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Revision as of 02:28, 2 October 2013
Names | |
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IUPAC names
α-Antiarin: (3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde
β-Antiarin: (3S,5S,8R,9S,10S,12R,13S,14S,17R)-5,12,14-trihydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
PubChem CID
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Properties | |
C29H42O11 | |
Molar mass | 566.64 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Antiarins are cardiac glycoside poisons produced by the upas tree (Antiaris toxicaria).[1] There are two forms, α-antiarin and β-antiarin.
References
- ^ Dolder, F.; Tamm, Ch.; Reichstein, T. (1955). "Glycosides and aglycons. CL. The glycosides of Antiaris toxicaria". Helvetica Chimica Acta. 38: 1364–96.
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: CS1 maint: multiple names: authors list (link)