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QuickView for Nadolol (compound)


PubChem
Name: Nadolol
PubChem Compound ID: 11255327
Description: A non-selective beta-adrenergic antagonist with a long half-life, used in cardiovascular disease to treat arrhythmias, angina pectoris, and hypertension. Nadolol is also used for MIGRAINE DISORDERS and for tremor.
Molecular formula: C17H27NO4
Molecular weight: 309.401 g/mol
DrugBank
Identification
Name: Nadolol
Name (isomeric): DB01203
Drug Type: small molecule
Description: A non-selective beta-adrenergic antagonist with a long half-life, used in cardiovascular disease to treat arrhythmias, angina pectoris, and hypertension. Nadolol is also used for MIGRAINE DISORDERS and for tremor.
Brand: Corgard, Anabet, Solgol
Brand name mixture: Corzide Tab W Nadolol 40mg(Bendroflumethiazide + Nadolol), Corzide Tab W Nadolol 80mg(Bendroflumethiazide + Nadolol)
Category: Sympatholytics, Adrenergic beta-Antagonists, Anti-Arrhythmia Agents, Antihypertensive Agents
CAS number: 42200-33-9
Pharmacology
Indication: Used in cardiovascular disease to treat arrhythmias, angina pectoris, and hypertension.
Pharmacology:
Nadolol is a nonselective beta-adrenergic receptor antagonist with a long half-life, and is structurally similar to propranolol. Clinical pharmacology studies have demonstrated beta-blocking activity by showing (1) reduction in heart rate and cardiac output at rest and on exercise, (2) reduction of systolic and diastolic blood pressure at rest and ...
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Mechanism of Action:
Like other beta-adrenergic antagonists, nadolol competes with adrenergic neurotransmitters such as catecholamines for binding at sympathetic receptor sites. Like propranolol and timolol, nadolol binds at beta(1)-adrenergic receptors in the heart and vascular smooth muscle, inhibiting the effects of the catecholamines epinephrine and norepinephrine ...
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Absorption: Absorption of nadolol after oral dosing is variable, averaging about 30 percent.
Protein binding: 30%
Biotransformation: Not metabolized by the liver and excreted unchanged primarily by the kidneys.
Route of elimination: Unlike many other beta-adrenergic blocking agents, nadolol is not metabolized by the liver and is excreted unchanged, principally by the kidneys. Nadolol is excreted predominantly in the urine.
Half Life: 14-24 hours
Toxicity: Oral, mouse: LD50 = 4500mg/kg. Symptoms of overdose include abdominal irritation, central nervous system depression, coma, extremely slow heartbeat, heart failure, lethargy, low blood pressure, and wheezing.
Affected organisms: Humans and other mammals
Interactions
Food interaction:
Avoid alcohol.
Take without regard to meals.
Magnesium, potassium and zinc needs increased.
Avoid natural licorice.
Drug interaction:
IbuprofenRisk of inhibition of renal prostaglandins
MethyldopaPossible hypertensive crisis
AcetohexamideThe beta-blocker, nadolol, may decrease symptoms of hypoglycemia.
ErgonovineIschemia with risk of gangrene
RepaglinideThe beta-blocker, nadolol, may decrease symptoms of hypoglycemia.
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Targets


Transporters