Isorhamnetin
Names | |
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IUPAC name
3,5,7-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one | |
Other names
3-methylquercetin 3-Methylquercetin Isorhamnetol isorhamentin isorhamnetine iso-rhamnetin 3'-Methoxyquercetin | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.006.860 |
PubChem CID |
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UNII | |
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Properties | |
C16H12O7 | |
Molar mass | 316.26 g/mol |
Melting point | 307 °C (585 °F; 580 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Isorhamnetin is an O-methylated flavon-ol from the class of flavonoids. A common food source of this 3'-methoxylated derivative of quercetin and its glucoside conjugates are pungent yellow or red onions, in which it is a minor pigment, quercetin-3,4'-diglucoside and quercetin-4'-glucoside and the aglucon quercetin being the major pigments.[1] An other source [2] is the spice, herbal medicinal [3] and psychedelic Mexican terragon (Tagetes lucida), which is described as accumulating isorhamnetin and its 7-O-glucoside derivate.[4]
Metabolism
The enzyme quercetin 3-O-methyltransferase uses S-adenosyl methionine and quercetin to produce S-adenosylhomocysteine and isorhamnetin.
The enzyme 3-methylquercetin 7-O-methyltransferase uses S-adenosyl methionine and 5,7,3',4'-tetrahydroxy-3-methoxyflavone (isorhamnetin) to produce S-adenosylhomocysteine and 5,3',4'-trihydroxy-3,7-dimethoxyflavone (rhamnazin).
Glycosides
- Isorhamnetin-3-O-rutinoside-7-O-glucoside
- Isorhamnetin-3-O-rutinoside-4'-O-glucoside
- Narcissin (Isorhamnetin-3-O-rutinoside)
See also
- Tamarixetin, the 4'-methyl analog
References
- ↑ Slimestad, R; Fossen, T; Vågen, IM (December 2007). "Onions: a source of unique dietary flavonoids". J. Agric. Food Chem. 55: 10067–80. PMID 17997520. doi:10.1021/jf0712503.
- ↑ Bohm, Bruce A.; Tod F. Stuessy (2007). Flavonoids of the sunflower family (Asteraceae). Springer. p. 597. ISBN 978-3-211-83479-4.
- ↑ http://pubs.acs.org/doi/full/10.1021/jf053071w?src=recsys
- ↑ Abdala, 1999