4-Methylcoumarin

Details

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Internal ID 96383d00-ca03-410f-880f-0de89b272cc3
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4-methylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O2/c1-7-6-10(11)12-9-5-3-2-4-8(7)9/h2-6H,1H3
InChI Key PSGQCCSGKGJLRL-UHFFFAOYSA-N
Popularity 360 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O2
Molecular Weight 160.17 g/mol
Exact Mass 160.052429494 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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607-71-6
4-Methyl-2H-chromen-2-one
4-methylchromen-2-one
4-Methylcumarin
COUMARIN, 4-METHYL-
4-Methyl-chromen-2-one
2H-1-Benzopyran-2-one, 4-methyl-
4-Methyl-2H-1-benzopyran-2-one
2YZ8R79U9H
NSC20100
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methylcoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9248 92.48%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5444 54.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9873 98.73%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8326 83.26%
P-glycoprotein inhibitior - 0.9731 97.31%
P-glycoprotein substrate - 0.9629 96.29%
CYP3A4 substrate - 0.5646 56.46%
CYP2C9 substrate - 0.6642 66.42%
CYP2D6 substrate - 0.8815 88.15%
CYP3A4 inhibition - 0.8046 80.46%
CYP2C9 inhibition - 0.7823 78.23%
CYP2C19 inhibition - 0.7306 73.06%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition + 0.9552 95.52%
CYP2C8 inhibition - 0.8777 87.77%
CYP inhibitory promiscuity - 0.8103 81.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9113 91.13%
Carcinogenicity (trinary) Warning 0.4933 49.33%
Eye corrosion - 0.8547 85.47%
Eye irritation + 0.9968 99.68%
Skin irritation + 0.7397 73.97%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6987 69.87%
Micronuclear + 0.6459 64.59%
Hepatotoxicity + 0.6698 66.98%
skin sensitisation - 0.7106 71.06%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5605 56.05%
Acute Oral Toxicity (c) III 0.8415 84.15%
Estrogen receptor binding - 0.8755 87.55%
Androgen receptor binding + 0.6703 67.03%
Thyroid receptor binding - 0.7916 79.16%
Glucocorticoid receptor binding - 0.7287 72.87%
Aromatase binding - 0.6243 62.43%
PPAR gamma - 0.6863 68.63%
Honey bee toxicity - 0.9528 95.28%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.8118 81.18%

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 97.10% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.15% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.71% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 92.66% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 91.77% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.60% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.20% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.17% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.18% 95.50%

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.
There are no matching plants.

Cross-Links

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PubChem 11833
LOTUS LTS0055562
wikiData Q27097965