Wikidata

(Q51617505)

English

(-)-epigallocatechin

chemical compound

In more languages

Statements

subclass of
flavan
0 references
mass
306.07395278799993 dalton
1 reference
based on heuristic
inferred from isomeric SMILES
chemical formula
C₁₅H₁₄O₇
0 references
canonical SMILES
OC=1C=C(O)C2=C(OC(C3=CC(O)=C(O)C(O)=C3)C(O)C2)C1
0 references
isomeric SMILES
C1[C@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O
0 references
found in taxon
Camellia sinensis
56 references
stated in
Quantitative analysis of the active constituents in green tea
stated in
Prevention of cytotoxicity and inhibition of intercellular communication by antioxidant catechins isolated from Chinese green tea.
stated in
Effect of green tea and (-)-epigallocatechin gallate on ethanol-induced toxicity in HepG2 cells.
stated in
1H and13C NMR Assignments of Some Green Tea Polyphenols
stated in
Epicatechin derivatives and fatty acid composition of a traditional product made in Sikkim from leaves ofCamellia sinensis
stated in
Simultaneous analysis of individual catechins and caffeine in green tea
stated in
Effects of crude drugs on experimental hypercholesterolemia. I. Tea and its active principles
stated in
Application of capillary electrophoresis to tea quality estimation
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
Epigallocatechin gallate and gallocatechin gallate in green tea catechins inhibit extracellular release of Vero toxin from enterohemorrhagic Escherichia coli O157:H7
stated in
Electrospray characterization of selected medicinal plant extracts
stated in
Survey of Catechins, Gallic Acid, and Methylxanthines in Green, Oolong, Pu-erh, and Black Teas
stated in
Novel antiallergic catechin derivatives isolated from oolong tea
stated in
HPLC determination of catechins and caffeine in tea. Differentiation of green, black and instant teas
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
SEPARATION OF EPIGALLOCATECHIN GALLATE FROM KOREAN GREEN TEA BY RP-HPLC
stated in
ANALYSIS OF GREEN TEA CONSTITUENTS BY HPLC-FTIR
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
Theaflavins in black tea and catechins in green tea are equally effective antioxidants
stated in
Relationship between antimutagenic activity and major components of various teas.
stated in
Inhibitory effect of six green tea catechins and caffeine on the growth of four selected human tumor cell lines
stated in
Anticaries Effects of Polyphenolic Compounds from Japanese Green Tea
stated in
Antiallergic constituents from oolong tea stem
stated in
Tannins and related compounds. XV. A new class of dimeric flavan-3-ol gallates, theasinensins A and B, and proanthocyanidin gallates from green tea leaf. (1).
stated in
Tannins and related compounds. LVI Isolation of four new acylated flavan-3-ols from oolong tea.
stated in
Tannins and related compounds. LXXVII. Novel chalcan-flavan dimers, assamicains A, B and C, and a new flavan-3-ol and proanthocyanidins from the fresh leaves of Camellia sinensis L. var. assamica Kitamura.
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
Indonesian medicinal plants. XXV. Cancer cell invasion inhibitory effects of chemical constituents in the parasitic plant Scurrula atropurpurea (Loranthaceae).
stated in
Quantitative Analysis of (-)-Epigallocatechin Gallate in Tea Leaves by High-Performance Liquid Chromatography
stated in
Separation of the components in black tea infusion by chromatography on Toyopearl.
stated in
Antibacterial substances in japanese green tea extract against Streptococcus mutans, a cariogenic bacterium.
stated in
Effects of a component of green tea on the proliferation of vascular smooth muscle cells
stated in
Protective effect of green tea extract and tea polyphenols against the cytotoxicity of 1,4-naphthoquinone in isolated rat hepatocytes
stated in
Tannins and related compounds. XC. 8-C-ascorbyl (-)-epigallocatechin 3-O-gallate and novel dimeric flavan-3-ols, oolonghomobisflavans A and B, from oolong tea.(3).
stated in
Identification of two novel proanthocyanidins in green Tea
stated in
Tea catechins and flavonoids from the leaves of Camellia sinensis inhibit yeast alcohol dehydrogenase
stated in
Black tea represents a major source of dietary phenolics among regular tea drinkers
stated in
Catechin contents of foods commonly consumed in The Netherlands. 2. Tea, wine, fruit juices, and chocolate milk
stated in
Characterisation of polyphenols in green, oolong, and black teas, and in coffee, using cyclic voltammetry
stated in
Characterization of the antioxidant functions of flavonoids and proanthocyanidins in Mauritian black teas
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
Determination of Green and Black Tea Composition by Capillary Electrophoresis
stated in
Estimation of black tea quality by analysis of chemical composition and colour difference of tea infusions
stated in
IDENTIFICATION AND DETERMINATION OF POLYPHENOLS IN TEA BY LIQUID CHROMATOGRAPHY WITH MULTI-CHANNEL ELECTROCHEMICAL DETECTION
stated in
Influence of catechins and theaflavins on the astringent taste of black tea brews
stated in
Isocratic elution system for the determination of catechins, caffeine and gallic acid in green tea using HPLC
stated in
Method for determining the content of catechins in tea infusions by high-performance liquid chromatography
stated in
On-line high-performance liquid chromatography analysis of the antioxidant activity of phenolic compounds in green and black tea.
stated in
Preliminary investigation into development of HPLC with UV and MS-electrospray detection for the analysis of tea catechins
stated in
Quantitative Analysis of Flavan-3-ols in Spanish Foodstuffs and Beverages
stated in
Survey of Catechins, Gallic Acid, and Methylxanthines in Green, Oolong, Pu-erh, and Black Teas
stated in
Total phenol, catechin, and caffeine contents of teas commonly consumed in the United kingdom
stated in
Variations in the amounts of individual flavanols in a range of green teas
stated in
Tannins and related compounds. LXXVII. Novel chalcan-flavan dimers, assamicains A, B and C, and a new flavan-3-ol and proanthocyanidins from the fresh leaves of Camellia sinensis L. var. assamica Kitamura.
stated in
Bioactive saponins and glycosides. XXV. Acylated oleanane-type triterpene saponins from the seeds of tea plant (Camellia sinensis)
stated in
Medicinal flowers. XIV. New acylated oleanane-type triterpene oligoglycosides with antiallergic activity from flower buds of chinese tea plant (Camellia sinensis).

Identifiers

PubChem CID
72277
0 references
Reaxys registry number
3655868
0 references
MassBank accession ID
BS003949
0 references
BS003950
0 references
BS003951
0 references
BS003952
0 references
NSC number
674039
0 references
EC number
619-254-4
1 reference
stated in
ECHA Substance Infocard database
ECHA Substance Infocard ID
100.129.752
retrieved
27 December 2018
title
2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-, (2R,3R)- (English)
quotation
CAS no.: 970-74-1 (English)
ECHA Substance Infocard ID
100.129.752
1 reference
stated in
ECHA Substance Infocard database
ECHA Substance Infocard ID
100.129.752
retrieved
27 December 2018
title
2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-, (2R,3R)- (English)
quotation
CAS no.: 970-74-1 (English)
DrugBank ID
03823
1 reference
stated in
DrugBank
DrugBank ID
03823
retrieved
6 July 2021
quotation
CAS no.: 970-74-1 (English)
title
Epigallocatechin (English)
KNApSAcK ID
C00008818
0 references
UNII
7Z197MG6QL
0 references
KEGG ID
C12136
0 references
PDB ligand ID
EGT
0 references
 
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