Phenethyl acetate

Details

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Internal ID e77b90d8-d5d9-42f8-9d9a-35afa95cbddc
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-phenylethyl acetate
SMILES (Canonical) CC(=O)OCCC1=CC=CC=C1
SMILES (Isomeric) CC(=O)OCCC1=CC=CC=C1
InChI InChI=1S/C10H12O2/c1-9(11)12-8-7-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3
InChI Key MDHYEMXUFSJLGV-UHFFFAOYSA-N
Popularity 651 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2-Phenylethyl acetate
103-45-7
2-Phenethyl acetate
Acetic acid, 2-phenylethyl ester
Benzylcarbinyl acetate
beta-Phenylethyl acetate
Acetic acid, phenethyl ester
Acetic Acid Phenethyl Ester
Phenethyl alcohol, acetate
Phenylethyl acetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenethyl acetate

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 + 0.8520 85.20%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7384 73.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9365 93.65%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6909 69.09%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9651 96.51%
CYP3A4 substrate - 0.6521 65.21%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9641 96.41%
CYP2C9 inhibition - 0.9320 93.20%
CYP2C19 inhibition - 0.8349 83.49%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition + 0.6451 64.51%
CYP2C8 inhibition - 0.8029 80.29%
CYP inhibitory promiscuity - 0.8098 80.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6391 63.91%
Eye corrosion + 0.7799 77.99%
Eye irritation + 0.9614 96.14%
Skin irritation + 0.8428 84.28%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7473 74.73%
Micronuclear - 0.9915 99.15%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.5465 54.65%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5527 55.27%
Acute Oral Toxicity (c) III 0.8560 85.60%
Estrogen receptor binding - 0.8116 81.16%
Androgen receptor binding - 0.6025 60.25%
Thyroid receptor binding - 0.9357 93.57%
Glucocorticoid receptor binding - 0.7415 74.15%
Aromatase binding - 0.6788 67.88%
PPAR gamma - 0.8561 85.61%
Honey bee toxicity - 0.9472 94.72%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8319 83.19%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 98.60% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.47% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.75% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.52% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 87.48% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 85.76% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.19% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.76% 95.56%

Cross-Links

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PubChem 7654
NPASS NPC170484
LOTUS LTS0136181
wikiData Q6856299