Summary

IMPPAT Phytochemical identifier: IMPHY011737

Phytochemical name: Epigallocatechin

Synonymous chemical names:
(-)-epi-gallo-catechol, (-)-epigallocatechin, (-)-epigallocatechol, catechin, gallo, epi, (-), epigallo catechin, epigallocatechin, epigallocatechin (-), epigallocatechin,, epigallocatechin, l-, epigallocatechin,(-)-, epigallocatechol, epigallocatechol, (-)-, epigallocatechol, l-, gallocatechin, epi (-)

External chemical identifiers:
CID:72277, ChEMBL:CHEMBL47386, ChEBI:42255, ZINC:ZINC000003870336, FDASRS:7Z197MG6QL, SureChEMBL:SCHEMBL19553, MolPort-003-665-790

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Chemical structure information

SMILES:
Oc1cc2O[C@H](c3cc(O)c(c(c3)O)O)[C@@H](Cc2c(c1)O)O

InChI:
InChI=1S/C15H14O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-4,12,15-21H,5H2/t12-,15-/m1/s1

InChIKey:
XMOCLSLCDHWDHP-IUODEOHRSA-N

DeepSMILES:
OcccO[C@H]cccO)ccc6)O))O)))))[C@@H]Cc6cc%10)O))))O

Functional groups:
CO, cO, cOC

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Molecular scaffolds

Scaffold Graph/Node/Bond level:
c1ccc(C2CCc3ccccc3O2)cc1

Scaffold Graph/Node level:
C1CCC(C2CCC3CCCCC3O2)CC1

Scaffold Graph level:
C1CCC(C2CCC3CCCCC3C2)CC1

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Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Flavonoids

ClassyFire Subclass: Flavans

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Flavonoids

NP Classifier Class: Flavan-3-ols

NP-Likeness score: 2.272

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Chemical structure download