K-Strophanthidin
| Names | |
|---|---|
| IUPAC name
3β,5,14-Trihydroxy-5β-card-20(22)-enolid-19-al | |
| Systematic IUPAC name
(1R,3aS,3bR,5aS,7S,9aS,9bS,11aR)-3a,5a,7-Trihydroxy-11a-methyl-1-(5-oxo-2,5-dihydrofuran-3-yl)hexadecahydro-9aH-cyclopenta[a]phenanthrene-9a-carbaldehyde | |
| Other names
3β,5,14-Trihydroxy-19-oxo-5β,20(22)-cardenolide, Cymarigenen, Strophanthidin | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.569 |
| MeSH | Strophanthidin |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C23H32O6 | |
| Molar mass | 404.5 g/mol |
| Density | 1.43 g/mL |
| Melting point | 169 °C (336 °F; 442 K) |
| Boiling point | 620.7 °C (1,149.3 °F; 893.9 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).
Infobox references | |
k-Strophanthidin is a cardenolide found in species of the genus Strophanthus. It is the aglycone of k-strophanthin, an analogue of ouabain. k-strophanthin is found in the ripe seeds of Strophanthus kombé and in the lily Convallaria.
K-Strophantidin can be differentiated into:
- k-Strophanthin-α, h-Strophanthin, Cymarin, Strophanthidin-D-cymarosid (CAS: 508-77-0)
- k-Strophanthin-β, k-Strophanthin, Strophosid, Strophanthidin-glucocymarosid (CAS: 560-53-2)
- k-Strophanthin-γ,k-Strophanthosid, Strophanthidin-diglucocymarosid (CAS: 33279-57-1)
- Convallatoxin or Strophanthidin-L-rhamnosid (CAS: 508-75-8)
- Convallosid or Strophanthidin-glucorhamnosid (CAS: 13473-51-3)
Strophantidin is a cardiac glycoside which mechanism of action is similar to Digitalis, Ouabain and digitoxin. It specifically inhibits the membrane protein Na+/ K+ ATPase in muscle tissue (heart) which can lead to Ca2+ overload, diastolic dysfunction, arrhythmias and ultimately to heart failure and death. Native African tribes used Strophantidin among other toxins as arrow poison.