5,7-Dihydroxy-8,3',5'trimethoxyflavone

Details

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Internal ID ad29cdf0-e544-4064-b3a6-f1836ea75a1f
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 2-(3,5-dimethoxyphenyl)-5,7-dihydroxy-8-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-22-10-4-9(5-11(6-10)23-2)15-8-13(20)16-12(19)7-14(21)17(24-3)18(16)25-15/h4-8,19,21H,1-3H3
InChI Key KLKPEJIOCCWGEY-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 2.90
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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LMPK12111336
5,7-dihydroxy-8,3',5'trimethoxy-flavone

2D Structure

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2D Structure of 5,7-Dihydroxy-8,3',5'trimethoxyflavone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9417 94.17%
Caco-2 + 0.7311 73.11%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6343 63.43%
OATP2B1 inhibitior - 0.7117 71.17%
OATP1B1 inhibitior + 0.9105 91.05%
OATP1B3 inhibitior + 0.8767 87.67%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6346 63.46%
P-glycoprotein inhibitior + 0.7979 79.79%
P-glycoprotein substrate - 0.8856 88.56%
CYP3A4 substrate - 0.5217 52.17%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.6154 61.54%
CYP2C9 inhibition - 0.7484 74.84%
CYP2C19 inhibition + 0.5640 56.40%
CYP2D6 inhibition - 0.7310 73.10%
CYP1A2 inhibition + 0.8610 86.10%
CYP2C8 inhibition - 0.7087 70.87%
CYP inhibitory promiscuity + 0.8068 80.68%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6142 61.42%
Eye corrosion - 0.9818 98.18%
Eye irritation + 0.7184 71.84%
Skin irritation - 0.7187 71.87%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6263 62.63%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6784 67.84%
Acute Oral Toxicity (c) III 0.5210 52.10%
Estrogen receptor binding + 0.9462 94.62%
Androgen receptor binding + 0.7822 78.22%
Thyroid receptor binding + 0.7371 73.71%
Glucocorticoid receptor binding + 0.8333 83.33%
Aromatase binding + 0.8004 80.04%
PPAR gamma + 0.7515 75.15%
Honey bee toxicity - 0.8472 84.72%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8724 87.24%

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 97.98% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.71% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.96% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.39% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.64% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.56% 89.00%
CHEMBL2581 P07339 Cathepsin D 86.43% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.08% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.84% 96.77%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.83% 94.45%
CHEMBL308 P06493 Cyclin-dependent kinase 1 82.69% 91.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.07% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.43% 86.33%
CHEMBL3194 P02766 Transthyretin 81.41% 90.71%

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.
Limnophila rugosa

Cross-Links

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PubChem 44258563
LOTUS LTS0085681
wikiData Q105142664