Description
A cardiac glycoside; inhibits human recombinant α1β1, α2β2, and α3β1 subunit-containing Na+/K+-ATPases (Kis = 250, 63, and 136 nM, respectively); also inhibits hERG in HEK293 cells expressing hERG (IC50 = 11.1 nM); enhances developed tension and contractile force in electrically stimulated isolated guinea pig left atrial muscle at 0.2 and 0.4 µM, respectively; metabolized to digoxin in isolated rat liver microsomes; attenuates congestive heart failure and reduces myocardial hypertrophy in a rat model of myocardial infarction induced by coronary artery ligation at ~1 mg/kg per day); cytotoxic to a panel of 10 human cancer cell lines (IC50s = 12-76 nM)
Formal name: (3β,5β)-3-[(O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-14-hydroxy-card-20(22)-enolide
Synonyms: Digitoxoside|Lanatoxin|NSC 7529
Molecular weight: 765
CAS: 71-63-6
Purity: ≥98%
Formulation: A solid
Product Type|Biochemicals|Ion Channel Modulation|Blockers||Product Type|Biochemicals|Natural Products|Glycosides||Product Type|Biochemicals|Small Molecule Inhibitors|ATPases||Product Type|Biochemicals|Transporter & Exchanger Modulators||Research Area|Cancer|Cell Death||Research Area|Cardiovascular System|Cardiovascular Diseases|Heart Failure||Research Area|Cardiovascular System|Cardiovascular Diseases|Myocardial Infarction||Research Area|Cardiovascular System|Heart|Arrhythmia||Research Area|Cardiovascular System|Heart|Myocardial Contractility||Research Area|Cardiovascular System|Heart|Myocardial Hypertrophy