3-Methylcoumarin

Details

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Internal ID 7795280b-4862-4be7-860d-b3ec93fb9633
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 3-methylchromen-2-one
SMILES (Canonical) CC1=CC2=CC=CC=C2OC1=O
SMILES (Isomeric) CC1=CC2=CC=CC=C2OC1=O
InChI InChI=1S/C10H8O2/c1-7-6-8-4-2-3-5-9(8)12-10(7)11/h2-6H,1H3
InChI Key VIIIJFZJKFXOGG-UHFFFAOYSA-N
Popularity 251 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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2445-82-1
3-METHYL-CHROMEN-2-ONE
Methyl-2-benzopyrone
3-Methyl-2H-chromen-2-one
COUMARIN, 3-METHYL-
3-methylchromen-2-one
2H-1-Benzopyran-2-one, 3-methyl-
3-Methyl-2H-1-benzopyran-2-one
1333-47-7
2H-1-Benzopyran-2-one, methyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-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 + 0.7875 78.75%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6866 68.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9604 96.04%
OATP1B3 inhibitior + 0.9883 98.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7585 75.85%
P-glycoprotein inhibitior - 0.9659 96.59%
P-glycoprotein substrate - 0.9834 98.34%
CYP3A4 substrate - 0.6821 68.21%
CYP2C9 substrate - 0.7281 72.81%
CYP2D6 substrate - 0.8595 85.95%
CYP3A4 inhibition - 0.8323 83.23%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.7065 70.65%
CYP2D6 inhibition - 0.9553 95.53%
CYP1A2 inhibition + 0.9516 95.16%
CYP2C8 inhibition - 0.9466 94.66%
CYP inhibitory promiscuity - 0.7171 71.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.4645 46.45%
Eye corrosion - 0.9613 96.13%
Eye irritation + 0.9660 96.60%
Skin irritation + 0.7383 73.83%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7157 71.57%
Micronuclear + 0.6018 60.18%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6143 61.43%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.5904 59.04%
Acute Oral Toxicity (c) III 0.6513 65.13%
Estrogen receptor binding - 0.7894 78.94%
Androgen receptor binding - 0.5336 53.36%
Thyroid receptor binding - 0.7187 71.87%
Glucocorticoid receptor binding - 0.7202 72.02%
Aromatase binding - 0.5116 51.16%
PPAR gamma - 0.7172 71.72%
Honey bee toxicity - 0.9638 96.38%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9173 91.73%

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
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 93.38% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 93.07% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.74% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.26% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.57% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.52% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.26% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.93% 99.23%
CHEMBL2039 P27338 Monoamine oxidase B 82.90% 92.51%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.77% 96.67%

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.
Thapsia garganica

Cross-Links

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PubChem 17130
LOTUS LTS0045925
wikiData Q27272861