S-METHYL HEXANETHIOATE
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | S-METHYL HEXANETHIOATE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 2432-77-1 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 75515 |
| IUPAC Name | S-methyl hexanethioate |
| InChI | InChI=1S/C7H14OS/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3 |
| InChI Key | AKGAHYLJHAOPKQ-UHFFFAOYSA-N |
| Canonical SMILES | CCCCCC(=O)SC |
| Molecular Formula | C7H14OS |
| Wikipedia | S-methyl hexanethioate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 146.248 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Complexity | 81.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g I 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 g Q A A A A A C A C A w A C C A A A A A A g I A A A Q A A A A A A A A A B A A A A E A A A A A A B I g A A A A A A A A A A A A A A E I 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 = = |
| Topological Polar Surface Area | 42.4 |
| Monoisotopic Mass | 146.077 |
| Exact Mass | 146.077 |
| XLogP3 | None |
| XLogP3-AA | 2.6 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| 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+ | 0.9895 |
| Human Intestinal Absorption | HIA+ | 0.9929 |
| Caco-2 Permeability | Caco2+ | 0.7834 |
| P-glycoprotein Substrate | Non-substrate | 0.6875 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9166 |
| Non-inhibitor | 0.9467 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9044 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.3503 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7970 |
| CYP450 2D6 Substrate | Non-substrate | 0.8358 |
| CYP450 3A4 Substrate | Non-substrate | 0.6691 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.5171 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8903 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9357 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9155 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9871 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.8775 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9390 |
| Non-inhibitor | 0.8282 | |
| AMES Toxicity | Non AMES toxic | 0.9690 |
| Carcinogens | Carcinogens | 0.5071 |
| Fish Toxicity | High FHMT | 0.8617 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.7986 |
| Honey Bee Toxicity | High HBT | 0.7896 |
| Biodegradation | Ready biodegradable | 0.5948 |
| Acute Oral Toxicity | III | 0.7927 |
| Carcinogenicity (Three-class) | Non-required | 0.7625 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.7058 | LogS |
| Caco-2 Permeability | 1.6283 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9845 | LD50, mol/kg |
| Fish Toxicity | 1.4571 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.2582 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acyl thioesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acyl thioesters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acyl thioester - Carbothioic s-ester - Thiocarboxylic acid ester - Sulfenyl compound - Thiocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acyl thioesters. These are thioester derivatives of a fatty acid with the general formula RC(=O)SR', where R is the fatty acyl chain. |
From ClassyFire