has_role benzenetriol organic heterocyclic compound antineoplastic agent (-)-epigallocatechin 3-gallate 0 458.08491 458.375 pubmed:12053219 pubmed:19784588 chemspider:58575 patent:CN102600212 pubmed:21080642 A gallate ester obtained by the formal condensation of gallic acid with the (3<i>R</i>)-hydroxy group of (−)-epigallocatechin. InChI=1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2/t18-,21-/m1/s1 pubmed:23834676 pubmed:19928918 pubmed:34553787 chebi_ontology pubmed:18716169 pubmed:21434603 (-)-epigallocatechin gallate MESH:C045651 pubmed:33268646 pubmed:15950188 EGCG reaxys:67944 pubmed:12918062 kegg.compound:C09731 epigallocatechin 3-gallate [(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate pubmed:18665171 pubmed:19539611 pubmed:19113837 pubmed:20565072 pubmed:22300765 O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(O)c(O)c(O)c1)c1cc(O)c(O)c(O)c1 L-epigallocatechin gallate pubmed:22876177 knapsack:C00000958 pubmed:21750208 NVP-XAA 723 pubmed:17157668 lipidmaps:LMPK12030005 3-O-galloyl-(-)-epigallocatechin NCIt:C1088 epigallocatechin 3-O-gallate pubmed:31503486 pubmed:14521154 pubmed:15024383 wikipedia.en:Epigallocatechin_gallate C22H18O11 cas:989-51-5 (-)-epigallocatechin-3-O-gallate epigallocatechin gallate WMBWREPUVVBILR-WIYYLYMNSA-N (-)-epigallocatechol gallate lincs.smallmolecule:LSM-5661 beilstein:3658838 pubmed:14633667 pubmed:19085685 (2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate CHEBI:4806 pubmed:19542563 patent:CN102763743 hmdb:HMDB0003153 (2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate pdb-ccd:KDH pubmed:33604623 pubmed:31767902 patent:US2012309821 pubmed:32635637 (-)-epigallocatechin 3-O-gallate