6-Methoxycoumarin

Details

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Internal ID 4cf3ff65-0d90-4403-9aae-bd9a2452e709
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-methoxychromen-2-one
SMILES (Canonical) COC1=CC2=C(C=C1)OC(=O)C=C2
SMILES (Isomeric) COC1=CC2=C(C=C1)OC(=O)C=C2
InChI InChI=1S/C10H8O3/c1-12-8-3-4-9-7(6-8)2-5-10(11)13-9/h2-6H,1H3
InChI Key VKVCJIMMVPXDQD-UHFFFAOYSA-N
Popularity 21 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 1.40
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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6-methoxy-2H-chromen-2-one
17372-53-1
6-methoxychromen-2-one
MFCD00016707
Coumarin, 6-methoxy-
CHEMBL496547
SCHEMBL1108372
DTXSID00459751
CHEBI:178005
VKVCJIMMVPXDQD-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-Methoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7663 76.63%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6672 66.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9328 93.28%
OATP1B3 inhibitior + 0.9913 99.13%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7232 72.32%
P-glycoprotein inhibitior - 0.9433 94.33%
P-glycoprotein substrate - 0.9773 97.73%
CYP3A4 substrate - 0.6675 66.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8151 81.51%
CYP3A4 inhibition - 0.8691 86.91%
CYP2C9 inhibition + 0.6716 67.16%
CYP2C19 inhibition + 0.6403 64.03%
CYP2D6 inhibition - 0.9135 91.35%
CYP1A2 inhibition + 0.9871 98.71%
CYP2C8 inhibition - 0.8878 88.78%
CYP inhibitory promiscuity - 0.6003 60.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9123 91.23%
Carcinogenicity (trinary) Warning 0.5007 50.07%
Eye corrosion - 0.6041 60.41%
Eye irritation + 0.9928 99.28%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9886 98.86%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6021 60.21%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5350 53.50%
skin sensitisation - 0.9182 91.82%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5059 50.59%
Acute Oral Toxicity (c) III 0.8099 80.99%
Estrogen receptor binding - 0.5450 54.50%
Androgen receptor binding + 0.7413 74.13%
Thyroid receptor binding - 0.7398 73.98%
Glucocorticoid receptor binding - 0.7042 70.42%
Aromatase binding - 0.5148 51.48%
PPAR gamma - 0.7321 73.21%
Honey bee toxicity - 0.9254 92.54%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8510 85.10%

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 94.98% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.48% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.22% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.36% 96.00%
CHEMBL4208 P20618 Proteasome component C5 85.63% 90.00%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 85.60% 85.30%
CHEMBL2581 P07339 Cathepsin D 85.32% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 84.06% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.45% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.83% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 82.37% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.48% 93.65%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 11240776
NPASS NPC87563