8-Methoxychromen-2-one

Details

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Internal ID 3fda6417-221a-45c7-a1bc-658e6ba42955
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 8-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O3/c1-12-8-4-2-3-7-5-6-9(11)13-10(7)8/h2-6H,1H3
InChI Key ODRDTKMYQDXVGG-UHFFFAOYSA-N
Popularity 23 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O3
Molecular Weight 176.17 g/mol
Exact Mass 176.047344113 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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2445-81-0
8-Methoxy-2H-chromen-2-one
8-methoxychromen-2-one
Coumarin, 8-methoxy-
2H-1-Benzopyran-2-one, 8-methoxy-
2H-1-Benzopyran-2-one,8-methoxy-
W3OIY9A2QE
8-Methoxy-2H-1-benzopyran-2-one
MFCD00016708
8-methoxy-coumarin
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 8-Methoxychromen-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 + 0.9943 99.43%
Caco-2 + 0.6131 61.31%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6606 66.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9657 96.57%
OATP1B3 inhibitior + 0.9850 98.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7653 76.53%
P-glycoprotein inhibitior - 0.9494 94.94%
P-glycoprotein substrate - 0.9623 96.23%
CYP3A4 substrate - 0.6375 63.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8151 81.51%
CYP3A4 inhibition - 0.8948 89.48%
CYP2C9 inhibition - 0.6180 61.80%
CYP2C19 inhibition + 0.5996 59.96%
CYP2D6 inhibition - 0.9095 90.95%
CYP1A2 inhibition + 0.9794 97.94%
CYP2C8 inhibition - 0.8530 85.30%
CYP inhibitory promiscuity - 0.5958 59.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9410 94.10%
Carcinogenicity (trinary) Warning 0.5320 53.20%
Eye corrosion - 0.6362 63.62%
Eye irritation + 0.9800 98.00%
Skin irritation + 0.5135 51.35%
Skin corrosion - 0.9843 98.43%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6094 60.94%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.8754 87.54%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.7152 71.52%
Acute Oral Toxicity (c) III 0.8239 82.39%
Estrogen receptor binding - 0.6774 67.74%
Androgen receptor binding - 0.4857 48.57%
Thyroid receptor binding - 0.7445 74.45%
Glucocorticoid receptor binding - 0.7969 79.69%
Aromatase binding - 0.7259 72.59%
PPAR gamma - 0.7441 74.41%
Honey bee toxicity - 0.9303 93.03%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8098 80.98%

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 93.52% 95.56%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 92.37% 94.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.36% 94.00%
CHEMBL2581 P07339 Cathepsin D 89.27% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.54% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.18% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.11% 86.33%
CHEMBL1907 P15144 Aminopeptidase N 84.66% 93.31%
CHEMBL1255126 O15151 Protein Mdm4 83.07% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.94% 96.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.31% 85.30%

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.
Fraxinus floribunda

Cross-Links

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PubChem 520130
LOTUS LTS0276399
wikiData Q82099986