8-[2-(5,7-Dihydroxy-4-oxochromen-2-yl)-5-methoxyphenyl]-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one

Details

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Internal ID 722c2663-1bbf-4fde-8037-378403dbe78d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 4-O-methylated flavonoids
IUPAC Name 8-[2-(5,7-dihydroxy-4-oxochromen-2-yl)-5-methoxyphenyl]-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H22O10/c1-39-17-5-3-15(4-6-17)26-13-25(38)31-23(36)12-22(35)29(32(31)42-26)20-11-18(40-2)7-8-19(20)27-14-24(37)30-21(34)9-16(33)10-28(30)41-27/h3-14,33-36H,1-2H3
InChI Key XJHTVPQTZGBBRZ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H22O10
Molecular Weight 566.50 g/mol
Exact Mass 566.12129689 g/mol
Topological Polar Surface Area (TPSA) 152.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.74
H-Bond Acceptor 10
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-[2-(5,7-Dihydroxy-4-oxochromen-2-yl)-5-methoxyphenyl]-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9325 93.25%
Caco-2 - 0.7457 74.57%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8148 81.48%
OATP2B1 inhibitior - 0.5645 56.45%
OATP1B1 inhibitior - 0.4226 42.26%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9651 96.51%
P-glycoprotein inhibitior + 0.8192 81.92%
P-glycoprotein substrate - 0.6299 62.99%
CYP3A4 substrate + 0.6504 65.04%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.5831 58.31%
CYP2C9 inhibition + 0.6590 65.90%
CYP2C19 inhibition + 0.6234 62.34%
CYP2D6 inhibition - 0.7411 74.11%
CYP1A2 inhibition + 0.6533 65.33%
CYP2C8 inhibition + 0.8470 84.70%
CYP inhibitory promiscuity + 0.6726 67.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.8303 83.03%
Skin irritation - 0.7256 72.56%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7743 77.43%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.9458 94.58%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6097 60.97%
Acute Oral Toxicity (c) III 0.6505 65.05%
Estrogen receptor binding + 0.9329 93.29%
Androgen receptor binding + 0.9468 94.68%
Thyroid receptor binding + 0.6611 66.11%
Glucocorticoid receptor binding + 0.8153 81.53%
Aromatase binding + 0.5708 57.08%
PPAR gamma + 0.8092 80.92%
Honey bee toxicity - 0.8038 80.38%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9066 90.66%

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 98.91% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.92% 91.49%
CHEMBL242 Q92731 Estrogen receptor beta 97.84% 98.35%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.90% 94.00%
CHEMBL308 P06493 Cyclin-dependent kinase 1 96.82% 91.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.61% 99.15%
CHEMBL1907 P15144 Aminopeptidase N 94.90% 93.31%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.81% 95.56%
CHEMBL3194 P02766 Transthyretin 94.21% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.21% 89.00%
CHEMBL4208 P20618 Proteasome component C5 90.44% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 90.28% 86.92%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.28% 96.21%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.03% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.84% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.63% 94.73%
CHEMBL6029 Q9BQI3 Eukaryotic translation initiation factor 2-alpha kinase 1 84.47% 88.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.74% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.21% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.96% 96.95%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.82% 97.28%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.75% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.01% 93.65%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.84% 95.78%

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.
Ginkgo biloba

Cross-Links

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PubChem 163084208
LOTUS LTS0239647
wikiData Q105328969