Summary

IMPPAT Phytochemical identifier: IMPHY011735

Phytochemical name: (+)-Gallocatechin

Synonymous chemical names:
(+) gallocatechin, (+)-gallocatechin, (+)-gallocatechol, (+)gallocatechol, (dl)-gallocatechin, +-gallocatechin, allocatechin 5-o-gallate, catechol,gallo, (+), gallo catechin, gallocatechin, gallocatechin, (+), gallocatechin, (+)-, gallocatechin,(+)-, gallocatechin,d, gallocatechol, gallocatechol,(+)-

External chemical identifiers:
CID:65084, ChEMBL:CHEMBL125743, ChEBI:31018, ZINC:ZINC000003870338, FDASRS:HEJ6575V1X, SureChEMBL:SCHEMBL3872234, MolPort-001-740-421

---

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+/m0/s1

InChIKey:
XMOCLSLCDHWDHP-SWLSCSKDSA-N

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

Functional groups:
CO, cO, cOC

---

Molecular scaffolds

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

Scaffold Graph/Node level:
C1CCC(C2CCC3CCCCC3O2)CC1

Scaffold Graph level:
C1CCC(C2CCC3CCCCC3C2)CC1

---

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

---

Chemical structure download