Repositioning Candidate Details

Candidate ID: R0399
Source ID: DB01092
Source Type: approved
Compound Type: small molecule
Compound Name: Ouabain
Synonyms: 3-(α-L-rhamnopyranosyloxy)-1β,5β,11α,14,19-pentahydroxy-5β-card-20(22)-enolide; G-Strophanthin; Ouabagenin L-Rhamnoside; Ouabain anhydrous; Ouabaine; Oubain
Molecular Formula: C29H44O12
SMILES: [H][C@@]12CC[C@]3(O)C[C@H](C[C@@H](O)[C@]3(CO)[C@@]1([H])[C@H](O)C[C@]1(C)[C@H](CC[C@]21O)C1=CC(=O)OC1)O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O
Structure:
DrugBank Description: A cardioactive glycoside consisting of rhamnose and ouabagenin, obtained from the seeds of Strophanthus gratus and other plants of the Apocynaceae; used like digitalis. It is commonly used in cell biological studies as an inhibitor of the NA(+)-K(+)-exchanging ATPase.
CAS Number: 630-60-4
Molecular Weight: 584.6525
DrugBank Indication: For the treatment of atrial fibrillation and flutter and heart failure
DrugBank Pharmacology: Ouabain, a cardiac glycoside similar to digitoxin, is used to treat congestive heart failure and supraventricular arrhythmias due to reentry mechanisms, and to control ventricular rate in the treatment of chronic atrial fibrillation.
DrugBank MoA: Ouabain inhibits the Na-K-ATPase membrane pump, resulting in an increase in intracellular sodium and calcium concentrations. Increased intracellular concentrations of calcium may promote activation of contractile proteins (e.g., actin, myosin). Ouabain also acts on the electrical activity of the heart, increasing the slope of phase 4 depolarization, shortening the action potential duration, and decreasing the maximal diastolic potential.
Targets: Sodium/potassium-transporting ATPase subunit alpha-1 inhibitor; Sodium/potassium-transporting ATPase subunit alpha-2 inhibitor; Sodium/potassium-transporting ATPase subunit alpha-3 inhibitor
Inclusion Criteria: Indication associated