5-ETHYL-2-HYDROXY-3-METHYLCYCLOPENT-2-EN-1-ONE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 5-ETHYL-2-HYDROXY-3-METHYLCYCLOPENT-2-EN-1-ONE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 53263-58-4 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 65427 |
| IUPAC Name | 5-ethyl-2-hydroxy-3-methylcyclopent-2-en-1-one |
| InChI | InChI=1S/C8H12O2/c1-3-6-4-5(2)7(9)8(6)10/h6,9H,3-4H2,1-2H3 |
| InChI Key | ARHWUYVUNJLMRR-UHFFFAOYSA-N |
| Canonical SMILES | CCC1CC(=C(C1=O)O)C |
| Molecular Formula | C8H12O2 |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 140.182 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Complexity | 191.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w M A A A A A A A A A A A A A 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 G g A A C A A A D Q S A g A A C A A A A A g C I A o B Q A A I A A A A g I A A A C A F A A E g A A B I A A A A A Q A A E g A A I A Q O I Q A A O 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 | 37.3 |
| Monoisotopic Mass | 140.084 |
| Exact Mass | 140.084 |
| XLogP3 | None |
| XLogP3-AA | 1.2 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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+ | 0.9397 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7144 |
| P-glycoprotein Substrate | Non-substrate | 0.5849 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.5354 |
| Non-inhibitor | 0.8579 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8797 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6155 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8465 |
| CYP450 2D6 Substrate | Non-substrate | 0.8736 |
| CYP450 3A4 Substrate | Substrate | 0.5181 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7520 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8091 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.7885 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.7938 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8806 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.5718 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9701 |
| Non-inhibitor | 0.8954 | |
| AMES Toxicity | Non AMES toxic | 0.8599 |
| Carcinogens | Non-carcinogens | 0.7961 |
| Fish Toxicity | High FHMT | 0.7695 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9833 |
| Honey Bee Toxicity | High HBT | 0.8389 |
| Biodegradation | Ready biodegradable | 0.7662 |
| Acute Oral Toxicity | III | 0.6760 |
| Carcinogenicity (Three-class) | Non-required | 0.5441 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.8359 | LogS |
| Caco-2 Permeability | 1.5724 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9573 | LD50, mol/kg |
| Fish Toxicity | 1.7505 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.0336 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones |
| Direct Parent | Cyclic ketones |
| Alternative Parents | |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Cyclic ketone - Enol - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety. |
From ClassyFire