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Penbutolol is an antagonist of β-adrenergic receptors (β-ARs; IC50 = 2.8 nM) and the serotonin (5-HT) receptor subtype 5-HT1A (IC50 = 9.9 nM).1 It inhibits adenylate cyclase activity induced by the β-AR agonist isoprenaline (isoproterenol; Item No. 15592) in guinea pig myocardial membranes with a Ki value of 2.4 nM.2 Penbutolol reduces basal renin activity and blood pressure in spontaneously hypertonic rats.3 It decreases isolation-induced aggressive behavior in mice (ED50 = 56 µmol/kg) and reverses reductions in aggression induced by 8-hydroxy-DPAT (Item No. 22608) and TFMPP with ED50 values of 8.1 and 2.1 µmol/kg, respectively.1 Formulations containing penbutolol were previously used in the treatment of arterial hypertension.
WARNING This product is not for human or veterinary use.
1. The antiaggressive potency of (–)-
2. β-
3. Pharmacology of the β-