Endomorphin-1 vs Neurotensin

Head-to-head comparison of Endomorphin-1 (Tyr-Pro-Trp-Phe-NH2) and Neurotensin (Neurotensin) — benefits, dosing, side effects, research data, and where to buy.

Research Score

PropertyEndomorphin-1Neurotensin
CategoryPain ManagementPain Management
Full NameTyr-Pro-Trp-Phe-NH2Neurotensin
Molecular Weight610.71 Da1672.94
Half-LifeMinutes in plasmaminutes
Amino Acids413
Typical Dose0.1-10 ug per animalN/A|N/A
RouteIntrathecal / subcutaneousIntranasal/experimental injection
Purity≥98%≥98%
Studies Count60081
Research StatusPre-clinicalPre-clinical

Endomorphin-1 Benefits

  • mu-opioid selectivity
  • potent antinociception
  • endogenous peptide scaffold
  • useful for receptor-discovery studies

Neurotensin Benefits

  • antinociceptive signaling
  • descending pain modulation
  • preclinical pain research

Endomorphin-1 Dosing

Intrathecal 0.1-10 ug per animal|Subcutaneous 0.1-5 ug per animal|In vitro 0.1-100 nM

Neurotensin Dosing

N/A|N/A

Endomorphin-1 Side Effects

  • respiratory depression at high exposure
  • sedation
  • tolerance and dependence potential

Neurotensin Side Effects

  • hypotension
  • nausea
  • hypothermia

Research Overview

Endomorphin-1

Endomorphin-1 is a key research peptide in studies of endogenous mu-opioid signaling and spinal analgesia. Like other peptide analgesics, its main translational hurdles are enzymatic instability, limited oral bioavailability, and delivery across barriers.

Neurotensin

Neurotensin has reproducible analgesic and neuromodulatory effects in preclinical studies, especially in inflammatory and neuropathic pain paradigms. It is not a standard clinical analgesic, but it is a real non-opioid peptide with pain-relevant biology.

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Common Stacking Partners

Endomorphin-1 stacks with:

gabapentinketamine

Neurotensin stacks with:

NTS
mu-opioidendogenous-peptideanalgesiapain-modulationnon-opioidneuropeptideanalgesic