Repositioning Candidate Details

Candidate ID: R0314
Source ID: DB00866
Source Type: experimental; withdrawn
Compound Type: small molecule
Compound Name: Alprenolol
Synonyms: (RS)-1-(2-allylphenoxy)-3-(isopropylamino)propan-2-ol; 1-(2-Allylphenoxy)-3-isopropylamino-2-propanol; 1-(o-Allylphenoxy)-3-(isopropylamino)-2-propanol; Aprenololo
Molecular Formula: C15H23NO2
SMILES: CC(C)NCC(O)COC1=CC=CC=C1CC=C
Structure:
DrugBank Description: One of the adrenergic beta-antagonists used as an antihypertensive, anti-anginal, and anti-arrhythmic agent. Alprenolol is no longer marketed by AstraZeneca, but may still be available in generic varieties.
CAS Number: 13655-52-2
Molecular Weight: 249.3486
DrugBank Indication: For the treatment of hypertension, angina, and arrhythmia
DrugBank Pharmacology: Alprenolol is a non-selective beta-blocker used in the treatment of hypertension, edema, ventricular tachycardias, and atrial fibrillation. Alprenolol impairs AV node conduction and decreases sinus rate and may also increase plasma triglycerides and decrease HDL-cholesterol levels. Alprenolol is nonpolar and hydrophobic, with low to moderate lipid solubility. Alprenolol has little to no intrinsic sympathomimetic activity and, unlike some other beta-adrenergic blocking agents, alprenolol has little direct myocardial depressant activity and does not have an anesthetic-like membrane-stabilizing action.
DrugBank MoA: Alprenolol non-selectively blocks beta-1 adrenergic receptors mainly in the heart, inhibiting the effects of epinephrine and norepinephrine resulting in a decrease in heart rate and blood pressure. Also, with a more minor effect, by binding beta-2 receptors in the juxtaglomerular apparatus, alprenolol inhibits the production of renin, thereby inhibiting angiotensin II and aldosterone production and therefore inhibits the vasoconstriction and water retention due to angiotensin II and aldosterone, respectively.
Targets: Beta-1 adrenergic receptor antagonist; Beta-2 adrenergic receptor antagonist; 5-hydroxytryptamine receptor 1A antagonist; Beta-3 adrenergic receptor antagonist
Inclusion Criteria: Indication associated