5-Methoxycoumarin

Details

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Internal ID b55de00c-51c9-476a-b0c0-ea79fa5efb36
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5-methoxychromen-2-one
SMILES (Canonical) COC1=CC=CC2=C1C=CC(=O)O2
SMILES (Isomeric) COC1=CC=CC2=C1C=CC(=O)O2
InChI InChI=1S/C10H8O3/c1-12-8-3-2-4-9-7(8)5-6-10(11)13-9/h2-6H,1H3
InChI Key XYFXTIBDEAZMAH-UHFFFAOYSA-N
Popularity 9 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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51559-36-5
5-methoxy-2H-chromen-2-one
Coumarin, 5-methoxy-
YUV63OTC0P
UNII-YUV63OTC0P
2H-1-Benzopyran-2-one, 5-methoxy-
5-methoxychromen-2-one
5-Methoxycumarin
CHEMBL502746
SCHEMBL1859616
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Methoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.8980 89.80%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6150 61.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9517 95.17%
OATP1B3 inhibitior + 0.9947 99.47%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9138 91.38%
P-glycoprotein inhibitior - 0.9464 94.64%
P-glycoprotein substrate - 0.8938 89.38%
CYP3A4 substrate - 0.5651 56.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8151 81.51%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.7471 74.71%
CYP2D6 inhibition - 0.8988 89.88%
CYP1A2 inhibition + 0.9923 99.23%
CYP2C8 inhibition - 0.8236 82.36%
CYP inhibitory promiscuity - 0.5348 53.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Warning 0.4614 46.14%
Eye corrosion + 0.5202 52.02%
Eye irritation + 0.9899 98.99%
Skin irritation + 0.5362 53.62%
Skin corrosion - 0.9842 98.42%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5772 57.72%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9244 92.44%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.7008 70.08%
Acute Oral Toxicity (c) III 0.8038 80.38%
Estrogen receptor binding - 0.6600 66.00%
Androgen receptor binding + 0.5541 55.41%
Thyroid receptor binding - 0.7733 77.33%
Glucocorticoid receptor binding - 0.6949 69.49%
Aromatase binding + 0.6740 67.40%
PPAR gamma - 0.5143 51.43%
Honey bee toxicity - 0.8951 89.51%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.8334 83.34%

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 95.48% 95.56%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 95.00% 94.03%
CHEMBL2581 P07339 Cathepsin D 91.55% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.42% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.19% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.30% 99.23%
CHEMBL2535 P11166 Glucose transporter 86.18% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.60% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.09% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.93% 94.45%
CHEMBL1255126 O15151 Protein Mdm4 82.32% 90.20%
CHEMBL1907 P15144 Aminopeptidase N 81.06% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.51% 89.00%

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 decursiva
Kitagawia praeruptora
Psorothamnus emoryi

Cross-Links

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PubChem 10899191
NPASS NPC128633
LOTUS LTS0101978
wikiData Q27294723