2-acetyloxyethyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate

Details

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Internal ID 733651c3-dd81-4915-8406-af62286518d8
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Coumaric acids and derivatives
IUPAC Name 2-acetyloxyethyl (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate
SMILES (Canonical) CC(=O)OCCOC(=O)C=CC1=CC(=C(C(=C1)OC)OC)OC
SMILES (Isomeric) CC(=O)OCCOC(=O)/C=C/C1=CC(=C(C(=C1)OC)OC)OC
InChI InChI=1S/C16H20O7/c1-11(17)22-7-8-23-15(18)6-5-12-9-13(19-2)16(21-4)14(10-12)20-3/h5-6,9-10H,7-8H2,1-4H3/b6-5+
InChI Key NHBLFEHDZKHAPC-AATRIKPKSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O7
Molecular Weight 324.32 g/mol
Exact Mass 324.12090297 g/mol
Topological Polar Surface Area (TPSA) 80.30 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-acetyloxyethyl (E)-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 + 0.9858 98.58%
Caco-2 + 0.7420 74.20%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8783 87.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9367 93.67%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6919 69.19%
P-glycoprotein inhibitior - 0.7360 73.60%
P-glycoprotein substrate - 0.9028 90.28%
CYP3A4 substrate - 0.5223 52.23%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.8644 86.44%
CYP3A4 inhibition - 0.7706 77.06%
CYP2C9 inhibition - 0.7761 77.61%
CYP2C19 inhibition + 0.5156 51.56%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition + 0.5210 52.10%
CYP2C8 inhibition + 0.6633 66.33%
CYP inhibitory promiscuity - 0.7885 78.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7171 71.71%
Carcinogenicity (trinary) Non-required 0.6187 61.87%
Eye corrosion - 0.9774 97.74%
Eye irritation - 0.7704 77.04%
Skin irritation - 0.8670 86.70%
Skin corrosion - 0.9831 98.31%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3682 36.82%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.7350 73.50%
skin sensitisation - 0.7566 75.66%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6530 65.30%
Acute Oral Toxicity (c) III 0.7000 70.00%
Estrogen receptor binding + 0.8439 84.39%
Androgen receptor binding + 0.5898 58.98%
Thyroid receptor binding + 0.6185 61.85%
Glucocorticoid receptor binding - 0.5179 51.79%
Aromatase binding + 0.7478 74.78%
PPAR gamma - 0.7480 74.80%
Honey bee toxicity - 0.8729 87.29%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9511 95.11%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.42% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.41% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.35% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.89% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.16% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.92% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.84% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.79% 95.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.77% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 80.90% 94.73%

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 23656803
LOTUS LTS0132074
wikiData Q105179290