3-(2-FURYL)ACROLEIN
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 3-(2-FURYL)ACROLEIN |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 623-30-3 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 1549521 |
| IUPAC Name | (E)-3-(furan-2-yl)prop-2-enal |
| InChI | InChI=1S/C7H6O2/c8-5-1-3-7-4-2-6-9-7/h1-6H/b3-1+ |
| InChI Key | VZIRCHXYMBFNFD-HNQUOIGGSA-N |
| Canonical SMILES | C1=COC(=C1)C=CC=O |
| Molecular Formula | C7H6O2 |
| Wikipedia | 2-furanacrolein |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 122.123 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Complexity | 118.0 |
| CACTVS Substructure Key Fingerprint | A A A D c Y B g 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 w B I A A B E C I A K h S g 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 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 = = |
| Topological Polar Surface Area | 30.2 |
| Monoisotopic Mass | 122.037 |
| Exact Mass | 122.037 |
| 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+ | 0.9911 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7452 |
| P-glycoprotein Substrate | Non-substrate | 0.8042 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8628 |
| Non-inhibitor | 0.8107 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8578 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.4997 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8068 |
| CYP450 2D6 Substrate | Non-substrate | 0.9242 |
| CYP450 3A4 Substrate | Non-substrate | 0.7892 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5122 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9179 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9473 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5504 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9769 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.5096 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9004 |
| Non-inhibitor | 0.9762 | |
| AMES Toxicity | Non AMES toxic | 0.9133 |
| Carcinogens | Non-carcinogens | 0.7117 |
| Fish Toxicity | Low FHMT | 0.5550 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9977 |
| Honey Bee Toxicity | High HBT | 0.7766 |
| Biodegradation | Ready biodegradable | 0.8557 |
| Acute Oral Toxicity | III | 0.8452 |
| Carcinogenicity (Three-class) | Warning | 0.4371 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -0.9201 | LogS |
| Caco-2 Permeability | 1.7519 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.1840 | LD50, mol/kg |
| Fish Toxicity | 1.0330 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.9042 | 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 - Enal - Alpha,beta-unsaturated aldehyde - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - 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