Relevant Data

Food Additives Approved by WHO:

Flavouring Substances Approved by European Union:

  • Guaiacyl phenylacetate [show]

General Information

MaintermGUAIACYL PHENYLACETATE
Doc TypeASP
CAS Reg.No.(or other ID)4112-89-4
Regnum 172.515

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID61331
IUPAC Name(2-methoxyphenyl) 2-phenylacetate
InChIInChI=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 KeyKNVYLIIBQXVDKC-UHFFFAOYSA-N
Canonical SMILESCOC1=CC=CC=C1OC(=O)CC2=CC=CC=C2
Molecular FormulaC15H14O3
Wikipediaguaiacyl phenylacetate

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight242.274
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Complexity259.0
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 Area35.5
Monoisotopic Mass242.094
Exact Mass242.094
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count18
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8864
Human Intestinal AbsorptionHIA+0.9927
Caco-2 PermeabilityCaco2+0.8469
P-glycoprotein SubstrateNon-substrate0.6540
P-glycoprotein InhibitorInhibitor0.5702
Non-inhibitor0.7503
Renal Organic Cation TransporterNon-inhibitor0.8162
Distribution
Subcellular localizationMitochondria0.9298
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7361
CYP450 2D6 SubstrateNon-substrate0.8710
CYP450 3A4 SubstrateNon-substrate0.5833
CYP450 1A2 InhibitorInhibitor0.8116
CYP450 2C9 InhibitorInhibitor0.5000
CYP450 2D6 InhibitorNon-inhibitor0.9468
CYP450 2C19 InhibitorInhibitor0.7968
CYP450 3A4 InhibitorNon-inhibitor0.8792
CYP Inhibitory PromiscuityHigh CYP Inhibitory Promiscuity0.6576
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9461
Non-inhibitor0.9069
AMES ToxicityNon AMES toxic0.9391
CarcinogensNon-carcinogens0.8761
Fish ToxicityHigh FHMT0.9304
Tetrahymena Pyriformis ToxicityHigh TPT0.9424
Honey Bee ToxicityHigh HBT0.7399
BiodegradationNot ready biodegradable0.5624
Acute Oral ToxicityIII0.8324
Carcinogenicity (Three-class)Non-required0.5103

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-3.4541LogS
Caco-2 Permeability0.9732LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.7441LD50, mol/kg
Fish Toxicity0.1820pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.2569pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassBenzenoids
ClassPhenol esters
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentPhenol esters
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsPhenol 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
DescriptionThis 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