1,8-OCTANEDITHIOL
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 1,8-OCTANEDITHIOL |
| Doc Type | NIL |
| CAS Reg.No.(or other ID) | 1191-62-4 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 14493 |
| IUPAC Name | octane-1,8-dithiol |
| InChI | InChI=1S/C8H18S2/c9-7-5-3-1-2-4-6-8-10/h9-10H,1-8H2 |
| InChI Key | PGTWZHXOSWQKCY-UHFFFAOYSA-N |
| Canonical SMILES | C(CCCCS)CCCS |
| Molecular Formula | C8H18S2 |
| Wikipedia | 1,8-octanedithiol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 178.352 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 7 |
| Complexity | 47.2 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w 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 C A C E Q A C A A A A A A A Q 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 I A A A A A A A A A A A A A A A E A g I 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 | 2.0 |
| Monoisotopic Mass | 178.085 |
| Exact Mass | 178.085 |
| XLogP3 | None |
| XLogP3-AA | 3.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.8751 |
| Human Intestinal Absorption | HIA+ | 0.9806 |
| Caco-2 Permeability | Caco2+ | 0.6796 |
| P-glycoprotein Substrate | Non-substrate | 0.7209 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9370 |
| Non-inhibitor | 0.7619 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8043 |
| Distribution | ||
| Subcellular localization | Lysosome | 0.6428 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8581 |
| CYP450 2D6 Substrate | Non-substrate | 0.7330 |
| CYP450 3A4 Substrate | Non-substrate | 0.8113 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7083 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8603 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9225 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8320 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9654 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7039 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8286 |
| Non-inhibitor | 0.8799 | |
| AMES Toxicity | Non AMES toxic | 0.8475 |
| Carcinogens | Non-carcinogens | 0.6048 |
| Fish Toxicity | High FHMT | 0.8608 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8900 |
| Honey Bee Toxicity | High HBT | 0.7779 |
| Biodegradation | Not ready biodegradable | 0.9036 |
| Acute Oral Toxicity | III | 0.5609 |
| Carcinogenicity (Three-class) | Non-required | 0.4795 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.9663 | LogS |
| Caco-2 Permeability | 1.3968 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.4278 | LD50, mol/kg |
| Fish Toxicity | 1.7694 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7549 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organosulfur compounds |
| Class | Thiols |
| Subclass | Alkylthiols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alkylthiols |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alkylthiol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as alkylthiols. These are organic compounds containing the thiol functional group linked to an alkyl chain. |
From ClassyFire