IMPPAT Phytochemical information: 
Euglobal G3

Euglobal G3
Summary

SMILES: O=Cc1c2O[C@@]3(CCc2c(c(c1O)C(=O)CC(C)C)O)CC[C@H]1C[C@@H]3C1(C)C
InChI: InChI=1S/C23H30O5/c1-12(2)9-16(25)18-19(26)14-6-8-23(28-21(14)15(11-24)20(18)27)7-5-13-10-17(23)22(13,3)4/h11-13,17,26-27H,5-10H2,1-4H3/t13-,17+,23+/m0/s1
InChIKey: XREJXBXJCWWRFP-OLJPZDALSA-N
DeepSMILES: O=CccO[C@@]CCc6ccc%10O))C=O)CCC)C)))))O)))))CC[C@H]C[C@@H]6C4C)C
Scaffold Graph/Node/Bond level: c1ccc2c(c1)CCC1(CCC3CC1C3)O2
Scaffold Graph/Node level: C1CCC2OC3(CCC4CC3C4)CCC2C1
Scaffold Graph level: C1CCC2CC3(CCC4CC3C4)CCC2C1
Functional groups: cC(C)=O; cC=O; cO; cOC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Benzenoids
ClassyFire Class: Benzene and substituted derivatives
ClassyFire Subclass: Butyrophenones
NP Classifier Biosynthetic pathway: Polyketides|Terpenoids
NP Classifier Superclass: Phloroglucinols
NP Classifier Class: Phloroglucinol-terpene hybrids
Synonymous chemical names:
euglobal g3
External chemical identifiers:
CID:164300; ChEMBL:CHEMBL1800847; ZINC:ZINC000015209942; SureChEMBL:SCHEMBL135155
Chemical structure download


Euglobal G3
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 386.49
Log P RDKit 4.66
Topological polar surface area (Å2) RDKit 83.83
Number of hydrogen bond acceptors RDKit 5
Number of hydrogen bond donors RDKit 2
Number of carbon atoms RDKit 23
Number of heavy atoms RDKit 28
Number of heteroatoms RDKit 5
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 3
Stereochemical complexity RDKit 0.13
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 8
Number of sp3 hybridized carbon atoms RDKit 15
Shape complexity RDKit 0.65
Number of rotatable bonds RDKit 4
Number of aliphatic carbocycles RDKit 3
Number of aliphatic heterocycles RDKit 1
Number of aliphatic rings RDKit 4
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 1
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


Euglobal G3
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 Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.5808


Euglobal G3
ADMET 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 -4.9
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 1.0
CYP1A2 inhibitor SwissADME No
CYP2C19 inhibitor SwissADME No
CYP2C9 inhibitor SwissADME Yes
CYP2D6 inhibitor SwissADME No
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME Yes