IMPPAT Phytochemical information: 
6Beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one

6Beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one
Summary

SMILES: C=CC1(C)CC(=O)C2(C(O1)(C)C(O)C(C1C2(C)CCCC1(C)C)O)O
InChI: InChI=1S/C20H32O5/c1-7-17(4)11-12(21)20(24)18(5)10-8-9-16(2,3)14(18)13(22)15(23)19(20,6)25-17/h7,13-15,22-24H,1,8-11H2,2-6H3
InChIKey: BEXJRVNGEWHUJR-UHFFFAOYSA-N
DeepSMILES: C=CCC)CC=O)CCO6)C)CO)CCC6C)CCCC6C)C)))))))O))))O
Scaffold Graph/Node/Bond level: O=C1CCOC2CCC3CCCCC3C12
Scaffold Graph/Node level: OC1CCOC2CCC3CCCCC3C12
Scaffold Graph level: CC1CCCC2CCC3CCCCC3C12
Functional groups: C=CC; CC(=O)C; COC; CO
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: Labdane diterpenoids
Synonymous chemical names:
6beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one
Chemical structure download


6Beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 352.47
Log P RDKit 1.98
Topological polar surface area (Å2) RDKit 86.99
Number of hydrogen bond acceptors RDKit 5
Number of hydrogen bond donors RDKit 3
Number of carbon atoms RDKit 20
Number of heavy atoms RDKit 25
Number of heteroatoms RDKit 5
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 7
Stereochemical complexity RDKit 0.35
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 3
Number of sp3 hybridized carbon atoms RDKit 17
Shape complexity RDKit 0.85
Number of rotatable bonds RDKit 1
Number of aliphatic carbocycles RDKit 2
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 3
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 3
Number of saturated carbocycles RDKit 2
Number of saturated heterocycles RDKit 1
Number of saturated rings RDKit 3
Number of Smallest Set of Smallest Rings (SSSR) RDKit 3


6Beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one
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 0.6283


6Beta,7beta,9alpha-trihydroxy-8,13-epoxy-labd-14-en-11-one
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
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 -7.19
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 1
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes