(2-Methoxyethyl)benzene

Details

Top
Internal ID f98e1ecc-10f8-4a39-9cd1-f936d91df81a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-methoxyethylbenzene
SMILES (Canonical) COCCC1=CC=CC=C1
SMILES (Isomeric) COCCC1=CC=CC=C1
InChI InChI=1S/C9H12O/c1-10-8-7-9-5-3-2-4-6-9/h2-6H,7-8H2,1H3
InChI Key CQLYXIUHVFRXLT-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O
Molecular Weight 136.19 g/mol
Exact Mass 136.088815002 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
3558-60-9
2-methoxyethylbenzene
Methyl phenethyl ether
2-Phenylethyl methyl ether
Benzene, (2-methoxyethyl)-
Phenylethyl methyl ether
Methyl phenylethyl ether
Kewda ether
Methyl phenethyl oxide
ETHER, METHYL PHENETHYL
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of (2-Methoxyethyl)benzene

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9335 93.35%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5376 53.76%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8535 85.35%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9187 91.87%
CYP3A4 substrate - 0.6789 67.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4397 43.97%
CYP3A4 inhibition - 0.9758 97.58%
CYP2C9 inhibition - 0.9522 95.22%
CYP2C19 inhibition - 0.7679 76.79%
CYP2D6 inhibition - 0.9360 93.60%
CYP1A2 inhibition + 0.5318 53.18%
CYP2C8 inhibition - 0.6661 66.61%
CYP inhibitory promiscuity - 0.8960 89.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7620 76.20%
Carcinogenicity (trinary) Non-required 0.5362 53.62%
Eye corrosion + 0.6721 67.21%
Eye irritation + 0.9919 99.19%
Skin irritation + 0.7235 72.35%
Skin corrosion - 0.9731 97.31%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6985 69.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation + 0.7216 72.16%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6941 69.41%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.6003 60.03%
Acute Oral Toxicity (c) III 0.8916 89.16%
Estrogen receptor binding - 0.8599 85.99%
Androgen receptor binding - 0.7913 79.13%
Thyroid receptor binding - 0.9016 90.16%
Glucocorticoid receptor binding - 0.9176 91.76%
Aromatase binding - 0.9273 92.73%
PPAR gamma - 0.8893 88.93%
Honey bee toxicity - 0.8525 85.25%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.4077 40.77%

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 94.63% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.92% 94.62%
CHEMBL2581 P07339 Cathepsin D 92.47% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 88.28% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.92% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 85.29% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 84.02% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 81.64% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.31% 95.56%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

Top
PubChem 19089
NPASS NPC6184