IMPPAT Phytochemical information: 
Vepinin

Vepinin
Summary

SMILES: CC(=O)O[C@H]1[C@@H]2OC3C4C2(C)[C@@H]([C@@]2([C@@H]1C(C)(C)C(=O)C=C2)C)CC[C@]4([C@@H](C3)c1ccoc1)C
InChI: InChI=1S/C28H36O5/c1-15(29)32-21-23-25(2,3)20(30)8-11-27(23,5)19-7-10-26(4)17(16-9-12-31-14-16)13-18-22(26)28(19,6)24(21)33-18/h8-9,11-12,14,17-19,21-24H,7,10,13H2,1-6H3/t17-,18?,19+,21+,22?,23-,24-,26-,27+,28?/m0/s1
InChIKey: JHEAMHIBUPEMCC-GXJVPLPWSA-N
DeepSMILES: CC=O)O[C@H][C@@H]OCCC5C)[C@@H][C@@][C@@H]9CC)C)C=O)C=C6)))))C))CC[C@]6[C@@H]C9)cccoc5))))))C
Scaffold Graph/Node/Bond level: O=C1C=CC2C(C1)CC1OC3CC(c4ccoc4)C4CCC2C1C34
Scaffold Graph/Node level: OC1CCC2C(C1)CC1OC3CC(C4CCOC4)C4CCC2C1C34
Scaffold Graph level: CC1CCC2C(C1)CC1CC3CC(C4CCCC4)C4CCC2C1C34
Functional groups: CC(=O)OC; COC; CC(=O)C=CC; coc
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: Triterpenoids
NP Classifier Class: Limonoids
Synonymous chemical names:
vepinin
External chemical identifiers:
CID:CID_185552
Chemical structure download


Vepinin
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 452.59
Log P RDKit 5.31
Topological polar surface area (Å2) RDKit 65.74
Number of hydrogen bond acceptors RDKit 5
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 28
Number of heavy atoms RDKit 33
Number of heteroatoms RDKit 5
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 10
Stereochemical complexity RDKit 0.36
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 8
Number of sp3 hybridized carbon atoms RDKit 20
Shape complexity RDKit 0.71
Number of rotatable bonds RDKit 3
Number of aliphatic carbocycles RDKit 4
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 5
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 1
Total number of rings RDKit 6
Number of saturated carbocycles RDKit 3
Number of saturated heterocycles RDKit 1
Number of saturated rings RDKit 4
Number of Smallest Set of Smallest Rings (SSSR) RDKit 6


Vepinin
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 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 0.569412


Vepinin
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Moderately soluble
Solubility class [Silicos-IT] SwissADME Moderately soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -5.39
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 0
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