METHYL ETHYL SULFIDE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | METHYL ETHYL SULFIDE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 624-89-5 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 12230 |
| IUPAC Name | methylsulfanylethane |
| InChI | InChI=1S/C3H8S/c1-3-4-2/h3H2,1-2H3 |
| InChI Key | WXEHBUMAEPOYKP-UHFFFAOYSA-N |
| Canonical SMILES | CCSC |
| Molecular Formula | C3H8S |
| Wikipedia | ethyl methyl sulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 76.157 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Complexity | 7.2 |
| CACTVS Substructure Key Fingerprint | A A A D c c B A A A B A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A G A Q A A A A A A A C E Q A C C A A A A A A g A A A A A A A A A A A A A A B A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 25.3 |
| Monoisotopic Mass | 76.035 |
| Exact Mass | 76.035 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 4 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9834 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7333 |
| P-glycoprotein Substrate | Non-substrate | 0.7521 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9478 |
| Non-inhibitor | 0.9540 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8955 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.6069 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8566 |
| CYP450 2D6 Substrate | Non-substrate | 0.8332 |
| CYP450 3A4 Substrate | Non-substrate | 0.7241 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7663 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8929 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9272 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8927 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9799 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8975 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9383 |
| Non-inhibitor | 0.9336 | |
| AMES Toxicity | Non AMES toxic | 0.9319 |
| Carcinogens | Carcinogens | 0.7235 |
| Fish Toxicity | High FHMT | 0.5099 |
| Tetrahymena Pyriformis Toxicity | Low TPT | 0.7997 |
| Honey Bee Toxicity | High HBT | 0.8242 |
| Biodegradation | Not ready biodegradable | 0.7148 |
| Acute Oral Toxicity | III | 0.7970 |
| Carcinogenicity (Three-class) | Non-required | 0.6118 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.7613 | LogS |
| Caco-2 Permeability | 1.6806 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4363 | LD50, mol/kg |
| Fish Toxicity | 2.8849 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -1.0466 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Thioethers |
| Subclass | Dialkylthioethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkylthioethers |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkylthioether - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. |
From ClassyFire