Methyl 3-phenylpropionate

Details

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Internal ID 20bb33a9-7713-4f9a-b394-0266e78cdfdc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl 3-phenylpropanoate
SMILES (Canonical) COC(=O)CCC1=CC=CC=C1
SMILES (Isomeric) COC(=O)CCC1=CC=CC=C1
InChI InChI=1S/C10H12O2/c1-12-10(11)8-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3
InChI Key RPUSRLKKXPQSGP-UHFFFAOYSA-N
Popularity 113 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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103-25-3
Methyl 3-phenylpropanoate
Methyl hydrocinnamate
Benzenepropanoic acid, methyl ester
3-Phenylpropionic Acid Methyl Ester
Methyl benzenepropanoate
Hydrocinnamic acid, methyl ester
Methyl dihydrocinnamate
3-Phenylpropanoic acid methyl ester
Methyl beta-phenylpropionate
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 3-phenylpropionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8662 86.62%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6074 60.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9230 92.30%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6873 68.73%
P-glycoprotein inhibitior - 0.9925 99.25%
P-glycoprotein substrate - 0.9068 90.68%
CYP3A4 substrate - 0.6537 65.37%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7965 79.65%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9678 96.78%
CYP2C19 inhibition - 0.9170 91.70%
CYP2D6 inhibition - 0.9544 95.44%
CYP1A2 inhibition - 0.6188 61.88%
CYP2C8 inhibition - 0.6826 68.26%
CYP inhibitory promiscuity - 0.8927 89.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6351 63.51%
Carcinogenicity (trinary) Non-required 0.6673 66.73%
Eye corrosion + 0.7317 73.17%
Eye irritation + 0.9665 96.65%
Skin irritation + 0.8223 82.23%
Skin corrosion - 0.9491 94.91%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6272 62.72%
Micronuclear - 0.9715 97.15%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation - 0.6261 62.61%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6558 65.58%
Acute Oral Toxicity (c) III 0.9029 90.29%
Estrogen receptor binding - 0.9274 92.74%
Androgen receptor binding - 0.7910 79.10%
Thyroid receptor binding - 0.8893 88.93%
Glucocorticoid receptor binding - 0.6847 68.47%
Aromatase binding - 0.8273 82.73%
PPAR gamma - 0.8433 84.33%
Honey bee toxicity - 0.9579 95.79%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7190 71.90%

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 96.59% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.63% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.51% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.50% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.40% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 87.35% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.90% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.67% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 84.38% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.08% 94.62%
CHEMBL5028 O14672 ADAM10 80.45% 97.50%

Cross-Links

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PubChem 7643
NPASS NPC308586
LOTUS LTS0184155
wikiData Q27162059