IMPPAT Phytochemical information: 
Chitanone
Chitanone
Summary

SMILES: CCC[C@H]1[C@@H](O)c2cccc(c2C(=O)[C@@]1(C)c1ccc(c2c1C(=O)C(=CC2=O)C)O)O
InChI: InChI=1S/C25H24O6/c1-4-6-15-23(30)13-7-5-8-16(26)19(13)24(31)25(15,3)14-9-10-17(27)21-18(28)11-12(2)22(29)20(14)21/h5,7-11,15,23,26-27,30H,4,6H2,1-3H3/t15-,23-,25-/m0/s1
InChIKey: PATAKNRHLQOFNB-RKPBBICVSA-N
DeepSMILES: CCC[C@H][C@@H]O)cccccc6C=O)[C@@]%10C)cccccc6C=O)C=CC6=O)))C)))))O))))))))O
Scaffold Graph/Node/Bond level: O=C1C=CC(=O)c2c1cccc2C1CCc2ccccc2C1=O
Scaffold Graph/Node level: OC1CCC(O)C2C1CCCC2C1CCC2CCCCC2C1O
Scaffold Graph level: CC1CCC(C)C2C1CCCC2C1CCC2CCCCC2C1C
Functional groups: CO; cC(=O)C; CC1=CC(=O)ccC1=O; cO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Benzenoids
ClassyFire Class: Naphthalenes
ClassyFire Subclass: Naphthoquinones
NP Classifier Biosynthetic pathway: Polyketides
NP Classifier Superclass: Naphthalenes
NP Classifier Class: Bisnaphthalenes|Naphthoquinones
Synonymous chemical names:
chitanone
External chemical identifiers:
CID:CID_100947538
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Chitanone
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 420.46
Log P RDKit 4.03
Topological polar surface area (Å2) RDKit 111.9
Number of hydrogen bond acceptors RDKit 6
Number of hydrogen bond donors RDKit 3
Number of carbon atoms RDKit 25
Number of heavy atoms RDKit 31
Number of heteroatoms RDKit 6
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 3
Stereochemical complexity RDKit 0.12
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 17
Number of sp3 hybridized carbon atoms RDKit 8
Shape complexity RDKit 0.32
Number of rotatable bonds RDKit 3
Number of aliphatic carbocycles RDKit 2
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 2
Number of aromatic carbocycles RDKit 2
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 2
Total number of rings RDKit 4
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 4
Chitanone
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 Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.69128
Chitanone
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Moderately soluble
Solubility class [Silicos-IT] SwissADME Poorly soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -5.61
Number of PAINS structural alerts SwissADME 2
Number of Brenk structural alerts SwissADME 0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes