Digitoxigenin
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Digitoxigenin | ||||||||||||||||||
other names |
3 β , 14 β -dihydroxy-5 β- card-20 (22) -enolide |
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Molecular formula | C 23 H 34 O 4 | ||||||||||||||||||
Brief description |
colorless, bitter-tasting prisms |
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properties | |||||||||||||||||||
Molar mass | 374.53 g · mol -1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
253 ° C |
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solubility |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Digitoxigenin is a steroid from the hydrolysis of the cardiac glycoside digitoxin , which occurs in the foxglove , digitalis lanata .
Structure and properties
Structurally, digitoxigenin belongs to the group of cardenolides , a group of steroids with an active effect on the heart, which have an unsaturated γ-lactone as a common structural feature .
Individual evidence
- ↑ a b c d Entry on digitalis glycosides. In: Römpp Online . Georg Thieme Verlag, accessed on December 28, 2014.
- ↑ a b Entry on digitoxigenin in the GESTIS substance database of the IFA , accessed on February 8, 2017(JavaScript required) .
- ^ Entry on digitoxigenin in the ChemIDplus database of the United States National Library of Medicine (NLM) .