4-(4-Hydroxy-3,5-dimethoxyphenyl)-3-buten-2-one

Details

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Internal ID dfb72dd3-6f5e-42c5-b642-ca376d797a1b
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives
IUPAC Name 4-(4-hydroxy-3,5-dimethoxyphenyl)but-3-en-2-one
SMILES (Canonical) CC(=O)C=CC1=CC(=C(C(=C1)OC)O)OC
SMILES (Isomeric) CC(=O)C=CC1=CC(=C(C(=C1)OC)O)OC
InChI InChI=1S/C12H14O4/c1-8(13)4-5-9-6-10(15-2)12(14)11(7-9)16-3/h4-7,14H,1-3H3
InChI Key OOFWCWCUKUVTKD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H14O4
Molecular Weight 222.24 g/mol
Exact Mass 222.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.01
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(4-Hydroxy-3,5-dimethoxyphenyl)-3-buten-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 + 0.9919 99.19%
Caco-2 + 0.6736 67.36%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8103 81.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9160 91.60%
OATP1B3 inhibitior + 0.9799 97.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6406 64.06%
P-glycoprotein inhibitior - 0.9520 95.20%
P-glycoprotein substrate - 0.9250 92.50%
CYP3A4 substrate - 0.6315 63.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8042 80.42%
CYP3A4 inhibition - 0.6527 65.27%
CYP2C9 inhibition - 0.9894 98.94%
CYP2C19 inhibition - 0.7557 75.57%
CYP2D6 inhibition - 0.9317 93.17%
CYP1A2 inhibition - 0.7057 70.57%
CYP2C8 inhibition - 0.6163 61.63%
CYP inhibitory promiscuity - 0.6951 69.51%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7825 78.25%
Carcinogenicity (trinary) Non-required 0.6474 64.74%
Eye corrosion - 0.5587 55.87%
Eye irritation + 0.9780 97.80%
Skin irritation + 0.5342 53.42%
Skin corrosion - 0.9686 96.86%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8020 80.20%
Micronuclear + 0.5233 52.33%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.7483 74.83%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5977 59.77%
Acute Oral Toxicity (c) III 0.6111 61.11%
Estrogen receptor binding + 0.5879 58.79%
Androgen receptor binding - 0.5906 59.06%
Thyroid receptor binding - 0.5551 55.51%
Glucocorticoid receptor binding - 0.7198 71.98%
Aromatase binding - 0.6288 62.88%
PPAR gamma - 0.5315 53.15%
Honey bee toxicity - 0.8912 89.12%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9324 93.24%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.82% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.41% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.35% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.85% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.94% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.41% 89.00%
CHEMBL3194 P02766 Transthyretin 83.23% 90.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.68% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.95% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.49% 94.73%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 80.03% 98.21%

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.
Isatis tinctoria

Cross-Links

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PubChem 71350958
LOTUS LTS0174786
wikiData Q105195354