Repositioning Candidate Details

Candidate ID: R0304
Source ID: DB00841
Source Type: approved
Compound Type: small molecule
Compound Name: Dobutamine
Synonyms: (±)-4-(2-((3-(p-hydroxyphenyl)-1-methylpropyl)amino)ethyl)pyrocatechol; 3,4-dihydroxy-N-[3-(4-hydroxyphenyl)-1-methylpropyl]-β-phenylethylamine; 4-{2-[3-(4-Hydroxy-phenyl)-1-methyl-propylamino]-ethyl}-benzene-1,2-diol; DL-dobutamine; rac-dobutamine; racemic-dobutamine
Molecular Formula: C18H23NO3
SMILES: CC(CCC1=CC=C(O)C=C1)NCCC1=CC(O)=C(O)C=C1
Structure:
DrugBank Description: A beta-1 agonist catecholamine that has cardiac stimulant action without evoking vasoconstriction or tachycardia. It is proposed as a cardiotonic after myocardial infarction or open heart surgery.
CAS Number: 34368-04-2
Molecular Weight: 301.3801
DrugBank Indication: Indicated when parenteral therapy is necessary for inotropic support in the short-term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures.
DrugBank Pharmacology: Dobutamine is a direct-acting inotropic agent whose primary activity results from stimulation of the beta-adrenoceptors of the heart while producing comparatively mild chronotropic, hypertensive, arrhythmogenic, and vasodilative effects. Dobutamine acts primarily on beta-1 adrenergic receptors, with negligible effects on beta-2 or alpha receptors. It does not cause the release of endogenous norepinephrine, as does dopamine.
DrugBank MoA: Dobutamine directly stimulates beta-1 receptors of the heart to increase myocardial contractility and stroke volume, resulting in increased cardiac output.
Targets: Beta-1 adrenergic receptor agonist; Beta-2 adrenergic receptor agonist; Alpha-1 adrenergic receptors agonist; Estrogen receptor alpha
Inclusion Criteria: Therapeutic strategy associated