IMPPAT Phytochemical information: 
6-Hydroxy-7,8,3',4'-tetramethoxyisoflavanquinone

6-Hydroxy-7,8,3',4'-tetramethoxyisoflavanquinone
Summary

SMILES: COC1=C(OC)C(=O)C(=CC1=O)C1COc2c(C1)cc(c(c2OC)OC)O
InChI: InChI=1S/C19H20O8/c1-23-16-13(21)7-11(14(22)18(16)25-3)10-5-9-6-12(20)17(24-2)19(26-4)15(9)27-8-10/h6-7,10,20H,5,8H2,1-4H3
InChIKey: JUJPNIDLVJQYEY-UHFFFAOYSA-N
DeepSMILES: COC=COC))C=O)C=CC6=O)))CCOccC6)cccc6OC)))OC)))O
Scaffold Graph/Node/Bond level: O=C1C=CC(=O)C(C2COc3ccccc3C2)=C1
Scaffold Graph/Node level: OC1CCC(O)C(C2COC3CCCCC3C2)C1
Scaffold Graph level: CC1CCC(C)C(C2CCC3CCCCC3C2)C1
Functional groups: COC1=C(OC)C(=O)C(C)=CC1=O; cOC; cO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Isoflavonoids
ClassyFire Subclass: Isoflavanquinones
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
Synonymous chemical names:
abruquinone-c
External chemical identifiers:
CID:CID_44257520; ChEBI:CHEBI:169313
Chemical structure download


6-Hydroxy-7,8,3',4'-tetramethoxyisoflavanquinone
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 376.36
Log P RDKit 1.54
Topological polar surface area (Å2) RDKit 100.52
Number of hydrogen bond acceptors RDKit 8
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 19
Number of heavy atoms RDKit 27
Number of heteroatoms RDKit 8
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 1
Stereochemical complexity RDKit 0.05
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 12
Number of sp3 hybridized carbon atoms RDKit 7
Shape complexity RDKit 0.37
Number of rotatable bonds RDKit 5
Number of aliphatic carbocycles RDKit 1
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 2
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 1
Total number of rings RDKit 3
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 3


6-Hydroxy-7,8,3',4'-tetramethoxyisoflavanquinone
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 0
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 0
Ghose filter RDKit Passed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.77273


6-Hydroxy-7,8,3',4'-tetramethoxyisoflavanquinone
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.56
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -7.36
Number of PAINS structural alerts SwissADME 1
Number of Brenk structural alerts SwissADME 1
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No