3,6-Dimethyl-1,2,4,5-tetrathiane
General Information
| Chemical name | 3,6-Dimethyl-1,2,4,5-tetrathiane |
| CAS number | 67411-27-2 |
| Flavouring type | substances |
| FL No. | 15.056 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 526613 |
| IUPAC Name | 3,6-dimethyl-1,2,4,5-tetrathiane |
| InChI | InChI=1S/C4H8S4/c1-3-5-7-4(2)8-6-3/h3-4H,1-2H3 |
| InChI Key | OLLSVBUNSGNIRV-UHFFFAOYSA-N |
| Canonical SMILES | CC1SSC(SS1)C |
| Molecular Formula | C4H8S4 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 184.348 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Complexity | 56.4 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g A A B w A A A A A A A A A A A A A A A A A A A A A A A k 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 | 101.0 |
| Monoisotopic Mass | 183.951 |
| Exact Mass | 183.951 |
| XLogP3 | None |
| XLogP3-AA | 2.4 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 8 |
| 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+ | 0.9761 |
| Human Intestinal Absorption | HIA+ | 0.9596 |
| Caco-2 Permeability | Caco2+ | 0.6232 |
| P-glycoprotein Substrate | Non-substrate | 0.7317 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9270 |
| Non-inhibitor | 0.9965 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9103 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5619 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7704 |
| CYP450 2D6 Substrate | Non-substrate | 0.8365 |
| CYP450 3A4 Substrate | Non-substrate | 0.7660 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5437 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.6726 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8136 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6454 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8131 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6603 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9646 |
| Non-inhibitor | 0.9524 | |
| AMES Toxicity | Non AMES toxic | 0.8280 |
| Carcinogens | Non-carcinogens | 0.7123 |
| Fish Toxicity | Low FHMT | 0.7620 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.6938 |
| Honey Bee Toxicity | High HBT | 0.8115 |
| Biodegradation | Not ready biodegradable | 0.8671 |
| Acute Oral Toxicity | II | 0.4868 |
| Carcinogenicity (Three-class) | Non-required | 0.6021 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.0542 | LogS |
| Caco-2 Permeability | 1.6617 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.3540 | LD50, mol/kg |
| Fish Toxicity | 1.6121 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.2092 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Tetrathianes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetrathianes |
| Alternative Parents | |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | 1,2,4,5-tetrathiane - Organic disulfide - Hydrocarbon derivative - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as tetrathianes. These are organic compounds containing a tetrathiane ring, which is a six-member saturated aliphatic ring made up of four sulfur atoms and two carbon atoms. |
From ClassyFire