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دیژیتوکسین

Structure via PubChem · Public domain (PubChem)

EntityQ423890· pop 28· linked from 673 articles

دیژیتوکسین

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Also known as digitoxoside, unidigin, Crystodigin (TN), Digitoxin, Digitoxinum, Digitoxoside, Crystodigin (tn), Digitoksin

Digitoxin is a cardiac glycoside used for the treatment of heart failure and certain kinds of heart arrhythmia. It is a phytosteroid and is similar in structure and effects to digoxin, though the effects are longer-lasting. Unlike digoxin, which is eliminated from the body via the kidneys, it is eliminated via the liver, and so can be used in patients with poor or erratic kidney function. While several controlled trials have shown digoxin to be effective in a proportion of patients treated for heart failure, the evidence base for digitoxin is not as strong, although it is presumed to be simila

Chemical data

Formula
C41H64O13
Molecular weight
764.9 g/mol
IUPAC name
3-[(3S,5R,8R,9S,10S,13R,14S,17R)-3-[(2R,4S,5S,6R)-5-[(2S,4S,5S,6R)-5-[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
SMILES
C[C@@H]1[C@H]([C@H](C[C@@H](O1)O[C@@H]2[C@H](O[C@H](C[C@@H]2O)O[C@@H]3[C@H](O[C@H](C[C@@H]3O)O[C@H]4CC[C@]5([C@@H](C4)CC[C@@H]6[C@@H]5CC[C@]7([C@@]6(CC[C@@H]7C8=CC(=O)OC8)O)C)C)C)C)O)O
InChIKey
WDJUZGPOPHTGOT-XUDUSOBPSA-N
XLogP
2.3
Polar surface area
183 Ų
H-bond donors
5
H-bond acceptors
13
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1982
Admin. routes
parenteral
Indications
cardiovascular disease, cystic fibrosis

via ChEMBL · EBI

Research

3,069 papers

via PubMed

Wikidata facts

Mass
764.434692
Has use
medication
Show 9 more facts
chemical formula
C₄₁H₆₄O₁₃
Commons category
Digitoxin
has characteristic
bitterness
World Health Organisation international non-proprietary name
digitoxin
found in taxon
Digitalis lanata
defined daily dose
0.1
isomeric SMILES
C[C@@H]1[C@H]([C@H](C[C@@H](O1)O[C@@H]2[C@H](O[C@H](C[C@@H]2O)O[C@@H]3[C@H](O[C@H](C[C@@H]3O)O[C@H]4CC[C@]5([C@@H](C4)CC[C@@H]6[C@@H]5CC[C@]7([C@@]6(CC[C@@H]7C8=CC(=O)OC8)O)C)C)C)C)O)O
canonical SMILES
CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C(C4)CCC6C5CCC7(C6(CCC7C8=CC(=O)OC8)O)C)C)C)C)O)O
subject has role
cardiotonic
Sources (7)

via Wikidata · CC0