Methyl 3-(2-ethenyl-4-methoxyphenyl)propanoate

Details

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Internal ID 2e1ddbfa-ef19-414d-b274-f8da51a8e750
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name methyl 3-(2-ethenyl-4-methoxyphenyl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O3/c1-4-10-9-12(15-2)7-5-11(10)6-8-13(14)16-3/h4-5,7,9H,1,6,8H2,2-3H3
InChI Key JPWMMPGBDKWYPX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O3
Molecular Weight 220.26 g/mol
Exact Mass 220.109944368 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.44
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-(2-ethenyl-4-methoxyphenyl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9255 92.55%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8810 88.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8947 89.47%
OATP1B3 inhibitior + 0.9596 95.96%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7898 78.98%
P-glycoprotein inhibitior - 0.9607 96.07%
P-glycoprotein substrate - 0.8341 83.41%
CYP3A4 substrate - 0.5562 55.62%
CYP2C9 substrate - 0.5969 59.69%
CYP2D6 substrate - 0.7822 78.22%
CYP3A4 inhibition - 0.7559 75.59%
CYP2C9 inhibition - 0.9111 91.11%
CYP2C19 inhibition - 0.6167 61.67%
CYP2D6 inhibition - 0.9151 91.51%
CYP1A2 inhibition - 0.5764 57.64%
CYP2C8 inhibition - 0.7660 76.60%
CYP inhibitory promiscuity - 0.6096 60.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7036 70.36%
Carcinogenicity (trinary) Non-required 0.6599 65.99%
Eye corrosion - 0.8553 85.53%
Eye irritation + 0.8859 88.59%
Skin irritation - 0.6537 65.37%
Skin corrosion - 0.9736 97.36%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5598 55.98%
Micronuclear - 0.8915 89.15%
Hepatotoxicity - 0.6439 64.39%
skin sensitisation - 0.7922 79.22%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.7719 77.19%
Acute Oral Toxicity (c) III 0.8341 83.41%
Estrogen receptor binding - 0.5795 57.95%
Androgen receptor binding - 0.5492 54.92%
Thyroid receptor binding - 0.6713 67.13%
Glucocorticoid receptor binding - 0.6836 68.36%
Aromatase binding - 0.5774 57.74%
PPAR gamma - 0.7585 75.85%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9825 98.25%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.64% 96.09%
CHEMBL4208 P20618 Proteasome component C5 93.63% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.33% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 90.83% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.79% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.77% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.43% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.19% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.64% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.59% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.75% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.71% 85.14%

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.
Gutierrezia solbrigii

Cross-Links

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PubChem 86144000
LOTUS LTS0258292
wikiData Q105133355