Xie L, Cao Y, Zhao Z, Ren C, Xing M, Wu B, et al. Involvement of MdUGT75B1 and MdUGT71B1 in flavonol galactoside/glucoside biosynthesis in apple fruit. Food Chem. 2020;312:126124 pubmed publisher

Krishnamoorthy R, Adisa A, Periasamy V, Athinarayanan J, Pandurangan S, Alshatwi A. Colonic Bacteria-Transformed Catechin Metabolite Response to Cytokine Production by Human Peripheral Blood Mononuclear Cells. Biomolecules. 2019;9: pubmed publisher

Riahi Chebbi I, Souid S, Othman H, Haoues M, Karoui H, Morel A, et al. The Phenolic compound Kaempferol overcomes 5-fluorouracil resistance in human resistant LS174 colon cancer cells. Sci Rep. 2019;9:195 pubmed publisher

Jun J, Xiao X, Rao X, Dixon R. Proanthocyanidin subunit composition determined by functionally diverged dioxygenases. Nat Plants. 2018;4:1034-1043 pubmed publisher

Yuzuak S, Ballington J, Xie D. HPLC-qTOF-MS/MS-Based Profiling of Flavan-3-ols and Dimeric Proanthocyanidins in Berries of Two Muscadine Grape Hybrids FLH 13-11 and FLH 17-66. Metabolites. 2018;8: pubmed publisher

Zhang M, Vervoort L, Moalin M, Mommers A, Douny C, den Hartog G, et al. The chemical reactivity of (-)-epicatechin quinone mainly resides in its B-ring. Free Radic Biol Med. 2018;124:31-39 pubmed publisher

Zhang C, Suen C, Yang C, Quek S. Antioxidant capacity and major polyphenol composition of teas as affected by geographical location, plantation elevation and leaf grade. Food Chem. 2018;244:109-119 pubmed publisher

Gao X, Lin X, Li X, Zhang Y, Chen Z, Li B. Cellular antioxidant, methylglyoxal trapping, and anti-inflammatory activities of cocoa tea (Camellia ptilophylla Chang). Food Funct. 2017;8:2836-2846 pubmed publisher

Chedea V, Pelmuş R, Lazar C, Pistol G, Călin L, Toma S, et al. Effects of a diet containing dried grape pomace on blood metabolites and milk composition of dairy cows. J Sci Food Agric. 2017;97:2516-2523 pubmed publisher

Quiñones M, Margalef M, Arola Arnal A, Muguerza B, Miguel M, Aleixandre A. The blood pressure effect and related plasma levels of flavan-3-ols in spontaneously hypertensive rats. Food Funct. 2015;6:3479-89 pubmed publisher

Takagaki A, Nanjo F. Bioconversion of (-)-epicatechin, (+)-epicatechin, (-)-catechin, and (+)-catechin by (-)-epigallocatechin-metabolizing bacteria. Biol Pharm Bull. 2015;38:789-94 pubmed publisher

Sashidhara K, Singh S, Misra S, Gupta J, Misra Bhattacharya S. Galactolipids from Bauhinia racemosa as a new class of antifilarial agents against human lymphatic filarial parasite, Brugia malayi. Eur J Med Chem. 2012;50:230-5 pubmed publisher

Hurst W, Krake S, Bergmeier S, Payne M, Miller K, Stuart D. Impact of fermentation, drying, roasting and Dutch processing on flavan-3-ol stereochemistry in cacao beans and cocoa ingredients. Chem Cent J. 2011;5:53 pubmed publisher

Liu Y, Nair M. An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds. J Nat Prod. 2010;73:1193-5 pubmed publisher

Arioka S, Sakagami M, Uematsu R, Yamaguchi H, Togame H, Takemoto H, et al. Potent inhibitor scaffold against Trypanosoma cruzi trans-sialidase. Bioorg Med Chem. 2010;18:1633-40 pubmed publisher

Larsen C, Bisson W, Dashwood R. Tea catechins inhibit hepatocyte growth factor receptor (MET kinase) activity in human colon cancer cells: kinetic and molecular docking studies. J Med Chem. 2009;52:6543-5 pubmed publisher

Shin E, Park J, Shin J, Cho D, Cho S, Shin D, et al. Catechin gallates are NADP+-competitive inhibitors of glucose-6-phosphate dehydrogenase and other enzymes that employ NADP+ as a coenzyme. Bioorg Med Chem. 2008;16:3580-6 pubmed publisher

Katavic P, Lamb K, Navarro H, Prisinzano T. Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships. J Nat Prod. 2007;70:1278-82 pubmed

Tasdemir D, Lack G, Brun R, Rüedi P, Scapozza L, Perozzo R. Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. J Med Chem. 2006;49:3345-53 pubmed

Seo W, Kim J, Kang J, Ryu H, Curtis Long M, Lee H, et al. Sulfonamide chalcone as a new class of alpha-glucosidase inhibitors. Bioorg Med Chem Lett. 2005;15:5514-6 pubmed