4,6-Dimethoxy-3,7-dimethylcoumarin

Details

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Internal ID 9545a8b5-328e-4ea1-a5b9-c7746c3c8c80
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4,6-dimethoxy-3,7-dimethylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14O4/c1-7-5-11-9(6-10(7)15-3)12(16-4)8(2)13(14)17-11/h5-6H,1-4H3
InChI Key GXMNZQIZQIFSLQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.43
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-3,7-dimethylcoumarin

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 + 0.9109 91.09%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5667 56.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9669 96.69%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7217 72.17%
P-glycoprotein inhibitior - 0.7875 78.75%
P-glycoprotein substrate - 0.9196 91.96%
CYP3A4 substrate - 0.5301 53.01%
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 - 0.8417 84.17%
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 + 0.9083 90.83%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.9908 99.08%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4064 40.64%
Micronuclear + 0.7759 77.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.9561 95.61%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7167 71.67%
Acute Oral Toxicity (c) II 0.7163 71.63%
Estrogen receptor binding + 0.8592 85.92%
Androgen receptor binding + 0.5804 58.04%
Thyroid receptor binding - 0.6276 62.76%
Glucocorticoid receptor binding + 0.6128 61.28%
Aromatase binding + 0.7606 76.06%
PPAR gamma + 0.6156 61.56%
Honey bee toxicity - 0.9047 90.47%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6100 61.00%
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 94.39% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.85% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.20% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.50% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.38% 93.65%
CHEMBL1871 P10275 Androgen Receptor 88.25% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.17% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.25% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 86.93% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.39% 85.14%
CHEMBL4302 P08183 P-glycoprotein 1 84.84% 92.98%
CHEMBL2535 P11166 Glucose transporter 83.90% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.62% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.27% 94.73%

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.
Colchicum decaisnei

Cross-Links

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PubChem 101609017
LOTUS LTS0116690
wikiData Q105023195