Butyl Benzoate

Details

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Internal ID 4434ffad-aea2-4de6-a71c-02a964bdfd32
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name butyl benzoate
SMILES (Canonical) CCCCOC(=O)C1=CC=CC=C1
SMILES (Isomeric) CCCCOC(=O)C1=CC=CC=C1
InChI InChI=1S/C11H14O2/c1-2-3-9-13-11(12)10-7-5-4-6-8-10/h4-8H,2-3,9H2,1H3
InChI Key XSIFPSYPOVKYCO-UHFFFAOYSA-N
Popularity 342 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O2
Molecular Weight 178.23 g/mol
Exact Mass 178.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.80
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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136-60-7
n-Butyl benzoate
Benzoic acid, butyl ester
Anthrapole AZ
Benzoic Acid Butyl Ester
Dai Cari XBN
Benzoic acid n-butyl ester
Butylester kyseliny benzoove
NSC 8474
HSDB 2089
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butyl 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 + 0.9816 98.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5654 56.54%
OATP2B1 inhibitior - 0.8688 86.88%
OATP1B1 inhibitior + 0.9281 92.81%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9201 92.01%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9552 95.52%
CYP3A4 substrate - 0.6660 66.60%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8123 81.23%
CYP3A4 inhibition - 0.9523 95.23%
CYP2C9 inhibition - 0.8690 86.90%
CYP2C19 inhibition + 0.5285 52.85%
CYP2D6 inhibition - 0.9238 92.38%
CYP1A2 inhibition + 0.8600 86.00%
CYP2C8 inhibition + 0.4540 45.40%
CYP inhibitory promiscuity - 0.7688 76.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.5463 54.63%
Eye corrosion + 0.7081 70.81%
Eye irritation + 0.9919 99.19%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9373 93.73%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6837 68.37%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.6321 63.21%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5194 51.94%
Acute Oral Toxicity (c) III 0.9186 91.86%
Estrogen receptor binding - 0.7126 71.26%
Androgen receptor binding - 0.5227 52.27%
Thyroid receptor binding - 0.6836 68.36%
Glucocorticoid receptor binding - 0.9435 94.35%
Aromatase binding - 0.8395 83.95%
PPAR gamma - 0.7007 70.07%
Honey bee toxicity - 0.9967 99.67%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9421 94.21%

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
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.34% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.45% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.43% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.75% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.33% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.39% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.37% 94.62%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.36% 92.08%

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.
Glycyrrhiza
Hamamelis virginiana
Spondias mombin

Cross-Links

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PubChem 8698
NPASS NPC276775
LOTUS LTS0062336
wikiData Q818506