Bryoamaride
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IUPAC name
(9R,10R,13R,14S,16R,17R)-17-(1,5-Dihydroxy-1,5-dimethyl-2-oxo-hexyl)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione
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Other names
Cucurbitacin L 2-O-β-D-glucopyranoside
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C36H54O12 | |
Molar mass | 678.816 g·mol−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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Bryoamaride is a chemical compound isolated from certain plants, notably Bryonia dioica. It can be seen as a derivative of the triterpene hydrocarbon cucurbitane (C
30H
54), more specifically from cucurbitacin L or 23,24-dihydrocucurbitacin I.[1]: 65
The derivative 25-O-acetylbryoamaride is found in Trichosanthes tricuspidata.[1]: 66
References
- ^ a b Jian Chao Chen, Ming Hua Chiu, Rui Lin Nie, Geoffrey A. Cordell and Samuel X. Qiu (2005), "Cucurbitacins and cucurbitane glycosides: structures and biological activities" Natural Product Reports, volume 22, pages 386-399 doi:10.1039/B418841C