GUAIACYL PHENYLACETATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | GUAIACYL PHENYLACETATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 4112-89-4 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61331 |
| IUPAC Name | (2-methoxyphenyl) 2-phenylacetate |
| InChI | InChI=1S/C15H14O3/c1-17-13-9-5-6-10-14(13)18-15(16)11-12-7-3-2-4-8-12/h2-10H,11H2,1H3 |
| InChI Key | KNVYLIIBQXVDKC-UHFFFAOYSA-N |
| Canonical SMILES | COC1=CC=CC=C1OC(=O)CC2=CC=CC=C2 |
| Molecular Formula | C15H14O3 |
| Wikipedia | guaiacyl phenylacetate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 242.274 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Complexity | 259.0 |
| 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 w Y A A A A A A A A A A B Q A A A G g A A A A A A D A S A m A I y D o A A B A C I A i D S C A A C C A A g I A A I i A E G i I g N J j K E N R q C O i K k w B E K q A e I y K C O A A A A A A A A Q A A A A A A A A A C A A A A A A A A A A A = = |
| Topological Polar Surface Area | 35.5 |
| Monoisotopic Mass | 242.094 |
| Exact Mass | 242.094 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 18 |
| 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+ | 0.8864 |
| Human Intestinal Absorption | HIA+ | 0.9927 |
| Caco-2 Permeability | Caco2+ | 0.8469 |
| P-glycoprotein Substrate | Non-substrate | 0.6540 |
| P-glycoprotein Inhibitor | Inhibitor | 0.5702 |
| Non-inhibitor | 0.7503 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8162 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.9298 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7361 |
| CYP450 2D6 Substrate | Non-substrate | 0.8710 |
| CYP450 3A4 Substrate | Non-substrate | 0.5833 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.8116 |
| CYP450 2C9 Inhibitor | Inhibitor | 0.5000 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9468 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.7968 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8792 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.6576 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9461 |
| Non-inhibitor | 0.9069 | |
| AMES Toxicity | Non AMES toxic | 0.9391 |
| Carcinogens | Non-carcinogens | 0.8761 |
| Fish Toxicity | High FHMT | 0.9304 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9424 |
| Honey Bee Toxicity | High HBT | 0.7399 |
| Biodegradation | Not ready biodegradable | 0.5624 |
| Acute Oral Toxicity | III | 0.8324 |
| Carcinogenicity (Three-class) | Non-required | 0.5103 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.4541 | LogS |
| Caco-2 Permeability | 0.9732 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7441 | LD50, mol/kg |
| Fish Toxicity | 0.1820 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.2569 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Phenol esters |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenol ester - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Carboxylic acid ester - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. |
From ClassyFire