Description
A nonpeptide antagonist of vasopressin V1 receptors (IC50 = 0.4 µM in rat liver membranes); selective for V1 over V2 receptors (IC50 = >100 µM in kidney membranes); selective for rat over human V1 receptors (Kis = 25 and 8,800 nM, respectively); inhibits pressor responses induced by arginine vasopressin in pithed rats at 0.03-1 mg/kg; inhibits arginine vasopressin-induced vasoconstriction in conscious rats (ID50 = 2 mg/kg); induces hypotension in aged SHRs and stroke-prone SHRs at 3 mg/kg
Formal name: N-[3-[4-[[4-(3,4-dihydro-2-oxo-1(2H)-quinolinyl)-1-piperidinyl]carbonyl]phenoxy]propyl]-acetamide
Synonyms:
Molecular weight: 449.5
CAS: 131631-89-5
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Cardiovascular System|Cardiovascular Diseases|Hypertension||Research Area|Cardiovascular System|Cardiovascular Diseases|Stroke||Research Area|Cardiovascular System|Vasculature|Vasodilation