2-Phenylethyl propionate

Details

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Internal ID 1ff90ac6-8246-4543-8ca0-fa2e59fcd697
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-phenylethyl propanoate
SMILES (Canonical) CCC(=O)OCCC1=CC=CC=C1
SMILES (Isomeric) CCC(=O)OCCC1=CC=CC=C1
InChI InChI=1S/C11H14O2/c1-2-11(12)13-9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
InChI Key HVGZQCSMLUDISR-UHFFFAOYSA-N
Popularity 112 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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122-70-3
Phenethyl propionate
2-Phenylethyl propanoate
Propanoic acid, 2-phenylethyl ester
Phenylethyl propionate
2-Phenethyl propionate
Benzylcarbinyl propionate
EcoPCO ACU
Phenethyl alcohol, propionate
PROPIONIC ACID, PHENETHYL 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 2-Phenylethyl propionate

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 + 0.9712 97.12%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5708 57.08%
OATP2B1 inhibitior - 0.8629 86.29%
OATP1B1 inhibitior + 0.9163 91.63%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7220 72.20%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9339 93.39%
CYP3A4 substrate - 0.6149 61.49%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9535 95.35%
CYP2C9 inhibition - 0.8343 83.43%
CYP2C19 inhibition - 0.8182 81.82%
CYP2D6 inhibition - 0.8775 87.75%
CYP1A2 inhibition + 0.5875 58.75%
CYP2C8 inhibition + 0.5491 54.91%
CYP inhibitory promiscuity - 0.6272 62.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5708 57.08%
Eye corrosion + 0.7160 71.60%
Eye irritation + 0.9263 92.63%
Skin irritation - 0.7112 71.12%
Skin corrosion - 0.9973 99.73%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5463 54.63%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6019 60.19%
skin sensitisation + 0.4872 48.72%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.8304 83.04%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.8024 80.24%
Acute Oral Toxicity (c) III 0.8571 85.71%
Estrogen receptor binding - 0.8670 86.70%
Androgen receptor binding - 0.7629 76.29%
Thyroid receptor binding - 0.8502 85.02%
Glucocorticoid receptor binding - 0.7655 76.55%
Aromatase binding - 0.7230 72.30%
PPAR gamma - 0.7741 77.41%
Honey bee toxicity - 0.9555 95.55%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9562 95.62%

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 97.13% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 96.16% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 94.71% 90.17%
CHEMBL2581 P07339 Cathepsin D 93.86% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.23% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.53% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.20% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.69% 94.73%

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.
Eucalyptus bridgesiana
Eucalyptus leucoxylon
Pelargonium endlicherianum

Cross-Links

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PubChem 31225
NPASS NPC121800
LOTUS LTS0176876
wikiData Q4596915