5,2',5'-Trihydroxy-7,8-dimethoxyflavone

Details

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Internal ID c856bbfa-f0a8-4fff-bb92-f042adf92be4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 2-(2,5-dihydroxyphenyl)-5-hydroxy-7,8-dimethoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O7/c1-22-14-7-12(21)15-11(20)6-13(24-17(15)16(14)23-2)9-5-8(18)3-4-10(9)19/h3-7,18-19,21H,1-2H3
InChI Key CNFKFBYQNXFUCI-UHFFFAOYSA-N
Popularity 6 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) 105.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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5,2',5'-trihydroxy-7,8-dimethoxyflavone

2D Structure

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2D Structure of 5,2',5'-Trihydroxy-7,8-dimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 + 0.7860 78.60%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8156 81.56%
OATP2B1 inhibitior - 0.5625 56.25%
OATP1B1 inhibitior + 0.8827 88.27%
OATP1B3 inhibitior + 0.9738 97.38%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4611 46.11%
P-glycoprotein inhibitior + 0.6872 68.72%
P-glycoprotein substrate - 0.7273 72.73%
CYP3A4 substrate + 0.5577 55.77%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.5571 55.71%
CYP2C9 inhibition + 0.7766 77.66%
CYP2C19 inhibition + 0.8962 89.62%
CYP2D6 inhibition - 0.7334 73.34%
CYP1A2 inhibition + 0.8679 86.79%
CYP2C8 inhibition + 0.6712 67.12%
CYP inhibitory promiscuity + 0.7750 77.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6135 61.35%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.8613 86.13%
Skin irritation - 0.6511 65.11%
Skin corrosion - 0.9662 96.62%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6361 63.61%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9410 94.10%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5605 56.05%
Acute Oral Toxicity (c) III 0.5602 56.02%
Estrogen receptor binding + 0.9026 90.26%
Androgen receptor binding + 0.8579 85.79%
Thyroid receptor binding + 0.7422 74.22%
Glucocorticoid receptor binding + 0.8690 86.90%
Aromatase binding + 0.6843 68.43%
PPAR gamma + 0.7540 75.40%
Honey bee toxicity - 0.8205 82.05%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.8898 88.98%

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 96.50% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.03% 94.00%
CHEMBL3194 P02766 Transthyretin 93.91% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.68% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.96% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.58% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.54% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.81% 99.17%
CHEMBL2535 P11166 Glucose transporter 87.86% 98.75%
CHEMBL2581 P07339 Cathepsin D 87.78% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 85.48% 98.35%
CHEMBL4208 P20618 Proteasome component C5 83.25% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.10% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.23% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 80.05% 94.73%

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.
Scutellaria baicalensis
Scutellaria rehderiana

Cross-Links

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PubChem 21122623
LOTUS LTS0103395
wikiData Q105168421