IMPPAT Phytochemical information: 
Boerhadiffusene

Boerhadiffusene
Summary

SMILES: CC(CCCC1CCCC(C1)(C)C)CCCC(C/C=C/C1=C(C)CCCC1(C)C)C
InChI: InChI=1S/C30H54/c1-24(15-9-18-27-19-12-21-29(4,5)23-27)13-8-14-25(2)16-10-20-28-26(3)17-11-22-30(28,6)7/h10,20,24-25,27H,8-9,11-19,21-23H2,1-7H3/b20-10+
InChIKey: CULXOYWCXZXOLD-KEBDBYFISA-N
DeepSMILES: CCCCCCCCCCC6)C)C)))))))))CCCCC/C=C/C=CC)CCCC6C)C))))))))))C
Scaffold Graph/Node/Bond level: C(=CC1=CCCCC1)CCCCCCCCCC1CCCCC1
Scaffold Graph/Node level: C(CCCCCC1CCCCC1)CCCCCC1CCCCC1
Scaffold Graph level: C(CCCCCC1CCCCC1)CCCCCC1CCCCC1
Functional groups: C/C=C/C(C)=C(C)C
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Prenol lipids
ClassyFire Subclass: Triterpenoids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Diterpenoids
NP Classifier Class: Cyclophytane diterpenoids|Labdane diterpenoids
Synonymous chemical names:
boerhadiffusene
External chemical identifiers:
CID:100933427
Chemical structure download


Boerhadiffusene
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


Boerhadiffusene
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 1
Lipinski’s rule of 5 filter RDKit Passed
Number of Ghose filter violations RDKit 3
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.3152


Boerhadiffusene
ADMET properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Poorly soluble
Solubility class [Silicos-IT] SwissADME Poorly soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -0.36
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 0.0
CYP1A2 inhibitor SwissADME Yes
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes