Ethyl 3-phenylpropionate

Details

Top
Internal ID 06b1ad5e-1cbc-4216-bbd5-52132731966c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 3-phenylpropanoate
SMILES (Canonical) CCOC(=O)CCC1=CC=CC=C1
SMILES (Isomeric) CCOC(=O)CCC1=CC=CC=C1
InChI InChI=1S/C11H14O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
InChI Key JAGZUIGGHGTFHO-UHFFFAOYSA-N
Popularity 133 references in papers

Physical and Chemical Properties

Top
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) 2.18
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
Ethyl 3-phenylpropanoate
2021-28-5
Ethyl hydrocinnamate
Benzenepropanoic acid, ethyl ester
3-Phenylpropionic Acid Ethyl Ester
Ethyl dihydrocinnamate
Hydrocinnamic acid, ethyl ester
ETHYL BENZENEPROPANOATE
Ethylhydrocinnamoate
ethyl benzylacetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Ethyl 3-phenylpropionate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9546 95.46%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5708 57.08%
OATP2B1 inhibitior - 0.8631 86.31%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7070 70.70%
P-glycoprotein inhibitior - 0.9926 99.26%
P-glycoprotein substrate - 0.9727 97.27%
CYP3A4 substrate - 0.6048 60.48%
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 - 0.6539 65.39%
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 + 0.9696 96.96%
Skin irritation - 0.7112 71.12%
Skin corrosion - 0.9973 99.73%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4879 48.79%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6265 62.65%
skin sensitisation + 0.4872 48.72%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8304 83.04%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.7394 73.94%
Acute Oral Toxicity (c) III 0.8571 85.71%
Estrogen receptor binding - 0.8750 87.50%
Androgen receptor binding - 0.8879 88.79%
Thyroid receptor binding - 0.8104 81.04%
Glucocorticoid receptor binding - 0.7536 75.36%
Aromatase binding - 0.7803 78.03%
PPAR gamma - 0.7952 79.52%
Honey bee toxicity - 0.9413 94.13%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5455 54.55%
Fish aquatic toxicity + 0.9562 95.62%

Targets

Top

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 95.57% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.36% 86.33%
CHEMBL2581 P07339 Cathepsin D 93.14% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.10% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.76% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.18% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.91% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.15% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.96% 94.62%

Plants that contains it

Top
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 salsoloides
Baccharis dracunculifolia

Cross-Links

Top
PubChem 16237
LOTUS LTS0187332
wikiData Q27261590