IMPPAT Phytochemical information: 
Heteroclitin F

Heteroclitin F
Summary

SMILES: COC(=O)/C=C/1\C[C@@H](C)[C@@H](C)[C@H](c2c3C1(COc3c1c(c2)OCO1)C(=O)C(=O)OC)OC(=O)/C(=C\C)/C
InChI: InChI=1S/C27H30O10/c1-7-13(2)25(30)37-21-15(4)14(3)8-16(9-19(28)32-5)27(24(29)26(31)33-6)11-34-23-20(27)17(21)10-18-22(23)36-12-35-18/h7,9-10,14-15,21H,8,11-12H2,1-6H3/b13-7-,16-9+/t14-,15-,21-,27?/m1/s1
InChIKey: WZHLOZOCPVZWTE-JFKIBXCKSA-N
DeepSMILES: COC=O)/C=C\C[C@@H]C)[C@@H]C)[C@H]ccC\8COc5ccc9)OCO5))))))))C=O)C=O)OC)))))))OC=O)/C=C\C))/C
Scaffold Graph/Node/Bond level: C=C1CCCCc2cc3c(c4c2C1CO4)OCO3
Scaffold Graph/Node level: CC1CCCCC2CC3OCOC3C3OCC1C23
Scaffold Graph level: CC1CCCCC2CC3CCCC3C3CCC1C23
Functional groups: COC(=O)/C=C(\C)C; cOC; c1cOCO1; COC(=O)C(C)=O; C/C=C(/C)C(=O)OC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organoheterocyclic compounds
ClassyFire Class: Benzodioxoles
Synonymous chemical names:
heteroclitin f
External chemical identifiers:
CID:CID_44575996; ChEMBL:CHEMBL519496
Chemical structure download


Heteroclitin F
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 514.53
Log P RDKit 3.11
Topological polar surface area (Å2) RDKit 123.66
Number of hydrogen bond acceptors RDKit 10
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 27
Number of heavy atoms RDKit 37
Number of heteroatoms RDKit 10
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 4
Stereochemical complexity RDKit 0.15
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 14
Number of sp3 hybridized carbon atoms RDKit 13
Shape complexity RDKit 0.48
Number of rotatable bonds RDKit 8
Number of aliphatic carbocycles RDKit 1
Number of aliphatic heterocycles RDKit 2
Number of aliphatic rings RDKit 3
Number of aromatic carbocycles RDKit 1
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 1
Total number of rings RDKit 4
Number of saturated carbocycles RDKit 0
Number of saturated heterocycles RDKit 0
Number of saturated rings RDKit 0
Number of Smallest Set of Smallest Rings (SSSR) RDKit 4


Heteroclitin F
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 1
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 0.250534


Heteroclitin F
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Moderately soluble
Solubility class [Silicos-IT] SwissADME Poorly soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -6.20
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 Yes
CYP3A4 inhibitor SwissADME No
P-glycoprotein substrate SwissADME No