5,7-Dimethoxy-8-(3-oxobut-1-enyl)chromen-2-one

Details

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Internal ID 60846a55-e3d8-4c46-83e9-1b99ed146c97
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5,7-dimethoxy-8-(3-oxobut-1-enyl)chromen-2-one
SMILES (Canonical) CC(=O)C=CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC
SMILES (Isomeric) CC(=O)C=CC1=C(C=C(C2=C1OC(=O)C=C2)OC)OC
InChI InChI=1S/C15H14O5/c1-9(16)4-5-10-12(18-2)8-13(19-3)11-6-7-14(17)20-15(10)11/h4-8H,1-3H3
InChI Key MNCJDGPGSIIWJA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 5
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 5,7-Dimethoxy-8-(3-oxobut-1-enyl)chromen-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 + 0.9860 98.60%
Caco-2 + 0.8129 81.29%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6156 61.56%
OATP2B1 inhibitior - 0.8656 86.56%
OATP1B1 inhibitior + 0.9366 93.66%
OATP1B3 inhibitior + 0.9908 99.08%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5100 51.00%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.8377 83.77%
CYP3A4 substrate - 0.5409 54.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.6456 64.56%
CYP2C9 inhibition - 0.8987 89.87%
CYP2C19 inhibition - 0.8719 87.19%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition + 0.9067 90.67%
CYP2C8 inhibition - 0.5631 56.31%
CYP inhibitory promiscuity + 0.6291 62.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Danger 0.4385 43.85%
Eye corrosion - 0.9709 97.09%
Eye irritation - 0.6017 60.17%
Skin irritation - 0.7908 79.08%
Skin corrosion - 0.9818 98.18%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3869 38.69%
Micronuclear + 0.7559 75.59%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9227 92.27%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6627 66.27%
Acute Oral Toxicity (c) II 0.7142 71.42%
Estrogen receptor binding + 0.7123 71.23%
Androgen receptor binding + 0.8342 83.42%
Thyroid receptor binding - 0.5976 59.76%
Glucocorticoid receptor binding + 0.6586 65.86%
Aromatase binding + 0.6989 69.89%
PPAR gamma + 0.5997 59.97%
Honey bee toxicity - 0.8549 85.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9881 98.81%

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 95.47% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.98% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.21% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.51% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.87% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.59% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.25% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.50% 94.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.74% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 80.66% 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.
Murraya paniculata
Toddalia asiatica

Cross-Links

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PubChem 86232416
LOTUS LTS0257110
wikiData Q105168275