IMPPAT Phytochemical information: 
Epoxyfarnachrol
Epoxyfarnachrol
Summary

SMILES: COc1cc2ccc(=O)oc2c(c1OCC1=C(C)CCC2=C1CCC1C2(C)O1)OC
InChI: InChI=1S/C24H26O6/c1-13-5-8-17-15(7-9-19-24(17,2)30-19)16(13)12-28-22-18(26-3)11-14-6-10-20(25)29-21(14)23(22)27-4/h6,10-11,19H,5,7-9,12H2,1-4H3
InChIKey: SXDAZBMPWBQUHL-UHFFFAOYSA-N
DeepSMILES: COcccccc=O)oc6cc%10OCC=CC)CCC=C6CCCC6C)O3))))))))))))))OC
Scaffold Graph/Node/Bond level: O=c1ccc2ccc(OCC3=CCCC4=C3CCC3OC43)cc2o1
Scaffold Graph/Node level: OC1CCC2CCC(OCC3CCCC4C3CCC3OC34)CC2O1
Scaffold Graph level: CC1CCC2CCC(CCC3CCCC4C3CCC3CC34)CC2C1
Functional groups: CC1=C(C)C2=C(CC1)C1(C)OC1CC2; c=O; cOC; coc
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Phenylpropanoids and polyketides
ClassyFire Class: Coumarins and derivatives
NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids
NP Classifier Superclass: Coumarins
NP Classifier Class: Simple coumarins
Synonymous chemical names:
epoxyfarnachrol
External chemical identifiers:
CID:14563784
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Epoxyfarnachrol
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 0
Log P RDKit 0
Topological polar surface area (Å2) RDKit
Number of hydrogen bond acceptors RDKit
Number of hydrogen bond donors RDKit
Number of carbon atoms RDKit
Number of heavy atoms RDKit
Number of heteroatoms RDKit
Number of nitrogen atoms RDKit
Number of sulfur atoms RDKit
Number of chiral carbon atoms RDKit
Stereochemical complexity RDKit 0
Number of sp hybridized carbon atoms RDKit
Number of sp2 hybridized carbon atoms RDKit
Number of sp3 hybridized carbon atoms RDKit
Shape complexity RDKit
Number of rotatable bonds RDKit
Number of aliphatic carbocycles RDKit
Number of aliphatic heterocycles RDKit
Number of aliphatic rings RDKit
Number of aromatic carbocycles RDKit
Number of aromatic heterocycles RDKit
Number of aromatic rings RDKit
Total number of rings RDKit
Number of saturated carbocycles RDKit
Number of saturated heterocycles RDKit
Number of saturated rings RDKit
Number of Smallest Set of Smallest Rings (SSSR) RDKit
Epoxyfarnachrol
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 0.5321
Epoxyfarnachrol
ADMET properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Soluble
Solubility class [Silicos-IT] SwissADME Poorly soluble
Blood Brain Barrier permeation SwissADME Yes
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -7.21
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 2.0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME Yes
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME Yes
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes