Back to Peptide Database
RecoveryInvestigational

Dalargin

Overview

Dalargin is a synthetic hexapeptide analog of leucine-enkephalin with enhanced metabolic stability due to D-amino acid substitutions. It acts as a selective delta opioid receptor agonist with peripheral and central effects, including modulation of stress responses, anti-inflammatory activity, and cytoprotection in gastrointestinal and vascular tissues. Unlike classical opioids, dalargin exhibits reduced central analgesic potency but pronounced tissue-protective properties.

Key Research Findings

Dalargin has been used clinically in Russia and some Eastern European countries for treatment of gastric ulcers, pancreatitis, and stress-related mucosal injury since the 1980s. Peer-reviewed evidence in Western literature is limited, with most data derived from Soviet-era clinical studies and pharmacological characterization in animal models.

Route of Administration

Intravenous, Intramuscular injection

Regulatory Status

Investigational

Interested in Dalargin?

Find a verified provider experienced with Dalargin protocols in your area. All providers are credentialed and use compliant sourcing.

Find a Dalargin Provider

Related Peptides

BPC-157

Research Phase

A synthetic gastric pentadecapeptide derived from a protein found in human gastric juice. BPC-157 promotes angiogenesis and the expression of growth factors including VEGF, EGF, and NO-mediated pathways. It has demonstrated cytoprotective and wound-healing properties across multiple tissue types in preclinical models, including tendon, muscle, ligament, and gastrointestinal mucosa.

TB-500 (Thymosin Beta-4)

In Clinical Trials

Thymosin Beta-4 is a 43-amino acid actin-sequestering protein involved in cell migration, differentiation, and tissue repair. It promotes wound healing by upregulating cell-building proteins such as actin and laminin, facilitating cell migration to sites of injury. TB-500 also has anti-inflammatory properties mediated through NF-kB pathway modulation.

GHK-Cu

Research Phase

A naturally occurring copper-binding tripeptide (glycyl-L-histidyl-L-lysine) found in human plasma, saliva, and urine. GHK-Cu activates tissue remodeling by stimulating collagen synthesis, glycosaminoglycan production, and angiogenesis while suppressing fibrinogen synthesis. It modulates the activity of matrix metalloproteinases and influences over 4,000 genes related to tissue repair.

DSIP (Delta Sleep-Inducing Peptide)

Research Phase

A naturally occurring nonapeptide (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) originally isolated from cerebral venous blood of rabbits during induced sleep. DSIP modulates sleep architecture by promoting delta wave (slow-wave) sleep through interactions with the GABAergic system and hypothalamic sleep centers. It also exhibits stress-protective, analgesic, and neuromodulatory properties.