IMPPAT Phytochemical information: 
Biflavanone

Biflavanone
Summary

SMILES: O=C1CC(Oc2c1cccc2)(c1ccccc1)C1(CC(=O)c2c(O1)cccc2)c1ccccc1
InChI: InChI=1S/C30H22O4/c31-25-19-29(21-11-3-1-4-12-21,33-27-17-9-7-15-23(25)27)30(22-13-5-2-6-14-22)20-26(32)24-16-8-10-18-28(24)34-30/h1-18H,19-20H2
InChIKey: VKXZCPLFHFDCCT-UHFFFAOYSA-N
DeepSMILES: O=CCCOcc6cccc6)))))))cccccc6))))))CCC=O)ccO6)cccc6))))))))cccccc6
Scaffold Graph/Node/Bond level: O=C1CC(c2ccccc2)(C2(c3ccccc3)CC(=O)c3ccccc3O2)Oc2ccccc21
Scaffold Graph/Node level: OC1CC(C2CCCCC2)(C2(C3CCCCC3)CC(O)C3CCCCC3O2)OC2CCCCC12
Scaffold Graph level: CC1CC(C2CCCCC2)(C2(C3CCCCC3)CC(C)C3CCCCC3C2)CC2CCCCC12
Functional groups: cC(=O)C; cOC
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: Flavanones
Synonymous chemical names:
biflavanone
External chemical identifiers:
CID:CID_10906409; SureChEMBL:SCHEMBL6704259
Chemical structure download


Biflavanone
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 446.5
Log P RDKit 6.11
Topological polar surface area (Å2) RDKit 52.6
Number of hydrogen bond acceptors RDKit 4
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 30
Number of heavy atoms RDKit 34
Number of heteroatoms RDKit 4
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 2
Stereochemical complexity RDKit 0.07
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 26
Number of sp3 hybridized carbon atoms RDKit 4
Shape complexity RDKit 0.13
Number of rotatable bonds RDKit 3
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 2
Number of aliphatic rings RDKit 2
Number of aromatic carbocycles RDKit 4
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 4
Total number of rings RDKit 6
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 6


Biflavanone
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 1
Lipinski’s rule of 5 RDKit Passed
Number of Ghose rule violations RDKit 1
Ghose rule RDKit Failed
Veber rule RDKit Good
Egan rule RDKit Bad
GSK 4/400 rule RDKit Bad
Pfizer 3/75 rule RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.38


Biflavanone
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Poorly soluble
Solubility class [Silicos-IT] SwissADME Insoluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -5.31
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 0
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME No