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Flavanonol

A flavonoid typically with no double bond between C-2 and C-3, with a carbonyl (C=O) function at C-4, and with a hydroxyl group at C-3.
National Institutes of Health

Papers overview

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2019
2019
A Method to Study the Distribution Patterns for Metabolites in Xylem and Phloem of Spatholobi Caulis
Spatholobi Caulis (SC), the vine stem of Spatholobus suberectus Dunn, is a widely used traditional Chinese medicine (TCM) for the… 
2017
2017
A pair of taxifolin-3-O-arabinofuranoside isomers from Juglans regia L.
Abstract Diaphragma juglandis Fructus has been known for its effect on tonifying kidney in traditional Uighur medicine. During… 
2015
2015
Antioxidant stilbenoid and flavanonol from stem of Erythrophleum suaveolens (Guill. & Perr.)
Keywords: NMR; 1H NMR; Caesalpiniaceae; Erythrophleum suaveolens; flavanonol; stilbenoid; radical scavenging activity 
2014
2014
Flavanonol Taxifolin Attenuates Proteasome Inhibition-Induced Apoptosis in Differentiated PC12 Cells by Suppressing Cell Death Process
The proteasomal dysfunction and mitochondrial impairment has been implicated in neuronal degeneration. Taxifolin has antioxidant… 
2014
2014
Two new flavanonols from the bark of Akschindlium godefroyanum
The first phytochemical investigation of the bark of Akschindlium godefroyanum (Kuntze) H. Ohashi (Fabaceae), a Thai herbal… 
2007
2007
Flavonoid glycosides and limonoids from Citrus molasses
Molasses of tangerine orange (Citrus unshiu Markovich) is obtained as a waste product in the course of tangerine orange juice… 
1996
1996
[Flavanonol glucosides of Smilax glabra Roxb].
Three flavanonol glucosides have been isolated from the rhizome of Smilax glabra. Their structures were identified as… 
1984
1984
A New Flavanonol Glycoside from Adansonia digitata Roots
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1978
1978
Pigment synthesis in maize aleurone from precursors fed to anthocyanin mutants
Aleurone tissue of c2 Pr, C2 pr, or c2 pr genotypes can utilize either of two flavanones (naringenin, homoeriodictyol) or a… 
1963
1963
Structural and chromatographic correlations of some flavonoid compounds.
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