(3-Methoxyphenyl) 3-(3,4,5-trimethoxyphenyl)prop-2-enoate

Details

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Internal ID 4fb17a69-64a1-4c07-9a52-2c8a03088cdc
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name (3-methoxyphenyl) 3-(3,4,5-trimethoxyphenyl)prop-2-enoate
SMILES (Canonical) COC1=CC(=CC=C1)OC(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC
SMILES (Isomeric) COC1=CC(=CC=C1)OC(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC
InChI InChI=1S/C19H20O6/c1-21-14-6-5-7-15(12-14)25-18(20)9-8-13-10-16(22-2)19(24-4)17(11-13)23-3/h5-12H,1-4H3
InChI Key MVWHPKDQHSIMPR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O6
Molecular Weight 344.40 g/mol
Exact Mass 344.12598835 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3-Methoxyphenyl) 3-(3,4,5-trimethoxyphenyl)prop-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 + 0.9944 99.44%
Caco-2 + 0.8797 87.97%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7974 79.74%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9562 95.62%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7710 77.10%
P-glycoprotein inhibitior + 0.7375 73.75%
P-glycoprotein substrate - 0.9367 93.67%
CYP3A4 substrate - 0.5134 51.34%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.8434 84.34%
CYP3A4 inhibition - 0.5407 54.07%
CYP2C9 inhibition - 0.9510 95.10%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9585 95.85%
CYP1A2 inhibition + 0.7597 75.97%
CYP2C8 inhibition + 0.7136 71.36%
CYP inhibitory promiscuity + 0.7482 74.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7514 75.14%
Carcinogenicity (trinary) Non-required 0.5035 50.35%
Eye corrosion - 0.9627 96.27%
Eye irritation - 0.6088 60.88%
Skin irritation - 0.8399 83.99%
Skin corrosion - 0.9925 99.25%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4289 42.89%
Micronuclear + 0.5707 57.07%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9241 92.41%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.5725 57.25%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.6463 64.63%
Acute Oral Toxicity (c) III 0.5384 53.84%
Estrogen receptor binding + 0.9469 94.69%
Androgen receptor binding + 0.6463 64.63%
Thyroid receptor binding + 0.7948 79.48%
Glucocorticoid receptor binding + 0.8468 84.68%
Aromatase binding + 0.7153 71.53%
PPAR gamma + 0.6196 61.96%
Honey bee toxicity - 0.8102 81.02%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5845 58.45%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.23% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.74% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.33% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.94% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.68% 91.11%
CHEMBL2535 P11166 Glucose transporter 89.23% 98.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 85.17% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.10% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 83.16% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.01% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.17% 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.
Oxalis pes-caprae

Cross-Links

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PubChem 73103092
LOTUS LTS0228548
wikiData Q105173387