Ethyl benzoate

Details

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Internal ID d42b6af9-8a5e-4517-8e1e-47024288dc30
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name ethyl benzoate
SMILES (Canonical) CCOC(=O)C1=CC=CC=C1
SMILES (Isomeric) CCOC(=O)C1=CC=CC=C1
InChI InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI Key MTZQAGJQAFMTAQ-UHFFFAOYSA-N
Popularity 1,257 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O2
Molecular Weight 150.17 g/mol
Exact Mass 150.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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93-89-0
Benzoic acid, ethyl ester
Benzoic ether
Ethyl benzenecarboxylate
Benzoic Acid Ethyl Ester
Benzoyl ethyl ether
Ethylester kyseliny benzoove
FEMA No. 2422
Ethyl benzoate (natural)
NSC 8884
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 benzoate

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 + 0.9115 91.15%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7797 77.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9572 95.72%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8658 86.58%
P-glycoprotein inhibitior - 0.9909 99.09%
P-glycoprotein substrate - 0.9915 99.15%
CYP3A4 substrate - 0.7168 71.68%
CYP2C9 substrate - 0.7945 79.45%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.9817 98.17%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.8897 88.97%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition + 0.7888 78.88%
CYP2C8 inhibition - 0.7175 71.75%
CYP inhibitory promiscuity - 0.7227 72.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5239 52.39%
Carcinogenicity (trinary) Non-required 0.6038 60.38%
Eye corrosion + 0.8185 81.85%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8823 88.23%
Skin corrosion - 0.8782 87.82%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8512 85.12%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5285 52.85%
skin sensitisation + 0.7518 75.18%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.5908 59.08%
Acute Oral Toxicity (c) III 0.9356 93.56%
Estrogen receptor binding - 0.7528 75.28%
Androgen receptor binding - 0.8428 84.28%
Thyroid receptor binding - 0.9140 91.40%
Glucocorticoid receptor binding - 0.9731 97.31%
Aromatase binding - 0.8040 80.40%
PPAR gamma - 0.9176 91.76%
Honey bee toxicity - 0.9884 98.84%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7055 70.55%
Fish aquatic toxicity + 0.9145 91.45%

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 93.89% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.14% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.44% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.00% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.41% 94.73%
CHEMBL4267 P37173 TGF-beta receptor type II 82.66% 88.18%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.08% 95.50%

Cross-Links

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PubChem 7165
NPASS NPC249912
LOTUS LTS0211245
wikiData Q421100