Compare Peptides

Select any two compounds for a side-by-side comparison of mechanism, uses, risks, and FDA regulatory status.

Popular comparisons

Emideltide

DSIP, Delta Sleep-Inducing Peptide

Pending PCAC
Sleep & Neurological

Pinealon

EDR peptide, Glu-Asp-Arg

Unregulated
Nootropic & Neuroprotective
Overview

A nonapeptide (9 amino acids) first isolated from rabbit cerebral venous blood in 1977. Originally studied for sleep-induction properties, it is now being investigated for opioid withdrawal and chronic insomnia.

A synthetic tripeptide (Glu-Asp-Arg) developed by the St. Petersburg Institute of Bioregulation and Gerontology — the same institution behind Epitalon. Pinealon is designed to target the central nervous system and pineal gland, with research focused on neuroprotection, cognitive function, and circadian rhythm regulation.

Mechanism of Action

Modulates the sleep-wake cycle through interactions with opioid, serotonin, and other neurotransmitter systems. Reduces the activity of stress-response systems. Mechanism is not fully characterized, but effects appear to be on circadian regulation and stress adaptation.

Penetrates the blood-brain barrier and accumulates in neurons. Modulates gene expression related to neuronal survival and function. Reduces oxidative stress in neural tissue. Appears to regulate melatonin synthesis through pineal gland activity, supporting circadian rhythm normalization.

Common Uses
  • Sleep quality improvement
  • Opioid withdrawal support
  • Stress and cortisol reduction
  • Chronic insomnia
  • Narcolepsy (investigational)
  • Cognitive enhancement and memory
  • Neuroprotection
  • Sleep quality improvement
  • Age-related cognitive decline
  • Stroke recovery support (preliminary research)
Known Risks
  • Limited human clinical data
  • Mechanism not fully understood
  • Potential interactions with opioid medications
  • Inconsistent results across studies
  • Long-term effects unknown
  • Very limited independent Western research
  • Most studies from Russian institutions
  • Long-term safety unknown
  • Mechanism not fully characterized
  • Injection site reactions
Regulatory Status
Pending PCAC

Removed from FDA 503A Category 2 effective April 22, 2026. Scheduled for PCAC review on July 24, 2026 for opioid withdrawal, chronic insomnia, and narcolepsy indications. Compounding not yet authorized — status is in regulatory gray zone pending PCAC recommendation.

PCAC: July 24, 2026

Unregulated

Not FDA-approved and not on any compounding list. Available as a research chemical. Research base is almost entirely from Russian institutions — independent replication is limited. Not affected by the 2026 regulatory changes.

This comparison is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before starting any peptide therapy.