DIETHYL TRISULFIDE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | DIETHYL TRISULFIDE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 3600-24-6 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 77151 |
| IUPAC Name | (ethyltrisulfanyl)ethane |
| InChI | InChI=1S/C4H10S3/c1-3-5-7-6-4-2/h3-4H2,1-2H3 |
| InChI Key | OPMRTBDRQRSNDN-UHFFFAOYSA-N |
| Canonical SMILES | CCSSSCC |
| Molecular Formula | C4H10S3 |
| Wikipedia | diethyl trisulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 154.304 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Complexity | 26.1 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g A A B g 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 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 A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 75.9 |
| Monoisotopic Mass | 153.994 |
| Exact Mass | 153.994 |
| XLogP3 | None |
| XLogP3-AA | 2.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 7 |
| 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+ | 0.9633 |
| Human Intestinal Absorption | HIA+ | 0.9956 |
| Caco-2 Permeability | Caco2+ | 0.5873 |
| P-glycoprotein Substrate | Non-substrate | 0.7894 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9245 |
| Non-inhibitor | 0.9813 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8933 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.4900 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8493 |
| CYP450 2D6 Substrate | Non-substrate | 0.8436 |
| CYP450 3A4 Substrate | Non-substrate | 0.7597 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7401 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.7358 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8853 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7664 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9562 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7057 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8527 |
| Non-inhibitor | 0.9325 | |
| AMES Toxicity | Non AMES toxic | 0.9196 |
| Carcinogens | Carcinogens | 0.8187 |
| Fish Toxicity | High FHMT | 0.8135 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9187 |
| Honey Bee Toxicity | High HBT | 0.8511 |
| Biodegradation | Not ready biodegradable | 0.8464 |
| Acute Oral Toxicity | III | 0.5926 |
| Carcinogenicity (Three-class) | Non-required | 0.5930 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.5298 | LogS |
| Caco-2 Permeability | 1.3169 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.1909 | LD50, mol/kg |
| Fish Toxicity | 1.4146 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.0267 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Organic trisulfides |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic trisulfides |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic trisulfide - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as organic trisulfides. These are organosulfur compounds with the general formula RSSSR' (R,R'=alkyl, aryl). |
From ClassyFire