Methyl phenylacetate

Details

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Internal ID 922467ff-7863-489f-bf0e-7381ab3c1ad2
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name methyl 2-phenylacetate
SMILES (Canonical) COC(=O)CC1=CC=CC=C1
SMILES (Isomeric) COC(=O)CC1=CC=CC=C1
InChI InChI=1S/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3
InChI Key CRZQGDNQQAALAY-UHFFFAOYSA-N
Popularity 253 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O2
Molecular Weight 150.17 g/mol
Exact Mass 150.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.40
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Methyl 2-phenylacetate
101-41-7
Benzeneacetic acid, methyl ester
Methyl benzeneacetate
Methyl alpha-toluate
Methyl phenylethanoate
Methyl benzeneethanoate
Phenylacetic Acid Methyl Ester
Phenylacetic acid, methyl ester
Acetic acid, phenyl-, methyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl phenylacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8151 81.51%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.6925 69.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9436 94.36%
OATP1B3 inhibitior + 0.9602 96.02%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8171 81.71%
P-glycoprotein inhibitior - 0.9917 99.17%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.7050 70.50%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7965 79.65%
CYP3A4 inhibition - 0.9861 98.61%
CYP2C9 inhibition - 0.9678 96.78%
CYP2C19 inhibition - 0.9269 92.69%
CYP2D6 inhibition - 0.9506 95.06%
CYP1A2 inhibition - 0.5288 52.88%
CYP2C8 inhibition - 0.8495 84.95%
CYP inhibitory promiscuity - 0.9019 90.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5226 52.26%
Carcinogenicity (trinary) Non-required 0.7147 71.47%
Eye corrosion + 0.8662 86.62%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.8846 88.46%
Skin corrosion - 0.9315 93.15%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7768 77.68%
Micronuclear - 0.9215 92.15%
Hepatotoxicity + 0.5284 52.84%
skin sensitisation + 0.6102 61.02%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.4603 46.03%
Acute Oral Toxicity (c) III 0.8419 84.19%
Estrogen receptor binding - 0.9408 94.08%
Androgen receptor binding - 0.8806 88.06%
Thyroid receptor binding - 0.9154 91.54%
Glucocorticoid receptor binding - 0.8787 87.87%
Aromatase binding - 0.8917 89.17%
PPAR gamma - 0.8227 82.27%
Honey bee toxicity - 0.9875 98.75%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.7914 79.14%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.17% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.47% 90.17%
CHEMBL2581 P07339 Cathepsin D 93.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.02% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.55% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.86% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.05% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.75% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.99% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aspalathus linearis
Coffea arabica
Conioselinum anthriscoides
Humulus lupulus
Ligusticum striatum
Lonicera japonica
Syzygium aromaticum
Trollius chinensis
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zea mays

Cross-Links

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PubChem 7559
NPASS NPC288903
LOTUS LTS0085009
wikiData Q390681