IMPPAT Phytochemical information: 
2-(Methylthio)ethanol

2-(Methylthio)ethanol
Summary

SMILES: CSCCO
InChI: InChI=1S/C3H8OS/c1-5-3-2-4/h4H,2-3H2,1H3
InChIKey: WBBPRCNXBQTYLF-UHFFFAOYSA-N
DeepSMILES: CSCCO
Functional groups: CSC; CO
Chemical classification
ClassyFire Kingdom: Organic compounds
ClassyFire Superclass: Organosulfur compounds
ClassyFire Class: Thioethers
ClassyFire Subclass: Dialkylthioethers
NP Classifier Biosynthetic pathway: Fatty acids
NP Classifier Superclass: Fatty acyls
NP Classifier Class: Fatty alcohols
Synonymous chemical names:
2-methylthioethanol
External chemical identifiers:
CID:CID_78925; ChEMBL:CHEMBL277871; ChEBI:CHEBI:63861; ZINC:ZINC000001577077; FDASRS:5K6TOE95UY; SureChEMBL:SCHEMBL61752; MolPort-001-779-998
Chemical structure download


2-(Methylthio)ethanol
Physicochemical properties
Property name Tool Property value
Molecular weight (g/mol) RDKit 92.16
Log P RDKit 0.34
Topological polar surface area (Å2) RDKit 20.23
Number of hydrogen bond acceptors RDKit 2
Number of hydrogen bond donors RDKit 1
Number of carbon atoms RDKit 3
Number of heavy atoms RDKit 5
Number of heteroatoms RDKit 2
Number of nitrogen atoms RDKit 0
Number of sulfur atoms RDKit 1
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 3
Shape complexity RDKit 1
Number of rotatable bonds RDKit 2
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-(Methylthio)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 3
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 0.529801


2-(Methylthio)ethanol
ADME properties
Property nameToolProperty value
Bioavailability score SwissADME 0.55
Solubility class [ESOL] SwissADME Very soluble
Solubility class [Silicos-IT] SwissADME Soluble
Blood Brain Barrier permeation SwissADME No
Gastrointestinal absorption SwissADME High
Log Kp (Skin permeation, cm/s) SwissADME -6.73
Number of PAINS structural alerts SwissADME 0
Number of Brenk structural alerts SwissADME 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-(Methylthio)ethanol
Human target proteins
Protein identifierHGNC symbolCombined score from STITCH database
ENSP00000217426AHCY900
The human target proteins were predicted using STITCH, a database of Chemical-Protein interaction networks.