Somatostatin vs Met-enkephalin

Head-to-head comparison of Somatostatin (Somatostatin-14) and Met-enkephalin (Tyr-Gly-Gly-Phe-Met) — benefits, dosing, side effects, research data, and where to buy.

Research Score

PropertySomatostatinMet-enkephalin
CategoryPain ManagementPain Management
Full NameSomatostatin-14Tyr-Gly-Gly-Phe-Met
Molecular Weight1637.85573.67 Da
Half-Life1-3 min1-5 minutes in plasma
Amino Acids145
Typical DoseN/A|N/A0.1-5 ug per animal
RouteIV/SCIntrathecal / intracerebroventricular
Purity≥98%≥98%
Studies Count841200
Research StatusApprovedPre-clinical

Somatostatin Benefits

  • nociceptive inhibition
  • anti-inflammatory signaling
  • visceral pain modulation

Met-enkephalin Benefits

  • endogenous opioid signaling
  • analgesic reference ligand
  • spinal antinociception
  • neurochemical pain-pathway probe

Somatostatin Dosing

N/A|N/A

Met-enkephalin Dosing

Intrathecal 0.1-5 ug per animal|Intracerebroventricular 0.1-2 ug per animal|In vitro 1-100 nM

Somatostatin Side Effects

  • hyperglycemia
  • bradycardia
  • GI upset

Met-enkephalin Side Effects

  • sedation at higher exposure
  • constipation-like opioid effects
  • rapid enzymatic degradation

Research Overview

Somatostatin

Somatostatin reduces release of multiple excitatory mediators and can suppress pain signaling in preclinical and limited translational work. Its analgesic use is not standard, but the peptide is real and mechanistically relevant to pain control.

Met-enkephalin

Met-enkephalin has been extensively used in receptor pharmacology and nociception studies to map mu and delta opioid biology. The main limitation in translational work is very short half-life from peptidase cleavage and poor systemic stability.

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Common Stacking Partners

Somatostatin stacks with:

SRIFGrowth hormone-inhibiting hormone

Met-enkephalin stacks with:

gabapentinketamine
non-opioidanalgesichormoneopioid-peptideenkephalinmu-opioidanalgesia