Gallocatechin gallate

Gallocatechin gallate is a lipid of Polyketides (PK) class.

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Current reference collection contains 413 references associated with Gallocatechin gallate in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
Peng Y et al. Nanoemulsion delivery system of tea polyphenols enhanced the bioavailability of catechins in rats. 2018 Food Chem pmid:29037724
Hung WL et al. Quantification of ascorbyl adducts of epigallocatechin gallate and gallocatechin gallate in bottled tea beverages. 2018 Food Chem pmid:29739590
Xin Z et al. UPLC-Orbitrap-MS/MS combined with chemometrics establishes variations in chemical components in green tea from Yunnan and Hunan origins. 2018 Food Chem pmid:30381222
Frost S et al. Characterization of Red Wine Proanthocyanidins Using a Putative Proanthocyanidin Database, Amide Hydrophilic Interaction Liquid Chromatography (HILIC), and Time-of-Flight Mass Spectrometry. 2018 Molecules pmid:30340402
Fang R et al. Variation of theanine, phenolic, and methylxanthine compounds in 21 cultivars of Camellia sinensis harvested in different seasons. 2017 Food Chem pmid:27855934
Gao X et al. Cellular antioxidant, methylglyoxal trapping, and anti-inflammatory activities of cocoa tea (Camellia ptilophylla Chang). 2017 Food Funct pmid:28725904
Hui X et al. Antimicrobial mechanism of epigallocatechin gallate and gallocatechin gallate: They target 1-deoxy-d-xylulose 5-phosphate reductoisomerase, the key enzyme of the MEP terpenoid biosynthetic pathway. 2017 Arch. Biochem. Biophys. pmid:28428039
Hui X et al. Inhibition of green tea and the catechins against 1-deoxy-d-xylulose 5-phosphate reductoisomerase, the key enzyme of the MEP terpenoid biosynthetic pathway. 2016 Fitoterapia pmid:27439219
Li K et al. Preparative separation of gallocatechin gallate from Camellia ptilophylla using macroporous resins followed by sephadex LH-20 column chromatography. 2016 J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. pmid:26744789
Pantelić MM et al. Identification and quantification of phenolic compounds in berry skin, pulp, and seeds in 13 grapevine varieties grown in Serbia. 2016 Food Chem pmid:27283628
Lall N et al. Extract from Ceratonia siliqua Exhibits Depigmentation Properties. 2015 Phytother Res pmid:26201055
Zhu YT et al. Fast identification of lipase inhibitors in oolong tea by using lipase functionalised Fe3O4 magnetic nanoparticles coupled with UPLC-MS/MS. 2015 Food Chem pmid:25466054
Kaneko YK et al. Structure-dependent inhibitory effects of green tea catechins on insulin secretion from pancreatic β-cells. 2015 Biol. Pharm. Bull. pmid:25757931
Menegazzi M et al. Direct interaction of natural and synthetic catechins with signal transducer activator of transcription 1 affects both its phosphorylation and activity. 2014 FEBS J. pmid:24255956
Jang JH et al. Analysis of green tea compounds and their stability in dentifrices of different pH levels. 2014 Chem. Pharm. Bull. pmid:24695342
Roman MC Determination of catechins and caffeine in camillia sinensis raw materials, extracts, and dietary supplements by HPLC-uv: single-laboratory validation. 2013 Sep-Oct J AOAC Int pmid:24282928
Cunha CA et al. Green tea extract supplementation induces the lipolytic pathway, attenuates obesity, and reduces low-grade inflammation in mice fed a high-fat diet. 2013 Mediators Inflamm. pmid:23431242
Lee LS et al. Optimization of ultrasonic extraction of phenolic antioxidants from green tea using response surface methodology. 2013 Molecules pmid:24184822
Zhang Y et al. Effects of (-)-gallocatechin-3-gallate on tetrodotoxin-resistant voltage-gated sodium channels in rat dorsal root ganglion neurons. 2013 Int J Mol Sci pmid:23652835
Nguyen TT et al. Flavonoid-mediated inhibition of SARS coronavirus 3C-like protease expressed in Pichia pastoris. 2012 Biotechnol. Lett. pmid:22350287
Boušová I et al. Naturally occurring flavonoids as inhibitors of purified cytosolic glutathione S-transferase. 2012 Xenobiotica pmid:22458346
Roh C A facile inhibitor screening of SARS coronavirus N protein using nanoparticle-based RNA oligonucleotide. 2012 Int J Nanomedicine pmid:22619553
Xu YQ et al. Irreversible sediment formation in green tea infusions. 2012 J. Food Sci. pmid:22329921
Salem MM et al. In vitro anti-uveal melanoma activity of phenolic compounds from the Egyptian medicinal plant Acacia nilotica. 2011 Fitoterapia pmid:21903153
Zoechling A et al. Red wine: a source of potent ligands for peroxisome proliferator-activated receptor γ. 2011 Food Funct pmid:21773583
Maruyama T et al. Supplementation of green tea catechins in dentifrices suppresses gingival oxidative stress and periodontal inflammation. 2011 Arch. Oral Biol. pmid:20869695
Tsutsumi H et al. Stereochemical structure and intermolecular interaction of complexes of (-)-Gallocatechin-3-O-gallate and caffeine. 2011 Chem. Pharm. Bull. pmid:21212555
Yoshino K et al. Preventive effects of C-2 epimeric isomers of tea catechins on mouse type I allergy. 2010 J. Nutr. Sci. Vitaminol. pmid:20651464
Tsutsumi H et al. Offset pi-pi interaction in crystal structure of (-)-gallocatechin-3-O-gallate. 2010 Chem. Pharm. Bull. pmid:20410646
Jiang F et al. The evaluation of catechins that contain a galloyl moiety as potential HIV-1 integrase inhibitors. 2010 Clin. Immunol. pmid:20832370
Ishizu T et al. NMR spectroscopic characterization of inclusion complexes comprising cyclodextrins and gallated catechins in aqueous solution: cavity size dependency. 2009 Magn Reson Chem pmid:19089883
van't Slot G and Humpf HU Degradation and metabolism of catechin, epigallocatechin-3-gallate (EGCG), and related compounds by the intestinal microbiota in the pig cecum model. 2009 J. Agric. Food Chem. pmid:19670865
Liu J et al. Borate complexation-assisted field-enhanced sample injection for on-line preconcentration of cis-diol-containing compounds in capillary electrophoresis. 2009 Talanta pmid:19836518
Rambold AS et al. Green tea extracts interfere with the stress-protective activity of PrP and the formation of PrP. 2008 J. Neurochem. pmid:18691383
Nomura S et al. Tea catechins enhance the mRNA expression of uncoupling protein 1 in rat brown adipose tissue. 2008 J. Nutr. Biochem. pmid:18479902
Lee SM et al. GCG-rich tea catechins are effective in lowering cholesterol and triglyceride concentrations in hyperlipidemic rats. 2008 Lipids pmid:18365267
Muzolf-Panek M et al. Role of catechin quinones in the induction of EpRE-mediated gene expression. 2008 Chem. Res. Toxicol. pmid:19548356
Ishizu T et al. Diastereomeric difference of inclusion modes between (-)-epicatechin gallate, (-)-epigallocatechin gallate and (+)-gallocatechin gallate, with beta-cyclodextrin in aqueous solvent. 2008 Magn Reson Chem pmid:18318450
Fujimura Y et al. The impact of the 67kDa laminin receptor on both cell-surface binding and anti-allergic action of tea catechins. 2008 Arch. Biochem. Biophys. pmid:18358230
Anton S et al. Epigallocatechin gallate (EGCG) mimics insulin action on the transcription factor FOXO1a and elicits cellular responses in the presence and absence of insulin. 2007 Cell. Signal. pmid:16950602
Hirai M et al. Protective effects of EGCg or GCg, a green tea catechin epimer, against postischemic myocardial dysfunction in guinea-pig hearts. 2007 Life Sci. pmid:17174345
Haginaka J et al. Uniformly-sized, molecularly imprinted polymers for (-)-epigallocatechin gallate, -epicatechin gallate and -gallocatechin gallate by multi-step swelling and polymerization method. 2007 J Chromatogr A pmid:17070533
Kotani A et al. Attomole catechins determination by capillary liquid chromatography with electrochemical detection. 2007 Anal Sci pmid:17297226
Hotta Y et al. Positive inotropic effect of purified green tea catechin derivative in guinea pig hearts: the measurements of cellular Ca2+ and nitric oxide release. 2006 Eur. J. Pharmacol. pmid:17059816
Yamamoto S et al. Arachidonate 12-lipoxygenases with reference to their selective inhibitors. 2005 Biochem. Biophys. Res. Commun. pmid:16171776
Wan SB et al. Structure-activity study of epi-gallocatechin gallate (EGCG) analogs as proteasome inhibitors. 2005 Bioorg. Med. Chem. pmid:15727870
Dell'agli M et al. A structure-activity study for the inhibition of metalloproteinase-9 activity and gene expression by analogues of gallocatechin-3-gallate. 2005 Cell. Mol. Life Sci. pmid:16314917
Liu S et al. Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41. 2005 Biochim. Biophys. Acta pmid:15823507
Tanaka T et al. A novel black tea pigment and two new oxidation products of epigallocatechin-3-O-gallate. 2005 J. Agric. Food Chem. pmid:16159188
Okamoto M et al. Inhibitory effect of green tea catechins on cysteine proteinases in Porphyromonas gingivalis. 2004 Oral Microbiol. Immunol. pmid:14871352
Chen L et al. Tea catechins protect against lead-induced ROS formation, mitochondrial dysfunction, and calcium dysregulation in PC12 cells. 2003 Chem. Res. Toxicol. pmid:12971804
Morré DJ et al. Tea catechin synergies in inhibition of cancer cell proliferation and of a cancer specific cell surface oxidase (ECTO-NOX). 2003 Pharmacol. Toxicol. pmid:12753411
Donà M et al. Neutrophil restraint by green tea: inhibition of inflammation, associated angiogenesis, and pulmonary fibrosis. 2003 J. Immunol. pmid:12682270
Ikeda I et al. Heat-epimerized tea catechins rich in gallocatechin gallate and catechin gallate are more effective to inhibit cholesterol absorption than tea catechins rich in epigallocatechin gallate and epicatechin gallate. 2003 J. Agric. Food Chem. pmid:14640575
Oku N et al. Inhibitory effect of green tea polyphenols on membrane-type 1 matrix metalloproteinase, MT1-MMP. 2003 Biol. Pharm. Bull. pmid:12951464
Nakagawa T et al. Protective activity of green tea against free radical- and glucose-mediated protein damage. 2002 J. Agric. Food Chem. pmid:11929306
Nakagawa T and Yokozawa T Direct scavenging of nitric oxide and superoxide by green tea. 2002 Food Chem. Toxicol. pmid:12419687
Sarni-Manchado P and Cheynier V Study of non-covalent complexation between catechin derivatives and peptides by electrospray ionization mass spectrometry. 2002 J Mass Spectrom pmid:12112743
Kim JH et al. Prolyl endopeptidase inhibitors from green tea. 2001 Arch. Pharm. Res. pmid:11534759
Sartippour MR et al. Green tea and its catechins inhibit breast cancer xenografts. 2001 Nutr Cancer pmid:11962250
Yang B et al. Determination of catechins in human urine subsequent to tea ingestion by high-performance liquid chromatography with electrochemical detection. 2000 Anal. Biochem. pmid:10929811
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