(−)-Epigallocatechin

Papers

Efficiency of foam fractionation for the enrichment of nonpolar compounds from aqueous extracts of plant materials. Marlène Backleh-Sohrt et al J. Nat. Prod. 68, 1386-9, (2005)

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Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. Deniz Tasdemir et al J. Med. Chem. 49, 3345-53, (2006)

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Green tea catechins inhibit bacterial DNA gyrase by interaction with its ATP binding site. Helena Gradisar et al J. Med. Chem. 50, 264-71, (2007)

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Green tea catechins potentiate triclosan binding to enoyl-ACP reductase from Plasmodium falciparum (PfENR). Shailendra Kumar Sharma et al J. Med. Chem. 50, 765-75, (2007)

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Flavonoids as opioid receptor ligands: identification and preliminary structure-activity relationships. Peter L Katavic et al J. Nat. Prod. 70, 1278-82, (2007)

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Small molecule obatoclax (GX15-070) antagonizes MCL-1 and overcomes MCL-1-mediated resistance to apoptosis. Mai Nguyen et al Proc. Natl. Acad. Sci. U. S. A. 104, 19512-7, (2007)

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Synthesis and biological activity of a 3,4,5-trimethoxybenzoyl ester analogue of epicatechin-3-gallate. Luís Sánchez-del-Campo et al J. Med. Chem. 51, 2018-26, (2008)

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New polyphenols active on beta-amyloid aggregation. Céline Rivière et al Bioorg. Med. Chem. Lett. 18, 828-31, (2008)

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Catechin gallates are NADP+-competitive inhibitors of glucose-6-phosphate dehydrogenase and other enzymes that employ NADP+ as a coenzyme. Eui Seok Shin et al Bioorg. Med. Chem. 16, 3580-6, (2008)

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Tea catechins inhibit hepatocyte growth factor receptor (MET kinase) activity in human colon cancer cells: kinetic and molecular docking studies. Christine A Larsen et al J. Med. Chem. 52, 6543-5, (2009)

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Proteasome inhibition in human breast cancer cells with high catechol-O-methyltransferase activity by green tea polyphenol EGCG analogs. Congde Huo et al Bioorg. Med. Chem. 18, 1252-8, (2010)

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Reliability of bond dissociation enthalpy calculated by the PM6 method and experimental TEAC values in antiradical QSAR of flavonoids. Dragan Ami? et al Bioorg. Med. Chem. 18, 28-35, (2010)

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Structural characteristics of green tea catechins for formation of protein carbonyl in human serum albumin. Takeshi Ishii et al Bioorg. Med. Chem. 18, 4892-6, (2010)

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Synthesis and antimicrobial activities of 3-O-alkyl analogues of (+)-catechin: improvement of stability and proposed action mechanism. Ki Duk Park et al Eur. J. Med. Chem. 45, 1028-33, (2010)

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New monoterpene glycosides and phenolic compounds from Distylium racemosum and their inhibitory activity against ribonuclease H. Jeong Ah Kim et al Bioorg. Med. Chem. Lett. 21, 2840-4, (2011)

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Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells. Hisashi Matsuda et al Bioorg. Med. Chem. 19, 2835-41, (2011)

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Tea catechins and flavonoids from the leaves of Camellia sinensis inhibit yeast alcohol dehydrogenase. Md Maniruzzaman Manir et al Bioorg. Med. Chem. 20, 2376-81, (2012)

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