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Description: A widely used non-cardioselective beta-adrenergic antagonist. Propranolol is used in the treatment or prevention of many disorders including acute myocardial infarction, arrhythmias, angina pectoris, hypertension, hypertensive emergencies, hyperthyroidism, migraine, pheochromocytoma, menopause, and anxiety. [PubChem]
Drug Type: Small Molecule; Approved; Investigational
Pharmacology: Propranolol, the prototype of the beta-adrenergic receptor antagonists, is a competitive, nonselective beta-blocker similar to nadolol without intrinsic sympathomimetic activity. Propanolol is a racemic compound; the l-isomer is responsible for adrenergic blocking activity.
Mechanism of Action: Like atenolol and metoprolol, propranolol competes with sympathomimetic neurotransmitters such as catecholamines for binding at beta(1)-adrenergic receptors in the heart and vascular smooth muscle, inhibiting sympathetic stimulation. This results in a reduction in resting heart rate, cardiac output, systolic and diastolic blood pressure, and reflex orthostatic hypotension. Higher doses of atenolol also competitively block beta(2)-adrenergic responses in the bronchial and vascular smooth muscles.
Indication: For the prophylaxis of migraine.
Half Life: 4 hours
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Thought leaders and organizations working on research involving propranolol.

  • Jaume Bosch
  • Juan G Abraldes
  • Ronei Jesus Poppi
  • Walter Everaerd
  • Patrícia Valderrama
  • National Institute of Mental Health (NIMH)
  • National Institute on Drug Abuse (NIDA)
  • Korea University
  • National Institute of Neurological Disorders and Stroke (NINDS)
  • Par Pharmaceutical, Inc.
  • University of São Paulo
  • Leiden University
  • University of Campinas
  • Vanderbilt University
  • Institute of Liver and Biliary Sciences

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