5-Hydroxy-2-(2-hydroxyphenyl)-3,6,7-trimethoxychromen-4-one

Details

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Internal ID 68d7fb01-91ef-4b68-be7c-4fc9cf1f8587
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-2-(2-hydroxyphenyl)-3,6,7-trimethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-22-12-8-11-13(14(20)17(12)23-2)15(21)18(24-3)16(25-11)9-6-4-5-7-10(9)19/h4-8,19-20H,1-3H3
InChI Key CYIGDLOKZNAESA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.90
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-(2-hydroxyphenyl)-3,6,7-trimethoxychromen-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 + 0.9711 97.11%
Caco-2 + 0.5888 58.88%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.5702 57.02%
OATP1B1 inhibitior + 0.9000 90.00%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5704 57.04%
P-glycoprotein inhibitior + 0.8007 80.07%
P-glycoprotein substrate - 0.6853 68.53%
CYP3A4 substrate + 0.5616 56.16%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition - 0.6863 68.63%
CYP2C19 inhibition + 0.6566 65.66%
CYP2D6 inhibition - 0.8329 83.29%
CYP1A2 inhibition + 0.8642 86.42%
CYP2C8 inhibition + 0.7887 78.87%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.7682 76.82%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis - 0.5864 58.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6237 62.37%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.9511 95.11%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7893 78.93%
Acute Oral Toxicity (c) III 0.4741 47.41%
Estrogen receptor binding + 0.8556 85.56%
Androgen receptor binding + 0.7853 78.53%
Thyroid receptor binding + 0.6458 64.58%
Glucocorticoid receptor binding + 0.8762 87.62%
Aromatase binding + 0.6815 68.15%
PPAR gamma + 0.7991 79.91%
Honey bee toxicity - 0.8702 87.02%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5049 50.49%
Fish aquatic toxicity + 0.8969 89.69%

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 98.59% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.78% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.74% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.30% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.55% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.29% 89.00%
CHEMBL2535 P11166 Glucose transporter 90.21% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 87.68% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.67% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.66% 85.14%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.38% 80.78%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.74% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.72% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.35% 99.15%
CHEMBL3194 P02766 Transthyretin 83.64% 90.71%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 83.08% 95.64%
CHEMBL1255126 O15151 Protein Mdm4 81.95% 90.20%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.56% 96.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.27% 96.09%

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 bungei

Cross-Links

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PubChem 10991540
LOTUS LTS0225587
wikiData Q104888790