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Flavonols

Known as: 3-hydroxy-4-keto-Flavonoids, 2 Phenyl 3 Hydroxy Benzopyran 4 Ones, Flavonols [Chemical/Ingredient] 
A group of 3-hydroxy-4-keto-FLAVONOIDS.
National Institutes of Health

Related topics

Related topics

47 relations

Narrower (38)

2'-fluoroflavonol3',4'-dihydroxyflavonol3-O-acetyl-7-O-methyl kaemferol3-hydroxyflavone

Broader (1)

Flavonoids
In BloodProcess of secretionagonistsantagonists & inhibitors

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2007
Highly Cited
2007
(J. Agric. Food. Chem.,55(18):7462-7468)Identification and Comparison of Phenolic Compounds in the Preparation of Oolong Tea Manufactured by Semifermentation and Drying Processes
Highly Cited
2006
Highly Cited
2006
Oxidative DNA cleavage induced by an iron(III) flavonoid complex: synthesis, crystal structure and characterization of chlorobis(flavonolato)(methanol) iron(III) complex.
Highly Cited
2002
Highly Cited
2002
Analysis of wine phenolics by high-performance liquid chromatography using a monolithic type column.
Highly Cited
2002
Highly Cited
2002
Amperometric biosensor based on a functionalized gold electrode for the detection of antioxidants.
Highly Cited
1999
Highly Cited
1999
Antioxidant capacity of flavanols and gallate esters: pulse radiolysis studies.
Highly Cited
1999
Highly Cited
1999
Acylated flavonol glycosides from leaves of Stenochlaena palustris.
From the leaves of Stenochlaena palustris five new O-acylated flavonol glycosides, stenopalustrosides A-E (1-5), have been… 
Highly Cited
1996
Highly Cited
1996
Comparative effects of flavonoids on the growth, viability and metabolism of a colonic adenocarcinoma cell line (HT29 cells).
Highly Cited
1991
Highly Cited
1991
Inhibitory Effects of Galloylated Flavonoids on Xanthine Oxidase
(uncorr.; from CHC13); {aI': + 59.8° (c 0.4, CHC13). Its UV spectrum (MeOH) Amax nm (loge) 398 (3.71), 332 (3.85), 300 (4.23… 
Highly Cited
1987
Highly Cited
1987
Structural classification of flavonoids in beverages by liquid chromatography with ultraviolet-visible and electrochemical detection.
Highly Cited
1958
Highly Cited
1958
Metabolic fate of hesperidin, eriodictyol, homoeridictyol, and diosmin.
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