3-OCTEN-2-ONE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 3-OCTEN-2-ONE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 1669-44-9 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5363229 |
| IUPAC Name | (E)-oct-3-en-2-one |
| InChI | InChI=1S/C8H14O/c1-3-4-5-6-7-8(2)9/h6-7H,3-5H2,1-2H3/b7-6+ |
| InChI Key | ZCFOBLITZWHNNC-VOTSOKGWSA-N |
| Canonical SMILES | CCCCC=CC(=O)C |
| Molecular Formula | C8H14O |
| Wikipedia | 3-octen-2-one |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 126.199 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Complexity | 103.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w 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 A A A A A A A A A A A G g A A A A A A C A S A g A A C A A A A A A C I A K B S A A A A A A A g A A A I C A A A A E g A A A I A A Q A A A A A A g A A I A Y 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 A A A = = |
| Topological Polar Surface Area | 17.1 |
| Monoisotopic Mass | 126.104 |
| Exact Mass | 126.104 |
| XLogP3 | None |
| XLogP3-AA | 2.3 |
| 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 | 1 |
| 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+ | 0.9913 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8794 |
| P-glycoprotein Substrate | Non-substrate | 0.6731 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8025 |
| Non-inhibitor | 0.6613 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8855 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.2941 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8163 |
| CYP450 2D6 Substrate | Non-substrate | 0.8480 |
| CYP450 3A4 Substrate | Non-substrate | 0.6463 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6440 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9478 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9501 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9310 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9893 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7242 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8818 |
| Non-inhibitor | 0.9040 | |
| AMES Toxicity | Non AMES toxic | 0.8832 |
| Carcinogens | Carcinogens | 0.6482 |
| Fish Toxicity | High FHMT | 0.7279 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9395 |
| Honey Bee Toxicity | High HBT | 0.7886 |
| Biodegradation | Ready biodegradable | 0.8808 |
| Acute Oral Toxicity | III | 0.7671 |
| Carcinogenicity (Three-class) | Non-required | 0.6612 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.3679 | LogS |
| Caco-2 Permeability | 1.6578 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.8392 | LD50, mol/kg |
| Fish Toxicity | 1.5213 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.6480 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Alpha,beta-unsaturated carbonyl compounds - Alpha,beta-unsaturated ketones |
| Direct Parent | Enones |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Enone - Acryloyl-group - Ketone - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as enones. These are compounds containing the enone functional group, with the structure RC(=O)CR'. |
From ClassyFire