5-Hydroxy-2-(4-hydroxyphenoxy)-7-methoxy-6-methylchromen-4-one

Details

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Internal ID 9d429aaf-c2df-4c45-828b-d45e25f11b4f
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5-hydroxy-2-(4-hydroxyphenoxy)-7-methoxy-6-methylchromen-4-one
SMILES (Canonical) CC1=C(C=C2C(=C1O)C(=O)C=C(O2)OC3=CC=C(C=C3)O)OC
SMILES (Isomeric) CC1=C(C=C2C(=C1O)C(=O)C=C(O2)OC3=CC=C(C=C3)O)OC
InChI InChI=1S/C17H14O6/c1-9-13(21-2)8-14-16(17(9)20)12(19)7-15(23-14)22-11-5-3-10(18)4-6-11/h3-8,18,20H,1-2H3
InChI Key ZPMUVYUNMBTMFO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.31
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-2-(4-hydroxyphenoxy)-7-methoxy-6-methylchromen-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 + 0.9612 96.12%
Caco-2 + 0.8090 80.90%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7720 77.20%
OATP2B1 inhibitior + 0.5564 55.64%
OATP1B1 inhibitior + 0.8459 84.59%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.5800 58.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6492 64.92%
P-glycoprotein inhibitior + 0.6706 67.06%
P-glycoprotein substrate - 0.7849 78.49%
CYP3A4 substrate + 0.5725 57.25%
CYP2C9 substrate - 0.6279 62.79%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.8039 80.39%
CYP2C9 inhibition - 0.6216 62.16%
CYP2C19 inhibition - 0.6869 68.69%
CYP2D6 inhibition - 0.8087 80.87%
CYP1A2 inhibition + 0.8176 81.76%
CYP2C8 inhibition + 0.6534 65.34%
CYP inhibitory promiscuity - 0.5148 51.48%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6265 62.65%
Eye corrosion - 0.9711 97.11%
Eye irritation + 0.6106 61.06%
Skin irritation - 0.6647 66.47%
Skin corrosion - 0.9813 98.13%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6226 62.26%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.7841 78.41%
skin sensitisation - 0.9576 95.76%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6695 66.95%
Acute Oral Toxicity (c) II 0.5325 53.25%
Estrogen receptor binding + 0.8775 87.75%
Androgen receptor binding + 0.8925 89.25%
Thyroid receptor binding + 0.6277 62.77%
Glucocorticoid receptor binding + 0.7301 73.01%
Aromatase binding + 0.7790 77.90%
PPAR gamma + 0.8317 83.17%
Honey bee toxicity - 0.8418 84.18%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9387 93.87%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.84% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.88% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.14% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.73% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.42% 99.15%
CHEMBL3194 P02766 Transthyretin 89.28% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.76% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.13% 86.33%
CHEMBL2535 P11166 Glucose transporter 88.05% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.52% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.49% 99.23%
CHEMBL4208 P20618 Proteasome component C5 85.66% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.24% 94.42%
CHEMBL2581 P07339 Cathepsin D 85.22% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.12% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.03% 96.21%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.08% 93.65%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.38% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.96% 93.99%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.90% 95.89%

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.
Piliostigma thonningii

Cross-Links

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PubChem 10615140
LOTUS LTS0041574
wikiData Q105381012