2-(4-Methoxyphenyl)ethyl 3-methylbut-2-enoate

Details

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Internal ID cc5f4ff1-c2b2-4964-a74f-eee314e07aec
Taxonomy Benzenoids > Phenols > Tyrosols and derivatives
IUPAC Name 2-(4-methoxyphenyl)ethyl 3-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H18O3/c1-11(2)10-14(15)17-9-8-12-4-6-13(16-3)7-5-12/h4-7,10H,8-9H2,1-3H3
InChI Key DTBNLWLTBZIUPM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.75
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 2-(4-Methoxyphenyl)ethyl 3-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9709 97.09%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.9326 93.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.9535 95.35%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6049 60.49%
P-glycoprotein inhibitior - 0.8998 89.98%
P-glycoprotein substrate - 0.8825 88.25%
CYP3A4 substrate - 0.5198 51.98%
CYP2C9 substrate - 0.5788 57.88%
CYP2D6 substrate - 0.8748 87.48%
CYP3A4 inhibition - 0.8573 85.73%
CYP2C9 inhibition - 0.8514 85.14%
CYP2C19 inhibition - 0.5422 54.22%
CYP2D6 inhibition - 0.9058 90.58%
CYP1A2 inhibition + 0.6401 64.01%
CYP2C8 inhibition - 0.7584 75.84%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7099 70.99%
Carcinogenicity (trinary) Non-required 0.6137 61.37%
Eye corrosion - 0.9392 93.92%
Eye irritation + 0.9180 91.80%
Skin irritation - 0.8796 87.96%
Skin corrosion - 0.9930 99.30%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4798 47.98%
Micronuclear - 0.8667 86.67%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.6931 69.31%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7900 79.00%
Acute Oral Toxicity (c) III 0.6048 60.48%
Estrogen receptor binding - 0.5786 57.86%
Androgen receptor binding + 0.8166 81.66%
Thyroid receptor binding - 0.5711 57.11%
Glucocorticoid receptor binding + 0.5890 58.90%
Aromatase binding - 0.6194 61.94%
PPAR gamma - 0.8193 81.93%
Honey bee toxicity - 0.9082 90.82%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8943 89.43%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.04% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.25% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.95% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.73% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.23% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.97% 96.00%
CHEMBL4208 P20618 Proteasome component C5 87.90% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.63% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.26% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.67% 96.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.41% 94.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.71% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.65% 86.92%

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.
Othonna obtusiloba

Cross-Links

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PubChem 86150026
LOTUS LTS0201257
wikiData Q104988172