Methoxymethane;2-methoxy-4-prop-2-enylphenol

Details

Top
Internal ID f7af6ba9-786f-4abe-abab-8320db9ef1c0
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name methoxymethane;2-methoxy-4-prop-2-enylphenol
SMILES (Canonical) COC.COC1=C(C=CC(=C1)CC=C)O
SMILES (Isomeric) COC.COC1=C(C=CC(=C1)CC=C)O
InChI InChI=1S/C10H12O2.C2H6O/c1-3-4-8-5-6-9(11)10(7-8)12-2;1-3-2/h3,5-7,11H,1,4H2,2H3;1-2H3
InChI Key RAXFJUTZIXCEPR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H18O3
Molecular Weight 210.27 g/mol
Exact Mass 210.125594432 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 0.00
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methoxymethane;2-methoxy-4-prop-2-enylphenol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.7512 75.12%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8694 86.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9237 92.37%
P-glycoprotein inhibitior - 0.9775 97.75%
P-glycoprotein substrate - 0.9201 92.01%
CYP3A4 substrate - 0.6231 62.31%
CYP2C9 substrate - 0.6075 60.75%
CYP2D6 substrate + 0.4421 44.21%
CYP3A4 inhibition - 0.5604 56.04%
CYP2C9 inhibition - 0.8762 87.62%
CYP2C19 inhibition - 0.5471 54.71%
CYP2D6 inhibition - 0.8391 83.91%
CYP1A2 inhibition - 0.6253 62.53%
CYP2C8 inhibition + 0.8149 81.49%
CYP inhibitory promiscuity - 0.6283 62.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7521 75.21%
Carcinogenicity (trinary) Non-required 0.6619 66.19%
Eye corrosion - 0.7127 71.27%
Eye irritation + 0.9919 99.19%
Skin irritation - 0.6209 62.09%
Skin corrosion - 0.8033 80.33%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7061 70.61%
Micronuclear - 0.8126 81.26%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.5632 56.32%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7867 78.67%
Acute Oral Toxicity (c) III 0.8138 81.38%
Estrogen receptor binding - 0.5513 55.13%
Androgen receptor binding - 0.8337 83.37%
Thyroid receptor binding - 0.8268 82.68%
Glucocorticoid receptor binding - 0.8509 85.09%
Aromatase binding - 0.7880 78.80%
PPAR gamma - 0.5879 58.79%
Honey bee toxicity - 0.8637 86.37%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9524 95.24%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.34% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.42% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.78% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.54% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.26% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 89.18% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.06% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 87.56% 90.20%
CHEMBL4208 P20618 Proteasome component C5 86.09% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.96% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.42% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.89% 95.50%
CHEMBL1951 P21397 Monoamine oxidase A 80.56% 91.49%

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.
There are no matching plants.

Cross-Links

Top
PubChem 21972505
NPASS NPC14930