Home Antiviral Plant Compound Database Epigallocatechin gallate

Epigallocatechin gallate

by impac.co.in

Indian Plant Antiviral Compound Database (IMPAC)

Indian Plant Antiviral Compound Description
InAVPCDB Accession Number AVD018
Compound Name Epigallocatechin gallate
Phytochemical category Polyphenol
PubChem Id 65064
IUPAC Name[(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
Molecular Formula C22H18O11
Canonical SMILES Notation 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
Binomial Name Camellia sinensis var. assamica
Vernacular Names Teyilai/Chai/Black tea
Plant Part Leaf
Family Theaceae
Description Influenza, Human immunodeficiency virus, Hepatitis C virus, and SARS-CoV-2.
Mechanism of action Its viral efficacy of EGCG is attributable to damage to the physical properties of the viral envelope and partial inhibition of the Neuraminidase surface glycoprotein; and inhibits reverse transcriptase mechanism.
Molecular weight 458.37 g/mol
XLOGP3 1.17
Num. H-bond acceptors 11
Num. H-bond donors 8
Rotatable bonds 4
Topological polar surface area 197.37 Ų
Bioavailability Score 0.17
Druglikeness No
Lipinski 2 violations
References Kim M, Kim SY, Lee HW, Shin JS, Kim P, Jung YS, Jeong HS, Hyun JK, Lee CK. Inhibition of influenza virus internalization by (?)-epigallocatechin-3-gallate. Antiviral research. 2013 Nov 1;100(2):460-72. Zhong Y, Ma CM, Shahidi F. Antioxidant and antiviral activities of lipophilic epigallocatechin gallate (EGCG) derivatives. Journal of Functional Foods. 2012 Jan 1;4(1):87-93. Li S, Hattori T, Kodama EN. Epigallocatechin gallate inhibits the HIV reverse transcription step. Antiviral Chemistry and Chemotherapy. 2011 Aug;21(6):239-43.

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