4,6-Dimethoxy-5-methylchromen-2-one

Details

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Internal ID 593f9658-7d09-4ac8-940c-95b9f013efa3
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4,6-dimethoxy-5-methylchromen-2-one
SMILES (Canonical) CC1=C(C=CC2=C1C(=CC(=O)O2)OC)OC
SMILES (Isomeric) CC1=C(C=CC2=C1C(=CC(=O)O2)OC)OC
InChI InChI=1S/C12H12O4/c1-7-8(14-2)4-5-9-12(7)10(15-3)6-11(13)16-9/h4-6H,1-3H3
InChI Key STOSKTSCSSXGEX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H12O4
Molecular Weight 220.22 g/mol
Exact Mass 220.07355886 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6-Dimethoxy-5-methylchromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9855 98.55%
Caco-2 + 0.7945 79.45%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5667 56.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9477 94.77%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7573 75.73%
P-glycoprotein inhibitior - 0.8369 83.69%
P-glycoprotein substrate - 0.9385 93.85%
CYP3A4 substrate - 0.6199 61.99%
CYP2C9 substrate - 0.7010 70.10%
CYP2D6 substrate - 0.8488 84.88%
CYP3A4 inhibition - 0.7598 75.98%
CYP2C9 inhibition - 0.8925 89.25%
CYP2C19 inhibition - 0.7503 75.03%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition + 0.9796 97.96%
CYP2C8 inhibition - 0.8180 81.80%
CYP inhibitory promiscuity + 0.6045 60.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.5837 58.37%
Eye corrosion - 0.9431 94.31%
Eye irritation + 0.8056 80.56%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.9908 99.08%
Ames mutagenesis + 0.5336 53.36%
Human Ether-a-go-go-Related Gene inhibition - 0.4053 40.53%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9561 95.61%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7033 70.33%
Acute Oral Toxicity (c) II 0.7163 71.63%
Estrogen receptor binding + 0.8170 81.70%
Androgen receptor binding + 0.6781 67.81%
Thyroid receptor binding - 0.7442 74.42%
Glucocorticoid receptor binding - 0.4874 48.74%
Aromatase binding + 0.6320 63.20%
PPAR gamma + 0.5502 55.02%
Honey bee toxicity - 0.9145 91.45%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9565 95.65%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.67% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.48% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.86% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.04% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.12% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.29% 91.11%
CHEMBL1255126 O15151 Protein Mdm4 83.79% 90.20%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.09% 93.99%
CHEMBL2535 P11166 Glucose transporter 83.03% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.01% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.80% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.49% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.41% 89.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 81.40% 85.00%

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.
Ekebergia capensis

Cross-Links

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PubChem 85977339
LOTUS LTS0010164
wikiData Q105260484