Results 211 to 220 of about 25,452 (252)
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Efficient Synthesis of Flavanone Glucuronides
Journal of Agricultural and Food Chemistry, 2009The first efficient synthesis of flavanone glucuronides as potential human metabolites is described. The synthetic strategy is based on acetyl protection, followed by a combination of chemical and enzymatic deprotection steps. As an example, the method is applied to a synthesis of 7,4'-di-O-methyleriodictyol 3'-O-beta-d-glucuronide.
Ahcene, Boumendjel +3 more
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The biliary excretion of flavanones in the rat
Xenobiotica, 19791. The major biliary metabolites of flavanones in the rat have been identified by chromatographic and spectral methods. 2. Evidence is presented that flavanones and flavanone glycosides, following oral or parenteral administration, undergo glucuronylation and are selectively excreted via the bile. 3.
A M, Hackett +3 more
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Microbiological Transformation of (±)-Flavanone and (±)-Isoflavanone
Journal of Natural Products, 1990The microbiological transformation of flavanone and isoflavanone was explored using a group of 80 microorganisms in the initial screening. Ten metabolites of flavanone were isolated and identified as 4'-hydroxyflavanone [3], 3',4'-dihydroxyflavanone [4], 3-hydroxyflavone [2], flavone [5], 2'-hydroxydihydrochalcone [7], 2',4-dihydroxydihydrochalcone [6],
A R, Ibrahim, Y J, Abul-Hajj
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Chemical Synthesis of Citrus Flavanone Glucuronides
Journal of Agricultural and Food Chemistry, 2010Flavanone glucuronides are the major phenolic metabolites detected in human plasma after consumption of citrus fruits. As such, they might display significant cardioprotective effects. In this work, glucuronides of naringenin (4'- and 7-O-beta-d-glucuronides) and hesperetin (3'- and 7-O-beta-d-glucuronides), the major flavanone aglycones in grapefruit ...
Khan, Muhammad +3 more
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Flavanones and Dihydroflavonols
1975This chapter is concerned with the closely related flavanones and dihydroflavonols. Flavanones are based upon structure (1), 2-phenylbenzopyran-4-one, which is flavanone itself. The parent compound is not known to be naturally occurring; the simplest plant flavanone has a hydroxy 1 group at position 7.
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Flavanones fromTephrosia leiocarpa
Phytochemistry, 1991Abstract Roots and aereal parts of Tephrosia leiocarpa afforded two new flavanones, 5-hydroxy-7-methoxy-8-(3-hydroxy-3-methyl- trans -but-1-enyl)flavanone and 5-hydroxy-7-methoxy-8-(3-methyl- trans -but-1,3-dienyl)flavanone, named tephroleocarpin A and B, respectively.
Federico Go´mez-Garibay +2 more
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Flavanones ofTanacetum sibiricum
Chemistry of Natural Compounds, 1981Six flavanones have been isolated for the first time from Siberian tansy, and two of them have proved to be new compounds.
T. A. Stepanova +3 more
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The reaction of flavanone with hydrazine
Tetrahedron, 1965Abstract The interaction of flavanone and hydrazine hydrate can be directed to yield flavanone hydrazone, 3-(o-hydroxyphenyl) 5-phenylpyrazoline, or flavanone azine as the main product. The structures of these compounds have been proved by hydrolysis, acetylation, and other simple reactions.
F. Kálly, G. Janzsó, I. Koczor
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Flavanones and Related Compounds. I. The Preparation of Polyhydroxychalcones and -Flavanones
Journal of the American Chemical Society, 1946T A, GEISSMAN, R O, CLINTON
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