3,4-Dimethoxy-6-(2-phenylethenyl)pyran-2-one

Details

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Internal ID 45c5bf9f-14b8-4ef3-b14c-581d29526f9b
Taxonomy Phenylpropanoids and polyketides > Kavalactones
IUPAC Name 3,4-dimethoxy-6-(2-phenylethenyl)pyran-2-one
SMILES (Canonical) COC1=C(C(=O)OC(=C1)C=CC2=CC=CC=C2)OC
SMILES (Isomeric) COC1=C(C(=O)OC(=C1)C=CC2=CC=CC=C2)OC
InChI InChI=1S/C15H14O4/c1-17-13-10-12(19-15(16)14(13)18-2)9-8-11-6-4-3-5-7-11/h3-10H,1-2H3
InChI Key ABRZDKKKCLXJFO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4-Dimethoxy-6-(2-phenylethenyl)pyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 + 0.9224 92.24%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7226 72.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9853 98.53%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5625 56.25%
P-glycoprotein inhibitior + 0.6504 65.04%
P-glycoprotein substrate - 0.9541 95.41%
CYP3A4 substrate - 0.5629 56.29%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.8582 85.82%
CYP3A4 inhibition - 0.5494 54.94%
CYP2C9 inhibition - 0.9177 91.77%
CYP2C19 inhibition + 0.8364 83.64%
CYP2D6 inhibition - 0.9133 91.33%
CYP1A2 inhibition + 0.7552 75.52%
CYP2C8 inhibition + 0.6263 62.63%
CYP inhibitory promiscuity + 0.8587 85.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.5208 52.08%
Eye corrosion - 0.9346 93.46%
Eye irritation - 0.6080 60.80%
Skin irritation - 0.7073 70.73%
Skin corrosion - 0.9829 98.29%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6595 65.95%
Micronuclear + 0.7459 74.59%
Hepatotoxicity + 0.5908 59.08%
skin sensitisation - 0.8928 89.28%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7184 71.84%
Acute Oral Toxicity (c) II 0.4862 48.62%
Estrogen receptor binding + 0.8403 84.03%
Androgen receptor binding + 0.7768 77.68%
Thyroid receptor binding - 0.6169 61.69%
Glucocorticoid receptor binding - 0.6523 65.23%
Aromatase binding + 0.7415 74.15%
PPAR gamma - 0.6325 63.25%
Honey bee toxicity - 0.8827 88.27%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9716 97.16%

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 97.54% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.06% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.12% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.95% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.48% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.11% 95.50%
CHEMBL2581 P07339 Cathepsin D 84.82% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.53% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 83.34% 94.73%
CHEMBL2535 P11166 Glucose transporter 82.76% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.91% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.69% 94.03%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.32% 100.00%

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.
Miliusa balansae

Cross-Links

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PubChem 86210813
LOTUS LTS0107778
wikiData Q104908794