Allyl benzoate

Details

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Internal ID e9600576-511c-4d91-bbed-1a970088b089
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name prop-2-enyl benzoate
SMILES (Canonical) C=CCOC(=O)C1=CC=CC=C1
SMILES (Isomeric) C=CCOC(=O)C1=CC=CC=C1
InChI InChI=1S/C10H10O2/c1-2-8-12-10(11)9-6-4-3-5-7-9/h2-7H,1,8H2
InChI Key LYJHVEDILOKZCG-UHFFFAOYSA-N
Popularity 90 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O2
Molecular Weight 162.18 g/mol
Exact Mass 162.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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583-04-0
Benzoic acid, 2-propenyl ester
prop-2-enyl benzoate
Benzoic acid, allyl ester
2-Propenyl benzoate
Benzoic Acid Allyl Ester
prop-2-en-1-yl benzoate
ALLYLBENZOATE
UNII-AQY5543KFE
AQY5543KFE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Allyl benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.8909 89.09%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5744 57.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9456 94.56%
OATP1B3 inhibitior + 0.9620 96.20%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8327 83.27%
P-glycoprotein inhibitior - 0.9866 98.66%
P-glycoprotein substrate - 0.9933 99.33%
CYP3A4 substrate - 0.7200 72.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8236 82.36%
CYP3A4 inhibition - 0.9127 91.27%
CYP2C9 inhibition - 0.9031 90.31%
CYP2C19 inhibition - 0.6943 69.43%
CYP2D6 inhibition - 0.9442 94.42%
CYP1A2 inhibition + 0.5875 58.75%
CYP2C8 inhibition + 0.5589 55.89%
CYP inhibitory promiscuity - 0.6561 65.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5184 51.84%
Carcinogenicity (trinary) Non-required 0.6972 69.72%
Eye corrosion + 0.8810 88.10%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8886 88.86%
Skin corrosion - 0.7924 79.24%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8137 81.37%
Micronuclear - 0.9141 91.41%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation + 0.9414 94.14%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5331 53.31%
Acute Oral Toxicity (c) III 0.8614 86.14%
Estrogen receptor binding - 0.7494 74.94%
Androgen receptor binding - 0.7646 76.46%
Thyroid receptor binding - 0.7648 76.48%
Glucocorticoid receptor binding - 0.9388 93.88%
Aromatase binding - 0.5326 53.26%
PPAR gamma - 0.7528 75.28%
Honey bee toxicity - 0.9395 93.95%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.6951 69.51%
Fish aquatic toxicity + 0.9793 97.93%

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
CHEMBL240 Q12809 HERG 98.87% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.28% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.17% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.55% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.82% 99.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.16% 94.62%
CHEMBL4267 P37173 TGF-beta receptor type II 80.34% 88.18%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Styrax benzoin

Cross-Links

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PubChem 11406
NPASS NPC270403