Phenetole

Details

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Internal ID 57b3cee0-8011-4674-9bc1-176b9eae9274
Taxonomy Benzenoids > Phenol ethers
IUPAC Name ethoxybenzene
SMILES (Canonical) CCOC1=CC=CC=C1
SMILES (Isomeric) CCOC1=CC=CC=C1
InChI InChI=1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI Key DLRJIFUOBPOJNS-UHFFFAOYSA-N
Popularity 801 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O
Molecular Weight 122.16 g/mol
Exact Mass 122.073164938 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Ethoxybenzene
103-73-1
Benzene, ethoxy-
Ethyl phenyl ether
Phenyl ethyl ether
Phenetol
Benzene, ethoxy
Phenoxyethane
A Phenoxyethane
Ether, ethyl phenyl
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Phenetole

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 + 0.9375 93.75%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7867 78.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9640 96.40%
OATP1B3 inhibitior + 0.9654 96.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8986 89.86%
P-glycoprotein inhibitior - 0.9940 99.40%
P-glycoprotein substrate - 0.9835 98.35%
CYP3A4 substrate - 0.6689 66.89%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate + 0.3972 39.72%
CYP3A4 inhibition - 0.9769 97.69%
CYP2C9 inhibition - 0.9249 92.49%
CYP2C19 inhibition - 0.6187 61.87%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition + 0.9317 93.17%
CYP2C8 inhibition - 0.7357 73.57%
CYP inhibitory promiscuity + 0.5257 52.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5958 59.58%
Carcinogenicity (trinary) Warning 0.5146 51.46%
Eye corrosion + 0.8494 84.94%
Eye irritation + 0.9922 99.22%
Skin irritation + 0.5455 54.55%
Skin corrosion - 0.8864 88.64%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6720 67.20%
Micronuclear - 0.9319 93.19%
Hepatotoxicity + 0.6526 65.26%
skin sensitisation + 0.8518 85.18%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.7627 76.27%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6339 63.39%
Acute Oral Toxicity (c) III 0.8919 89.19%
Estrogen receptor binding - 0.8861 88.61%
Androgen receptor binding - 0.7776 77.76%
Thyroid receptor binding - 0.8910 89.10%
Glucocorticoid receptor binding - 0.9203 92.03%
Aromatase binding - 0.8890 88.90%
PPAR gamma - 0.8753 87.53%
Honey bee toxicity - 0.9222 92.22%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.7982 79.82%

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 88.54% 90.17%
CHEMBL2581 P07339 Cathepsin D 88.39% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.05% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.92% 94.73%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.81% 94.62%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 85.64% 92.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.62% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.93% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.46% 99.17%

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.
Prunus persica
Scutellaria barbata

Cross-Links

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PubChem 7674
NPASS NPC299571
LOTUS LTS0012327
wikiData Q419340