7,2'-Dihydroxy-4'-methoxy-isoflavonol

Details

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Internal ID fc2f797e-9d3a-47d1-a402-1068f51d6baa
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Hydroxyisoflavonoids
IUPAC Name 4,7-dihydroxy-3-(2-hydroxy-4-methoxyphenyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O6/c1-21-9-3-5-10(12(18)7-9)14-15(19)11-4-2-8(17)6-13(11)22-16(14)20/h2-7,17-19H,1H3
InChI Key SREKTCXBYGRZOA-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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7,2'-dihydroxy-4'-methoxy-isoflavonol

2D Structure

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2D Structure of 7,2'-Dihydroxy-4'-methoxy-isoflavonol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 + 0.7151 71.51%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8430 84.30%
OATP2B1 inhibitior + 0.5708 57.08%
OATP1B1 inhibitior + 0.8317 83.17%
OATP1B3 inhibitior + 0.9714 97.14%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7309 73.09%
P-glycoprotein inhibitior - 0.7145 71.45%
P-glycoprotein substrate - 0.7123 71.23%
CYP3A4 substrate + 0.5490 54.90%
CYP2C9 substrate - 0.5385 53.85%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.8104 81.04%
CYP2C9 inhibition + 0.8378 83.78%
CYP2C19 inhibition + 0.6935 69.35%
CYP2D6 inhibition - 0.8851 88.51%
CYP1A2 inhibition + 0.7295 72.95%
CYP2C8 inhibition + 0.5938 59.38%
CYP inhibitory promiscuity + 0.6223 62.23%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.5359 53.59%
Eye corrosion - 0.9792 97.92%
Eye irritation + 0.8059 80.59%
Skin irritation - 0.6186 61.86%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8414 84.14%
Micronuclear + 0.9400 94.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.9731 97.31%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7522 75.22%
Acute Oral Toxicity (c) III 0.6240 62.40%
Estrogen receptor binding + 0.9236 92.36%
Androgen receptor binding + 0.9479 94.79%
Thyroid receptor binding + 0.7276 72.76%
Glucocorticoid receptor binding + 0.9032 90.32%
Aromatase binding + 0.7780 77.80%
PPAR gamma + 0.7346 73.46%
Honey bee toxicity - 0.9107 91.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9408 94.08%

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 99.72% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.65% 91.49%
CHEMBL242 Q92731 Estrogen receptor beta 95.87% 98.35%
CHEMBL2581 P07339 Cathepsin D 95.50% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 95.36% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.26% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.31% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 89.16% 93.31%
CHEMBL2535 P11166 Glucose transporter 88.66% 98.75%
CHEMBL4208 P20618 Proteasome component C5 88.08% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.56% 86.33%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 87.53% 93.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.34% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.28% 99.23%
CHEMBL2056 P21728 Dopamine D1 receptor 85.18% 91.00%
CHEMBL3194 P02766 Transthyretin 84.84% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.48% 95.89%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.12% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 81.38% 94.73%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.76% 95.53%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.54% 95.64%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.17% 96.67%

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.
Astragalus laxmannii

Cross-Links

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PubChem 69035380
LOTUS LTS0238109
wikiData Q105135155