3,4',6,7-Tetramethoxyflavone

Details

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Internal ID f078509e-2357-45dc-8c5e-33472cf2f634
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 3,6,7-trimethoxy-2-(4-methoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2=C(C(=O)C3=CC(=C(C=C3O2)OC)OC)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C2=C(C(=O)C3=CC(=C(C=C3O2)OC)OC)OC
InChI InChI=1S/C19H18O6/c1-21-12-7-5-11(6-8-12)18-19(24-4)17(20)13-9-15(22-2)16(23-3)10-14(13)25-18/h5-10H,1-4H3
InChI Key HXQFRQWEXDYZMZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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3,4',6,7-Tetramethoxyflavone

2D Structure

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2D Structure of 3,4',6,7-Tetramethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.8788 87.88%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7006 70.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7255 72.55%
P-glycoprotein inhibitior + 0.9566 95.66%
P-glycoprotein substrate - 0.7857 78.57%
CYP3A4 substrate + 0.5321 53.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.6138 61.38%
CYP2C9 inhibition - 0.7985 79.85%
CYP2C19 inhibition + 0.7445 74.45%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition + 0.9694 96.94%
CYP2C8 inhibition + 0.5973 59.73%
CYP inhibitory promiscuity + 0.8123 81.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.9682 96.82%
Eye irritation - 0.6777 67.77%
Skin irritation - 0.7565 75.65%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7794 77.94%
Micronuclear + 0.7759 77.59%
Hepatotoxicity - 0.5290 52.90%
skin sensitisation - 0.9439 94.39%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7979 79.79%
Acute Oral Toxicity (c) II 0.6245 62.45%
Estrogen receptor binding + 0.9270 92.70%
Androgen receptor binding + 0.9049 90.49%
Thyroid receptor binding + 0.7345 73.45%
Glucocorticoid receptor binding + 0.8622 86.22%
Aromatase binding + 0.7083 70.83%
PPAR gamma + 0.8122 81.22%
Honey bee toxicity - 0.9066 90.66%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9192 91.92%

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 96.94% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.87% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 92.67% 93.31%
CHEMBL2581 P07339 Cathepsin D 88.81% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.43% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.23% 86.33%
CHEMBL4302 P08183 P-glycoprotein 1 85.74% 92.98%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.31% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.07% 99.17%
CHEMBL2535 P11166 Glucose transporter 84.51% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.06% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.97% 99.15%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.74% 97.14%

Cross-Links

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PubChem 14887080
NPASS NPC177148