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Argipressin

peptide · headlineFDA-approved

Binds to V1 receptors on vascular smooth muscle to induce vasoconstriction

Summary

Argipressin (vasopressin) is a synthetic analog of antidiuretic hormone used in acute care to manage hypotension in vasodilatory shock and control excessive diuresis in diabetes insipidus. It acts on V1 and V2 receptors to regulate vascular tone and water reabsorption in the kidneys.

How it works

  • Binds to V1 receptors on vascular smooth muscle to induce vasoconstriction
  • Activates V2 receptors in renal collecting ducts, increasing aquaporin insertion and water reabsorption
  • Restores arterial pressure by elevating systemic vascular resistance in shock
  • Reduces free water clearance in the kidney without increasing sodium retention

Dosing

  • unit: units/min
    low dose: 0.01
    frequency: Continuous infusion
    high dose: 0.04
    standard dose: 0.03
    administration route: Intravenous (IV)

Cycling

  • Continuous infusion with titration between 0.01 to 0.04 units/min based on hemodynamic response. Monitoring is critical in ICU settings.

Side effects

common: ["Hyponatremia","Abdominal cramps","Headache","Flushing"]
warnings: ["Can cause water intoxication and electrolyte imbalance if not monitored closely","Use cautiously in patients with coronary artery disease or chronic kidney disease"]
long term: ["May cause long-term changes in renal sodium handling if misused","Tachyphylaxis may develop in prolonged shock states"]

Chemistry & PK

sequence: Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2
half life: 10 to 35 minutes
degradation: Rapid hepatic and renal enzymatic degradation
molecular weight: 1084.24
molecular formula: C46H65N15O12S2
tissue specificity: Targets vascular smooth muscle and renal collecting ducts

Verified citations

2 · PubMed-checked

Legal / compounding

FDA-approved

Legal status is a hard gate: non-compoundable or delisted agents cannot be filled and are blocked from protocol export. Keep 503A status current.