7-Methoxy-6-(3-methylbut-2-enoxy)chromen-2-one

Details

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Internal ID 4c0e0017-e5e7-4772-a731-425912a2a7bd
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-6-(3-methylbut-2-enoxy)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O4/c1-10(2)6-7-18-14-8-11-4-5-15(16)19-12(11)9-13(14)17-3/h4-6,8-9H,7H2,1-3H3
InChI Key TVQVDZKWITZCIB-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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16712-77-9
7-Methoxy-6-[(3-methyl-2-buten-1-yl)oxy]-2H-1-benzopyran-2-one
6-prenyloxy-7-methoxycoumarin
SCHEMBL18292782
AKOS000277619

2D Structure

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2D Structure of 7-Methoxy-6-(3-methylbut-2-enoxy)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 + 0.9910 99.10%
Caco-2 + 0.9550 95.50%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6969 69.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9367 93.67%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6552 65.52%
P-glycoprotein inhibitior - 0.6218 62.18%
P-glycoprotein substrate - 0.8011 80.11%
CYP3A4 substrate - 0.5718 57.18%
CYP2C9 substrate - 0.7071 70.71%
CYP2D6 substrate - 0.8388 83.88%
CYP3A4 inhibition - 0.6758 67.58%
CYP2C9 inhibition + 0.5649 56.49%
CYP2C19 inhibition + 0.9422 94.22%
CYP2D6 inhibition - 0.6148 61.48%
CYP1A2 inhibition + 0.9589 95.89%
CYP2C8 inhibition - 0.7012 70.12%
CYP inhibitory promiscuity + 0.8889 88.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7285 72.85%
Eye corrosion - 0.9791 97.91%
Eye irritation + 0.7100 71.00%
Skin irritation - 0.7969 79.69%
Skin corrosion - 0.9771 97.71%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6898 68.98%
Micronuclear - 0.5326 53.26%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7676 76.76%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5852 58.52%
Acute Oral Toxicity (c) III 0.6862 68.62%
Estrogen receptor binding + 0.7901 79.01%
Androgen receptor binding + 0.5625 56.25%
Thyroid receptor binding + 0.6332 63.32%
Glucocorticoid receptor binding + 0.7228 72.28%
Aromatase binding + 0.8341 83.41%
PPAR gamma + 0.6489 64.89%
Honey bee toxicity - 0.9263 92.63%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9927 99.27%

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 93.56% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.02% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.87% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.76% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.92% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.19% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.24% 96.00%
CHEMBL4208 P20618 Proteasome component C5 85.96% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.66% 94.45%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.54% 94.03%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.95% 90.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.99% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.03% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.04% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.51% 90.71%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.04% 92.38%

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.
Carduus tenuiflorus

Cross-Links

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PubChem 16638114
LOTUS LTS0021148
wikiData Q105265506