2-(3,4-Dihydroxyphenyl)-3,6,8-trihydroxy-7-methoxychromen-4-one

Details

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Internal ID aff5cef9-eac8-452e-8517-6ef59fc8bb80
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > Flavonols
IUPAC Name 2-(3,4-dihydroxyphenyl)-3,6,8-trihydroxy-7-methoxychromen-4-one
SMILES (Canonical) COC1=C(C=C2C(=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O
SMILES (Isomeric) COC1=C(C=C2C(=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O
InChI InChI=1S/C16H12O8/c1-23-16-10(19)5-7-11(20)12(21)14(24-15(7)13(16)22)6-2-3-8(17)9(18)4-6/h2-5,17-19,21-22H,1H3
InChI Key QUHROOHGMYKZRU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O8
Molecular Weight 332.26 g/mol
Exact Mass 332.05321734 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(3,4-Dihydroxyphenyl)-3,6,8-trihydroxy-7-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 + 0.9095 90.95%
Caco-2 + 0.5282 52.82%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6297 62.97%
OATP2B1 inhibitior + 0.5832 58.32%
OATP1B1 inhibitior + 0.9515 95.15%
OATP1B3 inhibitior + 0.9904 99.04%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8446 84.46%
P-glycoprotein inhibitior - 0.8426 84.26%
P-glycoprotein substrate - 0.8654 86.54%
CYP3A4 substrate + 0.5101 51.01%
CYP2C9 substrate - 0.8397 83.97%
CYP2D6 substrate - 0.7876 78.76%
CYP3A4 inhibition + 0.6330 63.30%
CYP2C9 inhibition - 0.7982 79.82%
CYP2C19 inhibition - 0.6361 63.61%
CYP2D6 inhibition - 0.8687 86.87%
CYP1A2 inhibition + 0.9091 90.91%
CYP2C8 inhibition + 0.6635 66.35%
CYP inhibitory promiscuity + 0.7089 70.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6208 62.08%
Eye corrosion - 0.9790 97.90%
Eye irritation + 0.7508 75.08%
Skin irritation - 0.6006 60.06%
Skin corrosion - 0.9153 91.53%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7520 75.20%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.9054 90.54%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7897 78.97%
Acute Oral Toxicity (c) III 0.6309 63.09%
Estrogen receptor binding + 0.7670 76.70%
Androgen receptor binding + 0.7799 77.99%
Thyroid receptor binding - 0.4918 49.18%
Glucocorticoid receptor binding + 0.8487 84.87%
Aromatase binding + 0.6410 64.10%
PPAR gamma + 0.8267 82.67%
Honey bee toxicity - 0.8699 86.99%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8562 85.62%

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 99.63% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.75% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.98% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.79% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.12% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.36% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.99% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.99% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.81% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.98% 99.23%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 86.87% 98.11%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 86.77% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 85.14% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.65% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.50% 99.17%

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 deltoidea

Cross-Links

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PubChem 162976223
LOTUS LTS0215689
wikiData Q105228186