epigallocatechin gallate (Q393339)

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chemical compound
  • EGCG
  • (-)-epigallocatechin-3-O-gallate
  • [(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
  • Epigallocatechin gallate，EGCG
  • Epigallocatechin gallate
  • Epigallocatechin Gallate
  • epi-gallocatechin-3gallate
edit
Language Label Description Also known as
English
epigallocatechin gallate
chemical compound
  • EGCG
  • (-)-epigallocatechin-3-O-gallate
  • [(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
  • Epigallocatechin gallate，EGCG
  • Epigallocatechin gallate
  • Epigallocatechin Gallate
  • epi-gallocatechin-3gallate

Statements

subclass of
flavan
0 references
proanthocyanidins
0 references
mass
458.085 dalton
1 reference
stated in
PubChem
PubChem CID
65064
language of work or name
English
title
EGCG (English)
retrieved
19 October 2016
chemical formula
C₂₂H₁₈O₁₁
1 reference
stated in
PubChem
PubChem CID
65064
language of work or name
English
title
EGCG (English)
retrieved
20 November 2016
canonical SMILES
C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O
1 reference
stated in
PubChem
PubChem CID
65064
language of work or name
English
title
EGCG (English)
retrieved
20 November 2016
isomeric SMILES
C1[C@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O
1 reference
stated in
PubChem
PubChem CID
65064
language of work or name
English
title
EGCG (English)
retrieved
20 November 2016
found in taxon
Camellia sinensis
60 references
stated in
Isolation and identification of acetyl-CoA carboxylase inhibitors from green tea (Camellia sinensis).
stated in
(-)-Epigallocatechin-3-gallate in Camellia sinensis leaves from Himalayan region of Sikkim: inhibitory effects against biochemical events and tumor initiation in Sencar mouse skin
stated in
Epicatechin derivatives and fatty acid composition of a traditional product made in Sikkim from leaves ofCamellia sinensis
stated in
Coffee, Tea, Cocoa
stated in
Green tea regulates cell cycle progression in oral leukoplakia.
stated in
Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea.
stated in
Quantitative analysis of the active constituents in green tea
stated in
Electrospray characterization of selected medicinal plant extracts
stated in
Separation of the components in black tea infusion by chromatography on Toyopearl.
stated in
Tannins and Related Compounds. CXIV. Structures of Novel Fermentation Products, Theogallinin, Theaflavonin and Desgalloyl Theaflavonin from Black Tea, and Changes of Tea Leaf Polyphenols during Fermentation.
stated in
Selection of column and gradient elution system for the separation of catechins in green tea using high-performance liquid chromatography
stated in
Relationship between antimutagenic activity and major components of various teas.
stated in
Survey of Catechins, Gallic Acid, and Methylxanthines in Green, Oolong, Pu-erh, and Black Teas
stated in
Quantitative Analysis of (-)-Epigallocatechin Gallate in Tea Leaves by High-Performance Liquid Chromatography
stated in
Simultaneous analysis of individual catechins and caffeine in green tea
stated in
Composition of Polyphenols in Fresh Tea Leaves and Associations of Their Oxygen-Radical-Absorbing Capacity with Antiproliferative Actions in Fibroblast Cells
stated in
Analysis of (-)-epigallocatechin gallate in human serum obtained after ingesting green tea
stated in
HPLC determination of catechins and caffeine in tea. Differentiation of green, black and instant teas
stated in
ANALYSIS OF GREEN TEA CONSTITUENTS BY HPLC-FTIR
stated in
Effects of crude drugs on experimental hypercholesterolemia. I. Tea and its active principles
stated in
Antitumor promoting activity of (−)-epigallocatechin gallate, the main constituent of “Tannin” in green tea
stated in
The effect of crude drugs on experimental hypercholesteremia: mode of action of (-)-epigallocatechin gallate in tea leaves
stated in
Novel antiallergic catechin derivatives isolated from oolong tea
stated in
Inhibitory effect of six green tea catechins and caffeine on the growth of four selected human tumor cell lines
stated in
Protective effect of green tea extract and tea polyphenols against the cytotoxicity of 1,4-naphthoquinone in isolated rat hepatocytes
stated in
Application of capillary electrophoresis to tea quality estimation
stated in
Effect of Tannins in Green Tea on the Urinary Methylguanidine Excretion in Rats Indicating a Possible Radical Scavenging Action
stated in
Effects of a component of green tea on the proliferation of vascular smooth muscle cells
stated in
Protecting effect of a green tea percolate and its main constituents against gamma ray-induced scission of DNA
stated in
Inhibition of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) mutagenicity by black and green tea extracts and polyphenols.
stated in
1H and13C NMR Assignments of Some Green Tea Polyphenols
stated in
Antiallergic constituents from oolong tea stem
stated in
Inhibitory effects and toxicity of green tea polyphenols for gastrointestinal carcinogenesis
stated in
Epigallocatechin gallate and gallocatechin gallate in green tea catechins inhibit extracellular release of Vero toxin from enterohemorrhagic Escherichia coli O157:H7
stated in
Inhibition of phorbol ester tumor promoter 12-O-tetradecanoylphorbol-13-acetate-caused inflammatory responses in SENCAR mouse skin by black tea polyphenols
stated in
SEPARATION OF EPIGALLOCATECHIN GALLATE FROM KOREAN GREEN TEA BY RP-HPLC
stated in
Theaflavins in black tea and catechins in green tea are equally effective antioxidants
stated in
Indonesian medicinal plants. XXV. Cancer cell invasion inhibitory effects of chemical constituents in the parasitic plant Scurrula atropurpurea (Loranthaceae).
stated in
Preparative separation of polyphenols from tea by high-speed countercurrent chromatography
stated in
Tannins and related compounds. LVI Isolation of four new acylated flavan-3-ols from oolong tea.
stated in
Antibacterial substances in japanese green tea extract against Streptococcus mutans, a cariogenic bacterium.
stated in
Anticaries Effects of Polyphenolic Compounds from Japanese Green Tea
stated in
Inhibition of rotavirus and enterovirus infections by tea extracts
stated in
Catechin contents of foods commonly consumed in The Netherlands. 2. Tea, wine, fruit juices, and chocolate milk
stated in
Black tea represents a major source of dietary phenolics among regular tea drinkers
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
Estimation of black tea quality by analysis of chemical composition and colour difference of tea infusions
stated in
Preliminary investigation into development of HPLC with UV and MS-electrospray detection for the analysis of tea catechins
stated in
IDENTIFICATION AND DETERMINATION OF POLYPHENOLS IN TEA BY LIQUID CHROMATOGRAPHY WITH MULTI-CHANNEL ELECTROCHEMICAL DETECTION
stated in
Total phenol, catechin, and caffeine contents of teas commonly consumed in the United kingdom
stated in
Method for determining the content of catechins in tea infusions by high-performance liquid chromatography
stated in
Characterization of the antioxidant functions of flavonoids and proanthocyanidins in Mauritian black teas
stated in
On-line high-performance liquid chromatography analysis of the antioxidant activity of phenolic compounds in green and black tea.
stated in
Characterisation of polyphenols in green, oolong, and black teas, and in coffee, using cyclic voltammetry
stated in
Influence of catechins and theaflavins on the astringent taste of black tea brews
stated in
Determination of Green and Black Tea Composition by Capillary Electrophoresis
stated in
Variations in the amounts of individual flavanols in a range of green teas
stated in
Isocratic elution system for the determination of catechins, caffeine and gallic acid in green tea using HPLC
stated in
Seasonal variations of phenolic compounds in Australia-grown tea (Camellia sinensis).
stated in
Tea polyphenols: Selective growth inhibitors of Clostridium spp.
has part(s)
carbon
0 references
Commons category
Epigallocatechin gallate
0 references

Identifiers

ChemSpider ID
58575
1 reference
stated in
ChemSpider
ChemSpider ID
58575
language of work or name
English
title
(−)-Epigallocatechin gallate (English)
retrieved
20 November 2016
Reaxys registry number
67944
1 reference
stated in
ChEBI
ChEBI ID
4806
language of work or name
English
title
(-)-epigallocatechin 3-gallate (English)
retrieved
19 October 2016
3658838
1 reference
stated in
ChEBI
ChEBI ID
4806
language of work or name
English
title
(-)-epigallocatechin 3-gallate (English)
retrieved
19 October 2016
ChEMBL ID
CHEMBL297453
1 reference
stated in
ChEMBL
ChEMBL ID
CHEMBL297453
language of work or name
English
title
EPIGALOCATECHIN GALLATE (English)
retrieved
20 November 2016
MassBank accession ID
BS003896
0 references
BS003897
0 references
BS003898
0 references
BS003899
0 references
BS003900
0 references
BS003901
0 references
EC number
619-381-5
0 references
CosIng number
56148
0 references
DrugBank ID
12116
1 reference
stated in
DrugBank
DrugBank ID
12116
language of work or name
English
title
Epigallocatechin Gallate (English)
publication date
3 July 2018
KNApSAcK ID
C00000958
1 reference
stated in
ChEBI
ChEBI ID
4806
language of work or name
English
title
(-)-epigallocatechin 3-gallate (English)
retrieved
19 October 2016
KEGG ID
C09731
1 reference
stated in
ChEBI
ChEBI ID
4806
language of work or name
English
title
(-)-epigallocatechin 3-gallate (English)
retrieved
19 October 2016
PDB ligand ID
KDH
0 references
Microsoft Academic ID
2777192995
0 references
2908789873
0 references
 
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                Retrieved from "https://www.wikidata.org/w/index.php?title=Q393339&oldid=2146969354"