ETHYL 2-FURANPROPIONATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | ETHYL 2-FURANPROPIONATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 10031-90-0 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61450 |
| IUPAC Name | ethyl 3-(furan-2-yl)propanoate |
| InChI | InChI=1S/C9H12O3/c1-2-11-9(10)6-5-8-4-3-7-12-8/h3-4,7H,2,5-6H2,1H3 |
| InChI Key | OWIWZQQFSTZZIG-UHFFFAOYSA-N |
| Canonical SMILES | CCOC(=O)CCC1=CC=CO1 |
| Molecular Formula | C9H12O3 |
| Wikipedia | ethyl 2-furanpropionate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 168.192 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Complexity | 145.0 |
| 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 S A A A A A A A A A A A A A A A A A B g A A A G g A A A A A A C A S g k A I y D I A A B E C I A K j S i A A C C A A k I A A I i A E G C M g M J j K E N R q C G S C k w B E I q Y f L y 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 = = |
| Topological Polar Surface Area | 39.4 |
| Monoisotopic Mass | 168.079 |
| Exact Mass | 168.079 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9750 |
| Human Intestinal Absorption | HIA+ | 0.9967 |
| Caco-2 Permeability | Caco2+ | 0.6594 |
| P-glycoprotein Substrate | Non-substrate | 0.6517 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7522 |
| Non-inhibitor | 0.5781 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7675 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7002 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8377 |
| CYP450 2D6 Substrate | Non-substrate | 0.8784 |
| CYP450 3A4 Substrate | Non-substrate | 0.6550 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.5645 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.5942 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9087 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5111 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9401 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.5681 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8385 |
| Non-inhibitor | 0.8249 | |
| AMES Toxicity | Non AMES toxic | 0.8891 |
| Carcinogens | Non-carcinogens | 0.7810 |
| Fish Toxicity | High FHMT | 0.5881 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9634 |
| Honey Bee Toxicity | High HBT | 0.6994 |
| Biodegradation | Ready biodegradable | 0.9414 |
| Acute Oral Toxicity | III | 0.8749 |
| Carcinogenicity (Three-class) | Non-required | 0.5613 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.4030 | LogS |
| Caco-2 Permeability | 1.0252 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7078 | LD50, mol/kg |
| Fish Toxicity | 1.6212 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.1237 | 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 | Aromatic heteromonocyclic compounds |
| Substituents | Fatty acid ester - Heteroaromatic compound - Furan - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic heteromonocyclic 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