DSIP is a nine-amino-acid peptide (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) that a Basel group isolated in 1977 from the cerebral venous blood of rabbits. Infused into other rabbits' brain ventricles, it increased slow-wave (delta) EEG activity, which gave it its name. Nearly 50 years later, nobody has found the gene that makes it, the protein it comes from, or a receptor it binds, so whether it is a real sleep signal in humans is still an open question.
Human testing happened mostly in the 1980s, by intravenous injection. One researcher reported that insomnia normalized over a week of injections, but two other double-blind trials found little: 16 patients in Amsterdam had slightly better sleep efficiency that the authors judged clinically unimportant, and a crossover study found no meaningful difference from placebo nights. Open-label reports in alcohol and opioid withdrawal and in chronic pain looked positive, but had no control group.
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DSIP is broken down in blood within minutes. Russia registers a nasal product, Deltaran, that mixes DSIP with glycine for stress and alcohol withdrawal. In the US it is unapproved. FDA reviewed it for compounding in July 2026. Its staff concluded the evidence did not support effectiveness for insomnia, narcolepsy or opioid withdrawal and that injectable safety is unknown, and the advisory committee voted 6-7 against listing it.
Structure9 residues
Hydrophobic
Polar
Negative charge
Gly / Pro / Cys
Sequence
Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu (WAGGDASGE)
Length
9 amino acids
Molecular weight
848.8 g/mol
Origin
Originally isolated from rabbit cerebral venous blood (Schoenenberger and Monnier, 1977); all products are synthetic. No precursor gene or protein has been identified.
Mechanism
How DSIP (Delta Sleep-Inducing Peptide) works
What it binds to, and what happens inside the body after that, step by step.
TargetUnknown receptor; indirect opioid (endorphin release) and possible neuroendocrine effects reported in animals
No DSIP receptor has been identified. In animals, its sleep and pain effects appear to run partly through the opioid system: FDA's review describes it stimulating calcium-dependent release of endorphins rather than binding opioid receptors directly, and animal work cited by the early withdrawal studies found the opioid blocker naloxone reversed its EEG effects. It also has reported effects on stress hormones in animals, but a human study found it did not change ACTH or cortisol responses.
1Injection or nasal doseHuman studies used intravenous injection; the Russian product is intranasal. A sheep study showed some passage from blood into cerebrospinal fluid via the choroid plexus.
2Rapid breakdownAminopeptidases cut DSIP from its N-terminal end. Plasma half-life is about 8 minutes in humans; 5-10 minutes in human serum in vitro.
3Opioid system activationIn animal work DSIP triggers endorphin release, which may explain reported analgesia and effects on withdrawal symptoms.
4EEG effect in rabbitsIntraventricular infusion increased delta and spindle EEG activity in rabbits; the effect on human sleep stages has been inconsistent.
The research
What the studies show
Human results and animal results are kept apart below. A result in rats tells you a mechanism is plausible. It does not tell you what happens in a person.
BEvidence
Small randomized, double-blind trials in chronic insomnia exist from the 1980s and 1990s, but the independent ones found little or no benefit over placebo, and FDA's 2026 review called the insomnia data inconclusive. The positive reports in withdrawal, pain and narcolepsy are uncontrolled case series or single cases. Grade B reflects that RCTs exist, not that they showed DSIP works.
How far the evidence reachesHighest rung: Regulatory approval
Cell studiesIn a dish None listed
Animal studiesRodents and other models 1 key study below
Small human studiesOpen-label, case series 2 key studies below
Preclinical: tells you a mechanism is plausibleHuman: tells you what happened in people (15 published studies, approx.)
In people 6
Randomized trial1992
Effects of delta sleep-inducing peptide on sleep of chronic insomniac patients. A double-blind study
16 adults with chronic insomnia, IV DSIP vs placebo for 3 nights
Sleep efficiency was slightly higher and sleep latency shorter with DSIP, but the effects were weak and subjective sleep quality did not change; authors concluded it is unlikely to be of major benefit.
Study of delta sleep-inducing peptide efficacy in improving sleep on short-term administration to chronic insomniacs
Chronic insomniacs, IV DSIP vs placebo for 4 nights, crossover
Total sleep time and stage 2 sleep rose, but the same differences existed at baseline; no meaningful difference from placebo, and slow-wave sleep was unchanged.
Author reported improved night sleep and daytime alertness reaching normal-control levels; this single investigator's positive results were not reproduced by other groups.
These are questions the published research has not answered.
01Whether DSIP is an endogenous human sleep signal at all: no gene, precursor protein or receptor has been found.
02Effect of subcutaneous injection, the way it is sold today: no human PK, efficacy or safety data.
03Why a peptide that clears in about 8 minutes would affect sleep hours later.
04Addiction or dependence potential, flagged by FDA because of its opioid-system effects.
05Long-term safety of repeated use.
History
DSIP (Delta Sleep-Inducing Peptide) from discovery to today
1977Schoenenberger and Monnier in Basel isolate and sequence DSIP from rabbit cerebral venous blood.
1983Open-label study reports IV DSIP improved alcohol and opioid withdrawal symptoms in 48 of 49 evaluable patients.
1987Double-blind crossover study in chronic insomniacs finds no clinically meaningful sleep effect.
1992Amsterdam double-blind trial in 16 insomniacs concludes DSIP is unlikely to be of major therapeutic benefit.
1998Deltaran (DSIP plus glycine nasal product) registered in Russia.
2006Review calls DSIP 'a still unresolved riddle': no gene, precursor or receptor found.
2023FDA places emideltide (DSIP) in 503A Category 2 in its September update.
2026FDA announces removal from Category 2 in April after nominations were withdrawn; at the July 24 advisory meeting FDA staff recommend against listing and the committee votes 6-7 against (per RAPS).
Approval or regulatory milestoneResearch milestone
Regulation
Legal and regulatory status
Approved outside US Approved as a medicine in another country, not by the FDA.
Approved products
Deltaran (DSIP plus glycine, intranasal)Stress-induced conditions; alcohol withdrawal and alcohol craving, as part of combination therapyRussia, 1998
Not FDA- or EMA-approved. The Russian product Deltaran is a DSIP plus glycine mixture; it was first registered in July 1998 (certificate 98/207/6) and is now sold under registration LP-016126 as a nonprescription product. FDA's 2026 review found that DSIP on its own (free base or acetate) is not a registered drug in any country it searched; the approved-elsewhere status here rests only on this DSIP plus glycine combination. DSIP is not named on the 2026 WADA Prohibited List. Because a DSIP-containing product is approved in Russia, WADA's S0 catch-all may not clearly apply, but athletes should confirm with their anti-doping authority.
Sport (WADA)
Not on the World Anti-Doping Agency prohibited list as a named substance.
Compounding pharmacies
Not legal to compound in the US. Emideltide (DSIP) was placed in 503A Category 2 (significant safety risks) in FDA's September 2023 update; after the nominations were withdrawn, FDA announced on April 15, 2026 that it would take it off Category 2. FDA reviewed it at the Pharmacy Compounding Advisory Committee on July 24, 2026 for opioid withdrawal, chronic insomnia and narcolepsy. FDA's briefing document concluded the criteria weigh against listing: it is not well characterized, there is no effectiveness evidence by the proposed subcutaneous route, and there are no safety data for that route. RAPS reported the committee voted 6-7, with one abstention, against recommending it.
Unknown for nasal and subcutaneous routes in humans
Notes
FDA's 2026 review cites a plasma half-life of about 8 minutes, with breakdown by aminopeptidases starting at the N-terminal tryptophan. In human serum in vitro the half-life was 5-10 minutes; in dogs 3-6 minutes and in rats and a monkey 2-3 minutes after IV dosing. FDA found no PK data for the subcutaneous route that clinics and online sellers use.
Single-dose clearance
How much of DSIP (Delta Sleep-Inducing Peptide) is left after a single dose
50%left after 7.8 min
Half-lifeAbout 8 minutes in plasma
About 97% cleared39 min
Simple first-order model from the published half-life. Real clearance varies with dose, route, kidney and liver function and formulation. This is not a dosing schedule.
Members
Doses used in published studies
This table records the doses that trials and approved labels used, with the source for each row. It is a record of research, not a recommendation, and it is open to free members.
Doses used in published research and approved labels5 rows
Study or labelDoseRouteFrequencyDurationSource
Checking membershipEach row names the trial or label, the dose, route, frequency, duration and a link to the source. Free account, no card.
HeadacheReported in withdrawal studies; FDA lists transient headache as common in those populations.Common
Nausea and vertigoReported as common in withdrawal studies, where symptoms overlap with withdrawal itself.Common
Low blood pressureFDA's review describes hypotension in two withdrawal patients at the start of the first IV injection and progressive hypotension in another after a second injection.Rare
Nasal irritation and allergic reactionsListed on the Russian Deltaran label.Frequency unknown
Immune reaction to impuritiesFDA flagged immunogenicity risk for injectable products due to aggregation and peptide impurities.Frequency unknown
Groups with specific risks
Pregnancy and breastfeeding (Russian Deltaran label)
Under 18 (Russian Deltaran label)
Severe bradycardia: not recommended (Russian Deltaran label)
Hypersensitivity
Interactions
Opioids and other sedatives: animal data suggest DSIP acts through endorphin release, so additive effects are plausible but unstudied in humans.
What people say online, checked against the studies
Tap a claim to see what the studies found.
The claim"DSIP gives you deep (delta) sleep."Not supportedThe evidence does not back this
The name comes from rabbit EEG experiments. In human trials, slow-wave sleep did not increase, and independent double-blind studies found little effect on sleep at all.
The claim"DSIP is a natural human sleep hormone."UntestedNobody has measured this in people
DSIP-like immunoreactivity is found in human blood and brain, but no gene or precursor protein has been identified, so this has never been established.
The claim"DSIP lowers cortisol and stress."Not supportedThe evidence does not back this
A human study found IV DSIP did not change ACTH or cortisol responses to CRH or a meal.
The claim"DSIP helps with opioid withdrawal."MixedSome studies agree, some do not
Early open-label reports were strongly positive, but there was no control group. FDA found the evidence insufficient in 2026.
The claim"DSIP improves insomnia over a course of injections."MixedSome studies agree, some do not
One Swiss investigator reported normalization; two independent double-blind trials found no clinically meaningful benefit.
Untested pairings
Combinations people discuss
These pairings come up often. Almost none have been tested together in a trial, and the evidence note on each says so plainly.
Sold online as a sleep and circadian pairing because epitalon is marketed for melatonin and DSIP for deep sleep.
EvidenceNo human study has tested the combination. Neither peptide has shown a clear sleep benefit in independent controlled trials.
Handling
Storage and stability
Dry powder (lyophilized)
FDA notes the substance is expected to be stable below -20 C. Keep frozen, dry and away from light.
Mixed with water (reconstituted)
No published stability data for home-made solutions. DSIP is poorly water-soluble and breaks down quickly in biological fluids; FDA cites a recommendation to add a carrier protein for storage. The Russian product is dissolved immediately before use and not stored.
New DSIP (Delta Sleep-Inducing Peptide) research, explained when it is published
One email when a trial reads out, a label changes or the FDA acts on a peptide. Free, no selling of peptides, unsubscribe any time.
Frequently asked questions
Does DSIP actually work for sleep?
The best trials say probably not in a way you would notice. Two independent double-blind studies in chronic insomnia found weak or no benefit over placebo. The positive results come largely from one investigator.
Is DSIP legal?
It is not FDA-approved and cannot be legally compounded in the US. In July 2026 FDA staff recommended against adding it to the compounding list and the advisory committee voted 6-7 against. It is sold online as a research chemical.
What is the half-life of DSIP?
About 8 minutes in human plasma. Enzymes break it down from the front end of the chain.
What is emideltide?
Emideltide is the name FDA and some suppliers use for DSIP. It is the same nine-amino-acid sequence.
Can DSIP be taken nasally?
Russia registers a nasal DSIP product mixed with glycine for stress and alcohol withdrawal. How much reaches the bloodstream or brain from the nose in humans has not been measured.
Is DSIP safe?
Short-term IV use in small studies caused headaches, nausea and occasional low blood pressure. Nothing is known about long-term or subcutaneous use.