FOR RESEARCH PURPOSES ONLY — This compound is not FDA approved. All data presented is from clinical trials for educational reference.
Plasma Concentration Studies
DSIP
Delta-Sleep Peptide
Emideltide
A 9-peptido acid peptide that modulates delta-wave sleep architecture and circadian rhythm signaling, studied for sleep onset mechanisms in research models. Premium Research Peptide.
Certificate of Analysis
Third Party Tested by Freedom Diagnostics
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59%
Sleep Increase
Within 130 minutes of administration
97%
Symptom Relief
Opiate withdrawal (107 patients)
86%
Pain Reduction
Chronic pain patients (6/7)
NoLD50
Safety Record
No lethal dose ever determined
9peptido acids
Nonapeptide
WAGGDASGE sequence
How DSIP Works
Third Party Tested by Freedom Diagnostics
The Science, Simplified
Natural Sleep Programming
DSIP is synthesized in the hypothalamus and targets multiple sites in the brainstem. Unlike sedatives, it promotes natural sleep architecture by modulating circadian rhythms, neurotransmitters, and stress-response systems — without causing dependence or tolerance.
CIRC
Circadian Pathway
Circadian Rhythm Modulation
Regulates sleep-wake cycles Normalizes disturbed sleep patterns. Effects persist for days after dosing
OPI
Opioid Pathway
Endogenous Opioid System
Modulates pain perception. Blocked by naloxone. Supports withdrawal management.
Unlike most peptides, DSIP freely crosses the blood-brain barrier and can be absorbed from the gut without enzymatic degradation. It’s even present in human breast milk at 10-30 ng/mL concentrations.
Key distinction: DSIP promotes sleep without sedation — it supports natural sleep mechanisms rather than forcing unconsciousness
What Research Has Shown
Clinical trials and human studies
📋
Human Clinical Trials
59%
Increase in Total Sleep Time Within 130 Minutes
Withdrawal Symptom Relief
Opiate Addicts
Alcohol Addicts
Trial details: 107 inpatients (60 opiate, 47 alcohol) received IV DSIP. Clinical symptoms and signs disappeared or improved markedly and rapidly in the vast majority of patients.
📈
Clinical Outcomes
Response Rates Across Indications
Consistent efficacy across multiple conditions
Showed symptom improvement Opiate withdrawal group
97% of subjects
Showed symptom improvement Alcohol withdrawal group
87% of subjects
Experienced pain reduction Chronic pain patients
86% of subjects
💡Key observation: DSIP’s effects persisted for days after treatment, suggesting it ‘reprograms’ natural sleep patterns rather than providing temporary relief.
DSIP demonstrates an exceptional safety profile. No lethal dose (LD50) has ever been determined because it has proven impossible to kill an animal with DSIP regardless of dose — a remarkable finding for any bioactive compound.
🤢 Common Digestive Issues
15%
Headache
10%
Nausea
8%
Vertigo/Dizziness
5%
Daytime Grogginess
🛡️
Safety Profile
No Lethal Dose
DSIP’s LD50 has never been determined because it has never proven possible to kill an animal regardless of the dose administered
Exceptional safety margin
No dependence or tolerance
Naturally occurring endogenous peptide
📊
Discontinuation Rates
Tolerability in Clinical Trials
Withdrawal studies
Well-tolerated
Insomnia studies
No significant AEs
Pain studies
Occasional headaches
💡 No tolerance development with repeated dosing.
💡 No withdrawal symptoms upon discontinuation.
💡 Naturally occurring peptide in human body.
🚫 Trial Exclusions
Research Considerations
Caution with ACE inhibitors (shared metabolic pathway)
Limited data on pregnancy/breastfeeding (present in milk)
Drug interactions not extensively studied
Long-term effects require more research
💡 Researcher Notes
Remarkably safe profile for a bioactive peptide
No serious adverse events reported in published studies
Naturally occurring substance found in human tissues
Present in breast milk — indicating natural safety profile
Compound Information
Technical specifications
🔬 Molecular Profile
What Is DSIP?
Naturally occurring nonapeptide first isolated from rabbit brain in 1977
Nonapeptide
Endogenous
Type
Synthetic nonapeptide
CAS Number
62568-57-4
Molecular Formula
C35H48N10O15
Molecular Weight
848.8 g/mol
Amino Acids
9 residues
Sequence
Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu
🧊 Storage Requirements
Stability Information
Handle with care to maintain potency
Light sensitive
Temperature sensitive
Lyophilized (powder)
-20°C • up to 2 years
Reconstituted
2-8°C
•
up to 30 days
Stability
15 minutes (plasma half-life)
📋
Research Status
Development History
First isolated from rabbit brain in 1977 by Schoenenberger & Monnier