FURFURYL PROPIONATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | FURFURYL PROPIONATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 623-19-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61166 |
| IUPAC Name | furan-2-ylmethyl propanoate |
| InChI | InChI=1S/C8H10O3/c1-2-8(9)11-6-7-4-3-5-10-7/h3-5H,2,6H2,1H3 |
| InChI Key | LGBXNZSSTFWRFS-UHFFFAOYSA-N |
| Canonical SMILES | CCC(=O)OCC1=CC=CO1 |
| Molecular Formula | C8H10O3 |
| Wikipedia | furfuryl propionate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 154.165 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Complexity | 133.0 |
| 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 I C C A A k I A A I i A F G C M g N J j K E N R 6 C G S C k w B E K q Y a I J A 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 = = |
| Topological Polar Surface Area | 39.4 |
| Monoisotopic Mass | 154.063 |
| Exact Mass | 154.063 |
| XLogP3 | None |
| XLogP3-AA | 1.2 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| 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+ | 0.9826 |
| Human Intestinal Absorption | HIA+ | 0.9971 |
| Caco-2 Permeability | Caco2+ | 0.5993 |
| P-glycoprotein Substrate | Non-substrate | 0.6452 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.6315 |
| Non-inhibitor | 0.7449 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8532 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7649 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8412 |
| CYP450 2D6 Substrate | Non-substrate | 0.8952 |
| CYP450 3A4 Substrate | Non-substrate | 0.6838 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.7824 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.5473 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9418 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5394 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9590 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.6720 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9718 |
| Non-inhibitor | 0.8509 | |
| AMES Toxicity | Non AMES toxic | 0.5628 |
| Carcinogens | Non-carcinogens | 0.6903 |
| Fish Toxicity | Low FHMT | 0.5518 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.7513 |
| Honey Bee Toxicity | High HBT | 0.6851 |
| Biodegradation | Ready biodegradable | 0.9261 |
| Acute Oral Toxicity | III | 0.7994 |
| Carcinogenicity (Three-class) | Warning | 0.4440 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.6721 | LogS |
| Caco-2 Permeability | 0.8947 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7985 | LD50, mol/kg |
| Fish Toxicity | 2.0568 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3932 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Heteroaromatic compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Heteroaromatic compounds |
| Alternative Parents | |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Heteroaromatic compound - Furan - Carboxylic acid ester - Oxacycle - 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 heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom. |
From ClassyFire