5-Hydroxy-3-(4-hydroxyphenyl)chromen-4-one

Details

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Internal ID 858090e5-fcb2-4125-90c9-8f738cdc40ef
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O4/c16-10-6-4-9(5-7-10)11-8-19-13-3-1-2-12(17)14(13)15(11)18/h1-8,16-17H
InChI Key GTKATHVTDOTYMV-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O4
Molecular Weight 254.24 g/mol
Exact Mass 254.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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148356-24-5
4',5-Dihydroxyisoflavone
SCHEMBL18676275
DTXSID801037024
AKOS015963320
AC-19588
3-(4-hydroxyphenyl)-5-oxidanyl-chromen-4-one
5-Hydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one
A827584
5-hydroxy-3-(4-hydroxyphenyl)-1-benzopyran-4-one

2D Structure

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2D Structure of 5-Hydroxy-3-(4-hydroxyphenyl)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 + 0.9853 98.53%
Caco-2 + 0.8177 81.77%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8516 85.16%
OATP2B1 inhibitior - 0.7035 70.35%
OATP1B1 inhibitior + 0.9390 93.90%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior + 0.6600 66.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7678 76.78%
P-glycoprotein inhibitior - 0.8928 89.28%
P-glycoprotein substrate - 0.9417 94.17%
CYP3A4 substrate - 0.5112 51.12%
CYP2C9 substrate - 0.6443 64.43%
CYP2D6 substrate - 0.8503 85.03%
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 + 0.5894 58.94%
CYP inhibitory promiscuity + 0.6929 69.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.6163 61.63%
Eye corrosion - 0.9915 99.15%
Eye irritation + 0.9820 98.20%
Skin irritation + 0.6467 64.67%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8987 89.87%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.6554 65.54%
skin sensitisation - 0.8894 88.94%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.8257 82.57%
Acute Oral Toxicity (c) II 0.5629 56.29%
Estrogen receptor binding + 0.9065 90.65%
Androgen receptor binding + 0.8954 89.54%
Thyroid receptor binding + 0.8238 82.38%
Glucocorticoid receptor binding + 0.8571 85.71%
Aromatase binding + 0.9187 91.87%
PPAR gamma + 0.9222 92.22%
Honey bee toxicity - 0.9262 92.62%
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
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 96.51% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.57% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.25% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.84% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 90.35% 98.35%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.62% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.03% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.63% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.51% 99.15%
CHEMBL1937 Q92769 Histone deacetylase 2 85.45% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 81.46% 94.73%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.87% 91.38%

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.
Pueraria montana var. lobata
Wisteria brachybotrys

Cross-Links

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PubChem 5702539
LOTUS LTS0075956
wikiData Q105018939