1-(2-FURYL)BUTAN-3-ONE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 1-(2-FURYL)BUTAN-3-ONE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 699-17-2 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 12780 |
| IUPAC Name | 4-(furan-2-yl)butan-2-one |
| InChI | InChI=1S/C8H10O2/c1-7(9)4-5-8-3-2-6-10-8/h2-3,6H,4-5H2,1H3 |
| InChI Key | GGJUJWSDTDBTLX-UHFFFAOYSA-N |
| Canonical SMILES | CC(=O)CCC1=CC=CO1 |
| Molecular Formula | C8H10O2 |
| Wikipedia | 4-(2-furyl)-2-butanone |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 138.166 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 120.0 |
| 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 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 e L y K 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 | 30.2 |
| Monoisotopic Mass | 138.068 |
| Exact Mass | 138.068 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| 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+ | 0.9914 |
| Human Intestinal Absorption | HIA+ | 0.9972 |
| Caco-2 Permeability | Caco2+ | 0.7705 |
| P-glycoprotein Substrate | Non-substrate | 0.6786 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8447 |
| Non-inhibitor | 0.6915 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7915 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4542 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7532 |
| CYP450 2D6 Substrate | Non-substrate | 0.8414 |
| CYP450 3A4 Substrate | Non-substrate | 0.6885 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6184 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8760 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9407 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5803 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9569 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7895 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7706 |
| Non-inhibitor | 0.9472 | |
| AMES Toxicity | Non AMES toxic | 0.9416 |
| Carcinogens | Non-carcinogens | 0.7751 |
| Fish Toxicity | Low FHMT | 0.6126 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9534 |
| Honey Bee Toxicity | High HBT | 0.6480 |
| Biodegradation | Ready biodegradable | 0.9031 |
| Acute Oral Toxicity | III | 0.8877 |
| Carcinogenicity (Three-class) | Non-required | 0.4358 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.4792 | LogS |
| Caco-2 Permeability | 1.6614 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7484 | LD50, mol/kg |
| Fish Toxicity | 1.3482 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.3794 | 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 - Ketone - Oxacycle - 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