ETHYL 2-METHYL-3-PENTENOATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | ETHYL 2-METHYL-3-PENTENOATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 1617-23-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5463855 |
| IUPAC Name | ethyl (E)-2-methylpent-3-enoate |
| InChI | InChI=1S/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h4,6-7H,5H2,1-3H3/b6-4+ |
| InChI Key | HOWBPXBYCPKWBL-GQCTYLIASA-N |
| Canonical SMILES | CCOC(=O)C(C)C=CC |
| Molecular Formula | C8H14O2 |
| Wikipedia | (3E)-ethyl 2-methyl-3-pentenoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 142.198 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Complexity | 127.0 |
| 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 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 D Q C g g A I C C A A A B A C I A C D S C A A A A A A g A A A I C A E A A A g A A A A A A Q A C A A A A Q A A I A A 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 | 26.3 |
| Monoisotopic Mass | 142.099 |
| Exact Mass | 142.099 |
| 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 | 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+ | 0.9804 |
| Human Intestinal Absorption | HIA+ | 0.9962 |
| Caco-2 Permeability | Caco2+ | 0.7280 |
| P-glycoprotein Substrate | Non-substrate | 0.7988 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8797 |
| Non-inhibitor | 0.8129 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9255 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6045 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8384 |
| CYP450 2D6 Substrate | Non-substrate | 0.9152 |
| CYP450 3A4 Substrate | Non-substrate | 0.6426 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.7329 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9393 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9535 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9506 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9655 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6946 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9704 |
| Non-inhibitor | 0.9545 | |
| AMES Toxicity | Non AMES toxic | 0.7516 |
| Carcinogens | Carcinogens | 0.7832 |
| Fish Toxicity | High FHMT | 0.6242 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.8820 |
| Honey Bee Toxicity | High HBT | 0.8707 |
| Biodegradation | Ready biodegradable | 0.7877 |
| Acute Oral Toxicity | III | 0.9267 |
| Carcinogenicity (Three-class) | Non-required | 0.5438 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.9851 | LogS |
| Caco-2 Permeability | 1.3562 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5536 | LD50, mol/kg |
| Fish Toxicity | 1.4708 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3673 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire