(-)-Epigallocatechin

(-)-Epigallocatechin is a lipid of Polyketides (PK) class. The involved functions are known as Protective Agents, inhibitors, Process, Drug Kinetics and Fermentation. (-)-epigallocatechin often locates in Hepatic, Blood, Membrane, Back and apical membrane. The associated genes with (-)-Epigallocatechin are ADRBK1 gene and FASTK Gene. The related lipids are 1,2-dilinolenoyl-3-(4-aminobutyryl)propane-1,2,3-triol. The related experimental models are Rodent Model and Transgenic Model.

Cross Reference

Introduction

To understand associated biological information of (-)-Epigallocatechin, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with (-)-Epigallocatechin?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with (-)-Epigallocatechin

MeSH term MeSH ID Detail
Adenocarcinoma D000230 166 associated lipids
Body Weight D001835 333 associated lipids
Glioblastoma D005909 27 associated lipids
Hemolysis D006461 131 associated lipids
Liver Diseases D008107 31 associated lipids
Lung Neoplasms D008175 171 associated lipids
Mammary Neoplasms, Experimental D008325 67 associated lipids
Pancreatic Neoplasms D010190 77 associated lipids
Total 8

PubChem Associated disorders and diseases

What pathways are associated with (-)-Epigallocatechin

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with (-)-Epigallocatechin?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with (-)-Epigallocatechin?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with (-)-Epigallocatechin?

Related references are published most in these journals:

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What genes are associated with (-)-Epigallocatechin?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with (-)-Epigallocatechin?

Rodent Model

Rodent Model are used in the study 'Dietary (-)-epicatechin as a potent inhibitor of βγ-secretase amyloid precursor protein processing.' (Cox CJ et al., 2015) and Rodent Model are used in the study 'Effects of dosing condition on the oral bioavailability of green tea catechins after single-dose administration of Polyphenon E in healthy individuals.' (Chow HH et al., 2005).

Transgenic Model

Transgenic Model are used in the study 'Dietary (-)-epicatechin as a potent inhibitor of βγ-secretase amyloid precursor protein processing.' (Cox CJ et al., 2015).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
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NCBI Entrez Crosslinks

All references with (-)-Epigallocatechin

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Authors Title Published Journal PubMed Link
Garbacki N et al. Inhibitory effects of proanthocyanidins from Ribes nigrum leaves on carrageenin acute inflammatory reactions induced in rats. 2004 BMC Pharmacol. pmid:15498105
Aneja R et al. Epigallocatechin, a green tea polyphenol, attenuates myocardial ischemia reperfusion injury in rats. 2004 Jan-Jun Mol. Med. pmid:15502883
Nimal Punyasiri PA et al. Exobasidium vexans infection of Camellia sinensis increased 2,3-cis isomerisation and gallate esterification of proanthocyanidins. 2004 Phytochemistry pmid:15504433
Zhang L et al. Investigation of intestinal absorption and disposition of green tea catechins by Caco-2 monolayer model. 2004 Int J Pharm pmid:15541906
Koyama Y et al. Effects of green tea on gene expression of hepatic gluconeogenic enzymes in vivo. 2004 Planta Med. pmid:15549673
Furuyashiki T et al. Tea catechin suppresses adipocyte differentiation accompanied by down-regulation of PPARgamma2 and C/EBPalpha in 3T3-L1 cells. 2004 Biosci. Biotechnol. Biochem. pmid:15564676
Taguri T et al. Antimicrobial activity of 10 different plant polyphenols against bacteria causing food-borne disease. 2004 Biol. Pharm. Bull. pmid:15577214
Zhou B et al. Evidence for alpha-tocopherol regeneration reaction of green tea polyphenols in SDS micelles. 2005 Free Radic. Biol. Med. pmid:15589374
Apak R et al. Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method. 2004 J. Agric. Food Chem. pmid:15612784
Wang R and Zhou W Stability of tea catechins in the breadmaking process. 2004 J. Agric. Food Chem. pmid:15612821
Lee K Transactivation of peroxisome proliferator-activated receptor alpha by green tea extracts. 2004 J. Vet. Sci. pmid:15613816
Proctor GB et al. Salivary proteins interact with dietary constituents to modulate tooth staining. 2005 J. Dent. Res. pmid:15615880
Navarro RE et al. Complexation of epigallocatechin gallate (a green tea extract, egcg) with Mn2+: nuclear spin relaxation by the paramagnetic ion. 2005 J. Inorg. Biochem. pmid:15621293
Kuo YC et al. Isolation and immunomodulatory effect of flavonoids from Syzygium samarangense. 2004 Planta Med. pmid:15643565
Hung PF et al. Antimitogenic effect of green tea (-)-epigallocatechin gallate on 3T3-L1 preadipocytes depends on the ERK and Cdk2 pathways. 2005 Am. J. Physiol., Cell Physiol. pmid:15647388
Babich H et al. Differential in vitro cytotoxicity of (-)-epicatechin gallate (ECG) to cancer and normal cells from the human oral cavity. 2005 Toxicol In Vitro pmid:15649637
Ikeda I et al. Tea catechins with a galloyl moiety suppress postprandial hypertriacylglycerolemia by delaying lymphatic transport of dietary fat in rats. 2005 J. Nutr. pmid:15671206
Lambert JD et al. Synthesis and biological activity of the tea catechin metabolites, M4 and M6 and their methoxy-derivatives. 2005 Bioorg. Med. Chem. Lett. pmid:15686878
Guendez R et al. An analytical survey of the polyphenols of seeds of varieties of grape (Vitis vinifera) cultivated in Greece: implications for exploitation as a source of value-added phytochemicals. Phytochem Anal pmid:15688951
Lee YK et al. VEGF receptors on chronic lymphocytic leukemia (CLL) B cells interact with STAT 1 and 3: implication for apoptosis resistance. 2005 Leukemia pmid:15703780