Names | |
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IUPAC name
3β,12β,14-Trihydroxy-5β-card-20(22)-enolide
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Systematic IUPAC name
4-[(1R,3aS,3bR,5aR,7S,9aS,9bS,11R,11aS)-3a,7,11-Trihydroxy-9a,11a-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]furan-2(5H)-one | |
Identifiers | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.279 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C23H34O5 | |
Molar mass | 390.51 g/mol |
log P | 2.57510[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Digoxigenin (DIG) is a steroid found exclusively in the flowers and leaves of the plants Digitalis purpurea, Digitalis orientalis and Digitalis lanata (foxgloves), where it is attached to sugars, to form the glycosides (e.g. digoxin, lanatoside C).[2]