Pratensein
Names | |
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IUPAC name 3′,5,7-Trihydroxy-4′-methoxyisoflavone | |
Systematic IUPAC name 5,7-Dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one | |
Other names 4′-Methoxy-3′,5,7-trihydroxyisoflavone | |
Identifiers | |
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ChEBI |
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ECHA InfoCard | 100.347.521 |
KEGG |
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InChI
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Properties | |
Chemical formula | C16H12O6 |
Molar mass | 300.26 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Pratensein is an O-methylated isoflavone, a type of flavonoid. It can be found in Trifolium pratense (red clover)[1] and can have effects for the prevention of atherosclerosis.[2]
References
- ^ Isoflavone contents of red and subterranean clovers. E. Wong, Journal of the Science of Food and Agriculture, Volume 14 Issue 6, Pages 376-379
- ^ Characterization of the Isoflavone Pratensein as a Novel Transcriptional Up-Regulator of Scavenger Receptor Class B Type I in HepG2 Cells. Yang Yuan, JIiang Wei, Wang Li, Hang Zhong-Bing, Si Shu-Yi and Hong Bin, Biological & pharmaceutical bulletin, 2009, vol. 32, no7, pp. 1289-1294
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Isoflavones and their glycosides
- Biochanin A
- Calycosin
- Formononetin
- Glycitein
- Irigenin
- 5-O-methylgenistein
- Pratensein
- Prunetin
- Psi-tectorigenin
- Retusin
- Tectorigenin
- Bidwillol A
- Derrubone
- Luteone
- 7-O-Methylluteone
- Wighteone
- Alpinumisoflavone
- Barbigerone
- Di-O-methylalpinumisoflavone
- 4'-methyl-alpinumisoflavone
- Anagyroidisoflavone A and B
- Irilone
- Pseudobaptigenin
- Rotenoids
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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