IMPPAT Phytochemical information: 
1,6-bis-O-galloyl-beta-D-glucose
1,6-bis-O-galloyl-beta-D-glucose
Summary

SMILES: O[C@@H]1[C@@H](COC(=O)c2cc(O)c(c(c2)O)O)O[C@H]([C@@H]([C@H]1O)O)OC(=O)c1cc(O)c(c(c1)O)O
InChI: InChI=1S/C20H20O14/c21-8-1-6(2-9(22)13(8)25)18(30)32-5-12-15(27)16(28)17(29)20(33-12)34-19(31)7-3-10(23)14(26)11(24)4-7/h1-4,12,15-17,20-29H,5H2/t12-,15-,16+,17-,20+/m1/s1
InChIKey: LYGRISUQIZNHGM-IVABAYMNSA-N
DeepSMILES: O[C@@H][C@@H]COC=O)cccO)ccc6)O))O))))))))O[C@H][C@@H][C@H]6O))O))OC=O)cccO)ccc6)O))O
Scaffold Graph/Node/Bond level: O=C(OCC1CCCC(OC(=O)c2ccccc2)O1)c1ccccc1
Scaffold Graph/Node level: OC(OCC1CCCC(OC(O)C2CCCCC2)O1)C1CCCCC1
Scaffold Graph level: CC(CCC1CCCC(CC(C)C2CCCCC2)C1)C1CCCCC1
Functional groups: CO; cO; cC(=O)OC; cC(=O)O[C@@H](C)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Tannins
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Phenolic acids (C6-C1)
NP Classifier Class: Gallotannins
Synonymous chemical names:
1,6-digalloylglucose-beta-d-pyranose-form, 1-6-di-galloyl-glucopyranose, 1-6-di-o-galloyl-beta-d-glucose, beta-d-1,6-di-o-galloylglucose
External chemical identifiers:
CID:CID_440221; ChEMBL:CHEMBL522251; ChEBI:CHEBI:15723; ZINC:ZINC000004096316; SureChEMBL:SCHEMBL10379318
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
1,6-bis-O-galloyl-beta-D-glucose
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 484.37
Log P RDKit -1.26
Topological polar surface area (Å2) RDKit 243.9
Number of hydrogen bond acceptors RDKit 14
Number of hydrogen bond donors RDKit 9
Number of carbon atoms RDKit 20
Number of heavy atoms RDKit 34
Number of heteroatoms RDKit 14
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 5
Stereochemical complexity RDKit 0.25
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 14
Number of sp3 hybridized carbon atoms RDKit 6
Shape complexity RDKit 0.3
Number of rotatable bonds RDKit 7
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 1
Number of aromatic carbocycles RDKit 2
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 2
Total number of rings RDKit 3
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 1
Number of saturated rings RDKit 1
Number of Smallest Set of Smallest Rings (SSSR) RDKit 3
1,6-bis-O-galloyl-beta-D-glucose
Drug-likeness
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 2
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 2
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.177667
1,6-bis-O-galloyl-beta-D-glucose
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.17
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -9.83
Number of PAINS structural alerts SwissADME 1
Number of Brenk structural alerts SwissADME 2
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No
1,6-bis-O-galloyl-beta-D-glucose
Phytochemical - Human target proteins supported by experimental evidence associations
Human target proteins supported by experimental evidence
IMPPAT target identifierGene identifierHGNC symbolEntrez Gene identifierSource
TAR_EXP_001215ENSG00000027075PRKCH5583ChEMBL
TAR_EXP_001207ENSG00000154229PRKCA5578BindingDB, ChEMBL
TAR_EXP_001209ENSG00000166501PRKCB5579ChEMBL
TAR_EXP_000496ENSG00000115825PRKD323683ChEMBL
TAR_EXP_001212ENSG00000163932PRKCD5580ChEMBL
TAR_EXP_001216ENSG00000163558PRKCI5584ChEMBL
TAR_EXP_001226ENSG00000065675PRKCQ5588ChEMBL, NPASS
TAR_EXP_001223ENSG00000184304PRKD15587ChEMBL
TAR_EXP_001214ENSG00000126583PRKCG5582ChEMBL
TAR_EXP_001840ENSG00000078269SYNJ28871ChEMBL, NPASS
TAR_EXP_001838ENSG00000159082SYNJ18867ChEMBL, NPASS
TAR_EXP_001227ENSG00000067606PRKCZ5590ChEMBL
TAR_EXP_001213ENSG00000171132PRKCE5581ChEMBL