7-Methoxy-4',4''',5,5'',7''-pentahydroxy-3',6''-biflavone

Details

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Internal ID 4a8885c5-ae7d-4674-b9db-dc962cfd3137
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Biflavonoids and polyflavonoids
IUPAC Name 5,7-dihydroxy-6-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenyl]-2-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)C4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)C4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O)O
InChI InChI=1S/C31H20O10/c1-39-17-9-20(34)29-22(36)11-25(41-26(29)10-17)15-4-7-19(33)18(8-15)28-21(35)13-27-30(31(28)38)23(37)12-24(40-27)14-2-5-16(32)6-3-14/h2-13,32-35,38H,1H3
InChI Key JOXJXCNVYDRXDT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H20O10
Molecular Weight 552.50 g/mol
Exact Mass 552.10564683 g/mol
Topological Polar Surface Area (TPSA) 163.00 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.44
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methoxy-4',4''',5,5'',7''-pentahydroxy-3',6''-biflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9430 94.30%
Caco-2 - 0.8413 84.13%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8174 81.74%
OATP2B1 inhibitior - 0.5589 55.89%
OATP1B1 inhibitior + 0.7984 79.84%
OATP1B3 inhibitior + 0.9706 97.06%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7911 79.11%
P-glycoprotein inhibitior + 0.7623 76.23%
P-glycoprotein substrate - 0.7584 75.84%
CYP3A4 substrate + 0.6145 61.45%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.5760 57.60%
CYP2C9 inhibition + 0.7647 76.47%
CYP2C19 inhibition + 0.7471 74.71%
CYP2D6 inhibition - 0.7766 77.66%
CYP1A2 inhibition + 0.8002 80.02%
CYP2C8 inhibition + 0.8699 86.99%
CYP inhibitory promiscuity + 0.6806 68.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5868 58.68%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.8037 80.37%
Skin irritation - 0.6647 66.47%
Skin corrosion - 0.9266 92.66%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6956 69.56%
Micronuclear + 0.8900 89.00%
Hepatotoxicity - 0.8375 83.75%
skin sensitisation - 0.9499 94.99%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7216 72.16%
Acute Oral Toxicity (c) III 0.6544 65.44%
Estrogen receptor binding + 0.8789 87.89%
Androgen receptor binding + 0.9426 94.26%
Thyroid receptor binding + 0.5953 59.53%
Glucocorticoid receptor binding + 0.8364 83.64%
Aromatase binding + 0.5298 52.98%
PPAR gamma + 0.7670 76.70%
Honey bee toxicity - 0.7658 76.58%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8837 88.37%

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 99.31% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 98.37% 99.15%
CHEMBL242 Q92731 Estrogen receptor beta 97.91% 98.35%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.12% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.76% 94.00%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL3194 P02766 Transthyretin 94.25% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.88% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.39% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.11% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.00% 96.21%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.74% 91.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.30% 94.45%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 84.60% 95.64%
CHEMBL3401 O75469 Pregnane X receptor 84.57% 94.73%
CHEMBL4208 P20618 Proteasome component C5 84.48% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.88% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.68% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.42% 93.65%
CHEMBL1907 P15144 Aminopeptidase N 82.88% 93.31%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.89% 86.92%
CHEMBL1951 P21397 Monoamine oxidase A 81.83% 91.49%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.04% 97.28%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.84% 95.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.52% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.49% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.33% 95.50%

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.
Dacrycarpus imbricatus
Selaginella willdenowii

Cross-Links

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PubChem 5320989
NPASS NPC230320
LOTUS LTS0055712
wikiData Q105132577