5-Hydroxy-2-(4-hydroxyphenoxy)-6,7-dimethoxychromen-4-one

Details

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Internal ID f3f12be6-1947-443e-be4b-89ac0f8d3028
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5-hydroxy-2-(4-hydroxyphenoxy)-6,7-dimethoxychromen-4-one
SMILES (Canonical) COC1=C(C(=C2C(=C1)OC(=CC2=O)OC3=CC=C(C=C3)O)O)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1)OC(=CC2=O)OC3=CC=C(C=C3)O)O)OC
InChI InChI=1S/C17H14O7/c1-21-13-8-12-15(16(20)17(13)22-2)11(19)7-14(24-12)23-10-5-3-9(18)4-6-10/h3-8,18,20H,1-2H3
InChI Key SDFLBBYWGIOMBJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-2-(4-hydroxyphenoxy)-6,7-dimethoxychromen-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 + 0.9388 93.88%
Caco-2 + 0.8062 80.62%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7158 71.58%
OATP2B1 inhibitior - 0.5799 57.99%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior + 0.5600 56.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6539 65.39%
P-glycoprotein inhibitior + 0.7318 73.18%
P-glycoprotein substrate - 0.8123 81.23%
CYP3A4 substrate + 0.5774 57.74%
CYP2C9 substrate - 0.6296 62.96%
CYP2D6 substrate - 0.8329 83.29%
CYP3A4 inhibition - 0.8307 83.07%
CYP2C9 inhibition - 0.8397 83.97%
CYP2C19 inhibition - 0.6971 69.71%
CYP2D6 inhibition - 0.7985 79.85%
CYP1A2 inhibition + 0.7985 79.85%
CYP2C8 inhibition + 0.7034 70.34%
CYP inhibitory promiscuity - 0.5594 55.94%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6175 61.75%
Eye corrosion - 0.9687 96.87%
Eye irritation + 0.6972 69.72%
Skin irritation - 0.6342 63.42%
Skin corrosion - 0.9748 97.48%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6121 61.21%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.8341 83.41%
skin sensitisation - 0.9361 93.61%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.5839 58.39%
Acute Oral Toxicity (c) II 0.5090 50.90%
Estrogen receptor binding + 0.9172 91.72%
Androgen receptor binding + 0.8690 86.90%
Thyroid receptor binding + 0.5972 59.72%
Glucocorticoid receptor binding + 0.8036 80.36%
Aromatase binding + 0.7781 77.81%
PPAR gamma + 0.7885 78.85%
Honey bee toxicity - 0.8423 84.23%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.9179 91.79%

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 98.26% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.22% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.79% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.80% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.53% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.55% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.59% 86.33%
CHEMBL3194 P02766 Transthyretin 89.45% 90.71%
CHEMBL2535 P11166 Glucose transporter 89.33% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.27% 99.15%
CHEMBL4208 P20618 Proteasome component C5 87.43% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.16% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 83.54% 94.73%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.10% 94.42%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.03% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.25% 93.99%
CHEMBL2581 P07339 Cathepsin D 80.74% 98.95%

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.
Artemisia capillaris

Cross-Links

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PubChem 5319541
NPASS NPC70066
LOTUS LTS0206100
wikiData Q105250615