5,3',4',5'-Tetrahydroxy-6,7-dimethoxyflavone

Details

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Internal ID 6a28060b-72a0-4fc6-8736-2c43b4b7edfa
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-6,7-dimethoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O8/c1-23-13-6-12-14(16(22)17(13)24-2)8(18)5-11(25-12)7-3-9(19)15(21)10(20)4-7/h3-6,19-22H,1-2H3
InChI Key IRXAPKVAVMWNLX-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 2.30
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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LMPK12111267

2D Structure

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2D Structure of 5,3',4',5'-Tetrahydroxy-6,7-dimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8965 89.65%
Caco-2 + 0.7483 74.83%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6457 64.57%
OATP2B1 inhibitior - 0.5567 55.67%
OATP1B1 inhibitior + 0.9320 93.20%
OATP1B3 inhibitior + 0.9828 98.28%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6451 64.51%
P-glycoprotein inhibitior - 0.5692 56.92%
P-glycoprotein substrate - 0.7971 79.71%
CYP3A4 substrate + 0.5073 50.73%
CYP2C9 substrate - 0.6887 68.87%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition + 0.6914 69.14%
CYP2C9 inhibition - 0.8489 84.89%
CYP2C19 inhibition - 0.6694 66.94%
CYP2D6 inhibition - 0.8174 81.74%
CYP1A2 inhibition + 0.8416 84.16%
CYP2C8 inhibition + 0.6689 66.89%
CYP inhibitory promiscuity + 0.6916 69.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6616 66.16%
Eye corrosion - 0.9801 98.01%
Eye irritation + 0.6845 68.45%
Skin irritation - 0.6619 66.19%
Skin corrosion - 0.9271 92.71%
Ames mutagenesis - 0.7064 70.64%
Human Ether-a-go-go-Related Gene inhibition - 0.7673 76.73%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9068 90.68%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8631 86.31%
Acute Oral Toxicity (c) III 0.5234 52.34%
Estrogen receptor binding + 0.8349 83.49%
Androgen receptor binding + 0.8045 80.45%
Thyroid receptor binding + 0.6222 62.22%
Glucocorticoid receptor binding + 0.8122 81.22%
Aromatase binding + 0.6854 68.54%
PPAR gamma + 0.7844 78.44%
Honey bee toxicity - 0.8499 84.99%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.8835 88.35%

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 99.32% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.58% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.98% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.27% 89.00%
CHEMBL3194 P02766 Transthyretin 90.74% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.11% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.91% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.42% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.35% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.39% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.03% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.08% 90.71%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.44% 98.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.30% 94.42%

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.
Gutierrezia sphaerocephala

Cross-Links

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PubChem 44258534
LOTUS LTS0164479
wikiData Q105119276