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DSIP 10mg vial
99% HPLC
Independent (3rd-party)
20%saved
Neuropeptides

DSIP

DSIP (Delta Sleep-Inducing Peptide) is a nonapeptide, Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu, isolated in 1977. No DSIP gene or receptor has ever been identified. Rodent work measures HPA-axis and antioxidant enzyme markers. Lyophilized powder, third-party CoA.

99.52%View COA

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For Research Use Only

This product is sold strictly for in-vitro research and laboratory use. Not intended for human consumption or any in-vivo application.

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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 rabbits during delta-wave EEG activity. That circumstance is where the name comes from.

Unresolved mechanism

After nearly fifty years of study, no DSIP gene and no single confirmed receptor have been identified (PMID 16539679), so there is no defined molecular target to reason from.

HPA-axis markers in rats

A rat model of emotional stress measured hypothalamic substance P and structural stress markers rather than a receptor readout (PMID 1382246).

Antioxidant enzyme readouts

Rat studies of cold and oxidative stress measure lipid peroxidation and the activity of SOD, catalase and glutathione peroxidase (PMID 11421812, PMID 21809625).

Very short half-life

Pharmacokinetic work gives intravenous half-lives of 4.0 minutes in dogs, 2.9 in monkeys and 2.0 in rats, at a clearance of about 30.7 ml/kg/min (PMID 6379493).

Regulatory status

Not an approved drug and not patented. As Emideltide, DSIP left the FDA 503A Category 2 list effective 22 April 2026, which is not a compounding clearance. A Pharmacy Compounding Advisory Committee review took place at the 23-24 July 2026 meeting.

Research areas

HPA axisSubstance POxidative stress markersRodent modelsPharmacokinetics

What is DSIP

DSIP is a nonapeptide with the sequence Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu. Schoenenberger and Monnier isolated it in 1977 from the blood of rabbits showing delta-wave EEG activity, and that circumstance, not an established function, is where the name Delta Sleep-Inducing Peptide comes from. A 2006 review in the Journal of Neurochemistry describes the underlying factor hypothesis as still unresolved and notes the possibility that a different, DSIP-like peptide accounts for some of the older animal findings (PMID 16539679).

DSIP is not an approved drug and is not patented. Under the pharmaceutical name Emideltide, covering both the acetate and the free-base form, it appeared on the FDA 503A Category 2 list for substances with significant safety concerns. The updated list published 15 April 2026 removed Emideltide from Category 2 effective 22 April 2026, as one of twelve peptides removed after their sponsors withdrew petitions. Removal from Category 2 is not by itself a compounding clearance: a Pharmacy Compounding Advisory Committee review took place at the 23-24 July 2026 meeting, and only addition to the 503A bulks list would open a compounding path.

We supply it as research-grade lyophilized powder with a batch-specific third-party certificate of analysis.

How it works

The honest answer is that the mechanism is unresolved. No DSIP gene and no single receptor have been identified in nearly fifty years of published work (PMID 16539679), so every statement about this peptide rests on observed readouts in model systems rather than on a defined molecular target.

At the level of the stress axis, a rat model of emotional stress measured hypothalamic substance P together with structural stress markers, adrenal and thymus tissue changes, rather than circulating hormone measurements (PMID 1382246). That distinction matters when reading secondary summaries, which often describe this work as a direct ACTH or cortisol measurement.

A second line of rodent findings is antioxidant. In rat studies of cold and oxidative stress, lipid peroxidation and the activity of superoxide dismutase, catalase and glutathione peroxidase were the measured endpoints (PMID 11421812). A longer rat study run over several months measured the same panel with ceruloplasmin added (PMID 21809625).

Pharmacokinetics sets a hard constraint on all of it: an enzyme-immunoassay study measured intravenous half-lives of 4.0 minutes in dogs, 2.9 in monkeys and 2.0 in rats, with clearance of about 30.7 ml/kg per minute (PMID 6379493). Whatever the downstream readouts depend on, it is not the parent peptide staying in circulation.

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

Typical storage (sealed)

-20 °C long-term, 2 to 8 °C short-term, light-protected

Typical storage (reconstituted)

2 to 8 °C, commonly used within 30 days

CoA

Batch-specific, third-party (Janoshik)
Independently tested (third-party lab)
99.52%
Purity
10.18 mg
Content / assay
Identity
Confirmed
DSP10626A (Clear cap) · Kovera Labs · 29 Jun 2026
Manufacturer third-party report
99.00%
Purity
11.94 mg
Content / assay
Identity
Confirmed
Yellow (10mg) · Janoshik · 15 Dec 2025

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.

Storage and stability

  • Dry, lyophilized vials keep for months refrigerated, or up to 24 months frozen at -20°C.
  • After reconstitution in bacteriostatic water, use within about 30 days at 2 to 8°C, and avoid repeated freeze-thaw.
See the full storage and stability timeline

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Frequently Asked Questions

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.