IMPPAT Phytochemical information: 
2-(2-Methoxyethoxy)ethanol

2-(2-Methoxyethoxy)ethanol
Summary

SMILES: COCCOCCO
InChI: InChI=1S/C5H12O3/c1-7-4-5-8-3-2-6/h6H,2-5H2,1H3
InChIKey: SBASXUCJHJRPEV-UHFFFAOYSA-N
DeepSMILES: COCCOCCO
Functional groups: CO; COC
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organic oxygen compounds
ClassyFire Class: Organooxygen compounds
ClassyFire Subclass: Ethers
Synonymous chemical names:
3-hydroxy-mugenic-acid
External chemical identifiers:
CID:8134; ChEMBL:CHEMBL1235250; ChEBI:44836; ZINC:ZINC000001577245; FDASRS:465DDJ8G8K; SureChEMBL:SCHEMBL15778; MolPort-001-793-101
Chemical structure download


2-(2-Methoxyethoxy)ethanol
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 120.15
Log P RDKit -0.36
Topological polar surface area (Å2) RDKit 38.69
Number of hydrogen bond acceptors RDKit 3
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 5
Number of heavy atoms RDKit 8
Number of heteroatoms RDKit 3
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 0
Number of sp3 hybridized carbon atoms RDKit 5
Shape complexity RDKit 1
Number of rotatable bonds RDKit 5
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


2-(2-Methoxyethoxy)ethanol
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 2
Ghose filter RDKit Failed
Veber filter RDKit Good
Pfizer 3/75 filter RDKit Bad
GSK 4/400 filter RDKit Good
Weighted quantitative estimate of drug-likeness (QEDw) score RDKit 0.5035


2-(2-Methoxyethoxy)ethanol
ADMET properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Highly soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -7.68
Number of PAINS structural alerts SwissADME 0.0
Number of Brenk structural alerts SwissADME 0.0
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


2-(2-Methoxyethoxy)ethanol
Predicted human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000229595ASF1A704
ENSP00000263382ASF1B704
ENSP00000300093PLK1800
ENSP00000303211ACHE795
ENSP00000343103PRMT7795
ENSP00000348821MYOM1800
ENSP00000364801HSPA1B800
ENSP00000371798FSCN1800
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.