Chemistry:Azaleatin
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| Names | |
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| IUPAC name
3,3′,4′,7-Tetrahydroxy-5-methoxyflavone
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| Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-4H-1-benzopyran-4-one | |
| Other names
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-4H-chromen-4-one
5-O-Methylquercetin Quercetin 5-methyl ether | |
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| Properties | |
| C16H12O7 | |
| Molar mass | 316.26 g/mol |
| Density | 1.634 g/mL |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Azaleatin is a chemical compound. It is an O-methylated flavonol, a type of flavonoid. It was first isolated from the flowers of Rhododendron mucronatum in 1956[1] and has since been recorded in 44 other Rhododendron species, in Plumbago capensis, in Ceratostigma willmottiana[2] and in Carya pecan.[3] It has also been found in the leaves of Eucryphia.[4]
Glycosides
Azalein is the 3-O-α-L-rhamnoside of azaleatin.
References
- ↑ Wada, Einosuke (1956). "On a Flavonol Glycoside Isolated from Flowers of a White Azalea (Rhododendron mucronatum G. Don)". Journal of the American Chemical Society 78 (18): 4725–6. doi:10.1021/ja01599a052.
- ↑ Harborne, J.B. (1962). "Plant polyphenols: 5. Occurrence of azalein and related pigments in flowers of Plumbago and Rhododendro species". Archives of Biochemistry and Biophysics 96: 171–8. doi:10.1016/0003-9861(62)90467-8. PMID 13904580.
- ↑ Sasaki, T; Mikami, M (1963). "Studies on the Components of Pecan (Carya Pecan Engl. & Graebn). I. On the Flavon Isolated from the Bark of Pecan". Yakugaku Zasshi 83: 897–900. doi:10.1248/yakushi1947.83.9_897. PMID 14085492.
- ↑ Bate-Smith, E. C.; Harborne, J. B.; Davenport, S. M. (1966). "Occurrence of Azaleatin and Caryatin in Eucryphia". Nature 212 (5066): 1065–6. doi:10.1038/2121065a0.
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