4-Ethylphenyl acetate

Details

Top
Internal ID eeacd34c-8a84-4c48-be63-2260975e378e
Taxonomy Benzenoids > Phenol esters
IUPAC Name (4-ethylphenyl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H12O2/c1-3-9-4-6-10(7-5-9)12-8(2)11/h4-7H,3H2,1-2H3
InChI Key ANMYMLIUCWWISO-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
3245-23-6
Acetic Acid 4-Ethylphenyl Ester
(4-ethylphenyl) acetate
p-Ethylphenyl acetate
Phenol, 4-ethyl-, acetate
Phenol, 4-ethyl-, 1-acetate
3F8A85YM2Z
NSC-6705
MFCD00026970
NSC 6705
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 4-Ethylphenyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9414 94.14%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8702 87.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9616 96.16%
OATP1B3 inhibitior + 0.9615 96.15%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8021 80.21%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9760 97.60%
CYP3A4 substrate - 0.6497 64.97%
CYP2C9 substrate - 0.6120 61.20%
CYP2D6 substrate - 0.8350 83.50%
CYP3A4 inhibition - 0.9634 96.34%
CYP2C9 inhibition - 0.8929 89.29%
CYP2C19 inhibition - 0.7779 77.79%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition + 0.7386 73.86%
CYP2C8 inhibition - 0.8615 86.15%
CYP inhibitory promiscuity - 0.6758 67.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5543 55.43%
Carcinogenicity (trinary) Non-required 0.5659 56.59%
Eye corrosion + 0.8419 84.19%
Eye irritation + 0.9845 98.45%
Skin irritation + 0.6528 65.28%
Skin corrosion - 0.8965 89.65%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5967 59.67%
Micronuclear - 0.8067 80.67%
Hepatotoxicity + 0.5160 51.60%
skin sensitisation + 0.8149 81.49%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.5546 55.46%
Acute Oral Toxicity (c) III 0.9297 92.97%
Estrogen receptor binding - 0.7586 75.86%
Androgen receptor binding - 0.6624 66.24%
Thyroid receptor binding - 0.8409 84.09%
Glucocorticoid receptor binding - 0.8261 82.61%
Aromatase binding - 0.7171 71.71%
PPAR gamma - 0.8225 82.25%
Honey bee toxicity - 0.8042 80.42%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9226 92.26%

Targets

Top

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 96.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.47% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.73% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.06% 94.45%
CHEMBL4208 P20618 Proteasome component C5 85.35% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.30% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.34% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.08% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.54% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 80.93% 94.73%

Plants that contains it

Top
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.
Leptolejeunea elliptica

Cross-Links

Top
PubChem 76731
LOTUS LTS0185728
wikiData Q82854428