Repositioning Candidate Details

Candidate ID: R0440
Source ID: DB01193
Source Type: approved; investigational
Compound Type: small molecule
Compound Name: Acebutolol
Synonyms: (±)-acebutolol; 3'-acetyl-4'-(2-hydroxy-3-(isopropylamino)propoxy)butyranilide; 5'-butyramido-2'-(2-hydroxy-3-isopropylaminopropoxy)acetophenone; Acebutolol; N-(3-acetyl-4-[2-hydroxy-3-(isopropylamino)propoxy]phenyl)butanamide; N-[3-acetyl-4-[2-hydroxy-3-[(1-methylethyl)amino]propoxy]phenyl]butanamide
Molecular Formula: C18H28N2O4
SMILES: CCCC(=O)NC1=CC=C(OCC(O)CNC(C)C)C(=C1)C(C)=O
Structure:
DrugBank Description: A cardioselective beta-adrenergic antagonist with little effect on the bronchial receptors. The drug has stabilizing and quinidine-like effects on cardiac rhythm as well as weak inherent sympathomimetic action.
CAS Number: 37517-30-9
Molecular Weight: 336.4259
DrugBank Indication: For the management of hypertension and ventricular premature beats in adults.
DrugBank Pharmacology: Acebutolol is a cardioselective, beta-adrenoreceptor blocking agent, which possesses mild intrinsic sympathomimetic activity (ISA) in its therapeutically effective dose range. In general, beta-blockers reduce the work the heart has to do and allow it to beat more regularly. Acebutolol has less antagonistic effects on peripheral vascular ß2-receptors at rest and after epinephrine stimulation than nonselective beta-antagonists. Low doses of acebutolol produce less evidence of bronchoconstriction than nonselective agents like propranolol but more than atenolol.
DrugBank MoA: Acebutolol is a selective β1-receptor antagonist. Activation of β1-receptors by epinephrine increases the heart rate and the blood pressure, and the heart consumes more oxygen. Acebutolol blocks these receptors, lowering the heart rate and blood pressure. This drug then has the reverse effect of epinephrine. In addition, beta blockers prevent the release of renin, which is a hormone produced by the kidneys which leads to constriction of blood vessels.
Targets: Beta-1 adrenergic receptor partial agonist; Beta-2 adrenergic receptor partial agonist
Inclusion Criteria: Indication associated