4-Hydroxy-5-methylcoumarin

Details

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Internal ID 729d98f8-5096-4703-8431-3cef0e6bbc4d
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 4-hydroxycoumarins
IUPAC Name 4-hydroxy-5-methylchromen-2-one
SMILES (Canonical) CC1=C2C(=CC=C1)OC(=O)C=C2O
SMILES (Isomeric) CC1=C2C(=CC=C1)OC(=O)C=C2O
InChI InChI=1S/C10H8O3/c1-6-3-2-4-8-10(6)7(11)5-9(12)13-8/h2-5,11H,1H3
InChI Key SGMVRLBDQDWGRZ-UHFFFAOYSA-N
Popularity 16 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) 46.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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24631-87-6
4-Hydroxy-5-methyl-2H-chromen-2-one
2-hydroxy-5-methyl-chromone
SCHEMBL5346812
SCHEMBL8537987
MFCD18450601
SY309884

2D Structure

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2D Structure of 4-Hydroxy-5-methylcoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.9456 94.56%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6005 60.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9435 94.35%
OATP1B3 inhibitior + 0.9920 99.20%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8942 89.42%
P-glycoprotein inhibitior - 0.9625 96.25%
P-glycoprotein substrate - 0.9530 95.30%
CYP3A4 substrate - 0.6161 61.61%
CYP2C9 substrate + 0.6360 63.60%
CYP2D6 substrate - 0.8834 88.34%
CYP3A4 inhibition - 0.8379 83.79%
CYP2C9 inhibition - 0.9070 90.70%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9725 97.25%
CYP1A2 inhibition + 0.9108 91.08%
CYP2C8 inhibition - 0.8646 86.46%
CYP inhibitory promiscuity - 0.8952 89.52%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.4806 48.06%
Eye corrosion - 0.9095 90.95%
Eye irritation + 0.9866 98.66%
Skin irritation + 0.7241 72.41%
Skin corrosion - 0.9735 97.35%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6589 65.89%
Micronuclear + 0.7959 79.59%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation - 0.8965 89.65%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5721 57.21%
Acute Oral Toxicity (c) III 0.8133 81.33%
Estrogen receptor binding + 0.5285 52.85%
Androgen receptor binding - 0.5808 58.08%
Thyroid receptor binding - 0.7291 72.91%
Glucocorticoid receptor binding + 0.6181 61.81%
Aromatase binding + 0.5255 52.55%
PPAR gamma + 0.5803 58.03%
Honey bee toxicity - 0.9777 97.77%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8608 86.08%

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 97.48% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.71% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 94.59% 94.73%
CHEMBL2581 P07339 Cathepsin D 94.55% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 93.76% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.45% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.58% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.32% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.67% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.54% 99.15%

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.
Ambrosia hispida
Coptis chinensis
Leibnitzia anandria
Lonicera morrowii

Cross-Links

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PubChem 54688203
NPASS NPC214456