IMPPAT Phytochemical information: 
Azedarachin B
Azedarachin B
Summary

SMILES: CC(=O)O[C@@H]1C[C@H](O)[C@]23[C@H]([C@]1(C)[C@@H](OC2)OC(=O)C(C)C)C[C@H]([C@@]1([C@@H]3C(=O)[C@H](O)[C@@]2([C@]31O[C@@H]3C[C@H]2c1ccoc1)C)C)O
InChI: InChI=1S/C32H42O11/c1-14(2)26(38)42-27-28(4)18-10-19(34)30(6)24(31(18,13-40-27)20(35)11-21(28)41-15(3)33)23(36)25(37)29(5)17(16-7-8-39-12-16)9-22-32(29,30)43-22/h7-8,12,14,17-22,24-25,27,34-35,37H,9-11,13H2,1-6H3/t17-,18-,19+,20-,21+,22+,24-,25-,27-,28-,29+,30+,31+,32+/m0/s1
InChIKey: IWWHKSITDUTKRB-JRWPYURWSA-N
DeepSMILES: CC=O)O[C@@H]C[C@H]O)[C@][C@H][C@]6C)[C@@H]OC6))OC=O)CC)C))))))C[C@H][C@@][C@@H]6C=O)[C@H]O)[C@@][C@@]6O[C@@H]3C[C@H]6cccoc5))))))))))C)))))C))O
Scaffold Graph/Node/Bond level: O=C1CC2C(c3ccoc3)CC3OC32C2CCC3C4CCCC3(COC4)C12
Scaffold Graph/Node level: OC1CC2C(C3CCOC3)CC3OC32C2CCC3C4CCCC3(COC4)C12
Scaffold Graph level: CC1CC2C(C3CCCC3)CC3CC32C2CCC3C4CCCC3(CCC4)C12
Functional groups: C[C@H]1O[C@@]1(C)C; CC(=O)OC; coc; CO; CO[C@@H](OC(C)=O)C; CC(=O)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: Triterpenoids
NP Classifier Class: Lanostane, Tirucallane and Euphane triterpenoids|Limonoids
Synonymous chemical names:
azedarachin b
External chemical identifiers:
CID:CID_102586008
Chemical structure download
2D:2D MOL2D MOL22D SDF
3D:3D MOL3D MOL23D SDF3D PDB3D PDBQT
Azedarachin B
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 602.68
Log P RDKit 2.1
Topological polar surface area (Å2) RDKit 165.26
Number of hydrogen bond acceptors RDKit 11
Number of hydrogen bond donors RDKit 3
Number of carbon atoms RDKit 32
Number of heavy atoms RDKit 43
Number of heteroatoms RDKit 11
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 14
Stereochemical complexity RDKit 0.44
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 7
Number of sp3 hybridized carbon atoms RDKit 25
Shape complexity RDKit 0.78
Number of rotatable bonds RDKit 6
Number of aliphatic carbocycles RDKit 4
Number of aliphatic heterocycles RDKit 2
Number of aliphatic rings RDKit 6
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 1
Number of aromatic rings RDKit 1
Total number of rings RDKit 7
Number of saturated carbocycles RDKit 4
Number of saturated heterocycles RDKit 2
Number of saturated rings RDKit 6
Number of Smallest Set of Smallest Rings (SSSR) RDKit 7
Azedarachin B
Drug-likeness properties
Property nameToolProperty value
Number of Lipinski’s rule of 5 violations RDKit 2
Lipinski’s rule of 5 filter RDKit Failed
Number of Ghose filter violations RDKit 3
Ghose filter RDKit Failed
Veber filter RDKit Bad
Pfizer 3/75 filter RDKit Good
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.341353
Azedarachin B
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.17
Solubility class [ESOL] SwissADME Moderately soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME Low
Log Kp (Skin permeation, cm/s) SwissADME -8.76
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 2
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME No
CYP2D6 inhibitor SwissADME Yes
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME Yes