Repositioning Candidate Details

Candidate ID: R1153
Source ID: DB08807
Source Type: experimental
Compound Type: small molecule
Compound Name: Bopindolol
Synonyms: Bopindolol
Molecular Formula: C23H28N2O3
SMILES: CC1=CC2=C(N1)C=CC=C2OCC(CNC(C)(C)C)OC(=O)C1=CC=CC=C1
Structure:
DrugBank Description: Bopindolol (INN) is an ester prodrug for the beta blocker .
CAS Number: 62658-63-3
Molecular Weight: 380.48
DrugBank Indication: For the management of hypertension, edema, ventricular tachycardias, and atrial fibrillation.
DrugBank Pharmacology: Bopindolol is a prodrug of pindolol. Pindolol is a non-selective beta-adrenergic antagonist (beta-blocker) which possesses intrinsic sympathomimetic activity (ISA) in therapeutic dosage ranges but does not possess quinidine-like membrane stabilizing activity. Pindolol impairs AV node conduction and decreases sinus rate and may also increase plasma triglycerides and decrease HDL-cholesterol levels. Pindolol is nonpolar and hydrophobic, with low to moderate lipid solubility. Pindolol has little to no intrinsic sympathomimetic activity and, unlike some other beta-adrenergic blocking agents, pindolol has little direct myocardial depressant activity and does not have an anesthetic-like membrane-stabilizing action.
DrugBank MoA: Bopindolol (as pindolol) 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. By binding beta-2 receptors in the juxtaglomerular apparatus, Pindolol 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 partial agonist; Beta-2 adrenergic receptor partial agonist; 5-hydroxytryptamine receptor 1A; 5-hydroxytryptamine receptor 1B; Beta-3 adrenergic receptor
Inclusion Criteria: Indication associated