IMPPAT Phytochemical information: 
Mollugogenol C
Mollugogenol C
Summary

SMILES: CC(C1=C2C=C[C@@]3([C@@H]([C@]2(CC1)C)CC[C@H]1[C@@]3(C)CC(=O)[C@@H]2[C@]1(C)CC[C@@H](C2(C)C)O)C)C
InChI: InChI=1S/C30H46O2/c1-18(2)19-11-14-27(5)20(19)12-16-29(7)22(27)9-10-23-28(6)15-13-24(32)26(3,4)25(28)21(31)17-30(23,29)8/h12,16,18,22-25,32H,9-11,13-15,17H2,1-8H3/t22-,23-,24+,25+,27+,28-,29-,30-/m1/s1
InChIKey: INOQPWGBFWQEMR-GVBFKZGCSA-N
DeepSMILES: CCC=CC=C[C@@][C@@H][C@]6CC9))C))CC[C@H][C@@]6C)CC=O)[C@@H][C@]6C)CC[C@@H]C6C)C))O)))))))))))))C))))))C
Scaffold Graph/Node/Bond level: O=C1CC2C3C=CC4=CCCC4C3CCC2C2CCCCC12
Scaffold Graph/Node level: OC1CC2C(CCC3C4CCCC4CCC32)C2CCCCC12
Scaffold Graph level: CC1CC2C(CCC3C4CCCC4CCC32)C2CCCCC12
Functional groups: CC(=C(C)C=CC)C; CC(=O)C; CO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Prenol lipids
ClassyFire Subclass: Hopanoids
NP Classifier Biosynthetic pathway: Terpenoids
NP Classifier Superclass: Triterpenoids
NP Classifier Class: Hopane and Moretane triterpenoids
Synonymous chemical names:
mollugogenol c, Mollugogenol C
External chemical identifiers:
CID:CID_101306755; ZINC:ZINC000255219886
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Mollugogenol C
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 438.7
Log P RDKit 7.12
Topological polar surface area (Å2) RDKit 37.3
Number of hydrogen bond acceptors RDKit 2
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 30
Number of heavy atoms RDKit 32
Number of heteroatoms RDKit 2
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 8
Stereochemical complexity RDKit 0.27
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 5
Number of sp3 hybridized carbon atoms RDKit 25
Shape complexity RDKit 0.83
Number of rotatable bonds RDKit 1
Number of aliphatic carbocycles RDKit 5
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 5
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 5
Number of saturated carbocycles RDKit 3
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 3
Number of Smallest Set of Smallest Rings (SSSR) RDKit 5
Mollugogenol C
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 Good
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.472871
Mollugogenol C
ADME 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 -4.10
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 No