DSIP (delta sleep-inducing peptide)
A nine-amino-acid peptide once proposed as a natural sleep factor; small insomnia trials found weak, mixed results.
What it is
Not established. A 2006 review noted that no DSIP gene, precursor protein or receptor had been identified. Rat studies summarised by FDA suggest effects run partly through release of the body's own opioid peptides, without direct opioid-receptor binding.
What it is studied for
DSIP was isolated from rabbit blood in the 1970s and studied as a possible natural sleep factor. Small human studies, mostly from the 1980s and 1990s, tested it in chronic insomnia; a single case report covered narcolepsy, and open-label studies covered alcohol and opioid withdrawal.
What the evidence says
Small, older human trials; mixed results
A double-blind study of 16 people with chronic insomnia found only weak effects, unlikely to be of major benefit. FDA's 2026 review found the evidence insufficient for insomnia, narcolepsy or opioid withdrawal, noted headache, nausea, vertigo and low blood pressure in withdrawal studies, and flagged possible immune reactions.
How it was studied
The human studies FDA reviewed gave DSIP by intravenous injection. FDA notes that injection and nasal-spray products are marketed in the US, but no sleep trial of a spray form, or of this four-ingredient spray, was found.
Regulatory status
No approved use. FDA's 2026 review states that neither emideltide nor emideltide acetate is a component of an FDA-approved drug, and FDA proposed not adding them to the list of bulk substances pharmacies may use for compounding.
Where to find it
Deep Sleep
- Spray DSIP 10 mg, pinealon 10 mg, melatonin 50 mg and GABA 250 mg per 10 mL bottle
Sold by USA Standard Research, the team behind PeptidesGenie, for research use only. Not for human or veterinary use.
Sources
- 1PubChem: Delta Sleep-Inducing Peptide, CID 68816 Chemical reference
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- 5FDA: Bulk substances that may present significant safety risks FDA safety information
Source-checked · 27 Oct 2026