IMPPAT Phytochemical information: 
Methyl (e)-11-methoxy-9-oxo-10-nonadecenoate

Methyl (e)-11-methoxy-9-oxo-10-nonadecenoate
Summary

SMILES: CCCCCCCC/C(=C\C(=O)CCCCCCCC(=O)OC)/OC
InChI: InChI=1S/C21H38O4/c1-4-5-6-7-10-13-16-20(24-2)18-19(22)15-12-9-8-11-14-17-21(23)25-3/h18H,4-17H2,1-3H3/b20-18+
InChIKey: ZMUBBDGDFMAIMP-CZIZESTLSA-N
DeepSMILES: CCCCCCCC/C=C\C=O)CCCCCCCC=O)OC))))))))))))/OC
Functional groups: CO/C(C)=C/C(C)=O; COC(C)=O
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Lipids and lipid-like molecules
ClassyFire Class: Fatty Acyls
ClassyFire Subclass: Fatty acid esters
NP Classifier Biosynthetic pathway: Fatty acids
NP Classifier Superclass: Fatty esters
NP Classifier Class: Wax monoesters
Synonymous chemical names:
methyl-(e)-11-methoxy-9-oxo-10-nonadecenoate
External chemical identifiers:
CID:CID_129847920; ZINC:ZINC000238737248
Chemical structure download


Methyl (e)-11-methoxy-9-oxo-10-nonadecenoate
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 354.53
Log P RDKit 5.74
Topological polar surface area (Å2) RDKit 52.6
Number of hydrogen bond acceptors RDKit 4
Number of hydrogen bond donors RDKit 0
Number of carbon atoms RDKit 21
Number of heavy atoms RDKit 25
Number of heteroatoms RDKit 4
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 0
Number of chiral carbon atoms RDKit 0
Stereochemical complexity RDKit 0
Number of sp hybridized carbon atoms RDKit 0
Number of sp2 hybridized carbon atoms RDKit 4
Number of sp3 hybridized carbon atoms RDKit 17
Shape complexity RDKit 0.81
Number of rotatable bonds RDKit 18
Number of aliphatic carbocycles RDKit 0
Number of aliphatic heterocycles RDKit 0
Number of aliphatic rings RDKit 0
Number of aromatic carbocycles RDKit 0
Number of aromatic heterocycles RDKit 0
Number of aromatic rings RDKit 0
Total number of rings RDKit 0
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 0


Methyl (e)-11-methoxy-9-oxo-10-nonadecenoate
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 Bad
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Bad
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.144584


Methyl (e)-11-methoxy-9-oxo-10-nonadecenoate
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.85
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 -4.11
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 No
CYP3A4 inhibitor SwissADME Yes
P-glycoprotein substrate SwissADME No