CID 11777207

Details

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Internal ID f8ad7c12-29b9-412e-a599-bc475f848683
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 7-hydroxy-3-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical) C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2=COC3=C(C2=O)C=[13CH][13C](=[13CH]3)O)O
InChI InChI=1S/C15H10O4/c16-10-3-1-9(2-4-10)13-8-19-14-7-11(17)5-6-12(14)15(13)18/h1-8,16-17H/i5+1,7+1,11+1
InChI Key ZQSIJRDFPHDXIC-QTFCXHRBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O4
Molecular Weight 257.21 g/mol
Exact Mass 257.06797330 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 11777207

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.9313 93.13%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8516 85.16%
OATP2B1 inhibitior + 0.5453 54.53%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7504 75.04%
P-glycoprotein inhibitior - 0.9166 91.66%
P-glycoprotein substrate - 0.9363 93.63%
CYP3A4 substrate - 0.5266 52.66%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.8000 80.00%
CYP3A4 inhibition - 0.6261 62.61%
CYP2C9 inhibition + 0.9757 97.57%
CYP2C19 inhibition + 0.8994 89.94%
CYP2D6 inhibition - 0.9199 91.99%
CYP1A2 inhibition + 0.9108 91.08%
CYP2C8 inhibition + 0.5356 53.56%
CYP inhibitory promiscuity + 0.6929 69.29%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6163 61.63%
Eye corrosion - 0.9915 99.15%
Eye irritation + 0.9755 97.55%
Skin irritation + 0.6467 64.67%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8644 86.44%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.6054 60.54%
skin sensitisation - 0.8894 88.94%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5960 59.60%
Acute Oral Toxicity (c) II 0.5629 56.29%
Estrogen receptor binding + 0.8905 89.05%
Androgen receptor binding + 0.9445 94.45%
Thyroid receptor binding + 0.7973 79.73%
Glucocorticoid receptor binding + 0.8970 89.70%
Aromatase binding + 0.8685 86.85%
PPAR gamma + 0.8418 84.18%
Honey bee toxicity - 0.9110 91.10%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9385 93.85%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293237 P54132 Bloom syndrome protein 501.2 nM
Potency
via Super-PRED
CHEMBL3729 P22748 Carbonic anhydrase IV 718.7 nM
Ki
via Super-PRED
CHEMBL2326 P43166 Carbonic anhydrase VII 4.2 nM
Ki
via Super-PRED
CHEMBL3242 O43570 Carbonic anhydrase XII 56.4 nM
Ki
via Super-PRED
CHEMBL1293235 P02545 Prelamin-A/C 5 nM
Potency
via Super-PRED
CHEMBL1075138 Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 354.8 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL242 Q92731 Estrogen receptor beta 98.12% 98.35%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.95% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.56% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.96% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 87.92% 91.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.59% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.25% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.98% 94.00%
CHEMBL3194 P02766 Transthyretin 81.53% 90.71%

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.
Epimedium pubescens
Glycine max
Medicago sativa
Piptanthus nepalensis
Toxicopueraria peduncularis
Trifolium pratense

Cross-Links

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PubChem 11777207
NPASS NPC147748