Benzyl methyl ether

Details

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Internal ID 03033cab-fa74-4d87-9f6a-9eabfec9dfb4
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzylethers
IUPAC Name methoxymethylbenzene
SMILES (Canonical) COCC1=CC=CC=C1
SMILES (Isomeric) COCC1=CC=CC=C1
InChI InChI=1S/C8H10O/c1-9-7-8-5-3-2-4-6-8/h2-6H,7H2,1H3
InChI Key GQKZBCPTCWJTAS-UHFFFAOYSA-N
Popularity 202 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 1.90
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(methoxymethyl)benzene
538-86-3
METHOXYMETHYLBENZENE
Methyl benzyl ether
Benzene, (methoxymethyl)-
Ether, benzyl methyl
alpha-Methoxytoluene
.alpha.-Methoxytoluene
1-(methoxymethyl)benzene
Benzylmethylether
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzyl methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9168 91.68%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5684 56.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9138 91.38%
P-glycoprotein inhibitior - 0.9928 99.28%
P-glycoprotein substrate - 0.9736 97.36%
CYP3A4 substrate - 0.7164 71.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3589 35.89%
CYP3A4 inhibition - 0.9834 98.34%
CYP2C9 inhibition - 0.9490 94.90%
CYP2C19 inhibition - 0.8173 81.73%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition + 0.5325 53.25%
CYP2C8 inhibition - 0.6622 66.22%
CYP inhibitory promiscuity - 0.8383 83.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6047 60.47%
Carcinogenicity (trinary) Non-required 0.4776 47.76%
Eye corrosion + 0.7204 72.04%
Eye irritation + 0.9908 99.08%
Skin irritation + 0.5939 59.39%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7068 70.68%
Micronuclear - 0.9341 93.41%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation + 0.8677 86.77%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5465 54.65%
Acute Oral Toxicity (c) III 0.8894 88.94%
Estrogen receptor binding - 0.9242 92.42%
Androgen receptor binding - 0.7706 77.06%
Thyroid receptor binding - 0.9204 92.04%
Glucocorticoid receptor binding - 0.9101 91.01%
Aromatase binding - 0.9036 90.36%
PPAR gamma - 0.9130 91.30%
Honey bee toxicity - 0.9286 92.86%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7068 70.68%

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 93.75% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.31% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.93% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.85% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.04% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.60% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.39% 99.17%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.34% 92.67%

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.
Crataegus pinnatifida
Gastrodia elata
Schisandra chinensis
Uvaria chamae

Cross-Links

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PubChem 10869
NPASS NPC292979
LOTUS LTS0250950
wikiData Q27277530