3,7,8-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one

Details

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Internal ID 940381ae-5aa7-4a17-8ce5-7d3c3b63a9fc
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 3,7,8-trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O8/c1-23-10-5-7(3-4-9(10)18)16-14(21)12(19)8-6-11(24-2)13(20)15(22)17(8)25-16/h3-6,18,20-22H,1-2H3
InChI Key GPOMYLGRWDKXBA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O8
Molecular Weight 346.30 g/mol
Exact Mass 346.06886740 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,8-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-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 + 0.9497 94.97%
Caco-2 - 0.5664 56.64%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7985 79.85%
OATP2B1 inhibitior - 0.5506 55.06%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9910 99.10%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7768 77.68%
P-glycoprotein inhibitior - 0.6145 61.45%
P-glycoprotein substrate - 0.8080 80.80%
CYP3A4 substrate + 0.5055 50.55%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition - 0.6426 64.26%
CYP2C9 inhibition - 0.6061 60.61%
CYP2C19 inhibition + 0.6079 60.79%
CYP2D6 inhibition - 0.8565 85.65%
CYP1A2 inhibition + 0.8621 86.21%
CYP2C8 inhibition + 0.7274 72.74%
CYP inhibitory promiscuity + 0.5928 59.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6148 61.48%
Eye corrosion - 0.9795 97.95%
Eye irritation + 0.5251 52.51%
Skin irritation - 0.6593 65.93%
Skin corrosion - 0.9509 95.09%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7892 78.92%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9292 92.92%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7839 78.39%
Acute Oral Toxicity (c) III 0.5027 50.27%
Estrogen receptor binding + 0.8890 88.90%
Androgen receptor binding + 0.7256 72.56%
Thyroid receptor binding + 0.6262 62.62%
Glucocorticoid receptor binding + 0.8262 82.62%
Aromatase binding + 0.7050 70.50%
PPAR gamma + 0.7745 77.45%
Honey bee toxicity - 0.8815 88.15%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9062 90.62%

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 99.11% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.68% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.57% 98.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.58% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.68% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.36% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.04% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.39% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.69% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.01% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.96% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.48% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.25% 90.71%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 80.68% 95.53%
CHEMBL1907 P15144 Aminopeptidase N 80.34% 93.31%

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.
Balsamorhiza macrophylla

Cross-Links

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PubChem 162943201
LOTUS LTS0003745
wikiData Q105015033