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DSIP
99% HPLC
Cognitive

DSIP

DSIP (Delta Sleep-Inducing Peptide), a nonapeptide isolated in 1977. Research material for sleep, HPA-axis, and stress regulation. Research-grade lyophilized powder, laboratory use only.

99.00%View COA

€39.99

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Nonapeptide

DSIP is a nonapeptide with the sequence Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu, isolated in 1977 from the blood of sleeping rabbits. That origin gave it the name Delta Sleep-Inducing Peptide.

Unresolved mechanism

Despite decades of research, no single receptor or DSIP gene has ever been identified (PMID 16539679). The exact mechanism of action remains unresolved.

HPA axis and stress

In animal models DSIP dampens HPA-axis reactivity: it lowers stress-induced ACTH and cortisol and raises substance P in the hypothalamus (PMID 1382246).

Antioxidant data

In rat studies DSIP inhibited lipid peroxidation and raised antioxidant enzymes such as SOD, catalase, and glutathione peroxidase (PMID 11421812, 21809625).

Very short half-life

Pharmacokinetic data show a very short half-life: dog 4.0 min, monkey 2.9 min, rat 2.0 min after intravenous dosing (PMID 6379493).

Regulatory status

Not an approved drug, not patented. As Emideltide, DSIP was removed from the FDA 503A Category 2 list effective 22 April 2026. That is not a compounding clearance. A PCAC review is scheduled for 24 July 2026.

Research areas

Sleep regulationHPA axisStress responseSubstance POxidative stress

What is DSIP

DSIP (Delta Sleep-Inducing Peptide) is a nonapeptide with the sequence Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu. It was isolated in 1977 from the blood of sleeping rabbits, which is where its name comes from. Despite that name, the peptide's role as a sleep factor is only weakly documented in the literature, and no clear receptor or associated gene has ever been found (PMID 16539679).

DSIP is not an approved drug and is not patented. Under the name Emideltide (acetate or free base) it was on the FDA 503A Category 2 list, which flags significant safety concerns. The updated 503A document (published 15 April 2026) removed Emideltide/DSIP from Category 2 effective 22 April 2026, as part of 12 peptides removed. Important: removal from Category 2 is not, by itself, a compounding clearance. A PCAC review of DSIP (together with Epitalon and Semax) is scheduled for 24 July 2026. Only addition to the 503A bulks list would open a clear compounding path.

We supply it as research-grade lyophilized powder.

How it works

The mechanism of action of DSIP is unresolved. Although the peptide has been studied since 1977, no single DSIP receptor and no DSIP gene have been identified (PMID 16539679). Statements about its activity therefore rest on observed functional effects rather than on a defined molecular target.

At the level of the stress axis, DSIP dampens hypothalamic-pituitary-adrenal reactivity in animal models. In rats it lowered stress-induced ACTH and cortisol, raised substance P in the hypothalamus, and reduced adrenal hypertrophy and thymus involution, with the strongest effect seen at the lower dose (PMID 1382246).

A second line of findings is antioxidant. In rat studies of cold and oxidative stress, DSIP inhibited lipid peroxidation and raised antioxidant enzymes such as superoxide dismutase, catalase, and glutathione peroxidase (PMID 11421812). In an ageing study run over several months, with dosing on five consecutive days per month, it suppressed lipid peroxidation and raised SOD, catalase, and ceruloplasmin (PMID 21809625), which forms the discussed geroprotective research angle.

Pharmacokinetically, DSIP is very short-lived. After intravenous dosing, half-lives were dog 4.0 min, monkey 2.9 min, and rat 2.0 min, at a clearance of about 30.7 ml/kg/min (PMID 6379493). In the sleep research that gave the peptide its name, a study in six chronic insomniacs reported longer sleep, better sleep quality, and fewer interruptions without daytime sedation after a single intravenous dose (PMID 7028502).

Often studied alongside

DSIP is studied in the context of CNS and stress regulation, and is therefore often considered alongside other neuromodulatory peptides. Selank and Semax are short regulatory peptides researched in anxiety- and stress-related models. Epitalon is the fourth peptide on the PCAC agenda for 24 July 2026, together with DSIP and Semax, and is studied in the context of ageing and antioxidant mechanisms.

For reconstitution, the standard solvent in published protocols is bacteriostatic water.

Documentation

Material specification

Purity

≥99% (HPLC)

Test method

HPLC + mass spectrometry

Form

Lyophilized powder

Storage (sealed)

2 to 8 °C, light-protected

Storage (reconstituted)

2 to 8 °C, use within 4 weeks

CoA

Batch-specific, third-party (Janoshik)

Lab Report (COA)

Batch NumberYellow (10mg)
Purity99.00%
Testing LabJanoshik
Test Date15 Dec 2025
Download COA
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Research use only

This material is sold strictly for in-vitro research and laboratory use. Not intended for human or animal consumption, medical, cosmetic, or household applications. Suitable only for professional laboratory environments.

Technical data sheet

CAS number
62568-57-4
Molecular formula
C₃₅H₄₈N₁₀O₁₅
Molar mass
848.8 g/mol
Type / receptor
Delta sleep-inducing nonapeptide
Form
White lyophilized powder
Solubility
Bacteriostatic water (BAC)
Storage
-20°C for up to 24 months; 30 days at 2-8°C after reconstitution

Identity data from public chemical references (PubChem). Per-batch purity: see lab reports below.