338/09
WADA Not on the Prohibited List Not on the Prohibited List
Family Mind Mind
Residues 9amino acids 7amino acids
Molecular weight 848.8 Da 751.9 Da
Formula C35H48N10O15 C33H57N11O9
Discovered 1977Isolated from rabbit blood during induced sleep and characterized by Schoenenberger and Monnier (PNAS 1977). Not on file
Routes studied Subcutaneous, Intramuscular Intranasal, Subcutaneous
Mechanism DSIP (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) has no identified gene, precursor protein, or specific receptor, so its mechanism and physiological role remain unresolved. Animal studies report effects on sleep, stress hormones, neurotransmitter levels, and opioid-related behaviors. Selank is a synthetic analog of the endogenous tetrapeptide tuftsin (Thr-Lys-Pro-Arg) with a C-terminal Pro-Gly-Pro extension for stability. It has been reported to modulate GABAergic neurotransmission and serotonin metabolism and to affect enkephalin-degrading activity in blood; it also retains immunomodulatory activity related to tuftsin.
Safety notes Human safety data are limited to small trials from the 1980s-1990s. Registered as an anxiolytic in Russia.
Cited studies 1 study 1 study
02

Questions

Which has stronger evidence, DSIP or Selank?
DSIP and Selank have the same evidence tier: both are tier A (Controlled human trials). DSIP: Small double-blind, placebo-controlled trials in chronic insomnia (e.g. Bes et al. 1992, n=16) found weak or no meaningful benefit; registered as a medicine in Russia but not FDA/EMA-approved. Selank: One small randomized trial (62 patients with anxiety disorders, selank vs medazepam, 2008; indexed in PubMed as an RCT), otherwise small Russian clinical studies; registered in Russia but not FDA/EMA-approved. Tiers rate the strength of published evidence, not effectiveness.
Is DSIP FDA-approved?
DSIP is not FDA-approved. Approvals listed outside the US: Russia — Deltaran® intranasal (registered 2016) for stress-related states and alcohol withdrawal.
Is Selank FDA-approved?
Selank is not FDA-approved. Approvals listed outside the US: Russia — Selank nasal drops 0.15% (Peptogen), registration ЛСР-003338/09.
Are DSIP and Selank banned in sport?
Neither DSIP nor Selank is on the WADA Prohibited List.
How do DSIP and Selank work?
DSIP (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) has no identified gene, precursor protein, or specific receptor, so its mechanism and physiological role remain unresolved. Selank is a synthetic analog of the endogenous tetrapeptide tuftsin (Thr-Lys-Pro-Arg) with a C-terminal Pro-Gly-Pro extension for stability.
esc
↑↓ navigate ↵ open