(2E)-3-(4-methoxyphenyl)prop-2-en-1-yl (2Z)-2-methylbut-2-enoate

Details

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Internal ID 9cedb2bd-e19e-4da6-a518-e990cae22d7e
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name [(E)-3-(4-methoxyphenyl)prop-2-enyl] (Z)-2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O3/c1-4-12(2)15(16)18-11-5-6-13-7-9-14(17-3)10-8-13/h4-10H,11H2,1-3H3/b6-5+,12-4-
InChI Key MZKARNAOCAPDSD-HSZUAVIASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O3
Molecular Weight 246.30 g/mol
Exact Mass 246.125594432 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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CHEMBL4174692
2-butenoic acid, 2-methyl-, (2E)-3-(4-methoxyphenyl)-2-propenyl ester, (2Z)-
InChI=1/C15H18O3/c1-4-12(2)15(16)18-11-5-6-13-7-9-14(17-3)10-8-13/h4-10H,11H2,1-3H3/b6-5+,12-4

2D Structure

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2D Structure of (2E)-3-(4-methoxyphenyl)prop-2-en-1-yl (2Z)-2-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 + 0.9972 99.72%
Caco-2 + 0.9247 92.47%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8855 88.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9000 90.00%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8000 80.00%
P-glycoprotein inhibitior - 0.8963 89.63%
P-glycoprotein substrate - 0.9634 96.34%
CYP3A4 substrate - 0.5409 54.09%
CYP2C9 substrate - 0.6211 62.11%
CYP2D6 substrate - 0.8581 85.81%
CYP3A4 inhibition - 0.8373 83.73%
CYP2C9 inhibition - 0.9225 92.25%
CYP2C19 inhibition - 0.7806 78.06%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition + 0.6128 61.28%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity + 0.6554 65.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6365 63.65%
Carcinogenicity (trinary) Non-required 0.6212 62.12%
Eye corrosion - 0.9458 94.58%
Eye irritation + 0.5779 57.79%
Skin irritation - 0.7477 74.77%
Skin corrosion - 0.9938 99.38%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7537 75.37%
Micronuclear - 0.6541 65.41%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.5858 58.58%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.6031 60.31%
Acute Oral Toxicity (c) III 0.8204 82.04%
Estrogen receptor binding + 0.7805 78.05%
Androgen receptor binding + 0.6718 67.18%
Thyroid receptor binding - 0.5923 59.23%
Glucocorticoid receptor binding - 0.6682 66.82%
Aromatase binding + 0.7747 77.47%
PPAR gamma - 0.9366 93.66%
Honey bee toxicity - 0.9238 92.38%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9599 95.99%

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 96.35% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.60% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.18% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.72% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.32% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.26% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.01% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.59% 95.50%

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.
Morina chinensis

Cross-Links

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PubChem 643822
LOTUS LTS0129636
wikiData Q105175716