Benzyl acetate

Details

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Internal ID d42bb4e9-6233-4bae-a50f-3be6adcead23
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyloxycarbonyls
IUPAC Name benzyl acetate
SMILES (Canonical) CC(=O)OCC1=CC=CC=C1
SMILES (Isomeric) CC(=O)OCC1=CC=CC=C1
InChI InChI=1S/C9H10O2/c1-8(10)11-7-9-5-3-2-4-6-9/h2-6H,7H2,1H3
InChI Key QUKGYYKBILRGFE-UHFFFAOYSA-N
Popularity 1,265 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 2.00
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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140-11-4
Benzyl ethanoate
Phenylmethyl acetate
Acetic acid benzyl ester
Acetic acid, phenylmethyl ester
Acetic acid, benzyl ester
Phenylmethyl ethanoate
alpha-Acetoxytoluene
benzylacetate
(Acetoxymethyl)benzene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzyl acetate

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 + 0.5964 59.64%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7946 79.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9490 94.90%
OATP1B3 inhibitior + 0.9608 96.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7254 72.54%
P-glycoprotein inhibitior - 0.9913 99.13%
P-glycoprotein substrate - 0.9899 98.99%
CYP3A4 substrate - 0.6911 69.11%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition - 0.9785 97.85%
CYP2C9 inhibition - 0.9360 93.60%
CYP2C19 inhibition - 0.8875 88.75%
CYP2D6 inhibition - 0.9449 94.49%
CYP1A2 inhibition + 0.7161 71.61%
CYP2C8 inhibition - 0.8693 86.93%
CYP inhibitory promiscuity - 0.8211 82.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5656 56.56%
Carcinogenicity (trinary) Non-required 0.7370 73.70%
Eye corrosion + 0.8853 88.53%
Eye irritation + 0.9702 97.02%
Skin irritation + 0.9147 91.47%
Skin corrosion - 0.9090 90.90%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7102 71.02%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation + 0.6174 61.74%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5695 56.95%
Acute Oral Toxicity (c) III 0.8584 85.84%
Estrogen receptor binding - 0.8682 86.82%
Androgen receptor binding - 0.7264 72.64%
Thyroid receptor binding - 0.9361 93.61%
Glucocorticoid receptor binding - 0.9046 90.46%
Aromatase binding - 0.7326 73.26%
PPAR gamma - 0.8904 89.04%
Honey bee toxicity - 0.9617 96.17%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6455 64.55%
Fish aquatic toxicity + 0.9404 94.04%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 19952.6 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.39% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.12% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.11% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.86% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.76% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.94% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 85.10% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 84.55% 94.73%

Cross-Links

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PubChem 8785
NPASS NPC58616
ChEMBL CHEMBL1233714
LOTUS LTS0185985
wikiData Q424223