Names | |
---|---|
IUPAC name
3β,14-Dihydroxy-5β-card-20(22)-enolide
| |
Systematic IUPAC name
4-[(1R,3aS,3bR,5aR,7S,9aS,9bS,11aR)-5a,7-Dihydroxy-9a,11a-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]furan-2(5H)-one | |
Other names
3-β,14-dihydroxy-5-β,14-β-card-20(22)-enolide
5β-Card-20(22)-enolide, 3β,14-dihydroxy- Card-20(22)-enolide, 3,14-dihydroxy-, (3β,5β)- NSC 407806 Δ20:22-3,14,21-Trihydroxynorcholenic acid lactone cerberigenin echujetin evonogenin thevetigenin | |
Identifiers | |
3D model (
JSmol)
|
|
95448 | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.005.095 |
EC Number |
|
PubChem
CID
|
|
RTECS number |
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C23H34O4 | |
Molar mass | 374.51 |
Appearance | solid[ citation needed] |
Melting point | 252 to 253 °C (486 to 487 °F; 525 to 526 K) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
|
Toxic |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Digitoxigenin, a cardenolide, is the aglycone of digitoxin.
Digitoxigenin can be used to prepare actodigin. [2]
In Lednicer's book on steroids, it is made from deoxycholic acid.
Names | |
---|---|
IUPAC name
3β,14-Dihydroxy-5β-card-20(22)-enolide
| |
Systematic IUPAC name
4-[(1R,3aS,3bR,5aR,7S,9aS,9bS,11aR)-5a,7-Dihydroxy-9a,11a-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-1-yl]furan-2(5H)-one | |
Other names
3-β,14-dihydroxy-5-β,14-β-card-20(22)-enolide
5β-Card-20(22)-enolide, 3β,14-dihydroxy- Card-20(22)-enolide, 3,14-dihydroxy-, (3β,5β)- NSC 407806 Δ20:22-3,14,21-Trihydroxynorcholenic acid lactone cerberigenin echujetin evonogenin thevetigenin | |
Identifiers | |
3D model (
JSmol)
|
|
95448 | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.005.095 |
EC Number |
|
PubChem
CID
|
|
RTECS number |
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C23H34O4 | |
Molar mass | 374.51 |
Appearance | solid[ citation needed] |
Melting point | 252 to 253 °C (486 to 487 °F; 525 to 526 K) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
|
Toxic |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Digitoxigenin, a cardenolide, is the aglycone of digitoxin.
Digitoxigenin can be used to prepare actodigin. [2]
In Lednicer's book on steroids, it is made from deoxycholic acid.