Ethyl 2-phenylpropionate

Details

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Internal ID d42e3de1-3a6c-4831-bd50-ee379a0ba3ee
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name ethyl 2-phenylpropanoate
SMILES (Canonical) CCOC(=O)C(C)C1=CC=CC=C1
SMILES (Isomeric) CCOC(=O)C(C)C1=CC=CC=C1
InChI InChI=1S/C11H14O2/c1-3-13-11(12)9(2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3
InChI Key UTUVIKZNQWNGIM-UHFFFAOYSA-N
Popularity 30 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 2.70
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Ethyl 2-phenylpropanoate
2510-99-8
Ethyl hydratropate
2-phenylpropionic acid ethyl ester
Ethyl hydrotropate
Hydratropic acid, ethyl ester
113085-12-4
Benzeneacetic acid, .alpha.-methyl-, ethyl ester
2-Phenyl-propionic acid ethyl ester
MFCD00795471
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl 2-phenylpropionate

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 + 0.8817 88.17%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7706 77.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9502 95.02%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8303 83.03%
P-glycoprotein inhibitior - 0.9919 99.19%
P-glycoprotein substrate - 0.9901 99.01%
CYP3A4 substrate - 0.7117 71.17%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8621 86.21%
CYP3A4 inhibition - 0.9735 97.35%
CYP2C9 inhibition - 0.9166 91.66%
CYP2C19 inhibition - 0.9377 93.77%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition + 0.6713 67.13%
CYP2C8 inhibition - 0.9874 98.74%
CYP inhibitory promiscuity - 0.6432 64.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5161 51.61%
Carcinogenicity (trinary) Non-required 0.6340 63.40%
Eye corrosion + 0.6309 63.09%
Eye irritation + 0.9311 93.11%
Skin irritation + 0.7104 71.04%
Skin corrosion - 0.9729 97.29%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6789 67.89%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.8179 81.79%
skin sensitisation + 0.8348 83.48%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity - 0.6964 69.64%
Acute Oral Toxicity (c) III 0.8626 86.26%
Estrogen receptor binding - 0.8283 82.83%
Androgen receptor binding - 0.6010 60.10%
Thyroid receptor binding - 0.9056 90.56%
Glucocorticoid receptor binding - 0.9395 93.95%
Aromatase binding - 0.8156 81.56%
PPAR gamma - 0.8726 87.26%
Honey bee toxicity - 0.9525 95.25%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5755 57.55%
Fish aquatic toxicity + 0.9356 93.56%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.90% 90.17%
CHEMBL2581 P07339 Cathepsin D 94.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.09% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.55% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.55% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.04% 86.33%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.87% 93.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.87% 95.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.97% 94.08%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.64% 96.00%
CHEMBL5028 O14672 ADAM10 81.35% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.02% 99.17%

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.
Artemisia sericea

Cross-Links

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PubChem 99643
LOTUS LTS0053080
wikiData Q72476728