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Deacetyllanatoside C. A cardiotonic glycoside from the leaves of Digitalis lanata.
- Mechanism
- Curator reviewed
Deslanoside 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). Deslanoside 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.
- Primary indication
- For the treatment and management of Congestive cardiac insufficiency, arrhythmias and heart failure.Curator reviewed
- Formula / weight
- C47H74O19 · 943.0791 g/mol (avg)
- Also known as
- Deacetyllanatoside C · Desacetyllanatoside C · Glucodigoxin
Resolves to
OBATZBGFDSVCJD-LALPQLPRSA-NSMILESC[C@H]1O[C@H](C[C@H](O)[C@@H]1O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](C)O2)[C@@H](C)O1)O[C@H]1CC[C@@]2(C)[C@H](CC[C@@H]3[C@@H]2C[C@@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1What you can answer from here — as of September 23, 2026
Which drugs share a target with Deslanoside, and which of those have an active Phase 3 trial?