5,7-Dihydroxy-8,2',6'-trimethoxyflavone

Details

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Internal ID 4d357f6a-8acc-44e3-a030-a1345c31da0b
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 2-(2,6-dimethoxyphenyl)-5,7-dihydroxy-8-methoxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-22-12-5-4-6-13(23-2)16(12)14-8-10(20)15-9(19)7-11(21)17(24-3)18(15)25-14/h4-8,19,21H,1-3H3
InChI Key ALVUROHRZICBSY-UHFFFAOYSA-N
Popularity 5 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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LMPK12111312

2D Structure

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2D Structure of 5,7-Dihydroxy-8,2',6'-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 + 0.6472 64.72%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6343 63.43%
OATP2B1 inhibitior - 0.5763 57.63%
OATP1B1 inhibitior + 0.9187 91.87%
OATP1B3 inhibitior + 0.8767 87.67%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6022 60.22%
P-glycoprotein inhibitior + 0.7051 70.51%
P-glycoprotein substrate - 0.8065 80.65%
CYP3A4 substrate + 0.5247 52.47%
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 + 0.4670 46.70%
CYP inhibitory promiscuity + 0.8068 80.68%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6142 61.42%
Eye corrosion - 0.9818 98.18%
Eye irritation + 0.8552 85.52%
Skin irritation - 0.7187 71.87%
Skin corrosion - 0.9573 95.73%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4901 49.01%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.9352 93.52%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.4897 48.97%
Acute Oral Toxicity (c) III 0.5210 52.10%
Estrogen receptor binding + 0.8953 89.53%
Androgen receptor binding + 0.7077 70.77%
Thyroid receptor binding + 0.7220 72.20%
Glucocorticoid receptor binding + 0.7903 79.03%
Aromatase binding + 0.6486 64.86%
PPAR gamma + 0.8293 82.93%
Honey bee toxicity - 0.8835 88.35%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
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 97.81% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.86% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.72% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.56% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.78% 98.95%
CHEMBL2535 P11166 Glucose transporter 90.78% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.19% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.52% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.72% 93.99%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 87.07% 94.03%
CHEMBL3401 O75469 Pregnane X receptor 85.28% 94.73%
CHEMBL3194 P02766 Transthyretin 85.20% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.29% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.96% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.46% 95.50%

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 discolor

Cross-Links

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PubChem 14180789
LOTUS LTS0136736
wikiData Q104914394