11H-Benzofuro(2,3-b)(1)benzopyran-11-one, 1, 3,8-trihydroxy-2-methoxy-

Details

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Internal ID 9394843e-4739-4132-ba92-bfe285a5d9b3
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 1,3,8-trihydroxy-2-methoxy-[1]benzofuro[2,3-b]chromen-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H10O7/c1-21-15-8(18)5-10-12(14(15)20)13(19)11-7-3-2-6(17)4-9(7)22-16(11)23-10/h2-5,17-18,20H,1H3
InChI Key CFHFUHISZSGRFT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H10O7
Molecular Weight 314.25 g/mol
Exact Mass 314.04265265 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.82
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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132915-54-9
DTXSID30157854

2D Structure

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2D Structure of 11H-Benzofuro(2,3-b)(1)benzopyran-11-one, 1, 3,8-trihydroxy-2-methoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9296 92.96%
Caco-2 + 0.7236 72.36%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6775 67.75%
OATP2B1 inhibitior - 0.5596 55.96%
OATP1B1 inhibitior + 0.8900 89.00%
OATP1B3 inhibitior + 0.9226 92.26%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8594 85.94%
P-glycoprotein inhibitior - 0.6895 68.95%
P-glycoprotein substrate - 0.7253 72.53%
CYP3A4 substrate + 0.5272 52.72%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6970 69.70%
CYP2C9 inhibition - 0.5362 53.62%
CYP2C19 inhibition + 0.7385 73.85%
CYP2D6 inhibition - 0.5245 52.45%
CYP1A2 inhibition + 0.7859 78.59%
CYP2C8 inhibition + 0.6328 63.28%
CYP inhibitory promiscuity + 0.7480 74.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.3797 37.97%
Eye corrosion - 0.9784 97.84%
Eye irritation + 0.7065 70.65%
Skin irritation - 0.6362 63.62%
Skin corrosion - 0.9486 94.86%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8383 83.83%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8392 83.92%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8735 87.35%
Acute Oral Toxicity (c) III 0.6064 60.64%
Estrogen receptor binding + 0.8841 88.41%
Androgen receptor binding + 0.8540 85.40%
Thyroid receptor binding + 0.6300 63.00%
Glucocorticoid receptor binding + 0.8858 88.58%
Aromatase binding + 0.7161 71.61%
PPAR gamma + 0.8310 83.10%
Honey bee toxicity - 0.8645 86.45%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8850 88.50%

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 99.20% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.76% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.31% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.68% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.38% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.20% 98.95%
CHEMBL3194 P02766 Transthyretin 88.43% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.10% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.48% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 86.36% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.70% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.40% 99.23%
CHEMBL2535 P11166 Glucose transporter 81.51% 98.75%
CHEMBL242 Q92731 Estrogen receptor beta 81.10% 98.35%

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.
Iris pseudacorus

Cross-Links

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PubChem 5491554
LOTUS LTS0232865
wikiData Q83026020